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韩国人群中黏蛋白 4 () 多态性与特发性复发性妊娠丢失的关联研究。

Association Study between Mucin 4 () Polymorphisms and Idiopathic Recurrent Pregnancy Loss in a Korean Population.

机构信息

Department of Obstetrics and Gynecology, CHA Bundang Medical Center, CHA University, Seongnam 13496, Korea.

Department of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.

出版信息

Genes (Basel). 2022 May 24;13(6):937. doi: 10.3390/genes13060937.

DOI:10.3390/genes13060937
PMID:35741699
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9222798/
Abstract

Recurrent pregnancy loss (RPL) is the loss of two or more consecutive pregnancies before 20 weeks of gestational age. Our study investigated whether mucin 4 (MUC4) polymorphisms are associated with RPL. MUC polymorphisms (rs882605 C>A, rs1104760 A>G, rs2688513 A>G, rs2258447 C>T, and rs2291652 A>G) were genotyped in 374 women with RPL and 239 controls of Korean ethnicity using polymerase chain reaction-restriction fragment length polymorphism analysis and the TaqMan probe SNP genotyping assay. Differences in genotype frequencies between cases of RPL and the controls were compared. MUC4 rs882605 C>A and rs1104760 A>G polymorphisms were associated with increased incidence of RPL in three and four or more pregnancy loss patients. The haplotype analyses showed a tendency for the allelic effect including the association of MUC4 rs882605 A and rs1104760 G alleles with increased incidence of RPL. In addition, the MUC4 rs882605 CA/MUC4 rs2258447 CC genotype combination was associated with increased RPL prevalence. The two exonic polymorphisms lead to amino acid changes of protein and may act as pathogenic variants for RPL. In conclusion, the MUC4 rs882605 C>A and MUC4 rs1104760 A>G polymorphisms were associated with the susceptibility of RPL and we considered them as potential biomarkers for RPL.

摘要

复发性妊娠丢失(RPL)是指在妊娠 20 周前连续两次或两次以上的妊娠丢失。我们的研究调查了粘蛋白 4(MUC4)多态性是否与 RPL 相关。使用聚合酶链反应-限制性片段长度多态性分析和 TaqMan 探针 SNP 基因分型检测,对 374 名 RPL 患者和 239 名韩国裔对照者的 MUC 多态性(rs882605 C>A、rs1104760 A>G、rs2688513 A>G、rs2258447 C>T 和 rs2291652 A>G)进行了基因分型。比较了 RPL 病例和对照组之间基因型频率的差异。MUC4 rs882605 C>A 和 rs1104760 A>G 多态性与三例及以上妊娠丢失患者 RPL 发生率增加有关。单体型分析显示,MUC4 rs882605 A 和 rs1104760 G 等位基因的等位基因效应与 RPL 发生率增加有关。此外,MUC4 rs882605 CA/MUC4 rs2258447 CC 基因型组合与 RPL 患病率增加有关。这两个外显子多态性导致蛋白质氨基酸的改变,可能作为 RPL 的致病变异。总之,MUC4 rs882605 C>A 和 MUC4 rs1104760 A>G 多态性与 RPL 的易感性相关,我们认为它们是 RPL 的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b3/9222798/c85411f31711/genes-13-00937-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b3/9222798/c85411f31711/genes-13-00937-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06b3/9222798/c85411f31711/genes-13-00937-g001.jpg

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