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中国中部 CAVD 患者中 CFTR 变异与 ART 结局的相关性。

Correlation between CFTR variants and outcomes of ART in patients with CAVD in Central China.

机构信息

Henan Provincial People's Hospital, Henan Provincial Reproductive Hospital, People's Hospital of Henan University, Zhengzhou, 450003, Henan, China.

出版信息

Sci Rep. 2023 Jan 5;13(1):64. doi: 10.1038/s41598-022-26384-8.

Abstract

Biallelic variants in Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) are the main pathogenic factor of congenital absence of the vas deferens (CAVD), including congenital bilateral absence of the vas deferens (CBAVD) and congenital unilateral absence of the vas deferens (CUAVD). However, there are few reports about the correlation between CFTR variant and outcomes of assisted reproductive technology (ART) in CAVD patients of China. In this study, 104 patients with CAVD were recruited in Central China, and provided gene detection by the whole-exome sequencing, among them 69% (72/104) carried at least one variant in CFTR and one carried adhesion G protein-coupled receptor G2 (ADGRG2) variant. A total of 81 CAVD patients were treated with ART, of which 21 and 60 carried none or at least one variant in CFTR, respectively. The fertilization rate, cleavage rate, effective embryo rate, implantation rate, clinical pregnancy rate and live birth rate per fresh embryo transfer were compared between patients with and without CFTR variants. It was found that the ART outcomes had no significant difference whether the patients carried the CFTR variant or not. In addition, all of the offspring were healthy after follow-up. In conclusion, rare CFTR variants may play a major role in patients with CAVD in Central China, which were greatly different from other descent. There was no significant difference in ART outcomes in CAVD patients with or without CFTR variants. The limitations of this study were that there was no statistical analysis of the sperm quality through TESA and conclusions were relatively limited due to the small sample size of the study.

摘要

双等位基因突变是先天性输精管缺如(CAVD)的主要致病因素,包括先天性双侧输精管缺如(CBAVD)和先天性单侧输精管缺如(CUAVD)。然而,关于中国 CAVD 患者 CFTR 变异与辅助生殖技术(ART)结局之间的相关性报道较少。本研究纳入了华中地区 104 例 CAVD 患者,通过全外显子组测序进行基因检测,其中 69%(72/104)患者携带至少一个 CFTR 变异和一个黏附 G 蛋白偶联受体 G2(ADGRG2)变异。共有 81 例 CAVD 患者接受了 ART 治疗,其中 21 例和 60 例患者分别携带 CFTR 无变异或至少一个变异。比较了 CFTR 变异患者和无 CFTR 变异患者之间的受精率、卵裂率、有效胚胎率、着床率、临床妊娠率和新鲜胚胎移植活产率。结果发现,无论患者是否携带 CFTR 变异,ART 结局均无显著差异。此外,随访后所有后代均健康。总之,罕见的 CFTR 变异可能在华中地区的 CAVD 患者中起主要作用,与其他人群有很大不同。在携带或不携带 CFTR 变异的 CAVD 患者中,ART 结局没有显著差异。本研究的局限性在于未对 TESA 中的精子质量进行统计学分析,并且由于研究样本量较小,结论相对有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53dd/9814922/3714c6c4dd4a/41598_2022_26384_Fig1_HTML.jpg

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