The importance of integrating genetic testing into reproductive medicine: a retrospective observational study investigating the monogenic causes of human infertility in couples considering ICSI

IF 2.3 3区 生物学 Q2 GENETICS & HEREDITY
Sara H. El-Dessouky, Wessam E. Sharaf-Eldin, Islam F. Soliman, Mona M. Aboulghar, Ahmed Abou El-Serour, Ashraf Ali, Sameh Senousy, Lova Matsa, Mohamed Maher, Dalia S. Zolfokar, Mohamed A. Youssef, Hatem A. Mousa, Maha M. Eid, Maha S. Zaki, Ebtesam M. Abdalla
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引用次数: 0

Abstract

The genetic landscape of human infertility is complex with diverse etiologies. Identifying the underlying etiology is crucial for guiding reproductive decisions and improving management for infertile couples. Here, we aim to report on the molecular spectrum of monogenic genetic causes of reproductive failure. Over a 3-year period, we recruited all infertile couples considering assisted reproductive technologies (ART) for whom the underlying genetic cause had been identified, in either partner, using exome sequencing (ES). Clinical data of all participants along with their hormonal profiles, sonographic findings and spermograms were recorded. The study included 50 couples with primary infertility. Clinically, male factor infertility was documented in 26 patients, female factor infertility in 10, while reproductive failure was unexplained in the remaining 14 couples. All participating couples had potentially disease-causing variants in infertility genes. ES identified variants related to male infertility in 26 men, while variants in female infertility-related genes were detected in the remaining couples (n = 24). According to ACMG classification criteria, 78% (39/50) of couples harbored pathogenic/likely pathogenic (P/LP) variants, whereas 22% (11/50) carried variants of uncertain significance (VUS). In view of the identified genetic etiologies, the cohort was stratified into two groups based on the predicted reproductive outcome: (1) couples with significantly impaired reproductive potential, and (2) couples who can have biological children using appropriate medical interventions. However, classifications involving VUS were interpreted cautiously and considered exploratory. This study provides further evidence for the molecular heterogeneity of human infertility and highlights the usefulness of genetic testing for infertile couples pursuing ARTs.
将基因检测纳入生殖医学的重要性:一项回顾性观察性研究调查了考虑ICSI的夫妇的人类不育的单基因原因。
人类不孕症的遗传景观是复杂的多种病因。确定潜在的病因对于指导生育决策和改善不孕夫妇的管理至关重要。在这里,我们的目的是报告单基因遗传原因生殖失败的分子谱。在3年的时间里,我们招募了所有考虑辅助生殖技术(ART)的不育夫妇,他们的潜在遗传原因已经被确定,在任何一方,使用外显子组测序(ES)。记录所有参与者的临床资料以及他们的激素谱、超声检查结果和精子图。该研究包括50对患有原发性不孕症的夫妇。临床上,男性因素导致的不孕26例,女性因素导致的不孕10例,其余14对夫妇不孕原因不明。所有参与研究的夫妇都有可能致病的不育基因变异。ES在26名男性中发现了与男性不育相关的变异,而在其余夫妇中发现了与女性不育相关的基因变异(n = 24)。根据ACMG分类标准,78%(39/50)的夫妇携带致病/可能致病(P/LP)变异,22%(11/50)携带不确定意义变异(VUS)。鉴于已确定的遗传病因,根据预测的生殖结果将队列分为两组:(1)生殖潜力明显受损的夫妇,(2)通过适当的医疗干预可以生育亲生子女的夫妇。然而,涉及VUS的分类被谨慎解释,并被认为是探索性的。这项研究为人类不孕症的分子异质性提供了进一步的证据,并强调了基因检测对寻求辅助生殖技术的不育夫妇的有用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Human Genetics
Journal of Human Genetics 生物-遗传学
CiteScore
7.20
自引率
0.00%
发文量
101
审稿时长
4-8 weeks
期刊介绍: The Journal of Human Genetics is an international journal publishing articles on human genetics, including medical genetics and human genome analysis. It covers all aspects of human genetics, including molecular genetics, clinical genetics, behavioral genetics, immunogenetics, pharmacogenomics, population genetics, functional genomics, epigenetics, genetic counseling and gene therapy. Articles on the following areas are especially welcome: genetic factors of monogenic and complex disorders, genome-wide association studies, genetic epidemiology, cancer genetics, personal genomics, genotype-phenotype relationships and genome diversity.
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