Genetic diagnosis and outcomes of intracytoplasmic sperm injection in South Chinese patients with congenital bilateral aplasia of the vas deferens.

IF 2.4 3区 医学 Q2 ANDROLOGY
Haishan Hu, Qing Zhou, Yanlin Ma, Lingxiao Zhang
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引用次数: 0

Abstract

Background: Obstructive azoospermia commonly is caused by CBAVD(Congenital Bilateral Aplasia of the Vas Deferens), mainly due to the cystic fibrosis transmembrane conductance regulator (CFTR) and adhesion G protein-coupled receptor G2(ADGRG2) mutations. The genetic landscape for Chinese CBAVD patients is unclear, leading to debates over genetic screening, counseling, and assisted reproduction strategies. This study investigates the prevalence of CFTR and ADGRG2 mutations in a southern Chinese cohort of CBAVD patients and evaluates the impact of CFTR mutations on intracytoplasmic sperm injection (ICSI) outcomes.

Results: CFTR mutations were identified in 71.4% (30/42) of CBAVD patients, with a total of 36 CFTR mutation sites across 13 types identified, including two novel mutations. A novel ADGRG2 mutation was also detected. Betweenthe CFTR mutation-CBAVD group and the non-CBAVD OA group, a significant difference was observed only in the 2 Pronuclei(2PN) rate (79.5% vs 86.2%, P = 0.0065), while fertilization rates, pregnancy rates, miscarriage rates, and live birth rates showed no significant differences. Between the CFTR mutation-CBAVD group and the CBAVD group without CFTR mutation, there were no significant differences in fertilization rates, 2PN rates, pregnancy rates, miscarriage rates, or live birth rates.

Conclusion: Chinese CBAVD patients primarily exhibit mutations in the CFTR and ADGRG2 genes. Therefore, targeted gene testing for CFTR and ADGRG2 is more suitable compared to WES for CBAVD patients. Considering that the genetic factors of approximately 30% of CBAVD patients remain unknown, it is recommended to perform massive parallel sequencing for patients who test negative for CFTR and ADGRG2 gene screening. Despite these genetic factors, ICSI outcomes were not adversely affected, except for the 2PN rate. However, genetic counseling remains crucial for Chinese CBAVD patients before undergoing assisted reproduction.

华南先天性双侧输精管发育不全患者的遗传学诊断和卵胞浆内单精子注射的结果。
背景:梗阻性无精子症通常由囊性纤维化跨膜传导调节因子(CFTR)和粘附G蛋白偶联受体G2(ADGRG2)突变引起。中国 CBAVD 患者的遗传情况尚不清楚,因此在遗传筛查、咨询和辅助生殖策略方面存在争议。本研究调查了中国南方CBAVD患者队列中CFTR和ADGRG2突变的发生率,并评估了CFTR突变对卵胞浆内单精子显微注射(ICSI)结果的影响:结果:71.4%的CBAVD患者(30/42)发现了CFTR突变,共发现了13种类型的36个CFTR突变位点,其中包括两个新型突变。此外还发现了一种新型 ADGRG2 突变。在CFTR突变-CBAVD组和非CBAVD OA组之间,仅在2 Pronuclei(2PN)率方面观察到显著差异(79.5% vs 86.2%,P = 0.0065),而受精率、妊娠率、流产率和活产率则无显著差异。CFTR突变-CBAVD组与无CFTR突变的CBAVD组在受精率、2PN率、妊娠率、流产率和活产率方面无显著差异:结论:中国CBAVD患者主要表现为CFTR和ADGRG2基因突变。结论:中国 CBAVD 患者主要表现为 CFTR 和 ADGRG2 基因突变,因此,与 WES 相比,CFTR 和 ADGRG2 的靶向基因检测更适合 CBAVD 患者。考虑到约30%的CBAVD患者的遗传因素仍然未知,建议对CFTR和ADGRG2基因筛查阴性的患者进行大规模平行测序。尽管存在这些遗传因素,但除了 2PN 率外,ICSI 的结果并未受到不利影响。然而,对于中国的CBAVD患者来说,在接受辅助生殖之前,遗传咨询仍然至关重要。
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
Basic and Clinical Andrology
Basic and Clinical Andrology Medicine-Urology
CiteScore
3.50
自引率
0.00%
发文量
21
审稿时长
22 weeks
期刊介绍: Basic and Clinical Andrology is an open access journal in the domain of andrology covering all aspects of male reproductive and sexual health in both human and animal models. The journal aims to bring to light the various clinical advancements and research developments in andrology from the international community.
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