Literature DB >> 31840934

Evaluation of the relationships of the WBP1L gene with schizophrenia and the general psychopathology scale based on a case-control study.

Fanglin Guan1,2, Tong Ni1,2, Wei Han1,2, Huali Lin3, Bo Zhang4, Gang Chen1,5, Li Zhu1,2, Dan Liu1,2, Tianxiao Zhang6.   

Abstract

WBP1L is a target of microRNA 137 (miR-137) and has been considered a candidate gene for schizophrenia (SCZ). To investigate the relationships between WBP1L and SCZ and its related symptom scales, a total of 5,993 Chinese Han subjects, including 2,128 SCZ patients and 3,865 controls, were enrolled. In addition, an independent sample set for replication study including 1,052 SCZ patients and 2,124 controls were also recruited. Thirty-two tag single nucleotide polymorphisms (SNPs) located within gene region of WBP1L were selected for genotyping and analyzing. The expression quantitative trait loci (eQTL) effects for the targeted SNPs were investigated with gene expression data from multiple human tissues. Rs4147157 (OR = 0.84, p = 1.51 × 10-5 ) and rs284854 (OR = 1.14, p = 7.00 × 10-4 ) were significantly associated with SCZ disease status and these association signals were replicated in our replication sample. A significant association was identified between rs4147157 and the general (β = -.66, p = .001) and total (β = -.8, p = .0042) scores of positive and negative syndrome scale scores in SCZ patients. Both SNPs were significant eQTL for genes around WBP1L in human brain tissues including ARL3 and AS3MT. To conclude, SNPs rs4147157 and rs284854 were associated with SCZ in the Chinese Han population. Additionally, rs4147157 was significantly associated with specific symptom features of SCZ.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  zzm321990WBP1L; PANSS; common polymorphisms; eQTL; schizophrenia

Mesh:

Year:  2019        PMID: 31840934     DOI: 10.1002/ajmg.b.32773

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  9 in total

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2.  Evaluation of genetic susceptibility of common variants in SOX9 in patients with congenital talipes equinovarus in the Han Chinese population.

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5.  Expression of the GZMB Gene Polymorphism, SNP rs8192917, in 990 Han Chinese Patients with Postoperative Keloids.

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7.  The effects of common variants in MDM2 and GNRH2 genes on the risk and survival of osteosarcoma in Han populations from Northwest China.

Authors:  Weilou Feng; Zhi Wang; Dongxu Feng; Yangjun Zhu; Kun Zhang; Wei Huang
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Authors:  Bin Tian; Xin Kang; Liang Zhang; Jiang Zheng; Zandong Zhao
Journal:  J Orthop Surg Res       Date:  2020-08-26       Impact factor: 2.359

9.  Common Variants in NUS1 and GP2 Genes Contributed to the Risk of Gestational Diabetes Mellitus.

Authors:  Tianxiao Zhang; Longrui Zhao; Shujin Wang; Juan Liu; Ying Chang; Louyan Ma; Jia Feng; Yu Niu
Journal:  Front Endocrinol (Lausanne)       Date:  2021-06-29       Impact factor: 5.555

  9 in total

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