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Nordmark, G., Bengtsson, C., Larsson, A., Karlsson, F. A., Sturfelt, G., Ronnblom, L. Effects of dehydroepiandrosterone supplement on health-related quality of life in glucocorticoid treated female patients with systemic lupus erythematosus. Autoimmunity 2005;38(7):531-540. View abstract.

Srinivasan, M., Irving, B. A., Frye, R. L., O'Brien, P., Hartman, S. J., McConnell, J. P., Nair, K. S. Effects on lipoprotein particles of long-term dehydroepiandrosterone in elderly men and women and testosterone in elderly men. J Clin Endocrinol Metab 2010;95(4):1617-25. View abstract.

Srinivasan, M., Irving, B. A., Dhatariya, K., Klaus, K. A., Hartman, S. J., McConnell, J. P., Nair, K. S. Effect of dehydroepiandrosterone replacement on lipoprotein profile in hypoadrenal women. J Clin Endocrinol Metab 2009;94(3):761-4. View abstract.

Jankowski, C. M., Gozansky, W. S., Van Pelt, R. E., Wolfe, P., Schwartz, R. S., Kohrt, W. M. Oral dehydroepiandrosterone replacement in older adults: effects on central adiposity, glucose metabolism and blood lipids. Clin Endocrinol (Oxf) 2011;75(4):456-63. View abstract.

Gomez-Santos, C., Hernandez-Morante, J. J., Tebar, F. J., Granero, E., Garaulet, M. Differential effect of oral dehydroepiandrosterone-sulphate on metabolic syndrome features in pre- and postmenopausal obese women. Clin Endocrinol (Oxf) 2012;77(4):548-54. View abstract.

McHenry, C. M., Bell, P. M., Hunter, S. J., Thompson, C. J., Courtney, C. H., Ennis, C. N., Sheridan, B., McCance, D. R., Mullan, K. R., Atkinson, A. B. Effects of dehydroepiandrosterone sulphate (DHEAS) replacement on insulin action and quality of life in hypopituitary females: a double-blind, placebo-controlled study. Clin Endocrinol (Oxf) 2012;77(3):423-9. View abstract.

Weiss, E. P., Villareal, D. T., Ehsani, A. A., Fontana, L., Holloszy, J. O. Dehydroepiandrosterone replacement therapy in older adults improves indices of arterial stiffness. Aging Cell 2012;11(5):876-84. View abstract.

Jankowski, C. M., Gozansky, W. S., Schwartz, R. S., Dahl, D. J., Kittelson, J. M., Scott, S. M., Van Pelt, R. E., Kohrt, W. M. Effects of dehydroepiandrosterone replacement therapy on bone mineral density in older adults: a randomized, controlled trial. J Clin Endocrinol Metab 2006;91(8):2986-93. View abstract.

Forsblad-d'Elia, H., Carlsten, H., Labrie, F., Konttinen, Y. T., Ohlsson, C. Low serum levels of sex steroids are associated with disease characteristics in primary Sjogren's syndrome; supplementation with dehydroepiandrosterone restores the concentrations. J Clin Endocrinol Metab 2009;94(6):2044-51. View abstract.

Finckh, A., Berner, I. C., Aubry-Rozier, B., So, A. K. A randomized controlled trial of dehydroepiandrosterone in postmenopausal women with fibromyalgia. J Rheumatol 2005;32(7):1336-40. View abstract.

Gebre-Medhin, G., Husebye, E. S., Mallmin, H., Helstrom, L., Berne, C., Karlsson, F. A., Kampe, O. Oral dehydroepiandrosterone (DHEA) replacement therapy in women with Addison's disease. Clin Endocrinol (Oxf) 2000;52(6):775-80. View abstract.

Lovas, K., Gebre-Medhin, G., Trovik, T. S., Fougner, K. J., Uhlving, S., Nedrebo, B. G., Myking, O. L., Kampe, O., Husebye, E. S. Replacement of dehydroepiandrosterone in adrenal failure: no benefit for subjective health status and sexuality in a 9-month, randomized, parallel group clinical trial. J Clin Endocrinol Metab 2003;88(3):1112-18. View abstract.

Pillemer, S. R., Brennan, M. T., Sankar, V., Leakan, R. A., Smith, J. A., Grisius, M., Ligier, S., Radfar, L., Kok, M. R., Kingman, A., Fox, P. C. Pilot clinical trial of dehydroepiandrosterone (DHEA) versus placebo for Sjogren's syndrome. Arthritis Rheum 2004;51(4):601-4. View abstract.

Christiansen, J. J., Andersen, N. H., Sorensen, K. E., Pedersen, E. M., Bennett, P., Andersen, M., Christiansen, J. S., Jorgensen, J. O., Gravholt, C. H. Dehydroepiandrosterone substitution in female adrenal failure: no impact on endothelial function and cardiovascular parameters despite normalization of androgen status. Clin Endocrinol (Oxf) 2007;66(3):426-33. View abstract.

Panjari, M., Bell, R. J., Jane, F., Wolfe, R., Adams, J., Morrow, C., Davis, S. R. A randomized trial of oral DHEA treatment for sexual function, well-being, and menopausal symptoms in postmenopausal women with low libido. J Sex Med 2009;6(9):2579-90. View abstract.

Mamas, L., Mamas, E. Dehydroepiandrosterone supplementation in assisted reproduction: rationale and results. Curr Opin Obstet Gynecol 2009;21(4):306-8. View abstract.

Hartkamp, A., Geenen, R., Godaert, G. L., Bootsma, H., Kruize, A. A., Bijlsma, J. W., Derksen, R. H. Effect of dehydroepiandrosterone administration on fatigue, well-being, and functioning in women with primary Sjogren syndrome: a randomised controlled trial. Ann Rheum Dis 2008;67(1):91-7. View abstract.

Yeung, T. W., Li, R. H., Lee, V. C., Ho, P. C., Ng, E. H. A randomized double-blinded placebo-controlled trial on the effect of dehydroepiandrosterone for 16 weeks on ovarian response markers in women with primary ovarian insufficiency. J Clin Endocrinol Metab 2013;98(1):380-8. View abstract.

Virkki, L. M., Porola, P., Forsblad-d'Elia, H., Valtysdottir, S., Solovieva, S. A., Konttinen, Y. T. Dehydroepiandrosterone (DHEA) substitution treatment for severe fatigue in DHEA-deficient patients with primary Sjogren's syndrome. Arthritis Care Res (Hoboken) 2010;62(1):118-24. View abstract.

Binder, G., Weber, S., Ehrismann, M., Zaiser, N., Meisner, C., Ranke, M. B., Maier, L., Wudy, S. A., Hartmann, M. F., Heinrich, U., Bettendorf, M., Doerr, H. G., Pfaeffle, R. W., Keller, E. Effects of dehydroepiandrosterone therapy on pubic hair growth and psychological well-being in adolescent girls and young women with central adrenal insufficiency: a double-blind, randomized, placebo-controlled phase III trial. J Clin Endocrinol Metab 2009;94(4):1182-90. View abstract.

Klove, K. L., Roy, S., Lobo, R. A. The effect of different contraceptive treatments on the serum concentration of dehydroepiandrosterone sulfate. Contraception 1984;29(4):319-24. View abstract.

Cibula, D., Fanta, M., Vrbikova, J., Stanicka, S., Dvorakova, K., Hill, M., Skrha, J., Zivny, J., Skrenkova, J. The effect of combination therapy with metformin and combined oral contraceptives (COC) versus COC alone on insulin sensitivity, hyperandrogenaemia, SHBG and lipids in PCOS patients. Hum Reprod 2005;20(1):180-4. View abstract.

White, T., Jain, J. K., Stanczyk, F. Z. Effect of oral versus transdermal steroidal contraceptives on androgenic markers. Am J Obstet Gynecol 2005;192(6):2055-9. View abstract.

Bonorden, M. J., Greany, K. A., Wangen, K. E., Phipps, W. R., Feirtag, J., Adlercreutz, H., Kurzer, M. S. Consumption of Lactobacillus acidophilus and Bifidobacterium longum do not alter urinary equol excretion and plasma reproductive hormones in premenopausal women. Eur J Clin Nutr 2004;58(12):1635-42. View abstract.

Dorgan, J. F., Reichman, M. E., Judd, J. T., Brown, C., Longcope, C., Schatzkin, A., Forman, M., Campbell, W. S., Franz, C., Kahle, L., Taylor, P. R. Relation of energy, fat, and fiber intakes to plasma concentrations of estrogens and androgens in premenopausal women. Am J Clin Nutr 1996;64(1):25-31. View abstract.

Wang, C., Catlin, D. H., Starcevic, B., Heber, D., Ambler, C., Berman, N., Lucas, G., Leung, A., Schramm, K., Lee, P. W., Hull, L., Swerdloff, R. S. Low-fat high-fiber diet decreased serum and urine androgens in men. J Clin Endocrinol Metab 2005;90(6):3550-9. View abstract.

Fischer, L., Mahoney, C., Jeffcoat, A. R., Koch, M. A., Thomas, B. E., Valentine, J. L., Stinchcombe, T., Boan, J., Crowell, J. A., Zeisel, S. H. Clinical characteristics and pharmacokinetics of purified soy isoflavones: multiple-dose administration to men with prostate neoplasia. Nutr Cancer 2004;48(2):160-70. View abstract.

Goldin, B. R., Brauner, E., Adlercreutz, H., Ausman, L. M., Lichtenstein, A. H. Hormonal response to diets high in soy or animal protein without and with isoflavones in moderately hypercholesterolemic subjects. Nutr Cancer 2005;51(1):1-6. View abstract.

Al-Dujaili, E. A., Kenyon, C. J., Nicol, M. R., Mason, J. I. Liquorice and glycyrrhetinic acid increase DHEA and deoxycorticosterone levels in vivo and in vitro by inhibiting adrenal SULT2A1 activity. Mol Cell Endocrinol 2011;336(1-2):102-9. View abstract.

Vacheron-Trystram, M. N., Cheref, S., Gauillard, J., Plas, J. [A case report of mania precipitated by use of DHEA]. Encephale 2002;28(6 Pt 1):563-6. View abstract.

Sasaki, K., Nakano, R., Kadoya, Y., Iwao, M., Shima, K., Sowa, M. Cervical ripening with dehydroepiandrosterone sulphate. Br J Obstet Gynaecol 1982;89(3):195-8. View abstract.

Arlt, W., Callies, F., Allolio, B. DHEA replacement in women with adrenal insufficiency--pharmacokinetics, bioconversion and clinical effects on well-being, sexuality and cognition. Endocr Res 2000;26(4):505-11. View abstract.

Dhatariya, K. K., Greenlund, L. J., Bigelow, M. L., Thapa, P., Oberg, A. L., Ford, G. C., Schimke, J. M., Nair, K. S. Dehydroepiandrosterone replacement therapy in hypoadrenal women: protein anabolism and skeletal muscle function. Mayo Clin Proc 2008;83(11):1218-25. View abstract.

Gurnell, E. M., Hunt, P. J., Curran, S. E., Conway, C. L., Pullenayegum, E. M., Huppert, F. A., Compston, J. E., Herbert, J., Chatterjee, V. K. Long-term DHEA replacement in primary adrenal insufficiency: a randomized, controlled trial. J Clin Endocrinol Metab 2008;93(2):400-9. View abstract.

van Thiel, S. W., Romijn, J. A., Pereira, A. M., Biermasz, N. R., Roelfsema, F., van Hemert, A., Ballieux, B., Smit, J. W. Effects of dehydroepiandrostenedione, superimposed on growth hormone substitution, on quality of life and insulin-like growth factor I in patients with secondary adrenal insufficiency: a randomized, placebo-controlled, cross-over trial. J Clin Endocrinol Metab 2005;90(6):3295-3303. View abstract.

Christiansen, J. J., Bruun, J. M., Christiansen, J. S., Jorgensen, J. O., Gravholt, C. H. Long-term DHEA substitution in female adrenocortical failure, body composition, muscle function, and bone metabolism: a randomized trial. Eur J Endocrinol 2011;165(2):293-300. View abstract.

Abrams, D. I., Shade, S. B., Couey, P., McCune, J. M., Lo, J., Bacchetti, P., Chang, B., Epling, L., Liegler, T., Grant, R. M. Dehydroepiandrosterone (DHEA) effects on HIV replication and host immunity: a randomized placebo-controlled study. AIDS Res Hum Retroviruses 2007;23(1):77-85. View abstract.

Kenny, A. M., Boxer, R. S., Kleppinger, A., Brindisi, J., Feinn, R., Burleson, J. A. Dehydroepiandrosterone combined with exercise improves muscle strength and physical function in frail older women. J Am Geriatr Soc 2010;58(9):1707-14. View abstract.

Bloch, M., Ish-Shalom, S., Greenman, Y., Klein, E., Latzer, Y. Dehydroepiandrosterone treatment effects on weight, bone density, bone metabolism and mood in women suffering from anorexia nervosa-a pilot study. Psychiatry Res 2012;200(2-3):544-9. View abstract.

Hartkamp, A., Geenen, R., Godaert, G. L., Bijl, M., Bijlsma, J. W., Derksen, R. H. The effect of dehydroepiandrosterone on lumbar spine bone mineral density in patients with quiescent systemic lupus erythematosus. Arthritis Rheum 2004;50(11):3591-95. View abstract.

Dumas de La Roque, E., Savineau, J. P., Metivier, A. C., Billes, M. A., Kraemer, J. P., Doutreleau, S., Jougon, J., Marthan, R., Moore, N., Fayon, M., Baulieu, E. E., Dromer, C. Dehydroepiandrosterone (DHEA) improves pulmonary hypertension in chronic obstructive pulmonary disease (COPD): a pilot study. Ann Endocrinol (Paris) 2012;73(1):20-2. View abstract.

Hirshman, E., Wells, E., Wierman, M. E., Anderson, B., Butler, A., Senholzi, M., Fisher, J. The effect of dehydroepiandrosterone (DHEA) on recognition memory decision processes and discrimination in postmenopausal women. Psychon Bull Rev 2003;10(1):125-34. View abstract.

Merritt, P., Stangl, B., Hirshman, E., Verbalis, J. Administration of dehydroepiandrosterone (DHEA) increases serum levels of androgens and estrogens but does not enhance short-term memory in post-menopausal women. Brain Res 11-5-2012;1483:54-62. View abstract.

Stangl, B., Hirshman, E., and Verbalis, J. Administration of dehydroepiandrosterone (DHEA) enhances visual-spatial performance in postmenopausal women. Behav Neurosci 2011;125(5):742-52. View abstract.

Wolf, O. T., Koster, B., Kirschbaum, C., Pietrowsky, R., Kern, W., Hellhammer, D. H., Born, J., Fehm, H. L. A single administration of dehydroepiandrosterone does not enhance memory performance in young healthy adults, but immediately reduces cortisol levels. Biol Psychiatry 1997;42(9):845-8. View abstract.

Rabijewski, M. Zgliczynski, W. [Dehydroepiandrosterone therapy in men with angiographically verified coronary heart disease: the effects on plasminogen activator inhibitor-1 (PAI-1), tissue plasminogen activator (tPA) and fibrinogen plasma concentrations]. Endokrynol Pol 2007;58(3):213-9. View abstract.

Kawano, H., Yasue, H., Kitagawa, A., Hirai, N., Yoshida, T., Soejima, H., Miyamoto, S., Nakano, M., Ogawa, H. Dehydroepiandrosterone supplementation improves endothelial function and insulin sensitivity in men. J Clin Endocrinol Metab 2003;88(7):3190-95. View abstract.

Fassati, P., Fassati, M., Sonka, J., Lesensky, K. [New approach to the treatment of angina pectoris by dehydroepiandrosterone-sulfate]. Cas Lek Cesk 1971;110(26):606-9. View abstract.

Fassati, P., Fassati, M., Sonka, J., Lesensky, K. Dehydroepiandrosterone sulphate--a new approach to some cases of angina pectoris therapy. Agressologie 1970;11(5):445-8. View abstract.

Wolkowitz, O. M., Reus, V. I., Roberts, E., Manfredi, F., Chan, T., Ormiston, S., Johnson, R., Canick, J., Brizendine, L., Weingartner, H. Antidepressant and cognition-enhancing effects of DHEA in major depression. Ann N Y Acad Sci 1995;774:337-9. View abstract.

Schmidt, P. J., Daly, R. C., Bloch, M., Smith, M. J., Danaceau, M. A., St Clair, L. S., Murphy, J. H., Haq, N., Rubinow, D. R. Dehydroepiandrosterone monotherapy in midlife-onset major and minor depression. Arch Gen Psychiatry 2005;62(2):154-62. View abstract.

Forrest AD, Drewery J, Fotherby K, Laverty SG. A clinical trial of dehydroepiandrosterone (Diandrone). J Neurol Neurosurg Psychiat 1960;23:52-5. View abstract.

Basu R., Dalla Man C., Campioni M., Basu A., Nair K. S., Jensen M. D., Khosla S., Klee G., Toffolo G., Cobelli C., Rizza R. A. Two years of treatment with dehydroepiandrosterone does not improve insulin secretion, insulin action, or postprandial glucose turnover in elderly men or women. Diabetes 2007;56(3):753-66. View abstract.

Talaei A., Amini M., Siavash M., Zare M. The effect of dehydroepiandrosterone on insulin resistance in patients with impaired glucose tolerance. Hormones (Athens) 2010;9(4):326-31. View abstract.

Usiskin K. S., Butterworth S., Clore J. N., Arad Y., Ginsberg H. N., Blackard W. G., Nestler J. E. Lack of effect of dehydroepiandrosterone in obese men. Int J Obes 1990;14(5):457-63. View abstract.

Shoptaw, S., Majewska, M. D., Wilkins, J., Twitchell, G., Yang, X., Ling, W. Participants receiving dehydroepiandrosterone during treatment for cocaine dependence show high rates of cocaine use in a placebo-controlled pilot study. Exp Clin Psychopharmacol 2004;12(2):126-35. View abstract.

Maayan, R., Touati-Werner, D., Shamir, D., Yadid, G., Friedman, A., Eisner, D., Weizman, A., Herman, I. The effect of DHEA complementary treatment on heroin addicts participating in a rehabilitation program: a preliminary study. Eur Neuropsychopharmacol 2008;18(6):406-13. View abstract.

Wiser, A., Gonen, O., Ghetler, Y., Shavit, T., Berkovitz, A., Shulman, A. Addition of dehydroepiandrosterone (DHEA) for poor-responder patients before and during IVF treatment improves the pregnancy rate: a randomized prospective study. Hum Reprod 2010;25(10):2496-2500. View abstract.

Sonmezer, M., Ozmen, B., Cil, A. P., Ozkavukcu, S., Tasci, T., Olmus, H., Atabekoglu, C. S. Dehydroepiandrosterone supplementation improves ovarian response and cycle outcome in poor responders. Reprod Biomed Online 2009;19(4):508-13. View abstract.

Artini, P. G., Simi, G., Ruggiero, M., Pinelli, S., Di Berardino, O. M., Papini, F., Papini, S., Monteleone, P., Cela, V. DHEA supplementation improves follicular microenviroment in poor responder patients. Gynecol Endocrinol 2012;28(9):669-73. View abstract.

Andus, T., Klebl, F., Rogler, G., Bregenzer, N., Scholmerich, J., Straub, R. H. Patients with refractory Crohn's disease or ulcerative colitis respond to dehydroepiandrosterone: a pilot study. Aliment Pharmacol Ther 2003;17(3):409-14. View abstract.

Genazzani, A. R., Stomati, M., Valentino, V., Pluchino, N., Pot, E., Casarosa, E., Merlini, S., Giannini, A., Luisi, M. Effect of 1-year, low-dose DHEA therapy on climacteric symptoms and female sexuality. Climacteric 2011;14(6):661-8. View abstract.

Gleicher, N., Ryan, E., Weghofer, A., Blanco-Mejia, S., Barad, D. H. Miscarriage rates after dehydroepiandrosterone (DHEA) supplementation in women with diminished ovarian reserve: a case control study. Reprod Biol Endocrinol 2009;7-108. View abstract.

Dayal, M., Sammel, M. D., Zhao, J., Hummel, A. C., Vandenbourne, K., Barnhart, K. T. Supplementation with DHEA: effect on muscle size, strength, quality of life, and lipids. J Womens Health (Larchmt) 2005;14(5):391-400. View abstract.

Igwebuike, A., Irving, B. A., Bigelow, M. L., Short, K. R., McConnell, J. P., Nair, K. S. Lack of dehydroepiandrosterone effect on a combined endurance and resistance exercise program in postmenopausal women. J Clin Endocrinol Metab 2008;93(2):534-8. View abstract.

Muller, M., van den Beld, A. W., van der Schouw, Y. T., Grobbee, D. E., Lamberts, S. W. Effects of dehydroepiandrosterone and atamestane supplementation on frailty in elderly men. J Clin Endocrinol Metab 2006;91(10):3988-91. View abstract.

Giltay, E. J., van Schaardenburg, D., Gooren, L. J., von Blomberg, B. M., Fonk, J. C., Touw, D. J., Dijkmans, B. A. Effects of dehydroepiandrosterone administration on disease activity in patients with rheumatoid arthritis. Br J Rheumatol 1998;37(6):705-6. View abstract.

Ritsner, M. S., Gibel, A., Shleifer, T., Boguslavsky, I., Zayed, A., Maayan, R., Weizman, A., Lerner, V. Pregnenolone and dehydroepiandrosterone as an adjunctive treatment in schizophrenia and schizoaffective disorder: an 8-week, double-blind, randomized, controlled, 2-center, parallel-group trial. J Clin Psychiatry 2010;71(10):1351-62. View abstract.

Morales, A., Black, A., Emerson, L., Barkin, J., Kuzmarov, I., Day, A. Androgens and sexual function: a placebo-controlled, randomized, double-blind study of testosterone vs. dehydroepiandrosterone in men with sexual dysfunction and androgen deficiency. Aging Male 2009;12(4):104-12. View abstract.

Hartkamp, A., Geenen, R., Godaert, G. L., Bijl, M., Bijlsma, J. W., Derksen, R. H. Effects of dehydroepiandrosterone on fatigue and well-being in women with quiescent systemic lupus erythematosus: a randomised controlled trial. Ann Rheum Dis 2010;69(6):1144-7. View abstract.

Suh-Burgmann, E., Sivret, J., Duska, L. R., Del Carmen, M., Seiden, M. V. Long-term administration of intravaginal dehydroepiandrosterone on regression of low-grade cervical dysplasia--a pilot study. Gynecol Obstet Invest 2003;55(1):25-31. View abstract.

Vogiatzi, M. G., Boeck, M. A., Vlachopapadopoulou, E., el-Rashid, R., New, M. I. Dehydroepiandrosterone in morbidly obese adolescents: effects on weight, body composition, lipids, and insulin resistance. Metabolism 1996;45(8):1011-5. View abstract.

Nouveau, S., Bastien, P., Baldo, F., de Lacharriere O. Effects of topical DHEA on aging skin: a pilot study. Maturitas 2008;59(2):174-81. View abstract.

Labrie, F., Archer, D., Bouchard, C., Fortier, M., Cusan, L., Gomez, J. L., Girard, G., Baron, M., Ayotte, N., Moreau, M., Dube, R., Cote, I., Labrie, C., Lavoie, L., Berger, L., Martel, C., Balser, J. High internal consistency and efficacy of intravaginal DHEA for vaginal atrophy. Gynecol Endocrinol 2010;26(7):524-32. View abstract.

Labrie, F., Archer, D., Bouchard, C., Fortier, M., Cusan, L., Gomez, J. L., Girard, G., Baron, M., Ayotte, N., Moreau, M., Dube, R., Cote, I., Labrie, C., Lavoie, L., Berger, L., Gilbert, L., Martel, C., Balser, J. Intravaginal dehydroepiandrosterone (Prasterone), a physiological and highly efficient treatment of vaginal atrophy. Menopause 2009;16(5):907-22. View abstract.

Scarpellini, L., Scarpellini, F., Spina, V. [Clinical evaluation of DHEA-S plasma levels and possible therapeutic value of the hormone in the third trimester]. Clin Ter 1993;143(5):383-8. View abstract.

Ishikawa, M., Shimizu, T. Dehydroepiandrosterone sulfate and induction of labor. Am J Perinatol 1989;6(2):173-5. View abstract.

Mochizuki, M., Honda, T., Deguchi, M., Morikawa, H., Tojo, S. A study on the effect of dehydroepiandrosterone sulfate on so-called cervical ripening. Acta Obstet Gynecol Scand 1978;57(5):397-401. View abstract.

Sugino, M., Ohsawa, N., Ito, T., Ishida, S., Yamasaki, H., Kimura, F., Shinoda, K. A pilot study of dehydroepiandrosterone sulfate in myotonic dystrophy. Neurology 1998;51(2):586-9. View abstract.

Holzmann, H., Morsches, B., Krapp, R., Hoede, N., Oertel, G. W. [Therapy of psoriasis with dehydroepiandrosterone-enanthate. II. Intramuscular depot application of 300 mg weekly (author's transl)]. Archiv fur Dermatol Forsch 1973;247(1):23-8. View abstract.

Bernardi, F., Pieri, M., Stomati, M., Luisi, S., Palumbo, M., Pluchino, N., Ceccarelli, C., Genazzani, A. R. Effect of different hormonal replacement therapies on circulating allopregnanolone and dehydroepiandrosterone levels in postmenopausal women. Gynecol Endocrinol 2003;17(1):65-77. View abstract.

Schlegel, W., Petersdorf, L. I., Junker, R., Schulte, H., Ebert, C., Von Eckardstein, A. The effects of six months of treatment with a low-dose of conjugated oestrogens in menopausal women. Clin Endocrinol (Oxf) 1999;51(5):643-51. View abstract.

Teede, H. J., Dalais, F. S., McGrath, B. P. Dietary soy containing phytoestrogens does not have detectable estrogenic effects on hepatic protein synthesis in postmenopausal women. Am J Clin Nutr 2004;79(3):396-401. View abstract.

Panjari, M., Davis, S. R. DHEA for postmenopausal women: a review of the evidence. Maturitas 2010;66(2):172-9. View abstract.

Guay, A. T. Decreased testosterone in regularly menstruating women with decreased libido: a clinical observation. J Sex Marital Ther 2001;27(5):513-9. View abstract.

Boxer, R. S., Kleppinger, A., Brindisi, J., Feinn, R., Burleson, J. A., Kenny, A. M. Effects of dehydroepiandrosterone (DHEA) on cardiovascular risk factors in older women with frailty characteristics. Age Ageing 2010;39(4):451-8. View abstract.

Huppert, F. A., Van Niekerk, J. K. Dehydroepiandrosterone (DHEA) supplementation for cognitive function (Cochrane Review). Cochrane Database (Issue 2) 2001;2:CD000304. View abstract.

Nissen, S. L., Sharp, R. L. Effect of dietary supplements on lean mass and strength gains with resistance exercise: a meta-analysis. J Appl Physiol 2003;94(2):651-9. View abstract.

Crosbie, D., Black, C., McIntyre, L., Royle, P. L., Thomas, S. Dehydroepiandrosterone for systemic lupus erythematosus. Cochrane Database Syst Rev 2007;(4):CD005114. View abstract.

Morales, A. J., Nolan, J. J., Nelson, J. C., Yen, S. S. Effects of replacement dose of dehydroepiandrosterone in men and women of advancing age. J Clin Endocrinol Metab 1994;78(6):1360-7. View abstract.

Azuma, T., Nagai, Y., Saito, T., Funauchi, M., Matsubara, T., and Sakoda, S. The effect of dehydroepiandrosterone sulfate administration to patients with multi-infarct dementia. J Neurol.Sci. 1-1-1999;162(1):69-73. View abstract.

Wellman, M., Shane-McWhorter, L., Orlando, and Jennings, J. P. The role of dehydroepiandrosterone in diabetes mellitus. Pharmacotherapy 1999;19(5):582-591. View abstract.

Lahita, R. G. Dehydroepiandrosterone (DHEA) for serious disease, a possibility? Lupus 1999;8(3):169-170. View abstract.

Tsuji, K., Furutama, D., Tagami, M., and Ohsawa, N. Specific binding and effects of dehydroepiandrosterone sulfate (DHEA-S) on skeletal muscle cells: possible implication for DHEA-S replacement therapy in patients with myotonic dystrophy. Life Sci. 1999;65(1):17-26. View abstract.

Giltay, E. J., van Schaardenburg, D., Gooren, L. J., and Dijkmans, B. A. Dehydroepiandrosterone sulfate in patients with rheumatoid arthritis. Ann N.Y.Acad.Sci. 6-22-1999;876:152-154. View abstract.

Corrigan, A. B. Dehydroepiandrosterone and sport. Med J Aust 8-16-1999;171(4):206-208. View abstract.

Brown, G. A., Vukovich, M. D., Sharp, R. L., Reifenrath, T. A., Parsons, K. A., and King, D. S. Effect of oral DHEA on serum testosterone and adaptations to resistance training in young men. J Appl.Physiol 1999;87(6):2274-2283. View abstract.

Kumpfel, T., Then, Bergh F., Friess, E., Uhr, M., Yassouridis, A., Trenkwalder, C., and Holsboer, F. Dehydroepiandrosterone response to the adrenocorticotropin test and the combined dexamethasone and corticotropin-releasing hormone test in patients with multiple sclerosis. Neuroendocrinology 1999;70(6):431-438. View abstract.

Hillen, T., Lun, A., Reischies, F. M., Borchelt, M., Steinhagen-Thiessen, E., and Schaub, R. T. DHEA-S plasma levels and incidence of Alzheimer's disease. Biol Psychiatry 1-15-2000;47(2):161-163. View abstract.

Elekima, O. T., Mills, C. O., Ahmad, A., Skinner, G. R., Ramsden, D. B., Bown, J., Young, T. W., and Elias, E. Reduced hepatic content of dehydroepiandrosterone sulphotransferase in chronic liver diseases. Liver 2000;20(1):45-50. View abstract.

Bernardi, F., Lanzone, A., Cento, R. M., Spada, R. S., Pezzani, I., Genazzani, A. D., Luisi, S., Luisi, M., Petraglia, F., and Genazzani, A. R. Allopregnanolone and dehydroepiandrosterone response to corticotropin- releasing factor in patients suffering from Alzheimer's disease and vascular dementia. Eur J Endocrinol 2000;142(5):466-471. View abstract.

Lee, K. S., Oh, K. Y., and Kim, B. C. Effects of dehydroepiandrosterone on collagen and collagenase gene expression by skin fibroblasts in culture. J Dermatol.Sci 2000;23(2):103-110. View abstract.

Chassany, O. [Does dehydroepiandrosterone improve well-being?]. Presse Med 7-8-2000;29(24):1354-1355. View abstract.

Burger, H. G., Dudley, E. C., Cui, J., Dennerstein, L., and Hopper, J. L. A prospective longitudinal study of serum testosterone, dehydroepiandrosterone sulfate, and sex hormone-binding globulin levels through the menopause transition. J Clin.Endocrinol.Metab 2000;85(8):2832-2838. View abstract.

Casson, P. R., Lindsay, M. S., Pisarska, M. D., Carson, S. A., and Buster, J. E. Dehydroepiandrosterone supplementation augments ovarian stimulation in poor responders: a case series. Hum.Reprod. 2000;15(10):2129-2132. View abstract.

Straub, R. H., Scholmerich, J., and Zietz, B. Replacement therapy with DHEA plus corticosteroids in patients with chronic inflammatory diseases--substitutes of adrenal and sex hormones. Z Rheumatol. 2000;59 Suppl 2:II/108-II/118. View abstract.

Oberbeck, R., Dahlweid, M., Koch, R., van Griensven, M., Emmendorfer, A., Tscherne, H., and Pape, H. C. Dehydroepiandrosterone decreases mortality rate and improves cellular immune function during polymicrobial sepsis. Crit Care Med 2001;29(2):380-384. View abstract.

Sulcova, J., Hill, M., Hampl, R., Masek, Z., Novacek, A., Ceska, R., and Starka, L. Effects of transdermal application of DHEA on the levels of steroids, gonadotropins and lipids in men. Physiol Res 2000;49(6):685-693. View abstract.

Murialdo, G., Barreca, A., Nobili, F., Rollero, A., Timossi, G., Gianelli, M. V., Copello, F., Rodriguez, G., and Polleri, A. Relationships between cortisol, dehydroepiandrosterone sulphate and insulin-like growth factor-I system in dementia. J Endocrinol Invest 2001;24(3):139-146. View abstract.

Wang, M. J., Huang, H. M., Chen, H. L., Kuo, J. S., and Jeng, K. C. Dehydroepiandrosterone inhibits lipopolysaccharide-induced nitric oxide production in BV-2 microglia. J Neurochem. 2001;77(3):830-838. View abstract.

Fitzpatrick, J. L., Ripp, S. L., Smith, N. B., Pierce, W. M., Jr., and Prough, R. A. Metabolism of DHEA by cytochromes P450 in rat and human liver microsomal fractions. Arch.Biochem Biophys. 5-15-2001;389(2):278-287. View abstract.

Van Niekerk, J. K., Huppert, F. A., and Herbert, J. Salivary cortisol and DHEA: association with measures of cognition and well-being in normal older men, and effects of three months of DHEA supplementation. Psychoneuroendocrinology 2001;26(6):591-612. View abstract.

van Weering, H. G., Gutknecht, D. R., and Schats, R. Augmentation of ovarian response by dehydroepiandrosterone. Hum Reprod. 2001;16(7):1537-1539. View abstract.

Ciotta, L., Calogero, A. E., Farina, M., De, Leo, V, La Marca, A., and Cianci, A. Clinical, endocrine and metabolic effects of acarbose, an alpha- glucosidase inhibitor, in PCOS patients with increased insulin response and normal glucose tolerance. Hum Reprod. 2001;16(10):2066-2072. View abstract.

Luboshitzky, R., Qupti, G., Ishay, A., Shen-Orr, Z., and Herer, P. Increased urinary 6-sulfatoxymelatonin excretion in women with non- classical steroid 21-hydroxylase deficiency. Neuroendocrinol.Lett 2001;22(5):332-336. View abstract.

Barbetta, L., Dall'Asta, C., Re, T., Colombo, P., Travaglini, P., and Ambrosi, B. Androgen secretion in ectopic ACTH syndrome and in Cushing's disease: modifications before and after surgery. Horm.Metab Res 2001;33(10):596-601. View abstract.

Umezaki, H., Hess, D. L., Valenzuela, G. J., and Ducsay, C. A. Fetectomy alters maternal pituitary-adrenal function in pregnant rhesus macaques. Biol Reprod. 2001;65(5):1616-1621. View abstract.

Morrison, M. F., Ten Have, T., Freeman, E. W., Sammel, M. D., and Grisso, J. A. DHEA-S levels and depressive symptoms in a cohort of African American and Caucasian women in the late reproductive years. Biol Psychiatry 11-1-2001;50(9):705-711. View abstract.

Bhattoa, H. P., Kiss, E., Bettembuk, P., and Balogh, A. Bone mineral density, biochemical markers of bone turnover, and hormonal status in men with systemic lupus erythematosus. Rheumatol.Int 2001;21(3):97-102. View abstract.

Dorner, G., Gotz, F., Rohde, W., Plagemann, A., Lindner, R., Peters, H., and Ghanaati, Z. Genetic and epigenetic effects on sexual brain organization mediated by sex hormones. Neuroendocrinol.Lett 2001;22(6):403-409. View abstract.

Feldman, H. A., Longcope, C., Derby, C. A., Johannes, C. B., Araujo, A. B., Coviello, A. D., Bremner, W. J., and McKinlay, J. B. Age trends in the level of serum testosterone and other hormones in middle-aged men: longitudinal results from the Massachusetts male aging study. J Clin Endocrinol.Metab 2002;87(2):589-598. View abstract.

Munarriz, R., Talakoub, L., Flaherty, E., Gioia, M., Hoag, L., Kim, N. N., Traish, A., Goldstein, I., Guay, A., and Spark, R. Androgen replacement therapy with dehydroepiandrosterone for androgen insufficiency and female sexual dysfunction: androgen and questionnaire results. J Sex Marital Ther 2002;28 Suppl 1:165-173. View abstract.

Liu, D. and Dillon, J. S. Dehydroepiandrosterone activates endothelial cell nitric-oxide synthase by a specific plasma membrane receptor coupled to Galpha(i2,3). J Biol.Chem 6-14-2002;277(24):21379-21388. View abstract.

Takayanagi, R., Goto, K., Suzuki, S., Tanaka, S., Shimoda, S., and Nawata, H. Dehydroepiandrosterone (DHEA) as a possible source for estrogen formation in bone cells: correlation between bone mineral density and serum DHEA-sulfate concentration in postmenopausal women, and the presence of aromatase to be enhanced by 1,25-dihydroxyvitamin D3 in human osteoblasts. Mech.Ageing Dev. 4-30-2002;123(8):1107-1114. View abstract.

Josipovic, B. and Josipovic, A. Basal levels of DHEAS as a marker for disease activity in premenopausal women with recent onset rheumatoid arthritis. J Rheumatol. 2002;29(8):1803-1805. View abstract.

Chang, D. M., Lan, J. L., Lin, H. Y., and Luo, S. F. Dehydroepiandrosterone treatment of women with mild-to-moderate systemic lupus erythematosus: a multicenter randomized, double-blind, placebo-controlled trial. Arthritis Rheum. 2002;46(11):2924-2927. View abstract.

Mayer, D., Forstner, K., and Kopplow, K. Induction and modulation of hepatic preneoplasia and neoplasia in the rat by dehydroepiandrosterone. Toxicol.Pathol. 2003;31(1):103-112. View abstract.

Rommler, A. [Adrenopause and dehydroepiandrosterone: pharmacological therapy versus replacement therapy]. Gynakol.Geburtshilfliche Rundsch. 2003;43(2):79-90. View abstract.

Valtysdottir, S. T., Wide, L., and Hallgren, R. Mental wellbeing and quality of sexual life in women with primary Sjogren's syndrome are related to circulating dehydroepiandrosterone sulphate. Ann Rheum.Dis 2003;62(9):875-879. View abstract.

Rao, M. S., Subbarao, V., Yeldandi, A. V., and Reddy, J. K. Hepatocarcinogenicity of dehydroepiandrosterone in the rat. Cancer Res. 5-15-1992;52(10):2977-2979. View abstract.

Howard, J. S., III. Severe psychosis and the adrenal androgens. Integr Physiol Behav.Sci 1992;27(3):209-215. View abstract.

ROBERTS, K. D., VANDEWIELE, R. L., and Lieberman, S. The conversion in vivo of dehydroisoandrosterone sulfate to androsterone and etiocholanolone glucuronidates. J Biol.Chem 1961;236:2213-2215. View abstract.

Tagliaferro, A. R., Roebuck, B. D., Ronan, A. M., and Meeker, L. D. Enhancement of pancreatic carcinogenesis by dehydroepiandrosterone. Adv.Exp.Med Biol. 1992;322:119-129. View abstract.

Danenberg, H. D., Alpert, G., Lustig, S., and Ben Nathan, D. Dehydroepiandrosterone protects mice from endotoxin toxicity and reduces tumor necrosis factor production. Antimicrob Agents Chemother 1992;36(10):2275-2279. View abstract.

Maayan, R., Yoran-Hegesh, R., Strous, R., Nechmad, A., Averbuch, E., Weizman, A., and Spivak, B. Three-month treatment course of methylphenidate increases plasma levels of dehydroepiandrosterone (DHEA) and dehydroepiandrosterone-sulfate (DHEA-S) in attention deficit hyperactivity disorder. Neuropsychobiology 2003;48(3):111-115. View abstract.

Gobbi, D., Rhoden, E. L., Menti, E., Lulhier, F., and Rhoden, C. Effects of the chronic use of dehydroepiandrosterone (DHEA) on testicular weight and spermatogenesis: experimental study in rats. Int.Urol.Nephrol. 2003;35(1):119-122. View abstract.

Leal, A. M., Magalhaes, P. K., Souza, C. S., and Foss, N. T. Adrenocortical hormones and interleukin patterns in leprosy. Parasite Immunol. 2003;25(8-9):457-461. View abstract.

Armanini, D., Vecchio, F., Basso, A., Milone, F. F., Simoncini, M., Fiore, C., Mattarello, M. J., Sartorato, P., and Karbowiak, I. Alzheimer's disease: pathophysiological implications of measurement of plasma cortisol, plasma dehydroepiandrosterone sulfate, and lymphocytic corticosteroid receptors. Endocrine. 2003;22(2):113-118. View abstract.

Sullivan, D. A., Belanger, A., Cermak, J. M., Berube, R., Papas, A. S., Sullivan, R. M., Yamagami, H., Dana, M. R., and Labrie, F. Are women with Sjogren's syndrome androgen-deficient? J Rheumatol. 2003;30(11):2413-2419. View abstract.

Defay, R., Pinchinat, S., Lumbroso, S., Sultan, C., Papoz, L., and Delcourt, C. Relationships between hormonal status and cataract in french postmenopausal women: the POLA study. Ann.Epidemiol. 2003;13(9):638-644. View abstract.

Dolecek, R., Tymonova, J., Adamkova, M., Kadlcik, M., Pohlidal, A., and Zavodna, R. Endocrine changes after burns: the bone involvement. Acta Chir Plast. 2003;45(3):95-103. View abstract.

Miller, K. K., Cai, J., Ripp, S. L., Pierce, W. M., Jr., Rushmore, T. H., and Prough, R. A. Stereo- and regioselectivity account for the diversity of dehydroepiandrosterone (DHEA) metabolites produced by liver microsomal cytochromes P450. Drug Metab Dispos. 2004;32(3):305-313. View abstract.

Straub, R. H., Weidler, C., Demmel, B., Herrmann, M., Kees, F., Schmidt, M., Scholmerich, J., and Schedel, J. Renal clearance and daily excretion of cortisol and adrenal androgens in patients with rheumatoid arthritis and systemic lupus erythematosus. Ann Rheum.Dis 2004;63(8):961-968. View abstract.

Morgan, C. A., III, Southwick, S., Hazlett, G., Rasmusson, A., Hoyt, G., Zimolo, Z., and Charney, D. Relationships among plasma dehydroepiandrosterone sulfate and cortisol levels, symptoms of dissociation, and objective performance in humans exposed to acute stress. Arch.Gen.Psychiatry 2004;61(8):819-825. View abstract.

Buster, J. E., Casson, P. R., Straughn, A. B., Dale, D., Umstot, E. S., Chiamori, N., and Abraham, G. E. Postmenopausal steroid replacement with micronized dehydroepiandrosterone: preliminary oral bioavailability and dose proportionality studies. Am J Obstet Gynecol 1992;166(4):1163-1170. View abstract.

Rasmussen, K. R., Arrowood, M. J., and Healey, M. C. Effectiveness of dehydroepiandrosterone in reduction of cryptosporidial activity in immunosuppressed rats. Antimicrob.Agents Chemother 1992;36(1):220-222. View abstract.

Williams, M. R., Dawood, T., Ling, S., Dai, A., Lew, R., Myles, K., Funder, J. W., Sudhir, K., and Komesaroff, P. A. Dehydroepiandrosterone increases endothelial cell proliferation in vitro and improves endothelial function in vivo by mechanisms independent of androgen and estrogen receptors. J.Clin.Endocrinol.Metab 2004;89(9):4708-4715. View abstract.

Osmanagaoglu, M. A., Okumus, B., Osmanagaoglu, T., and Bozkaya, H. The relationship between serum dehydroepiandrosterone sulfate concentration and bone mineral density, lipids, and hormone replacement therapy in premenopausal and postmenopausal women. J Womens Health (Larchmt.) 2004;13(9):993-999. View abstract.

Goyal, R. O., Sagar, R., Ammini, A. C., Khurana, M. L., and Alias, A. G. Negative correlation between negative symptoms of schizophrenia and testosterone levels. Ann.N Y.Acad.Sci 2004;1032:291-294. View abstract.

Carlsen, S. M., Romundstad, P., and Jacobsen, G. Early second-trimester maternal hyperandrogenemia and subsequent preeclampsia: a prospective study. Acta Obstet Gynecol.Scand. 2005;84(2):117-121. View abstract.

Dhatariya, K., Bigelow, M. L., and Nair, K. S. Effect of dehydroepiandrosterone replacement on insulin sensitivity and lipids in hypoadrenal women. Diabetes 2005;54(3):765-769. View abstract.

Hammer, F., Subtil, S., Lux, P., Maser-Gluth, C., Stewart, P. M., Allolio, B., and Arlt, W. No evidence for hepatic conversion of dehydroepiandrosterone (DHEA) sulfate to DHEA: in vivo and in vitro studies. J Clin Endocrinol.Metab 2005;90(6):3600-3605. View abstract.

Christiansen, J. J., Gravholt, C. H., Fisker, S., Moller, N., Andersen, M., Svenstrup, B., Bennett, P., Ivarsen, P., Christiansen, J. S., and Jorgensen, J. O. Very short term dehydroepiandrosterone treatment in female adrenal failure: impact on carbohydrate, lipid and protein metabolism. Eur J Endocrinol. 2005;152(1):77-85. View abstract.

Yanase, T., Suzuki, S., Goto, K., Nawata, H., and Takayanagi, R. [DHEA and bone metabolism]. Clin Calcium 2003;13(11):1419-1424. View abstract.

Hampl, R., Sulcova, J., Bilek, R., and Hill, M. How short-term transdermal treatment of men with 7-oxo-dehydroepiandrosterone influence thyroid function. Physiol Res 2006;55(1):49-54. View abstract.

Fukui, M., Kitagawa, Y., Nakamura, N., Kadono, M., Yoshida, M., Hirata, C., Wada, K., Hasegawa, G., and Yoshikawa, T. Serum dehydroepiandrosterone sulfate concentration and carotid atherosclerosis in men with type 2 diabetes. Atherosclerosis 2005;181(2):339-344. View abstract.

Hsiao, C. C. Difference in pre- and post-treatment plasma DHEA levels were significantly and positively correlated with difference in pre- and post-treatment Hamilton depression scores following successful therapy for major depression. Psychoneuroendocrinology 2006;31(7):839-846. View abstract.

Villareal, D. T. and Holloszy, J. O. DHEA enhances effects of weight training on muscle mass and strength in elderly women and men. Am J Physiol Endocrinol.Metab 2006;291(5):E1003-E1008. View abstract.

Solano, M. E., Elia, E., Luchetti, C. G., Sander, V., Di, Girolamo G., Gonzalez, C., and Motta, A. B. Metformin prevents embryonic resorption induced by hyperandrogenisation with dehydroepiandrosterone in mice. Reprod.Fertil.Dev. 2006;18(5):533-544. View abstract.

Brooke, A. M., Kalingag, L. A., Miraki-Moud, F., Camacho-Hubner, C., Maher, K. T., Walker, D. M., Hinson, J. P., and Monson, J. P. Dehydroepiandrosterone improves psychological well-being in male and female hypopituitary patients on maintenance growth hormone replacement. J Clin Endocrinol.Metab 2006;91(10):3773-3779. View abstract.

Yehuda, R., Brand, S. R., Golier, J. A., and Yang, R. K. Clinical correlates of DHEA associated with post-traumatic stress disorder. Acta Psychiatr.Scand. 2006;114(3):187-193. View abstract.

Ritsner, M. S., Gibel, A., Ratner, Y., Tsinovoy, G., and Strous, R. D. Improvement of sustained attention and visual and movement skills, but not clinical symptoms, after dehydroepiandrosterone augmentation in schizophrenia: a randomized, double-blind, placebo-controlled, crossover trial. J Clin Psychopharmacol. 2006;26(5):495-499. View abstract.

Stewart, P. M. Aging and fountain-of-youth hormones. N Engl.J Med 10-19-2006;355(16):1724-1726. View abstract.

Kocis, P. Prasterone. Am J Health Syst.Pharm. 11-15-2006;63(22):2201-2210. View abstract.

Gray, A., Feldman, H. A., McKinlay, J. B., and Longcope, C. Age, disease, and changing sex hormone levels in middle-aged men: results of the Massachusetts Male Aging Study. J Clin.Endocrinol.Metab 1991;73(5):1016-1025. View abstract.

Zenk, J. L., Frestedt, J. L., and Kuskowski, M. A. HUM5007, a novel combination of thermogenic compounds, and 3-acetyl-7-oxo-dehydroepiandrosterone: each increases the resting metabolic rate of overweight adults. J Nutr Biochem 2007;18(9):629-634. View abstract.

Olff, M., de Vries, G. J., Guzelcan, Y., Assies, J., and Gersons, B. P. Changes in cortisol and DHEA plasma levels after psychotherapy for PTSD. Psychoneuroendocrinology 2007;32(6):619-626. View abstract.

Huppert, F. A. and Van Niekerk, J. K. WITHDRAWN: Dehydroepiandrosterone (DHEA) supplementation for cognitive function. Cochrane Database.Syst.Rev. 2006;(2):CD000304. View abstract.

Ahboucha, S., Pomier-Layrargues, G., Vincent, C., Hassoun, Z., Tamaz, R., Baker, G., and Butterworth, R. F. Reduced plasma dehydroepiandrosterone sulfate levels are significantly correlated with fatigue severity in patients with primary biliary cirrhosis. Neurochem.Int. 2008;52(4-5):569-574. View abstract.

Lee, M. S., Yang, J. W., Ko, Y. H., Han, C., Kim, S. H., Lee, M. S., Joe, S. H., and Jung, I. K. Effects of methylphenidate and bupropion on DHEA-S and cortisol plasma levels in attention-deficit hyperactivity disorder. Child Psychiatry Hum.Dev. 2008;39(2):201-209. View abstract.

Maggio, M., Lauretani, F., Ceda, G. P., Bandinelli, S., Ling, S. M., Metter, E. J., Artoni, A., Carassale, L., Cazzato, A., Ceresini, G., Guralnik, J. M., Basaria, S., Valenti, G., and Ferrucci, L. Relationship between low levels of anabolic hormones and 6-year mortality in older men: the aging in the Chianti Area (InCHIANTI) study. Arch.Intern.Med 11-12-2007;167(20):2249-2254. View abstract.

Bremner, D., Vermetten, E., and Kelley, M. E. Cortisol, dehydroepiandrosterone, and estradiol measured over 24 hours in women with childhood sexual abuse-related posttraumatic stress disorder. J Nerv.Ment.Dis 2007;195(11):919-927. View abstract.

Barad, D., Brill, H., and Gleicher, N. Update on the use of dehydroepiandrosterone supplementation among women with diminished ovarian function. J Assist.Reprod.Genet. 2007;24(12):629-634. View abstract.

Davis, S. R., Shah, S. M., McKenzie, D. P., Kulkarni, J., Davison, S. L., and Bell, R. J. Dehydroepiandrosterone sulfate levels are associated with more favorable cognitive function in women. J Clin Endocrinol.Metab 2008;93(3):801-808. View abstract.

Bednarek-Tupikowska, G., Tworowska-Bardzinska, U., Tupikowski, K., Bohdanowicz-Pawlak, A., Szymczak, J., Kubicka, E., Skoczynska, A., and Milewicz, A. The correlations between endogenous dehydroepiandrosterone sulfate and some atherosclerosis risk factors in premenopausal women. Med Sci Monit. 2008;14(1):CR37-CR41. View abstract.

Charlton, M., Angulo, P., Chalasani, N., Merriman, R., Viker, K., Charatcharoenwitthaya, P., Sanderson, S., Gawrieh, S., Krishnan, A., and Lindor, K. Low circulating levels of dehydroepiandrosterone in histologically advanced nonalcoholic fatty liver disease. Hepatology 2008;47(2):484-492. View abstract.

Kawano, H., Nagayoshi, Y., Soejima, H., Tanaka, Y., Yamabe, H., Kinoshita, Y., and Ogawa, H. Dehydroepiandrosterone levels vary according as heart failure condition in patients with idiopathic dilated cardiomyopathy. Int.J Cardiol. 4-10-2008;125(2):277-279. View abstract.

Risdon, G., Kumar, V., and Bennett, M. Differential effects of dehydroepiandrosterone (DHEA) on murine lymphopoiesis and myelopoiesis. Exp.Hematol. 1991;19(2):128-131. View abstract.

Haning, R. V., Jr., Carlson, I. H., Flood, C. A., Hackett, R. J., and Longcope, C. Metabolism of dehydroepiandrosterone sulfate (DS) in normal women and women with high DS concentrations. J Clin Endocrinol.Metab 1991;73(6):1210-1215. View abstract.

Pluchino, N., Ninni, F., Stomati, M., Freschi, L., Casarosa, E., Valentino, V., Luisi, S., Genazzani, A. D., Poti, E., and Genazzani, A. R. One-year therapy with 10mg/day DHEA alone or in combination with HRT in postmenopausal women: effects on hormonal milieu. Maturitas 4-20-2008;59(4):293-303. View abstract.

Enomoto, M., Adachi, H., Fukami, A., Furuki, K., Satoh, A., Otsuka, M., Kumagae, S., Nanjo, Y., Shigetoh, Y., and Imaizumi, T. Serum dehydroepiandrosterone sulfate levels predict longevity in men: 27-year follow-up study in a community-based cohort (Tanushimaru study). J Am Geriatr.Soc 2008;56(6):994-998. View abstract.

Page, J. H., Ma, J., Rexrode, K. M., Rifai, N., Manson, J. E., and Hankinson, S. E. Plasma dehydroepiandrosterone and risk of myocardial infarction in women. Clin Chem 2008;54(7):1190-1196. View abstract.

Buford, T. W. and Willoughby, D. S. Impact of DHEA(S) and cortisol on immune function in aging: a brief review. Appl.Physiol Nutr Metab 2008;33(3):429-433. View abstract.

Acosta, E. G., Bruttomesso, A. C., Bisceglia, J. A., Wachsman, M. B., Galagovsky, L. R., and Castilla, V. Dehydroepiandrosterone, epiandrosterone and synthetic derivatives inhibit Junin virus replication in vitro. Virus Res 2008;135(2):203-212. View abstract.

Kodama, M., Oyama, A., and Takagi, H. Control of interstitial pneumonia by drip infusion of megadose vitamin C, dehydroepiandrosterone and cortisol. A short review of our experience. In Vivo 2008;22(2):263-267. View abstract.

Jian, Z. W., Wu, S. Z., and Ruan, Y. J. [Relationship between dehydroepiandrosterone and arteriosclerosis in premenopausal and postmenopausal women]. Nan.Fang Yi.Ke.Da.Xue.Xue.Bao. 2008;28(6):942-943. View abstract.

Brzoza, Z., Kasperska-Zajac, A., Badura-Brzoza, K., Matysiakiewicz, J., Hese, R. T., and Rogala, B. Decline in dehydroepiandrosterone sulfate observed in chronic urticaria is associated with psychological distress. Psychosom.Med 2008;70(6):723-728. View abstract.

Kasperska-Zajac, A., Brzoza, Z., and Rogala, B. Lower serum dehydroepiandrosterone sulphate concentration in chronic idiopathic urticaria: a secondary transient phenomenon? Br.J Dermatol. 2008;159(3):743-744. View abstract.

Dhatariya, K. Dehydroepiandrosterone sulfate has not been substantiated as an anabolic hormone. Arch.Intern.Med 7-14-2008;168(13):1470. View abstract.

Sawalha, A. H. and Kovats, S. Dehydroepiandrosterone in systemic lupus erythematosus. Curr Rheumatol.Rep. 2008;10(4):286-291. View abstract.

Romanutti, C., Bruttomesso, A. C., Castilla, V., Bisceglia, J. A., Galagovsky, L. R., and Wachsman, M. B. In vitro antiviral activity of dehydroepiandrosterone and its synthetic derivatives against vesicular stomatitis virus. Vet.J 2009;182(2):327-335. View abstract.

Izawa, S., Sugaya, N., Shirotsuki, K., Yamada, K. C., Ogawa, N., Ouchi, Y., Nagano, Y., Suzuki, K., and Nomura, S. Salivary dehydroepiandrosterone secretion in response to acute psychosocial stress and its correlations with biological and psychological changes. Biol.Psychol. 2008;79(3):294-298. View abstract.

Chen, H., Lin, A. S., Li, Y., Reiter, C. E., Ver, M. R., and Quon, M. J. Dehydroepiandrosterone stimulates phosphorylation of FoxO1 in vascular endothelial cells via phosphatidylinositol 3-kinase- and protein kinase A-dependent signaling pathways to regulate ET-1 synthesis and secretion. J Biol.Chem 10-24-2008;283(43):29228-29238. View abstract.

Porola, P., Virkki, L., Przybyla, B. D., Laine, M., Patterson, T. A., Pihakari, A., and Konttinen, Y. T. Androgen deficiency and defective intracrine processing of dehydroepiandrosterone in salivary glands in Sjogren's syndrome. J Rheumatol. 2008;35(11):2229-2235. View abstract.

Karp, G., Bentov, Y., Masalha, R., and Ifergane, G. Onset of late posttraumatic seizure after dehydroepiandrosterone treatment. Fertil.Steril. 2009;91(3):931-932. View abstract.

Calvo, E., Luu-The, V., Morissette, J., Martel, C., Labrie, C., Bernard, B., Bernerd, F., Deloche, C., Chaussade, V., Leclaire, J., and Labrie, F. Pangenomic changes induced by DHEA in the skin of postmenopausal women. J Steroid Biochem Mol.Biol. 2008;112(4-5):186-193. View abstract.

Li, Y., Xia, Z., and Wang, M. Dehydroepiandrosterone inhibits CD40/CD40L expression on human umbilical vein endothelial cells induced by interferon gamma. Int.Immunopharmacol. 2009;9(2):168-172. View abstract.

Hirao, T., Urata, Y., Kageyama, K., Ikezaki, M., Kawakatsu, M., Matsuse, M., Matsuo, T., Akishita, M., Nagata, I., and Kondo, T. Dehydroepiandrosterone augments sensitivity to gamma-ray irradiation in human H4 neuroglioma cells through down-regulation of Akt signaling. Free Radic.Res 2008;42(11-12):957-965. View abstract.

Stanczyk, F. Z., Slater, C. C., Ramos, D. E., Azen, C., Cherala, G., Hakala, C., Abraham, G., and Roy, S. Pharmacokinetics of dehydroepiandrosterone and its metabolites after long-term oral dehydroepiandrosterone treatment in postmenopausal women. Menopause. 2009;16(2):272-278. View abstract.

Gill, J., Vythilingam, M., and Page, G. G. Low cortisol, high DHEA, and high levels of stimulated TNF-alpha, and IL-6 in women with PTSD. J Trauma Stress. 2008;21(6):530-539. View abstract.

Spaan, M., Porola, P., Laine, M., Rozman, B., Azuma, M., and Konttinen, Y. T. Healthy human salivary glands contain a DHEA-sulphate processing intracrine machinery, which is deranged in primary Sjogren's syndrome. J Cell Mol.Med 2009;13(7):1261-1270. View abstract.

Rice, S. P., Agarwal, N., Bolusani, H., Newcombe, R., Scanlon, M. F., Ludgate, M., and Rees, D. A. Effects of dehydroepiandrosterone replacement on vascular function in primary and secondary adrenal insufficiency: a randomized crossover trial. J Clin Endocrinol.Metab 2009;94(6):1966-1972. View abstract.

Gonzales, G. F., Gasco, M., Tapia, V., and Gonzales-Castaneda, C. High serum testosterone levels are associated with excessive erythrocytosis of chronic mountain sickness in men. Am J Physiol Endocrinol.Metab 2009;296(6):E1319-E1325. View abstract.

Strous, R. D., Maayan, R., Kaminsky, M., Blumensohn, R., Weizman, A., and Spivak, B. DHEA and DHEA-S levels in hospitalized adolescents with first-episode schizophrenia and conduct disorder: a comparison study. Eur Neuropsychopharmacol. 2009;19(7):499-503. View abstract.

Alexaki, V. I., Charalampopoulos, I., Panayotopoulou, M., Kampa, M., Gravanis, A., and Castanas, E. Dehydroepiandrosterone protects human keratinocytes against apoptosis through membrane binding sites. Exp.Cell Res 8-1-2009;315(13):2275-2283. View abstract.

Grasfeder, L. L., Gaillard, S., Hammes, S. R., Ilkayeva, O., Newgard, C. B., Hochberg, R. B., Dwyer, M. A., Chang, C. Y., and McDonnell, D. P. Fasting-induced hepatic production of DHEA is regulated by PGC-1alpha, ERRalpha, and HNF4alpha. Mol.Endocrinol. 2009;23(8):1171-1182. View abstract.

Panjari, M., Bell, R. J., Jane, F., Adams, J., Morrow, C., and Davis, S. R. The safety of 52 weeks of oral DHEA therapy for postmenopausal women. Maturitas 7-20-2009;63(3):240-245. View abstract.

Labrie, F., Archer, D., Bouchard, C., Fortier, M., Cusan, L., Gomez, J. L., Girard, G., Baron, M., Ayotte, N., Moreau, M., Dube, R., Cote, I., Labrie, C., Lavoie, L., Berger, L., Gilbert, L., Martel, C., and Balser, J. Effect of intravaginal dehydroepiandrosterone (Prasterone) on libido and sexual dysfunction in postmenopausal women. Menopause. 2009;16(5):923-931. View abstract.

Butterworth, R. F., Lalonde, R., Power, C., Baker, G. B., Gamrani, H., and Ahboucha, S. Dehydroepiandrosterone sulphate improves cholestasis-associated fatigue in bile duct ligated rats. Neurogastroenterol.Motil. 2009;21(12):1319-1325. View abstract.

Mizokami, A., Koh, E., Izumi, K., Narimoto, K., Takeda, M., Honma, S., Dai, J., Keller, E. T., and Namiki, M. Prostate cancer stromal cells and LNCaP cells coordinately activate the androgen receptor through synthesis of testosterone and dihydrotestosterone from dehydroepiandrosterone. Endocr.Relat Cancer 2009;16(4):1139-1155. View abstract.

Torricelli, M., Voltolini, C., Galleri, L., Biliotti, G., Giovannelli, A., De, Bonis M., De, Pascalis F., Centini, G., and Petraglia, F. Amniotic fluid urocortin, CRF, oestriol, dehydroepiandrosterone sulfate and cortisol concentrations at mid-trimester: putative relationship with preterm delivery. Eur J Obstet.Gynecol.Reprod.Biol. 2009;146(2):169-173. View abstract.

Valenti, G., Ferrucci, L., Lauretani, F., Ceresini, G., Bandinelli, S., Luci, M., Ceda, G., Maggio, M., and Schwartz, R. S. Dehydroepiandrosterone sulfate and cognitive function in the elderly: The InCHIANTI Study. J Endocrinol.Invest 2009;32(9):766-772. View abstract.

Kasperska-Zajac, A. E., Brzoza, Z. K., Koczy-Baron, E., and Jagodzinska, J. Dehydroepiandrosterone in therapy of allergic diseases. Recent Pat Inflamm.Allergy Drug Discov. 2009;3(3):211-213. View abstract.

Ritsner, M. S. and Strous, R. D. Neurocognitive deficits in schizophrenia are associated with alterations in blood levels of neurosteroids: a multiple regression analysis of findings from a double-blind, randomized, placebo-controlled, crossover trial with DHEA. J Psychiatr.Res 2010;44(2):75-80. View abstract.

Aldred, S. and Mecocci, P. Decreased dehydroepiandrosterone (DHEA) and dehydroepiandrosterone sulfate (DHEAS) concentrations in plasma of Alzheimer's disease (AD) patients. Arch.Gerontol.Geriatr. 2010;51(1):e16-e18. View abstract.

Cappola, A. R., O'Meara, E. S., Guo, W., Bartz, T. M., Fried, L. P., and Newman, A. B. Trajectories of dehydroepiandrosterone sulfate predict mortality in older adults: the cardiovascular health study. J Gerontol.A Biol.Sci Med Sci 2009;64(12):1268-1274. View abstract.

Kellner, M., Muhtz, C., Peter, F., Dunker, S., Wiedemann, K., and Yassouridis, A. Increased DHEA and DHEA-S plasma levels in patients with post-traumatic stress disorder and a history of childhood abuse. J Psychiatr.Res 2010;44(4):215-219. View abstract.

Bonnet, S., Paulin, R., Sutendra, G., Dromparis, P., Roy, M., Watson, K. O., Nagendran, J., Haromy, A., Dyck, J. R., and Michelakis, E. D. Dehydroepiandrosterone reverses systemic vascular remodeling through the inhibition of the Akt/GSK3-{beta}/NFAT axis. Circulation 9-29-2009;120(13):1231-1240. View abstract.

Sonmezer, M., Cil, A. P., and Oktay, K. Ongoing pregnancies from early retrieval of prematurely developing antral follicles after DHEA supplementation. Reprod.Biomed.Online. 2009;19(6):816-819. View abstract.

Chen, Y. C., Chang, H. H., Wen, C. J., Lin, W. Y., Chen, C. Y., Hong, B. S., and Huang, K. C. Elevated serum dehydroepiandrosterone sulphate level correlates with increased risk for metabolic syndrome in the elderly men. Eur J Clin Invest 2010;40(3):220-225. View abstract.

Ruckert, C., Stuepp, Cdos S., Gottardi, B., Rosa, J., Cisilotto, J., Borges, F. P., Rosemberg, D. B., Bogo, M. R., Tasca, T., De Carli, G. A., and Bonan, C. D. Trichomonas vaginalis: dehydroepiandrosterone sulfate and 17beta-estradiol alter NTPDase activity and gene expression. Exp.Parasitol. 2010;125(3):187-195. View abstract.

Sanders, J. L., Boudreau, R. M., Cappola, A. R., Arnold, A. M., Robbins, J., Cushman, M., and Newman, A. B. Cardiovascular disease is associated with greater incident dehydroepiandrosterone sulfate decline in the oldest old: the cardiovascular health study all stars study. J Am Geriatr.Soc 2010;58(3):421-426. View abstract.

Rice, S. P., Zhang, L., Grennan-Jones, F., Agarwal, N., Lewis, M. D., Rees, D. A., and Ludgate, M. Dehydroepiandrosterone (DHEA) treatment in vitro inhibits adipogenesis in human omental but not subcutaneous adipose tissue. Mol.Cell Endocrinol. 5-14-2010;320(1-2):51-57. View abstract.

Liu, X., Arnold, J. T., and Blackman, M. R. Dehydroepiandrosterone administration or G{alpha}q overexpression induces {beta}-catenin/T-Cell factor signaling and growth via increasing association of estrogen receptor-{beta}/Dishevelled2 in androgen-independent prostate cancer cells. Endocrinology 2010;151(4):1428-1440. View abstract.

Romanutti, C., Bruttomesso, A. C., Castilla, V., Galagovsky, L. R., and Wachsman, M. B. Anti-adenovirus activity of epiandrosterone and dehydroepiandrosterone derivatives. Chemotherapy 2010;56(2):158-165. View abstract.

Sanders, J. L., Cappola, A. R., Arnold, A. M., Boudreau, R. M., Chaves, P. H., Robbins, J., Cushman, M., and Newman, A. B. Concurrent change in dehydroepiandrosterone sulfate and functional performance in the oldest old: results from the Cardiovascular Health Study All Stars study. J Gerontol.A Biol.Sci Med Sci 2010;65(9):976-981. View abstract.

Phillips, A. C., Carroll, D., Gale, C. R., Lord, J. M., Arlt, W., and Batty, G. D. Cortisol, DHEA sulphate, their ratio, and all-cause and cause-specific mortality in the Vietnam Experience Study. Eur J Endocrinol. 2010;163(2):285-292. View abstract.

Patte-Mensah, C., Meyer, L., Kibaly, C., and Mensah-Nyagan, A. G. Regulatory effect of dehydroepiandrosterone on spinal cord nociceptive function. Front Biosci (Elite.Ed) 2010;2:1528-1537. View abstract.

Cho, S. H., Choi, M. H., Sim, W. Y., Lee, W. Y., and Chung, B. C. Metabolic alterations of DHEA and cholesterol sulphates in the hair of patients with acne measured by liquid chromatography-mass spectrometry. Exp.Dermatol. 7-1-2010;19(7):694-696. View abstract.

Gleicher, N., Weghofer, A., and Barad, D. H. Improvement in diminished ovarian reserve after dehydroepiandrosterone supplementation. Reprod.Biomed.Online. 2010;21(3):360-365. View abstract.

El-Alfy, M., Deloche, C., Azzi, L., Bernard, B. A., Bernerd, F., Coutet, J., Chaussade, V., Martel, C., Leclaire, J., and Labrie, F. Skin responses to topical dehydroepiandrosterone: implications in antiageing treatment? Br.J Dermatol. 2010;163(5):968-976. View abstract.

Shufelt, C., Bretsky, P., Almeida, C. M., Johnson, B. D., Shaw, L. J., Azziz, R., Braunstein, G. D., Pepine, C. J., Bittner, V., Vido, D. A., Stanczyk, F. Z., and Bairey Merz, C. N. DHEA-S levels and cardiovascular disease mortality in postmenopausal women: results from the National Institutes of Health--National Heart, Lung, and Blood Institute (NHLBI)-sponsored Women's Ischemia Syndrome Evaluation (WISE). J Clin Endocrinol.Metab 2010;95(11):4985-4992. View abstract.

Wang, L. J., Huang, Y. S., Hsiao, C. C., Chiang, Y. L., Wu, C. C., Shang, Z. Y., and Chen, C. K. Salivary dehydroepiandrosterone, but not cortisol, is associated with attention deficit hyperactivity disorder. World J Biol.Psychiatry 2011;12(2):99-109. View abstract.

Sumida, Y., Yonei, Y., Kanemasa, K., Hara, T., Inada, Y., Sakai, K., Imai, S., Hibino, S., Yamaguchi, K., Mitsuyoshi, H., Yasui, K., Minami, M., Itoh, Y., Naito, Y., Yoshikawa, T., and Okanoue, T. Lower circulating levels of dehydroepiandrosterone, independent of insulin resistance, is an important determinant of severity of non-alcoholic steatohepatitis in Japanese patients. Hepatol.Res 2010;40(9):901-910. View abstract.

Chen, M. J., Chen, C. D., Yang, J. H., Chen, C. L., Ho, H. N., Yang, W. S., and Yang, Y. S. High serum dehydroepiandrosterone sulfate is associated with phenotypic acne and a reduced risk of abdominal obesity in women with polycystic ovary syndrome. Hum.Reprod. 2011;26(1):227-234. View abstract.

Roth, M. Y., Page, S. T., Lin, K., Anawalt, B. D., Matsumoto, A. M., Marck, B., Bremner, W. J., and Amory, J. K. The effect of gonadotropin withdrawal and stimulation with human chorionic gonadotropin on intratesticular androstenedione and DHEA in normal men. J Clin Endocrinol.Metab 2011;96(4):1175-1181. View abstract.

Wang, F., Koskela, A., Hamalainen, E., Turpeinen, U., Savolainen-Peltonen, H., Mikkola, T. S., Vihma, V., Adlercreutz, H., and Tikkanen, M. J. Quantitative determination of dehydroepiandrosterone fatty acyl esters in human female adipose tissue and serum using mass spectrometric methods. J Steroid Biochem Mol.Biol. 2011;124(3-5):93-98. View abstract.

Farah, M. J., Givens, J. R., and Kitabchi, A. E. Bimodal correlation between the circulating insulin level and the production rate of dehydroepiandrosterone: positive correlation in controls and negative correlation in the polycystic ovary syndrome with acanthosis nigricans. J Clin Endocrinol Metab 1990;70(4):1075-1081. View abstract.

Daynes, R. A., Dudley, D. J., and Araneo, B. A. Regulation of murine lymphokine production in vivo. II. Dehydroepiandrosterone is a natural enhancer of interleukin 2 synthesis by helper T cells. Eur.J Immunol 1990;20(4):793-802. View abstract.

May, M., Holmes, E., Rogers, W., and Poth, M. Protection from glucocorticoid induced thymic involution by dehydroepiandrosterone. Life Sci 1990;46(22):1627-1631. View abstract.

Davis, S. R., Panjari, M., and Stanczyk, F. Z. Clinical review: DHEA replacement for postmenopausal women. J Clin Endocrinol.Metab 2011;96(6):1642-1653. View abstract.

Sunkara, S. K., Pundir, J., and Khalaf, Y. Effect of androgen supplementation or modulation on ovarian stimulation outcome in poor responders: a meta-analysis. Reprod.Biomed.Online. 2011;22(6):545-555. View abstract.

Hartkamp, A., Geenen, R., Kruize, A. A., Bossema, E. R., Godaert, G. L., Bootsma, H., Bijlsma, J. W., and Derksen, R. H. Serum dehydroepiandrosterone sulphate levels and laboratory and clinical parameters indicating expression of disease are not associated with fatigue, well-being and functioning in patients with primary Sjogren's syndrome. Clin Exp.Rheumatol. 2011;29(2):318-321. View abstract.

Estabrook, R. W., Milewich, L., and Prough, R. A. Cytochrome P-450s as toxicogenic catalysts: the influence of dehydroepiandrosterone. Princess Takamatsu Symp. 1990;21:33-44. View abstract.

Taylor, M. K., Padilla, G. A., Stanfill, K. E., Markham, A. E., Khosravi, J. Y., Ward, M. D., and Koehler, M. M. Effects of dehydroepiandrosterone supplementation during stressful military training: a randomized, controlled, double-blind field study. Stress. 2012;15(1):85-96. View abstract.

Gomez-Santos, C., Larque, E., Granero, E., Hernandez-Morante, J. J., and Garaulet, M. Dehydroepiandrosterone-sulphate replacement improves the human plasma fatty acid profile in plasma of obese women. Steroids 12-11-2011;76(13):1425-1432. View abstract.

Koetz, K. R., Ventz, M., Diederich, S., and Quinkler, M. Bone mineral density is not significantly reduced in adult patients on low-dose glucocorticoid replacement therapy. J Clin Endocrinol.Metab 2012;97(1):85-92. View abstract.

Traish, A. M., Kang, H. P., Saad, F., and Guay, A. T. Dehydroepiandrosterone (DHEA)--a precursor steroid or an active hormone in human physiology. J Sex Med 2011;8(11):2960-2982. View abstract.

Gonzalez, F., Nair, K. S., Daniels, J. K., Basal, E., and Schimke, J. M. Hyperandrogenism sensitizes mononuclear cells to promote glucose-induced inflammation in lean reproductive-age women. Am J Physiol Endocrinol.Metab 2-1-2012;302(3):E297-E306. View abstract.

Ovsiukova, M. V., Obut, T. A., and Saryg, S. K. [The dehydroepiandrosterone sulfate influence on anxiety and depressive behaviour: participation of mu-opioid receptors]. Ross.Fiziol.Zh.Im I.M.Sechenova 2011;97(9):903-913. View abstract.

Divasta, A. D., Feldman, H. A., Giancaterino, C., Rosen, C. J., Leboff, M. S., and Gordon, C. M. The effect of gonadal and adrenal steroid therapy on skeletal health in adolescents and young women with anorexia nervosa. Metabolism 2012;61(7):1010-1020. View abstract.

Xu, B., Yang, R., Chang, F., Chen, L., Xie, G., Sokabe, M., and Chen, L. Neurosteroid PREGS protects neurite growth and survival of newborn neurons in the hippocampal dentate gyrus of APPswe/PS1dE9 mice. Curr Alzheimer Res 2012;9(3):361-372. View abstract.

Bradley, M., McElhiney, M., and Rabkin, J. DHEA and cognition in HIV-positive patients with non-major depression. Psychosomatics 2012;53(3):244-249. View abstract.

Bosdou, J. K., Venetis, C. A., Kolibianakis, E. M., Toulis, K. A., Goulis, D. G., Zepiridis, L., and Tarlatzis, B. C. The use of androgens or androgen-modulating agents in poor responders undergoing in vitro fertilization: a systematic review and meta-analysis. Hum Reprod.Update. 2012;18(2):127-145. View abstract.

Papierska, L., Rabijewski, M., Kasperlik-Zaluska, A., and Zgliczynski, W. Effect of DHEA supplementation on serum IGF-1, osteocalcin, and bone mineral density in postmenopausal, glucocorticoid-treated women. Adv.Med Sci 6-1-2012;57(1):51-57. View abstract.

Nestler, J. E., Usiskin, K. S., Barlascini, C. O., Welty, D. F., Clore, J. N., and Blackard, W. G. Suppression of serum dehydroepiandrosterone sulfate levels by insulin: an evaluation of possible mechanisms. J Clin Endocrinol Metab 1989;69(5):1040-1046. View abstract.

Nestler, J. E., Clore, J. N., Strauss, J. F., III, and Blackard, W. G. The effects of hyperinsulinemia on serum testosterone, progesterone, dehydroepiandrosterone sulfate, and cortisol levels in normal women and in a woman with hyperandrogenism, insulin resistance, and acanthosis nigricans. J Clin Endocrinol Metab 1987;64(1):180-184. View abstract.

Devogelaer, J. P., Crabbe, J., and de Deuxchaisnes. Bone mineral density in Addison's disease: evidence for an effect of adrenal androgens on bone mass. Br.Med J (Clin.Res.Ed) 3-28-1987;294(6575):798-800. View abstract.

Nestler, J. E., Barlascini, C. O., Clore, J. N., and Blackard, W. G. Dehydroepiandrosterone reduces serum low density lipoprotein levels and body fat but does not alter insulin sensitivity in normal men. J Clin.Endocrinol.Metab 1988;66(1):57-61. View abstract.

Loria, R. M., Inge, T. H., Cook, S. S., Szakal, A. K., and Regelson, W. Protection against acute lethal viral infections with the native steroid dehydroepiandrosterone (DHEA). J Med Virol. 1988;26(3):301-314. View abstract.

Mochizuki, M. and Maruo, T. Effect of dehydroepiandrosterone sulfate on uterine cervical ripening in late pregnancy. Acta Physiol Hung. 1985;65(3):267-274. View abstract.

Haning, R. V., Jr., Austin, C. W., Carlson, I. H., Kuzma, D. L., and Zweibel, W. J. Role of dehydroepiandrosterone sulfate as a prehormone for ovarian steroidogenesis. Obstet.Gynecol. 1985;65(2):199-205. View abstract.

Nordin, B. E., Robertson, A., Seamark, R. F., Bridges, A., Philcox, J. C., Need, A. G., Horowitz, M., Morris, H. A., and Deam, S. The relation between calcium absorption, serum dehydroepiandrosterone, and vertebral mineral density in postmenopausal women. J Clin Endocrinol Metab 1985;60(4):651-657. View abstract.

Marchandise, B. and Lederer, J. [Gynecomastia produced by dehydroepiandrosterone excess]. Rev Fr.Endocrinol Clin 1966;7(5):383-387. View abstract.

Menzel, P. and Oertel, G. W. [Steroids in plasma and urine after i.m. injection of dehydroepiandrosterone-enanthate]. Arzneimittelforschung. 1971;21(7):1034-1037. View abstract.

Selye, H., Tache, Y., and Szabo, S. Interruption of pregnancy by various steroids. Fertil.Steril. 1971;22(11):735-740. View abstract.

Rosenfeld, R. S., Hellman, L., and Gallagher, T. F. Metabolism and interconversion of dehydroisoandrosterone and dehydroisoandrosterone sulfate. J Clin Endocrinol Metab 1972;35(2):187-193. View abstract.

Abraham, G. E. Ovarian and adrenal contribution to peripheral androgens during the menstrual cycle. J Clin.Endocrinol.Metab 1974;39(2):340-346. View abstract.

Foldes, J., Feher, T., Feher, K. G., Kollin, E., and Bodrogi, L. Dehydroepiandrosterone sulphate (DS), dehydroepiandrosterone (D) and "free" dehydroepiandrosterone (FD) in the plasma of patients with thyroid diseases. Horm Metab Res 1983;15(12):623-624. View abstract.

Dunn, P. J., Mahood, C. B., Speed, J. F., and Jury, D. R. Dehydroepiandrosterone sulphate concentrations in asthmatic patients: pilot study. N.Z.Med J 11-28-1984;97(768):805-808. View abstract.

Hoffman, D. I., Klove, K., and Lobo, R. A. The prevalence and significance of elevated dehydroepiandrosterone sulfate levels in anovulatory women. Fertil.Steril. 1984;42(1):76-81. View abstract.

Belisle, S., Schiff, I., and Tulchinsky, D. The use of constant infusion of unlabeled dehydroepiandrosterone for the assessment of its metabolic clearance rate, its half-life, and its conversion into estrogens. J Clin Endocrinol Metab 1980;50(1):117-121. View abstract.

Parker, C. R., Jr., Simpson, E. R., Bilheimer, D. W., Leveno, K., Carr, B. R., and MacDonald, P. C. Inverse relation between low-density lipoprotein-cholesterol and dehydroisoandrosterone sulfate in human fetal plasma. Science 5-2-1980;208(4443):512-514. View abstract.

Mattson, L. A., Cullberg, G., Tangkeo, P., Zador, G., and Samsioe, G. Administration of dehydroepiandrosterone enanthate to oophorectomized women--effects on sex hormones and lipid metabolism. Maturitas 1980;2(4):301-309. View abstract.

Tagliaferro, A. R., Ronan, A. M., Payne, J., Meeker, L. D., and Tse, S. Increased lipolysis to beta-adrenergic stimulation after dehydroepiandrosterone treatment in rats. Am J Physiol 1995;268(6 Pt 2):R1374-R1380. View abstract.

Yang, J. Y., Schwartz, A., and Henderson, E. E. Inhibition of HIV-1 latency reactivation by dehydroepiandrosterone (DHEA) and an analog of DHEA. AIDS Res Hum Retroviruses 1993;9(8):747-754. View abstract.

Hata, T., Hashimoto, M., Senoh, D., Hata, K., Kitao, M., and Masumura, S. Effect of dehydroepiandrosterone sulfate on ophthalmic artery flow velocity waveforms in full-term pregnant women. Am J Perinatol. 1995;12(2):135-137. View abstract.

Suzuki, T., Suzuki, N., Engleman, E. G., Mizushima, Y., and Sakane, T. Low serum levels of dehydroepiandrosterone may cause deficient IL-2 production by lymphocytes in patients with systemic lupus erythematosus (SLE). Clin Exp Immunol 1995;99(2):251-255. View abstract.

Nestler, J. E., Beer, N. A., Jakubowicz, D. J., Colombo, C., and Beer, R. M. Effects of insulin reduction with benfluorex on serum dehydroepiandrosterone (DHEA), DHEA sulfate, and blood pressure in hypertensive middle-aged and elderly men. J Clin.Endocrinol.Metab 1995;80(2):700-706. View abstract.

Nestler, J. E. and Kahwash, Z. Sex-specific action of insulin to acutely increase the metabolic clearance rate of dehydroepiandrosterone in humans. J Clin.Invest 1994;94(4):1484-1489. View abstract.

Hautanen, A., Manttari, M., Manninen, V., Tenkanen, L., Huttunen, J. K., Frick, M. H., and Adlercreutz, H. Adrenal androgens and testosterone as coronary risk factors in the Helsinki Heart Study. Atherosclerosis 1994;105(2):191-200. View abstract.

Regelson, W., Loria, R., and Kalimi, M. Dehydroepiandrosterone (DHEA)--the "mother steroid". I. Immunologic action. Ann N.Y.Acad.Sci. 5-31-1994;719:553-563. View abstract.

Regelson, W. and Kalimi, M. Dehydroepiandrosterone (DHEA)--the multifunctional steroid. II. Effects on the CNS, cell proliferation, metabolic and vascular, clinical and other effects. Mechanism of action? Ann N.Y.Acad.Sci. 5-31-1994;719:564-575. View abstract.

Wisniewski, T. L., Hilton, C. W., Morse, E. V., and Svec, F. The relationship of serum DHEA-S and cortisol levels to measures of immune function in human immunodeficiency virus-related illness. Am J Med Sci 1993;305(2):79-83. View abstract.

Nestler, J. E., Beer, N. A., Jakubowicz, D. J., and Beer, R. M. Effects of a reduction in circulating insulin by metformin on serum dehydroepiandrosterone sulfate in nondiabetic men. J Clin Endocrinol Metab 1994;78(3):549-554. View abstract.

Haffner, S. M., Valdez, R. A., Mykkanen, L., Stern, M. P., and Katz, M. S. Decreased testosterone and dehydroepiandrosterone sulfate concentrations are associated with increased insulin and glucose concentrations in nondiabetic men. Metabolism 1994;43(5):599-603. View abstract.

Buffington, C. K., Pourmotabbed, G., and Kitabchi, A. E. Case report: amelioration of insulin resistance in diabetes with dehydroepiandrosterone. Am J Med Sci. 1993;306(5):320-324. View abstract.

de la, Torre B., Hedman, M., Nilsson, E., Olesen, O., and Thorner, A. Relationship between blood and joint tissue DHEAS levels in rheumatoid arthritis and osteoarthritis. Clin Exp Rheumatol. 1993;11(6):597-601. View abstract.

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