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DC Field | Value | Language |
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dc.contributor.author | Narkwichean A. | |
dc.contributor.author | Maalouf W. | |
dc.contributor.author | Baumgarten M. | |
dc.contributor.author | Polanski L. | |
dc.contributor.author | Raine-Fenning N. | |
dc.contributor.author | Campbell B. | |
dc.contributor.author | Jayaprakasan K. | |
dc.date.accessioned | 2021-04-05T03:21:59Z | - |
dc.date.available | 2021-04-05T03:21:59Z | - |
dc.date.issued | 2017 | |
dc.identifier.issn | 3012115 | |
dc.identifier.other | 2-s2.0-85029532377 | |
dc.identifier.uri | https://ir.swu.ac.th/jspui/handle/123456789/13001 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85029532377&doi=10.1016%2fj.ejogrb.2017.09.006&partnerID=40&md5=9356158b78b61815f6d573dc4e140642 | |
dc.description.abstract | Objective To evaluate the effect of DHEA supplementation on In-Vitro Fertilisation (IVF) outcome as assessed by ovarian response, oocyte developmental competence and live birth rates in women predicted to have poor ovarian reserve (OR). The feasibility of conducting a large trial is also assessed by evaluating the recruitment rates and compliance of the recruited participants with DHEA/placebo intake and follow-up rates. Study design A single centre, double blinded, placebo controlled, randomized trial was performed over two years with 60 women undergoing in-vitro fertilisation (IVF). Subjects were randomized, based on a computer-generated pseudo-random code to receive either DHEA or placebo with both capsules having similar colour, size and appearance. 60 women with poor OR based on antral follicle count or anti-Mullerian hormone thresholds undergoing IVF were recruited. They were randomised to receive DHEA 75 mg/day or placebo for at-least 12 weeks before starting ovarian stimulation. They had long protocol using hMG 300 IU/day. Data analysed by “intention to treat”. Ovarian response, live birth rates and molecular markers of oocyte quality were compared between the study and control groups. Results The recruitment rate was 39% (60/154). A total of 52 participants (27 versus 25 in the study and placebo groups) were included in the final analysis after excluding eight. While the mean (standard deviation) DHEA levels were similar at recruitment (9.4 (5) versus 7.5 (2.4) ng/ml; P = 0.1), the DHEA levels at pre-stimulation were higher in the study group than in the controls (16.3 (5.8) versus 11.1 (4.5) ng/ml; P < 0.01). The number (median, range) of oocytes retrieved (4, 0–18 versus 4, 0–15 respectively; P = 0.54) and live birth rates (7/27, 26% versus 8/25, 32% respectively; RR (95% CI): 0.74 (0.22-2.48) and mRNA expression of developmental biomarkers in granulosa and cumulus cells were similar between the groups. Conclusion Pre-treatment DHEA supplementation, albeit statistical power in this study is low, did not improve the response to controlled ovarian hyperstimulation or oocyte quality or live birth rates during IVF treatment with long protocol in women predicted to have poor OR. © 2017 | |
dc.subject | ampiregulin | |
dc.subject | betaregulin | |
dc.subject | biological marker | |
dc.subject | buserelin | |
dc.subject | chorionic gonadotropin | |
dc.subject | cyclooxygenase 2 | |
dc.subject | epiregulin | |
dc.subject | follitropin receptor | |
dc.subject | GREM1 protein | |
dc.subject | human menopausal gonadotropin | |
dc.subject | hyaluronan synthase 2 | |
dc.subject | luteinizing hormone receptor | |
dc.subject | messenger RNA | |
dc.subject | molecular marker | |
dc.subject | Muellerian inhibiting factor | |
dc.subject | nafarelin | |
dc.subject | nafarelin acetate | |
dc.subject | pentraxin 3 | |
dc.subject | placebo | |
dc.subject | prasterone | |
dc.subject | progesterone | |
dc.subject | PTGS2 protein | |
dc.subject | somatomedin C | |
dc.subject | unclassified drug | |
dc.subject | androgen | |
dc.subject | prasterone | |
dc.subject | acne | |
dc.subject | adult | |
dc.subject | antral follicle count | |
dc.subject | Article | |
dc.subject | birth rate | |
dc.subject | clinical outcome | |
dc.subject | controlled study | |
dc.subject | cumulus cell | |
dc.subject | double blind procedure | |
dc.subject | drug efficacy | |
dc.subject | drug withdrawal | |
dc.subject | embryo | |
dc.subject | embryo transfer | |
dc.subject | female | |
dc.subject | follow up | |
dc.subject | gastrointestinal symptom | |
dc.subject | gene expression profiling | |
dc.subject | granulosa cell | |
dc.subject | human | |
dc.subject | in vitro fertilization | |
dc.subject | intention to treat analysis | |
dc.subject | intracytoplasmic sperm injection | |
dc.subject | live birth | |
dc.subject | major clinical study | |
dc.subject | nausea | |
dc.subject | oily skin | |
dc.subject | oocyte development | |
dc.subject | oocyte retrieval | |
dc.subject | ovarian reserve | |
dc.subject | ovary hyperstimulation | |
dc.subject | pregnancy outcome | |
dc.subject | priority journal | |
dc.subject | randomized controlled trial | |
dc.subject | single embryo transfer | |
dc.subject | aging | |
dc.subject | drug effect | |
dc.subject | metabolism | |
dc.subject | oocyte | |
dc.subject | ovary | |
dc.subject | ovulation induction | |
dc.subject | pregnancy | |
dc.subject | procedures | |
dc.subject | Adult | |
dc.subject | Aging | |
dc.subject | Androgens | |
dc.subject | Dehydroepiandrosterone | |
dc.subject | Double-Blind Method | |
dc.subject | Female | |
dc.subject | Fertilization in Vitro | |
dc.subject | Humans | |
dc.subject | Intention to Treat Analysis | |
dc.subject | Live Birth | |
dc.subject | Oocyte Retrieval | |
dc.subject | Oocytes | |
dc.subject | Ovarian Reserve | |
dc.subject | Ovary | |
dc.subject | Ovulation Induction | |
dc.subject | Pregnancy | |
dc.title | Efficacy of Dehydroepiandrosterone (DHEA) to overcome the effect of ovarian ageing (DITTO): A proof of principle double blinded randomized placebo controlled trial | |
dc.type | Article | |
dc.rights.holder | Scopus | |
dc.identifier.bibliograpycitation | European Journal of Obstetrics and Gynecology and Reproductive Biology. Vol 218, (2017), p.39-48 | |
dc.identifier.doi | 10.1016/j.ejogrb.2017.09.006 | |
Appears in Collections: | Scopus 1983-2021 |
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