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正常体重女性在体外受精和胚胎移植前单次口服维生素 D 补充剂:SUNDRO 随机对照试验。

Single oral dose of vitamin D supplementation prior to in vitro fertilization and embryo transfer in normal weight women: the SUNDRO randomized controlled trial.

机构信息

Università degli Studi di Milano, Milan, Italy; Fondazione Istituto di Ricovero e Cura Carattere Scientifico Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.

IRCCS San Raffaele Scientific Institute, Milan, Italy.

出版信息

Am J Obstet Gynecol. 2021 Sep;225(3):283.e1-283.e10. doi: 10.1016/j.ajog.2021.04.234. Epub 2021 Apr 21.

DOI:10.1016/j.ajog.2021.04.234
PMID:33894153
Abstract

BACKGROUND

Improving in vitro fertilization success is an unmet need. Observational studies have suggested that women with deficient or insufficient vitamin D have lower chances of in vitro fertilization success, but whether supplementation improves clinical pregnancy rate remains unclear.

OBJECTIVE

This study aimed to determine whether oral vitamin D supplementation improves clinical pregnancy in women undergoing an in vitro fertilization cycle.

STUDY DESIGN

The "supplementation of vitamin D and reproductive outcome" trial is a 2-center randomized superiority double-blind placebo-controlled trial. Subjects were recruited between October 2016 and January 2019. Participants were women aged 18 to 39 years with low vitamin D (peripheral 25-hydroxyvitamin D of <30 ng/mL), serum calcium of ≥10.6 mg/dL, body mass index of 18 to 25 kg/m, and antimüllerian hormone levels of >0.5 ng/mL and starting their first, second, or third treatment cycle of conventional in vitro fertilization or intracytoplasmic sperm injection. The primary outcome was the cumulative clinical pregnancy rate per cycle. Pregnancies obtained with both fresh or frozen embryo transfers were included. Clinical pregnancy was defined as an intrauterine gestational sac with a viable fetus. The primary analysis was performed according to the intention-to-treat principle and could also include natural conceptions. Secondary outcomes included total dose of gonadotropins used, embryologic variables (number of oocytes retrieved, number of suitable oocytes retrieved, fertilization rate, and rate of top-quality embryos), and clinical outcomes (miscarriage rate and live birth rate).

RESULTS

Overall, 630 women were randomized 2 to 12 weeks before the initiation of the in vitro fertilization cycle to receive either a single dose of 600,000 IU of vitamin D (n=308) or placebo (n=322). Interestingly, 113 (37%) and 130 (40%) women achieved a clinical pregnancy in the treatment and placebo groups, respectively (P=.37). The risk ratio of clinical pregnancy in women receiving vitamin D was 0.91 (95% confidence interval, 0.75-1.11). Compared with the placebo, vitamin D supplementation did not improve the rate of clinical pregnancy. Exploratory subgroup analyses for body mass index, age, indication to in vitro fertilization, ovarian reserve, interval between drug administration and initiation of the cycle, and basal levels of 25-hydroxyvitamin D failed to highlight any clinical situation that could benefit from the supplementation.

CONCLUSION

In women with normal weight with preserved ovarian reserve and low vitamin D levels undergoing in vitro fertilization cycles, a single oral dose of 600,000 IU of vitamin D did not improve the rate of clinical pregnancy. Although the findings do not support the use of vitamin D supplementation to improve in vitro fertilization success rates, further studies are required to rule out milder but potentially interesting benefits and explore the effectiveness of alternative modalities of supplementation.

摘要

背景

提高体外受精成功率是一项未满足的需求。观察性研究表明,维生素 D 缺乏或不足的女性体外受精成功率较低,但补充维生素 D 是否能提高临床妊娠率尚不清楚。

目的

本研究旨在确定口服维生素 D 补充剂是否能提高接受体外受精周期治疗的女性的临床妊娠率。

研究设计

“维生素 D 补充与生殖结局”试验是一项 2 中心随机优势双盲安慰剂对照试验。研究对象于 2016 年 10 月至 2019 年 1 月期间招募。参与者为年龄在 18 至 39 岁之间、维生素 D 水平低(外周 25-羟维生素 D<30ng/ml)、血清钙≥10.6mg/dL、体重指数 18 至 25kg/m²和抗苗勒管激素水平>0.5ng/ml 的女性,她们正在进行第一次、第二次或第三次常规体外受精或胞浆内精子注射治疗周期。主要结局为每个周期的累积临床妊娠率。包括新鲜或冷冻胚胎移植获得的妊娠。临床妊娠定义为宫内妊娠囊伴活胎。主要分析按照意向治疗原则进行,也可包括自然妊娠。次要结局包括使用的促性腺激素总剂量、胚胎学变量(获卵数、可受精卵数、受精率和优质胚胎率)和临床结局(流产率和活产率)。

结果

总体而言,630 名女性在体外受精周期开始前 2 至 12 周随机分为两组,分别接受单次 600000IU 维生素 D(n=308)或安慰剂(n=322)治疗。有趣的是,治疗组和安慰剂组分别有 113(37%)和 130(40%)名女性实现了临床妊娠(P=.37)。接受维生素 D 治疗的女性临床妊娠的风险比为 0.91(95%置信区间,0.75-1.11)。与安慰剂相比,维生素 D 补充剂并未提高临床妊娠率。对体重指数、年龄、体外受精指征、卵巢储备、药物治疗与周期开始之间的间隔以及 25-羟维生素 D 基础水平的探索性亚组分析未能突出任何可能受益于补充的临床情况。

结论

在接受体外受精周期治疗的体重正常、卵巢储备正常且维生素 D 水平较低的女性中,单次口服 600000IU 维生素 D 并不能提高临床妊娠率。尽管这些发现不支持使用维生素 D 补充剂来提高体外受精成功率,但仍需要进一步研究以排除更温和但可能有趣的益处,并探讨替代补充方式的有效性。

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