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荟萃分析:编码血清素转运蛋白活性的基因中的一个功能多态性与肠易激综合征无关。

Meta-analysis: a functional polymorphism in the gene encoding for activity of the serotonin transporter protein is not associated with the irritable bowel syndrome.

作者信息

Van Kerkhoven L A S, Laheij R J F, Jansen J B M J

机构信息

Department of Gastroenterology and Hepatology, Radboud University, Nijmegen Medical Center, Nijmegen, The Netherlands.

出版信息

Aliment Pharmacol Ther. 2007 Oct 1;26(7):979-86. doi: 10.1111/j.1365-2036.2007.03453.x.

Abstract

BACKGROUND

Serotonin is associated with symptoms of the irritable bowel syndrome, its action is terminated by the serotonin transporter protein.

AIM

To assess the association between a functional polymorphism in the gene encoding for activity of the serotonin transporter protein and the irritable bowel syndrome.

METHODS

Meta-analysis of studies identified through a Medline, PubMed and Web of Science search, describing the prevalence of a polymorphism in the serotonin transporter gene creating long and short alleles.

RESULTS

Eight eligible studies described a total of 1034 patients with the irritable bowel syndrome, and 1377 healthy controls. Presence of the short allele is not associated with an increased risk for the irritable bowel syndrome: OR 1.0; 95% CI: 0.7-1.4 for homozygous subjects, and OR 1.0; 95% CI: 0.8-1.2 for homozygous subjects and heterozygotes together. Although Caucasians and Asians had diverging genotypic frequencies, no association with the shot allele and irritable bowel syndrome was observed in subgroups: Asians OR 1.2; 95% CI: 0.9-1.6 and OR 1.1; 95% CI: 0.2-5.9; Caucasians OR 0.9; 95% CI: 0.5-1.7 and OR 0.9; 95% CI: 0.7-1.2, respectively, for homozygous subjects alone and for homozygous subjects and heterozygotes together.

CONCLUSION

A genetic polymorphism in the gene encoding for activity of the serotonin transporter protein is not associated with the irritable bowel.

摘要

背景

血清素与肠易激综合征的症状相关,其作用通过血清素转运蛋白终止。

目的

评估血清素转运蛋白活性编码基因中的功能多态性与肠易激综合征之间的关联。

方法

通过对Medline、PubMed和科学网搜索所确定的研究进行荟萃分析,描述血清素转运基因中产生长等位基因和短等位基因的多态性患病率。

结果

八项符合条件的研究共描述了1034例肠易激综合征患者和1377例健康对照。短等位基因的存在与肠易激综合征风险增加无关:纯合子受试者的比值比为1.0;95%置信区间:0.7 - 1.4,纯合子受试者和杂合子合在一起的比值比为1.0;95%置信区间:0.8 - 1.2。尽管白种人和亚洲人的基因型频率不同,但在亚组中未观察到短等位基因与肠易激综合征的关联:亚洲人单独纯合子受试者的比值比为1.2;95%置信区间:0.9 - 1.6,纯合子受试者和杂合子合在一起的比值比为1.1;95%置信区间:0.2 - 5.9;白种人单独纯合子受试者的比值比为0.9;95%置信区间:0.5 - 1.7,纯合子受试者和杂合子合在一起的比值比为0.9;95%置信区间:0.7 - 1.2。

结论

血清素转运蛋白活性编码基因中的遗传多态性与肠易激综合征无关。

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