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体外受精和卵胞浆内单精子注射中精子 DNA 损伤的临床意义:更新的系统评价和荟萃分析。

Clinical implications of sperm DNA damage in IVF and ICSI: updated systematic review and meta-analysis.

机构信息

Biotechnology of Animal and Human Reproduction (TechnoSperm), Institute of Food and Agricultural Technology, University of Girona, Jaume Casadamont Building, Door E, 15 Pic de Peguera St, Girona, ES-17003, Spain.

Unit of Cell Biology, Department of Biology, Faculty of Sciences, University of Girona, Sciences Building, 69 Maria Aurèlia Capmany, Girona, ES-17003, Spain.

出版信息

Biol Rev Camb Philos Soc. 2021 Aug;96(4):1284-1300. doi: 10.1111/brv.12700. Epub 2021 Mar 1.

Abstract

The clinical effect of sperm DNA damage in assisted reproduction has been a controversial topic during recent decades, leading to a variety of clinical practice recommendations. While the latest European Society of Human Reproduction and Embryology (ESHRE) position report concluded that DNA damage negatively affects assisted reproduction outcomes, the Practice Committee of the American Society for Reproductive Medicine (ASRM) does not recommend the routine testing of DNA damage for in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI). Herein, our aim was to perform a systematic review and meta-analysis of studies investigating whether sperm DNA damage affects clinical outcomes in IVF and ICSI, in order to contribute objectively to a consistent clinical recommendation. A comprehensive systematic search was conducted according to PRISMA guidelines from the earliest available online indexing year until March 2020, using the MEDLINE-PubMed and EMBASE databases. We included studies analysing IVF and/or ICSI treatments performed in infertile couples in which sperm DNA damage was well defined and assessed. Studies also had to include information about pregnancy, implantation or live birth rates as primary outcomes. The NHLBI-NIH quality assessment tool was used to assess the quality of each study. Meta-analyses were conducted using the Mantel-Haenszel method with random-effects models to evaluate the Risk Ratio (RR) between high-DNA-damage and control groups, taking into account the 95% confidence intervals. Heterogeneity among studies was evaluated using the I statistic. We also conducted sensitivity analyses and post-hoc subgroup analyses according to different DNA fragmentation assessment techniques. We identified 78 articles that met our inclusion and quality criteria and were included in the qualitative analysis, representing a total of 25639 IVF/ICSI cycles. Of these, 32 articles had sufficient data to be included in the meta-analysis, comprising 12380 IVF/ICSI cycles. Meta-analysis revealed that, considering IVF and ICSI results together, implantation rate (RR = 0.74; 95% CI = 0.61-0.91; I  = 69) and pregnancy rate (RR = 0.83; 0.73-0.94; I  = 58) are negatively influenced by sperm DNA damage, although after adjustment for publication bias the relationship for pregnancy rate was no longer significant. The results showed a non-significant but detrimental tendency (RR = 0.78; 0.58-1.06; I  = 72) on live birth rate. Meta-analysis also showed that IVF outcomes are negatively influenced by sperm DNA damage, with a statistically significant impact on implantation (RR = 0.68; 0.52-0.89; I  = 50) and pregnancy rates (RR = 0.72; 0.55-0.95; I  = 72), although the latter was no longer significant after correction for publication bias. While it did not quite meet our threshold for significance, a negative trend was also observed for live birth rate (RR = 0.48; 0.22-1.02; I  = 79). In the case of ICSI, non-significant trends were observed for implantation (RR = 0.79; 0.60-1.04; I  = 72) or pregnancy rates (RR = 0.89; 0.78-1.02; I  = 44), and live birth rate (RR = 0.92; 0.67-1.27; I  = 70). The current review provides the largest evidence to date supporting a negative association between sperm DNA damage and conventional IVF treatments, significantly reducing implantation and pregnancy rates. The routine use of sperm DNA testing is therefore justified, since it may help improve the outcomes of IVF treatments and/or allow a given couple to be advised on the most suitable treatment. Further well-designed controlled studies on a larger number of patients are required to allow us to reach more precise conclusions, especially in the case of ICSI treatments.

摘要

精子 DNA 损伤对辅助生殖临床效果的影响一直是近几十年来备受争议的话题,这导致了各种临床实践建议。虽然最新的欧洲人类生殖与胚胎学会(ESHRE)立场报告得出结论,DNA 损伤对辅助生殖结果有负面影响,但美国生殖医学学会(ASRM)的实践委员会不建议常规检测体外受精(IVF)或胞浆内精子注射(ICSI)的 DNA 损伤。在此,我们旨在对研究精子 DNA 损伤是否影响 IVF 和 ICSI 临床结局的研究进行系统评价和荟萃分析,以便客观地为一致性的临床推荐提供依据。根据 PRISMA 指南,我们从最早的在线索引年份开始进行了全面的系统搜索,直到 2020 年 3 月,使用了 MEDLINE-PubMed 和 EMBASE 数据库。我们纳入了分析在不孕夫妇中进行的 IVF 和/或 ICSI 治疗的研究,其中精子 DNA 损伤有明确的定义和评估。研究还必须包括妊娠、着床或活产率等主要结局的信息。我们使用 NHLBI-NIH 质量评估工具来评估每个研究的质量。使用 Mantel-Haenszel 方法进行荟萃分析,采用随机效应模型评估高 DNA 损伤组和对照组之间的风险比(RR),并考虑 95%置信区间。使用 I 统计量评估研究之间的异质性。我们还根据不同的 DNA 碎片评估技术进行了敏感性分析和事后亚组分析。我们确定了 78 篇符合我们的纳入和质量标准的文章,并进行了定性分析,共有 25639 个 IVF/ICSI 周期。其中,32 篇文章有足够的数据纳入荟萃分析,包括 12380 个 IVF/ICSI 周期。荟萃分析表明,综合考虑 IVF 和 ICSI 的结果,着床率(RR=0.74;95%CI=0.61-0.91;I=69)和妊娠率(RR=0.83;0.73-0.94;I=58)受到精子 DNA 损伤的负面影响,尽管调整发表偏倚后,妊娠率的相关性不再显著。结果显示,活产率呈非显著但不利的趋势(RR=0.78;0.58-1.06;I=72)。荟萃分析还表明,精子 DNA 损伤对 IVF 结局有负面影响,对着床率(RR=0.68;0.52-0.89;I=50)和妊娠率(RR=0.72;0.55-0.95;I=72)有统计学显著影响,尽管后者在纠正发表偏倚后不再显著。虽然它没有达到我们的显著性阈值,但活产率也呈现出负向趋势(RR=0.48;0.22-1.02;I=79)。对于 ICSI,着床率(RR=0.79;0.60-1.04;I=72)或妊娠率(RR=0.89;0.78-1.02;I=44)和活产率(RR=0.92;0.67-1.27;I=70)的趋势不显著。本综述提供了迄今为止最大的证据,支持精子 DNA 损伤与常规 IVF 治疗之间存在负相关,显著降低了着床率和妊娠率。因此,常规使用精子 DNA 检测是合理的,因为它可以帮助改善 IVF 治疗的结局,或允许一对夫妇就最合适的治疗方法提供建议。需要进一步设计良好的、针对更多患者的对照研究,以便我们得出更精确的结论,特别是在 ICSI 治疗方面。

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