Suppr超能文献

应激相关基因多态性与非综合征性唇裂伴或不伴腭裂的风险

Polymorphisms of stress-related genes and the risk of nonsyndromic cleft lip with or without cleft palate.

作者信息

Mostowska Adrianna, Hozyasz Kamil K, Wojcicka Karolina, Lianeri Margarita, Jagodzinski Pawel P

机构信息

Department of Biochemistry and Molecular Biology, Poznan University of Medical Sciences, Poznan, Poland.

出版信息

Birth Defects Res A Clin Mol Teratol. 2011 Nov;91(11):948-55. doi: 10.1002/bdra.20843. Epub 2011 Aug 24.

Abstract

BACKGROUND

Nonsyndromic cleft lip with or without cleft palate (NCL/P) is a common structural malformation with a complex and multifactorial etiology. It has been shown that maternal psychological stress in the periconceptional period can contribute to an increase in the risk of NCL/P affecting pregnancy.

METHODS

Twenty-four single nucleotide polymorphisms of 11 stress-related genes (COMT, CRHR1, FKBP5, GABRA6, HSD11β2, MAOA, NPY, NR3C1, SERPINA6, SLC6A4, and TPH2) were investigated in 220 healthy mothers of children with facial clefts and 210 matched controls using restriction fragment-length polymorphism and high-resolution melting analysis.

RESULTS

We found that polymorphisms in SLC6A4, TPH2, and SERPINA6 appear to be maternal factors increasing the risk of having a child with facial clefts. The closest correlations with NCL/P were found for the SLC6A4 rs2020942 and TPH2 rs10879357 gene variants (odds ratio [OR], 1.720; 95% confidence interval [CI], 1.158-2.553; p = 0.0069; p(trend) = 0.0036; and OR, 1.837; 95% CI, 1.226-2.753, p = 0.0030, p(trend) = 0.0057; respectively). Moreover, haplotype analysis revealed that several combinations of markers in SLC6A4, TPH2, and SERPINA6 might be significantly associated with the risk of NCL/P affected pregnancies. However, these associations were not statistically significant after correction for multiple testing.

CONCLUSION

This study suggests that nucleotide variants of genes encoding components of the hypothalamus-pituitary-adrenal axis and serotoninergic system have a role in the etiology of NCL/P in the Polish population. SLC6A4, TPH2, and SERPINA6 might be novel candidate genes for this common congenital anomaly.

摘要

背景

非综合征性唇裂伴或不伴腭裂(NCL/P)是一种常见的结构畸形,其病因复杂且具有多因素性。研究表明,受孕期间母亲的心理压力会增加影响妊娠的NCL/P风险。

方法

采用限制性片段长度多态性和高分辨率熔解分析,对220名面部裂隙患儿的健康母亲和210名匹配对照进行了11个应激相关基因(COMT、CRHR1、FKBP5、GABRA6、HSD11β2、MAOA、NPY、NR3C1、SERPINA6、SLC6A4和TPH2)的24个单核苷酸多态性研究。

结果

我们发现SLC6A4、TPH2和SERPINA6基因多态性似乎是增加生育面部裂隙患儿风险的母体因素。SLC6A4 rs2020942和TPH2 rs10879357基因变异与NCL/P的相关性最为密切(优势比[OR],1.720;95%置信区间[CI],1.158 - 2.553;p = 0.0069;p(趋势)= 0.0036;以及OR,1.837;95% CI,1.226 - 2.753,p = 0.0030,p(趋势)= 0.0057;)。此外,单倍型分析显示,SLC6A4、TPH2和SERPINA6中几个标记的组合可能与受NCL/P影响的妊娠风险显著相关。然而,在进行多重检验校正后,这些关联无统计学意义。

结论

本研究表明,编码下丘脑 - 垂体 - 肾上腺轴和5 - 羟色胺能系统成分的基因的核苷酸变异在波兰人群NCL/P的病因学中起作用。SLC6A4、TPH2和SERPINA6可能是这种常见先天性异常的新候选基因。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验