Dehydroepiandrosterone (DHEA) supplementation in diminished ovarian reserve (DOR)

Norbert Gleicher, David H Barad, Norbert Gleicher, David H Barad

Abstract

Background: With infertility populations in the developed world rapidly aging, treatment of diminished ovarian reserve (DOR) assumes increasing clinical importance. Dehydroepiandrosterone (DHEA) has been reported to improve pregnancy chances with DOR, and is now utilized by approximately one third of all IVF centers world-wide. Increasing DHEA utilization and publication of a first prospectively randomized trial now warrants a systematic review.

Methods: PubMed, Cochrane and Ovid Medline were searched between 1995 and 2010 under the following strategy: [<dehydroepiandrosterone or DHEA or androgens or testosterone > and <ovarian reserve or diminished ovarian reserve or ovarian function >]. Bibliographies of relevant publications were further explored for additional relevant citations. Since only one randomized study has been published, publications, independent of evidence levels and quality assessment, were reviewed.

Results: Current best available evidence suggests that DHEA improves ovarian function, increases pregnancy chances and, by reducing aneuploidy, lowers miscarriage rates. DHEA over time also appears to objectively improve ovarian reserve. Recent animal data support androgens in promoting preantral follicle growth and reduction in follicle atresia.

Discussion: Improvement of oocyte/embryo quality with DHEA supplementation potentially suggests a new concept of ovarian aging, where ovarian environments, but not oocytes themselves, age. DHEA may, thus, represent a first agent beneficially affecting aging ovarian environments. Others can be expected to follow.

Figures

Figure 1
Figure 1
Oocyte and embryo counts in index patient. The patient underwent nine consecutive IVF cycles and increased oocytes and embryo yields from cycle to cycle, starting with one egg and embryo, respectively, and ending up with 17 oocytes and 16 embryos in her ninth cycle. Gonadotropin stimulation was reduced in her last cycle for concerns about possible ovarian hyperstimulation. The patients advised us of her DHEA supplementation only after her sixth cycle. The figure is modified from Barad and Gleicher, with permission, [10].
Figure 2
Figure 2
Cumulative pregnancy rates in women with DOR with and without DHEA supplementation. The figure demonstrates on the left side cumulative pregnancy rates in DHEA and control patients with POA (for definition see text). The right side of the figure demonstrates cumulative pregnancy rates in women above age 40 years. Both patient populations demonstrate similar treatment benefits for DHEA, though POA patients appear to have a slight pregnancy advantage, further confirmed in later data presentations. Modified with permission from Barad et al [17].
Figure 3
Figure 3
Age-stratified miscarriage rates in DHEA supplemented DOR patient in comparison to national U.S. IVF pregnancies. DHEA pretreated patients demonstrated significantly lower miscarriage rates at all ages. The difference was, however, relatively small under age 35 years and progressively increased after that age. Modified with permission from Gleicher et al [28].
Figure 4
Figure 4
Spontaneous pregnancy loss in spontaneous and IVF pregnancies at various AMH levels. The figure depicts at various AMH levels in the left column IVF pregnancies (IVF), as previously reported [Gleicher et al. (31)], and in the right column spontaneously conceived pregnancies (SP). Each column represents 100% of all pregnancies established, separated for live births (black section), voluntary termination of pregnancy (TOP; usually for aneuploidy) and spontaneous miscarriages (SAB). The figure demonstrates that at very low AMH levels (≤0.40 ng/mL) and at AMH ≥ 1.06 ng/mL. IVF pregnancies led to significantly higher live birth rates than spontaneously conceived DHEA pregnancies. Lowest pregnancy and live birth rates were observed with IVF and spontaneously between AMH 0.41-1.05 ng/mL, with no spontaneous DHEA pregnancies at all at AMH 0.81-1.05 ng/mL. While in IVF pregnancies miscarriage rates were clearly reduced at very low and at higher AMH, miscarriages appeared unaffected (~50%) in spontaneously conceived pregnancies.
Figure 5
Figure 5
AMH in POA and DOR patients over time of DHEA exposure. As the figure demonstrates, AMH increases significantly with length of DHEA treatment (------). This effect is more pronounce in young POA patients (- - -) than older DOR patients (......). Modified with permission from Gleicher et al [32].
Figure 6
Figure 6
Trends in patient characteristics of our center's IVF population. Panel A demonstrates mean ages for IVF patients between 2005 and year-to-date 2009. Panel B demonstrates proportional shift from younger patients (<39 years) to older women (≥ 40 years). Panel C demonstrates that this age shift is also accompanied by a significant fall in AMH levels in younger women (ages 31-35 years) and, therefore, increasing DOR in these younger (POA) patients. Combined, these data explain why in 2009 close to 90% of the center's population was affected by either POA or DOR.

References

    1. Casson PR, Lindsay MS, Pisarska MD, Carson SA, Buster JE. Dehydroepiandrosterone supplementation augments ovarian stimulation in poor responders: a case series. Hum Reprod. 2000;15:2129–2132. doi: 10.1093/humrep/15.10.2129.
    1. Buster JE, Casson PR, Straughn AB, Dale D, Umstot ES, Chiamori N, Abraham GE. Postmenopausal steroid replacement with micronized dehydroepiandrosterone: preliminary oral bioavailability and dose proportionality studies. Am J Obstet Gynecol. 1992;66:1163–1168.
    1. Casson PR, Andersen RN, Herrod HG, Stentz FB, Straughn AB, Abraham GE, Buster JE. Oral dehydroepiandrosterone in physiologic doses modulates immune function in postmenopausal women. Am J Obstet Gynecol. 1993;169:1536–1539.
    1. Crosbie D, Black C, McIntyre L, Royle PL, Thomas S. Dehydroepiandrosterone for systemic lupus erythematosus. Cochrane Database Syst Rev. 2007. p. CD005114.
    1. Harding G, Mak YT, Evans B, Cheung J, MacDonald D, Hampson G. The effects of dexamethasone and dehydroepiandrosterone (DHEA) on cytokines and receptor expression in a human osteoblastic cell line: potential steroid-sparing role of DHEA. Cytokine. 2006;36:57–68. doi: 10.1016/j.cyto.2006.10.012.
    1. Casson PR, Straughn AB, Umstot ES, Abraham GE, Carson SA, Buster JE. Delivery of dehydroepiandrosterone to premenopausal women: effect of micronization and nonoral administration. Am J Obstet Gynecol. 1996;174:649–653. doi: 10.1016/S0002-9378(96)70444-1.
    1. Casson PR, Kristiansen SB, Umstot E, Carson SA, Buster JE. Ovarian hyperstimulation augments adrenal dehydroepiandrosterone sulfate secretion. Fertil Steril. 1996;65:950–953.
    1. Casson PR, Santoro N, Elkind-Hirsch K, Carson SA, Hornsby PJ, Abraham G, Buster JE. Postmenopausal dehydroepiandrosterone administration increases free insulin-like growth factor-I and decreases high-density lipoprotein: a six-month trial. Fertil Steril. 1998;70:107–110. doi: 10.1016/S0015-0282(98)00121-6.
    1. Harper AJ, Buster JE, Casson PR. Changes in adrenocortical function with aging and therapeutic implications. Semin Reprod Endocrinol. 1999;17:327–38.
    1. Barad DH, Gleicher N. Increased oocytes production after treatment with dehydroepiandrosterone. Fertil Steril. 2005;84:756.e1–3. doi: 10.1016/j.fertnstert.2005.02.049.
    1. Patrizio P, Leong M. Survey: Poor responders: How to define, diagnose and treat?
    1. 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;25:2496–2500. doi: 10.1093/humrep/deq220.
    1. Sen A, Hammes SR. Granulosa cell-specific androgen receptors are critical regulators of development and function. Mol Endocrinol. 2010;24:1393–1403. doi: 10.1210/me.2010-0006.
    1. Faddy MJ, Gosden RG. A mathematical model of follicle dynamics in the human ovary. Hum Reprod. 1995;10:770–775.
    1. Coccia ME, Rizzello F. Ovarian reserve. Ann N Y Acad Sci. 2008;1127:27–30. doi: 10.1196/annals.1434.011.
    1. Barad D, Gleicher N. Effect of dehydroepinadrosterone on oocytes and embryo yields, embryo grade and cell number in IVF. Hum Reprod. 2006;21:2845–2849. doi: 10.1093/humrep/del254.
    1. Barad DH, Brill H, Gleicher N. Update on the use of dehydroepiandrosterone supplementation among women with diminished ovarian function. J Assist Reprod Genet. 2007;24:629–634. doi: 10.1007/s10815-007-9178-x.
    1. Bedaiwy MA, Ryan E, Shaaban O, Claessens EA, Blanco-Mejia S, Casper RF. Follicular conditioning with dehydroepiandrosterone co-treatment improves IUI outcome in clomiphene citrate patients. 55th Annual Meeting of the Canadian Fertility and Andrology Society, Montreal, Canada, November 18-21, 2009.
    1. Sönmezer M, Özmen B, Cil AP, Özkavukcu, Tasci T, Olmus H, Atabekoğlu CS. Dehydroepiandrosterone supplementation improves ovarian response and cycle outcome in poor responders. RBM Online. 2009;19:508–513.
    1. Nelson LM. Clinical practice. Primary ovarian insufficiency. N Engl J Med. 2009;360:606–614. doi: 10.1056/NEJMcp0808697.
    1. Mamas L, Mamas E. Premature ovarian failure and dehydroepiandrosterone. Fertil Steril. 2009;91:644–646. doi: 10.1016/j.fertnstert.2007.11.055.
    1. Barad DH, Weghofer A, Gleicher N. Premature ovarian failure and dehydroepinadrosterone. Fertil Steril. 2009;91:e14. doi: 10.1016/j.fertnstert.2008.12.134.
    1. Mamas L, Mamas E. Dehydroepiandrosterone supplementation in assisted reproduction: rational and results. Curr Opin Obstet Gynecol. 2009;21:306–308. doi: 10.1097/GCO.0b013e32832e0785.
    1. Gleicher N, Weghofer A, Barad D. Preimplantation screening: "established" and ready for prime time? Fertil Steril. 2008;89:780–788. doi: 10.1016/j.fertnstert.2008.01.072.
    1. Gleicher N, Weghofer A, Barad D. Increased euploid embryos after supplementation with dehydroepiandrosterone (DHEA) in women with premature ovarian aging. Fertil Steril. 2007;88(Suppl1):S232.
    1. Gleicher N, Weghofer A, Barad DH. Dehydroepiandrosterone (DHEA) reduces embryo aneuploidy: Direct evidence from preimplantation genetic screening (PGS) Reprod Biol Endocrinol. 2010;8:140. doi: 10.1186/1477-7827-8-140.
    1. Marquard K, Westphal LM, Milki AA, Lathi RB. Etiology of recurrent pregnancy loss in women over the age of 35 years. Fertil Steril. 2010;94:1474–1477.
    1. Gleicher N, Ryan E, Weghofer A, Blanco-Mejia S, Barad DH. Miscarriage rates after dehydroepiandrosterone (DHEA) supplementation in women with diminished ovarian reserve: a case control study. Reprod Biol Endocrinol. 2009;7:108. doi: 10.1186/1477-7827-7-108.
    1. Levi AJ, Raynault MF, Bergh PA, Drews MR, Miller BT, Scott RT Jr. Reproductive outcome in patients with diminished ovarian reserve. Fertil Steril. 2001;76:666–669. doi: 10.1016/S0015-0282(01)02017-9.
    1. Nybo Andersen AM, Wohlfahrt J, Christens P, Olsen J, Melbye M. Maternal age and fetal loss: population register linkage study. BMJ. 2000;320:1708–1712. doi: 10.1136/bmj.320.7251.1708.
    1. Gleicher N, Weghofer A, Barad DH. Anti-Müllerian hormone (AMH) defines, independent of age, low versus good live birth chances in women with severely ovarian reserve. Fertil Steril. 2010;94:2824–2827. doi: 10.1016/j.fertnstert.2010.04.067.
    1. Gleicher N, Weghofer A, Barad DH. Improvement in diminished ovarian reserve after dehydroepiandrosterone (DHEA) supplementation. Reprod Biomed Online. 2010;21:360–365. doi: 10.1016/j.rbmo.2010.04.006.
    1. Ethics Committee of the American Society for Reproductive Medicine. Fertility treatment when the prognosis is very poor or futile. Fertil Steril. 2009;92:1194–1197.
    1. Stanczyk FZ, Slater CC, Ramos DE, Azen Z, Cherala G, Hakala C, Abraham G, Roy S. Pharamcokinetiks of dehydroepiandrosterone and its metabolites after long-term oral dehydroepiandrosterone treatment in postmenopausal women. Menopause. 2009;16:272–278. doi: 10.1097/gme.0b013e31818adb3f.
    1. Lifrak ET, Parker LN. Analysis of nonprescription capsules purported to contain an androgen. Am J Hosp Pharm. 1985;42:587–589.
    1. Karp G, Bentov Y, Masalha R, Ifergane G. Onset of posttraumatic seizure after dehydroepiandrosterone treatment. Fertil Steril. 2009;91:e1–2. 931.
    1. Panjari M, Bell RJ, Jane F, Adams J, Morrow C, Davis SR. The safety of 52 weeks of oral DHEA therapy for postmenopausal women. Maturitas. 2009;63:240–245. doi: 10.1016/j.maturitas.2009.03.020.
    1. Meldrum DR, Chang RJ, deZiegler D, Schoolcraft WB, Scott RT Jr, Pellicier A. Adjuncts for ovarian stimulation: when do we adopt "orphan indications" for approved drugs. Fertil Steril. 2009;92:1308.
    1. Hodges CA, Ilagan A, Jenninger D, Keri R, Nilson J, Hunt PA. Experimental evidence that changes in oocytes growth influence meiotic chromosome segregation. Hum Reprod. 2002;17:1171–1180. doi: 10.1093/humrep/17.5.1171.
    1. Bahceci M, Ulug U, Turan E, Akman MA. Comparisons of follicular levels of sex steroids, gonadotropins and insulin like growth factor-1 (IGF-1) and epidermal growth factor (EGF) in poor responders and normoresponders patients undergoing ovarian stimulation with GnRH antagonist. Eur J Obstet Gynecol Reprod Biol. 2007;130:93–98. doi: 10.1016/j.ejogrb.2006.04.032.
    1. Ware VC. The role of androgens in follicular development in the ovary. I. A quantitative analysis oocytes ovulation. J Exp Zoology. 1982;222:155–167. doi: 10.1002/jez.1402220207.
    1. Andersen CY, Lossi K. Increased intrafollicular androgen levels affect human granulose secretion of anti-Müllerian hormone and inhibin-B. Fertil Steril. 2008;89:1760–1765. doi: 10.1016/j.fertnstert.2007.05.003.
    1. Otala M, Mäkinen S, Tuuri T, Sjöberg J, Pentikäinen V, Matikainen T, Dunkel L. Effects of testosterone, dihydrotestosterone, and 17 beta-estradiol on human ovarian tissue survival in culture. Fertil Steril. 2004;82(Suppl 3):1077–85.
    1. Orvieto R, Fisch N, Yulzari-Roll V, LaMarca A. Ovarian androgens but not estrogens correlate with the degree of systemic inflammation observed during controlled ovarian stimulation. Gynecol Endocrinol. 2005;21:170–3. doi: 10.1080/09513590500279667.
    1. Frattarelli JL, Peterson EH. Effect of androgen levels on in vitro fertilization cycles. Fertil Steril. 2004;81:1713–1714. doi: 10.1016/j.fertnstert.2003.11.032.
    1. Frattarelli JL, Gerber MD. Basal and cycle androgen levels correlate with in vitro fertilization stimulation parameters but do not predict pregnancy outcome. Fertil Steril. 2006;86:51–57. doi: 10.1016/j.fertnstert.2005.12.028.
    1. Hossein Rashidi B, Hormoz B, Shahrokh Tehraninejad E, Shariat M, Mahdavi A. Testosterone and dehydroepiandrosterone sulphate levels and IVF/ICSI results. Gynecol Endocrinol. 2009;25:194–198. doi: 10.1080/09513590802582644.
    1. Lossl K, Andersen AN, Loft A, Freiesleben NL, Bangsbøll S, Andersen CY. Androgen priming using aromatase inhibitor and hCG during early-follicular-phase GnRH antagonist down-regulation in modified antagonist protocol. Hum Reprod. 2006;21:2593–2600. doi: 10.1093/humrep/del221.
    1. Lossl K, Andersen CY, Loft A, Freiesleben NL, Bangsbøll S, Andersen AN. Short-term androgen priming with use of aromatase inhibitor and hCG before controlled ovarian stimulation for IVF. A randomized controlled trial. Hum Reprod. 2008;23:1820–1829. doi: 10.1093/humrep/den131.
    1. Massin N, Cedrin-Durnerin I, Coussieu C, Galey-Fontaine J, Wolf JP, Hugues JN. Effects of transdermal testosterone application on the ovarian response to FSH in poor responders undergoing assisted reproduction-technique-a prospective, randomized, double-blind study. Hum Reprod. 2006;21:1204–1211. doi: 10.1093/humrep/dei481.
    1. Balasch J, Fábreques F, Peñarrubia J, Carmona F, Casamitjana R, Creus M, Manau D, Casals G, Vanrell JA. Pretreatment with transdermal testosterone may improve ovarian response to gonadotrophins in poor-responder IVF patients with normal basal concentrations of FSH. Hum Reprod. 2006;21:1884–1893. doi: 10.1093/humrep/del052.
    1. Fábreques F, Peñarurubia J, Creus M, Manau D, Caals G, Carmone F, Balasch J. Transdermal testosterone may improve ovarian response to gonadotrophins in low-responder IVF patients: a randomized, clinical trial. Hum Reprod. 2009;24:349–359. doi: 10.1093/humrep/den428.
    1. Kim CH, Howles CM, Lee HA. The effect of transdermal testosterone gel pretreatment on controlled ovarian stimulation and IVF outcome in low responders. Fertil Steril. 2011;95:679–683. doi: 10.1016/j.fertnstert.2010.07.1077.
    1. Gleicher N, Oleske DM, Tur-Kaspa I, Vidali A, Karande V. Reducing the risk of high-order multiple pregnancy after ovarian stimulation with gonadotropins. N Engl J Med. 2000;343:2–7. doi: 10.1056/NEJM200007063430101.
    1. Gleicher N, Weghofer A, Barad D. Too old for IVF: are we discriminating against older women? J Assist Reprod Genet. 2007;24:639–644. doi: 10.1007/s10815-007-9182-1.
    1. Broekmans FJ, Soules MR, Fauser BC. Ovarian aging: mechanisms and clinical consequences. Endocr Rev. 2009;30:465–493. doi: 10.1210/er.2009-0006.
    1. Weghofer A, Barad D, Li J, Gleicher N. Aneuploidy rates in embryos from women with prematurely declining ovarian function: a pilot study. Fertil Steril. 2007;88:90–94. doi: 10.1016/j.fertnstert.2006.11.081.
    1. Walker M, Anderson D, Herndon J, Walker L. Ovarian aging in Squirrel monkeys (Saimiri sclureus) Reproduction. 2009;138:793–799. doi: 10.1530/REP-08-0449.
    1. Bentov Y, Esfandiari N, Burstein E, Casper RF. The use of mitochondrial nutrients to improve the outcome of infertility treatment in older patients. Fertil Steril. 2010;93:272–275. doi: 10.1016/j.fertnstert.2009.07.988.
    1. Pitteloud N, Mootha VK, Dwyer AA, Hardin M, Lee H, Eriksson KF, Tripathy D, Yialamas M, Groop L, Elahi D, Hayes FJ. Relationship between testosterone levels, insulin sensitivity, and mitochondrial function in men. Diabetes Care. 2005;28:1636–1642. doi: 10.2337/diacare.28.7.1636.
    1. Xu M, Bnc A, Woodruff TK, Shea LD. Secondary follicle growth and oocytes maturation by culture in alginate hydrogel following cryopreservation of the ovary or individual follicles. Biotechnol Bioeng. 2009;103:378–386. doi: 10.1002/bit.22250.
    1. Wolff T, Witkop CT, Miller T, Syed SB. U.S. Preventive Services Task Force. Folic acid supplementation for the prevention of neural tube defects: an update of the evidence for the U.S. Preventive Task Force. Ann Intern Med. 2009;150:632–539.
    1. Scott JR. Evidence-based medicine under attack. Obstet Gynecol. 2009;113:1202–1203.
    1. Vintzileos AM. Evidence-based compared with reality-based medicine in obstetrics. Obstet Gynecol. 2009;113:1335–1340.
    1. Gleicher N, Barad DH. Misplaced obsession with prospectively randomized studies. RBM Online. 2010;21:440–443.

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