P53 p.a g72pro变异在复发性妊娠丢失、复发性植入失败和体外受精结果中的作用

N. Kaur, M. Eltom, Karen Cheung, S. Banka, L. Mohiyiddeen
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摘要

p53 p.a g72pro变异在复发性妊娠丢失、复发性植入失败和IVF结局中的作用存在争议,目前的研究结果也不一致。本系统综述旨在总结TP53 p.a g72pro变异在自然受孕和辅助受孕后复发性妊娠丢失中的作用。在MEDLINE、EMBASE和CENTRAL电子数据库中检索1998年至2020年4月间发表的文献。建立了纳入和排除标准及检索词。人工检索检索到的文章的参考文献,以确定其他相关论文,包括会议摘要。共纳入9项病例对照研究(1041例)、6项病例对照研究(382例)和7项研究(3403例),分别探讨了TP53 p.a g72pro变异在复发性妊娠丢失、复发性植入失败和IVF结局中的作用。综合基因型频率提示Pro/Pro基因型与复发性流产和Arg/Pro基因型与复发性植入失败之间可能存在关联。然而,TP53 p.a g72pro变异与复发性妊娠丢失、复发性植入失败或IVF结果之间的关系尚未明确确立。总之,TP53变异基因分型患者可能使我们能够确定原因不明的复发性妊娠丢失患者的病因,并在IVF治疗开始前发现有复发性植入失败风险的个体。此外,探索p53蛋白的作用机制可能为我们提供潜在的治疗方法。
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Role of P53 p.Arg72Pro Variant in Recurrent Pregnancy Loss, Recurrent Implantation Failure and IVF Outcome
The role of p53 p.Arg72Pro variant in recurrent pregnancy loss, recurrent implantation failure and IVF outcome is controversial and research so far has yielded inconsistent results. This systematic review aims to summarise the literature on the role of TP53 p.Arg72Pro variant in recurrent pregnancy loss following natural and assisted conception. A comprehensive literature search was conducted on MEDLINE, EMBASE and CENTRAL electronic databases for literature published between 1998 and April 2020. Inclusion and exclusion criteria and search terms were established. References of retrieved articles were hand searched to identify other relevant papers including conference abstracts. In total, 9 case control studies (1041 patients), 6 case control studies (382 patients) and 7 studies (3403) were included examining the role of TP53 p.Arg72Pro variant in recurrent pregnancy loss, recurrent implantation failure and IVF outcome respectively. Combined genotype frequencies suggest that there may be an association between Pro/Pro genotype and recurrent pregnancy loss and Arg/Pro genotype and recurrent implantation failure. However, the association between TP53 p.Arg72Pro variant and recurrent pregnancy loss, recurrent implantation failure or IVF outcomes has not been clearly established. In conclusion, genotyping patients for the TP53 variant may enable us to identify an aetiology for patients experiencing unexplained recurrent pregnancy loss and detect individuals at risk of recurrent implantation failure before IVF treatment is initiated. Furthermore, exploring the mechanisms of action of the p53 protein may provide us with an insight into potential treatments.
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