Department of Biology and Medical Genetics, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Department of Biology and Medical Genetics, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.
Fertil Steril. 2017 Jan;107(1):150-159.e2. doi: 10.1016/j.fertnstert.2016.10.007. Epub 2016 Nov 11.
Systematic review and meta-analysis.
Not applicable.
PATIENT(S): Couples with IRSA and their spontaneously aborted embryos.
INTERVENTION(S): Summary odds ratios (ORs) were calculated by means of fixed- or random-effects models.
MAIN OUTCOME MEASURE(S): Association of genetic variants with IRSA.
RESULT(S): The systematic review included 428 case-control studies (1990-2015), which differed substantially regarding RSA definition, clinical evaluation of patients, and selection of control subjects. In women, 472 variants in 187 genes were investigated. Meta-analyses were performed for 36 variants in 16 genes. Association with IRSA defined as three or more spontaneous abortions (SAs) was detected for 21 variants in genes involved in immune response (IFNG, IL10, KIR2DS2, KIR2DS3, KIR2DS4, MBL, TNF), coagulation (F2, F5, PAI-1, PROZ), metabolism (GSTT1, MTHFR), and angiogenesis (NOS3, VEGFA). However, ORs were modest (0.51-2.37), with moderate or weak epidemiologic credibility. Minor differences in summary ORs were detected between IRSA defined as two or more and as three or more SAs. Male partners were included in 12.1% of studies, and one study included spontaneously aborted embryos.
CONCLUSION(S): Candidate gene studies show moderate associations with IRSA. Owing to large differences in RSA definition and selection criteria for participants, consensus is needed. Future GASs should include both partners and spontaneously aborted embryos. Genome-wide association studies and large-scale replications of identified associations are recommended.
1)对特发性复发性自然流产(IRSA)的遗传关联研究(GAS)进行首次全面的系统评价;2)根据复发性自然流产(RSA)的定义以及患者和对照选择标准对研究进行分析;3)对候选基因与 IRSA 的关联进行荟萃分析。
系统评价和荟萃分析。
不适用。
IRSA 患者及其自然流产的胚胎。
通过固定或随机效应模型计算汇总比值比(OR)。
遗传变异与 IRSA 的关联。
系统综述共纳入 428 项病例对照研究(1990-2015 年),这些研究在 RSA 定义、患者临床评估和对照选择方面存在很大差异。在女性中,研究了 187 个基因中的 472 个变异。对 16 个基因中的 36 个变异进行了荟萃分析。在涉及免疫反应(IFNG、IL10、KIR2DS2、KIR2DS3、KIR2DS4、MBL、TNF)、凝血(F2、F5、PAI-1、PROZ)、代谢(GSTT1、MTHFR)和血管生成(NOS3、VEGFA)的基因中,与定义为三次或更多次自然流产(SA)的 IRSA 相关的 21 个变异被检测到。然而,OR 值适中(0.51-2.37),具有中等或较弱的流行病学可信度。在定义为两次或更多次和三次或更多次 SA 的 IRSA 之间,汇总 OR 差异较小。12.1%的研究纳入了男性伴侣,一项研究纳入了自然流产的胚胎。
候选基因研究显示与 IRSA 有中等相关性。由于 RSA 定义和参与者选择标准存在较大差异,因此需要达成共识。未来的 GAS 应同时包括男性和女性伴侣以及自然流产的胚胎。建议进行全基因组关联研究和对已确定的关联进行大规模复制。