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脱氢表雄酮(DHEA)克服卵巢衰老影响的疗效(DITTO):一项原理验证性双盲随机安慰剂对照试验。

Efficacy of Dehydroepiandrosterone (DHEA) to overcome the effect of ovarian ageing (DITTO): A proof of principle double blinded randomized placebo controlled trial.

作者信息

Narkwichean Amarin, Maalouf Walid, Baumgarten Miriam, Polanski Lukasz, Raine-Fenning Nick, Campbell Bruce, Jayaprakasan Kannamannadiar

机构信息

Division of Obstetrics and Gynaecology, Faculty of Medicine & Health Sciences, University of Nottingham, Nottingham, Nottinghamshire, NG7 2UH, United Kingdom; Department of Obstetrics and Gynaecology, Faculty of Medicine, Srinakharinwirot University, Nakhon-Nayok, 26120, Thailand.

Division of Obstetrics and Gynaecology, Faculty of Medicine & Health Sciences, University of Nottingham, Nottingham, Nottinghamshire, NG7 2UH, United Kingdom.

出版信息

Eur J Obstet Gynecol Reprod Biol. 2017 Nov;218:39-48. doi: 10.1016/j.ejogrb.2017.09.006. Epub 2017 Sep 8.

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 75mg/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.

摘要

目的

评估补充脱氢表雄酮(DHEA)对预计卵巢储备功能不良(OR)女性体外受精(IVF)结局的影响,该结局通过卵巢反应、卵母细胞发育能力和活产率进行评估。还通过评估招募率、招募参与者对DHEA/安慰剂摄入的依从性以及随访率来评估进行大型试验的可行性。

研究设计

一项单中心、双盲、安慰剂对照的随机试验进行了两年,有60名接受体外受精(IVF)的女性参与。根据计算机生成的伪随机代码将受试者随机分组,以接受DHEA或安慰剂,两种胶囊具有相似的颜色、大小和外观。招募了60名根据窦卵泡计数或抗苗勒管激素阈值判断为卵巢储备功能不良且正在接受IVF的女性。在开始卵巢刺激前,她们被随机分配接受75mg/天的DHEA或安慰剂至少12周。她们采用每天300IU人绝经期促性腺激素(hMG)的长方案。数据按“意向性分析”进行分析。比较研究组和对照组之间的卵巢反应、活产率和卵母细胞质量的分子标志物。

结果

招募率为39%(60/154)。排除8名参与者后,共有52名参与者(研究组27名,安慰剂组25名)纳入最终分析。虽然招募时平均(标准差)DHEA水平相似(9.4(5)对7.5(2.4)ng/ml;P = 0.1),但研究组刺激前的DHEA水平高于对照组(16.3(5.8)对11.1(4.5)ng/ml;P<0.01)。回收的卵母细胞数量(中位数,范围)(分别为4,0 - 18对4,0 - 15;P = 0.54)和活产率(分别为7/27,26%对8/25,32%;相对危险度(95%可信区间):0.74(0.22 - 2.48))以及颗粒细胞和卵丘细胞中发育生物标志物的mRNA表达在两组之间相似。

结论

尽管本研究的统计效力较低,但预处理补充DHEA并不能改善预计卵巢储备功能不良的女性在采用长方案进行IVF治疗期间对控制性卵巢过度刺激的反应、卵母细胞质量或活产率。

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