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伊朗男性极重度少精子症与 CFTR、AR 基因常见突变、Y 染色体微缺失和核型异常的关系。

The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian men.

机构信息

Department of Biology, Arsanjan Branch, Islamic Azad University, Arsanjan, Iran.

Department of Biology, Borujerd Branch, Islamic Azad University, Borujerd, Iran.

出版信息

Genes Genomics. 2023 Apr;45(4):519-529. doi: 10.1007/s13258-022-01300-6. Epub 2022 Aug 18.

Abstract

BACKGROUND

Male infertility due to very severe oligozoospermia has been associated with some genetic risk factors.

OBJECTIVE

To investigate the distribution of the mutations in the CFTR gene, the CAG-repeat expansion of the AR gene, also Y chromosome microdeletions and karyotyping abnormalities in very severe oligozoospermia patients.

METHODS

In the present case-control study, 200 patients and 200 fertile males were enrolled. All patients and control group were karyotyped. Microdeletions were evaluated using multiplex PCR. Five common CFTR mutations were genotyped using the ARMS-PCR technique. The CAG-repeat expansion in the AR gene was evaluated for each individual using sequencing.

RESULTS

Overall 4% of cases shows a numerical and structural abnormality. 7.5% of patients had a deletion in one of the AZF regions on Yq, and 3.5% had a deletion in two regions. F508del was the most common (4.5%) CFTR gene mutation; G542X, and W1282X were detected with 1.5% and 1% respectively. One patient was found to have AZFa microdeletion and F508del in heterozygote form; one patient had AZFb microdeletion with F508del. F508del was seen as compound heterozygous with G542X in one patient and with W1282X in the other patient. The difference in the mean of the CAG-repeats in the AR gene in patients and control groups was statistically significant (P = 0.04).

CONCLUSION

Our study shows the genetic mutations in men with severe oligozoospermia and given the possibility of transmission of these disorders to the next generation by fertilization, counseling and genetic testing are suggested for these couples before considering ICSI.

摘要

背景

严重少精子症导致的男性不育与一些遗传风险因素有关。

目的

研究严重少精子症患者中 CFTR 基因突变、AR 基因 CAG 重复扩增、Y 染色体微缺失和核型异常的分布情况。

方法

在本病例对照研究中,纳入了 200 例患者和 200 例正常生育男性。所有患者和对照组均进行核型分析。采用多重 PCR 评估微缺失情况。使用 ARMS-PCR 技术对 5 种常见的 CFTR 基因突变进行基因分型。使用测序技术评估 AR 基因中的 CAG 重复扩增情况。

结果

总体而言,4%的病例存在数量和结构异常。7.5%的患者在 Yq 上的一个 AZF 区域存在缺失,3.5%的患者在两个区域存在缺失。F508del 是最常见的(4.5%)CFTR 基因突变;G542X 和 W1282X 的检出率分别为 1.5%和 1%。一名患者被发现存在杂合形式的 AZFa 微缺失和 F508del;一名患者存在 AZFb 微缺失和 F508del。F508del 与 G542X 复合杂合存在于一名患者中,与 W1282X 复合杂合存在于另一名患者中。患者和对照组之间 AR 基因中 CAG 重复的平均值差异具有统计学意义(P=0.04)。

结论

我们的研究显示了严重少精子症男性中的遗传突变,并且由于这些疾病有可能通过受精传递给下一代,因此建议这些夫妇在考虑 ICSI 之前进行咨询和基因测试。

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