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5-羟色胺受体3A和5-羟色胺受体3E基因多态性与腹泻型肠易激综合征风险:一项荟萃分析的证据

HTR3A and HTR3E gene polymorphisms and diarrhea predominant irritable bowel syndrome risk: evidence from a meta-analysis.

作者信息

Guan Tangming, Li Ting, Cai Weiming, Huang Dong, Ouyang Peipei, Wang Yan, Chen Huayan, Wu Kefeng, Ma Xiaoli

机构信息

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

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

出版信息

Oncotarget. 2017 Jul 29;8(59):100459-100468. doi: 10.18632/oncotarget.19682. eCollection 2017 Nov 21.

Abstract

Several studies have reported an association between serotonin receptor type 3 (5-HT) subunit genes (rs1062613) and (rs62625044) and diarrhea predominant irritable bowel syndrome (IBS-D). However, the results remain inconclusive and controversial, particularly for the data derived from different ethnicities and genders. Therefore, we performed a meta-analysis to evaluate this association. All eligible case-control studies that met the search criteria were retrieved from multiple databases, and five 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 associations of (rs1062613) and (rs62625044) polymorphisms with IBS-D risk. Our results revealed statistically significant associations of the (rs1062613, C/T) polymorphism with a decreased risk of IBS-D in all genetic models. Additionally, the HTR3E (rs62625044, G/A) polymorphism was also found to be significantly associated with a decreased risk of IBS-D in the allele and recessive models. Subgroup analysis revealed that these associations held true especially for Asians and female. In conclusion, this meta-analysis suggested that the C allele of (rs1062613) and the G allele of (rs62625044) are associated with a decreased risk of IBS-D.

摘要

多项研究报告了血清素3型受体(5-HT)亚基基因(rs1062613)和(rs62625044)与腹泻型肠易激综合征(IBS-D)之间的关联。然而,结果仍无定论且存在争议,尤其是来自不同种族和性别的数据。因此,我们进行了一项荟萃分析来评估这种关联。从多个数据库中检索出所有符合搜索标准的合格病例对照研究,并纳入五项病例对照研究进行详细评估。计算合并比值比(OR)及其95%置信区间(95%CI),以评估(rs1062613)和(rs62625044)多态性与IBS-D风险关联的强度。我们的结果显示,在所有遗传模型中,(rs1062613,C/T)多态性与IBS-D风险降低存在统计学显著关联。此外,还发现HTR3E(rs62625044,G/A)多态性在等位基因模型和隐性模型中也与IBS-D风险降低显著相关。亚组分析表明,这些关联尤其在亚洲人和女性中成立。总之,这项荟萃分析表明,(rs1062613)的C等位基因和(rs62625044)的G等位基因与IBS-D风险降低相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f9f/5725034/cf7cf11ff3b7/oncotarget-08-100459-g001.jpg

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