Literature DB >> 28830823

Lack of association between SLC5A7 polymorphisms and Tourette syndrome in a Chinese Han population.

Wenmiao Liu1, Shiyan Qiu2, Chuanping Gao3, Guiju Wang4, Shiguo Liu5, Hongzai Guan6.   

Abstract

Although Tourette syndrome (TS) is a chronic neuropsychiatric disorder whose pathogenesis remains unclear, genetic factors play an important role in the occurrence and development. A variety of studies have been shown that the candidate genes related to cholinergic neurons may be associated with the onset of TS. To investigate the association between the SLC5A7 polymorphisms and Tourette syndrome (TS) in the Chinese Han population, the SNP rs1013940, rs2433718, and rs4676169 were genotyped in 401 TS trios and 400 controls. The transmission disequilibrium test (TDT) and haplotype relative risk (HRR) compared genetic distributions of trios, while the chi-square test compared patients and controls. However, no transmission disequilibrium was found between the three SLC5A7 SNPs and TS. Therefore, we think that this gene may not be the main risk factor on the onset of TS. However, these results should be further validated in different populations.
Copyright © 2017. Published by Elsevier B.V.

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Keywords:  Case–control study; Family-based study; Haplotype relative risk; SLC5A7 gene; Tourette syndrome; Transmission disequilibrium test

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Year:  2017        PMID: 28830823     DOI: 10.1016/j.neulet.2017.08.041

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  1 in total

1.  ASH1L may contribute to the risk of Tourette syndrome: Combination of family-based analysis and case-control study.

Authors:  Wenmiao Liu; Lulu Xu; Cheng Zhang; Lu Shen; Jicheng Dong; Han Zhang; Shiguo Liu; Fengyuan Che; Xueping Zheng
Journal:  Brain Behav       Date:  2022-03-20       Impact factor: 3.405

  1 in total

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