Associations of SLC6A20 genetic polymorphisms with Hirschsprung's disease in a Southern Chinese population

被引：0
作者：
Xie, Xiaoli [1 ]
He, Qiuming [1 ]
Huang, Lihua [1 ]
Li, Le [1 ]
Yao, Yuxiao [1 ]
Xia, Huimin [1 ]
Zhao, Jinglu [1 ]
Zhong, Wei [1 ]
Zhang, Yan [1 ]
机构：
[1] Guangzhou Med Univ, Guangzhou Inst Pediat, Dept Pediat Surg, Guangzhou Women & Childrens Med Ctr, Guangzhou 510623, Guangdong, Peoples R China
来源：
BIOSCIENCE REPORTS | 2019年 / 39卷
基金：
中国国家自然科学基金; 中国博士后科学基金;
关键词：
IDENTIFICATION; EXPRESSION; BOWEL; RET;
D O I：
10.1042/BSR20182290
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
Hirschsprung's disease (HSCR) is a neurodevelopmental disorder characterized by the absence of nerves in intestine with strong genetic components. SLC6A20 was found to be associated with HSCR in Korean population waiting for replication in an independent cohort. In the present study, ten single nucleotide polymorphisms (SNPs) in the SLC6A20 were selected from Southern Chinese with 1470 HSCR cases and 1473 ethnically matched healthy controls. Our results indicated that SNP rs7640009 was associated with HSCR and SLC6A20 has a gene-dose effect in the extent of the aganglionic segment during enteric nervous system (ENS) development. It is the first time to reveal the relationship between SNP rs2191026 and HSCR-associated enterocolitis (HAEC) susceptibility.
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