Oncotarget

Meta-Analysis:

G protein beta 3(GNβ3) C825T polymorphism and irritable bowel syndrome susceptibility: an updated meta-analysis based on eleven case-control studies

Dongbo Jiang, Dong Huang, Weiming Cai, Ting Li, Yan Wang, Huayan Chen, Tangming Guan _ and Xiaoli Ma

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Oncotarget. 2018; 9:2770-2781. https://doi.org/10.18632/oncotarget.23449

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Abstract

Dongbo Jiang1,*, Dong Huang1,*, Weiming Cai1,2, Ting Li1, Yan Wang1, Huayan Chen1, Tangming Guan1,2 and Xiaoli Ma1,3

1Department of Pharmacy, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong Province 524001, China

2Laboratory of Clinical Pharmacy, Guangdong Medical University, Zhanjiang, Guangdong Province 524001, China

3Department of Clinical Pharmacy, Guangdong Medical University, Zhanjiang, Guangdong Province 524001, China

*These authors contributed equally to this work

Correspondence to:

Tangming Guan, email: gdmcgtm@163.com

Xiaoli Ma, email: gdmu_maxiaoli@163.com

Keywords: GNβ3; polymorphism; irritable bowel syndrome; case-control; meta-analysis

Received: September 06, 2017     Accepted: October 31, 2017     Published: December 15, 2017

ABSTRACT

Several studies have reported an association between GNβ3 C825T polymorphism and irritable bowel syndrome (IBS). However, the results remain inconclusive and controversial, particularly for the data derived from different ethnicities and IBS subtypes. Therefore, we performed an updated meta-analysis to evaluate this association. All eligible case-control studies that met the search criteria were retrieved from multiple databases, and eleven case-control studies were included for detailed evaluation. The pooled odds ratios (ORs) with 95% confidence intervals (95% CIs) were calculated to assess the strengths of the association between GNβ3 C825T polymorphism and susceptibility to IBS and its subtypes. Our meta-analysis found no significantly associations of GNβ3 C825T polymorphism with IBS risk in all populations. Whereas the C allele was demonstrated to be a decreased risk factor for constipation predominant IBS (IBS-C) in allele model. Additionally, the CC genotype was found to be associated with increased diarrhea predominant IBS (IBS-D) risk in recessive model. Subgroup analysis by ethnicity revealed that these associations held true for the Asian subpopulation. In conclusion, this meta-analysis suggests the C allele of GNβ3 C825T might be associated with a decreased risk of IBS-C, and the CC genotype of GNβ3 might be associated with increased IBS-D risk.


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