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β3 - 肾上腺素能受体与毒蕈碱型胆碱能受体3基因多态性在肠易激综合征中的遗传关联。

A genetic association between ß3-aderenoceptor and cholinergic receptor muscarinic 3 polymorphisms in irritable bowel syndrome.

作者信息

Onodera Saori, Chiba Toshimi, Sugai Tamotsu, Habano Wataru

机构信息

Department of Internal Medicine, Iwate Medical University, Iwate, Japan.

出版信息

Hepatogastroenterology. 2011 Sep-Oct;58(110-111):1474-8. doi: 10.5754/hge10153. Epub 2011 Jul 15.

Abstract

BACKGROUND/AIMS: We examined the association of ß3-adrenoceptor (ß3-AR) and cholinergic receptor muscarinic 3 (CHRM3) polymorphisms with irritable bowel syndrome (IBS).

METHODOLOGY

DNA was obtained from 81 IBS patients (39 diarrhea type, IBS-D; 25 constipation type, IBS-C, 5 mixed type, IBS-M; and 12 unsubtyped, IBS-U) and 73 controls. For the analyses IBS-(M + U) was combined into one group (NonDNonC). ß3-AR and CHRM3 polymorphisms were determined by the polymerase chain reaction (PCR)-based restriction fragment length polymorphism (RFLP) method.

RESULTS

The ß3-AR genotype frequencies of T/C in IBS patients were significantly higher compared to those in controls. The distribution of the CHRM3 genotypes, C/C, T/C and T/T, was not significantly different between IBS patients and controls. The distribution of the ß3-AR and CHRM3 genotypes was not significantly different between IBS-D, IBS-C and NonDNonC. The frequencies of the CHRM3 genotypes in IBS were significantly different between disease duration greater than and less than 3 years.

CONCLUSIONS

ß3-AR polymorphisms in IBS patients are different compared to controls, and CHRM3 polymorphisms are also likely associated with disease duration in IBS. ß3-AR and CHRM3 polymorphisms could be associated with IBS.

摘要

背景/目的:我们研究了β3-肾上腺素能受体(β3-AR)和毒蕈碱型胆碱能受体3(CHRM3)基因多态性与肠易激综合征(IBS)的关联。

方法

从81例IBS患者(39例腹泻型,IBS-D;25例便秘型,IBS-C;5例混合型,IBS-M;12例未分型,IBS-U)和73例对照中获取DNA。分析时,将IBS-(M + U)合并为一组(非腹泻非便秘型)。采用基于聚合酶链反应(PCR)的限制性片段长度多态性(RFLP)方法测定β3-AR和CHRM3基因多态性。

结果

IBS患者中β3-AR基因T/C基因型频率显著高于对照组。IBS患者和对照组之间CHRM3基因型C/C、T/C和T/T的分布无显著差异。IBS-D、IBS-C和非腹泻非便秘型之间β3-AR和CHRM3基因型的分布无显著差异。IBS患者中CHRM3基因型频率在病程大于和小于3年之间存在显著差异。

结论

IBS患者的β3-AR基因多态性与对照组不同,CHRM3基因多态性也可能与IBS的病程有关。β3-AR和CHRM3基因多态性可能与IBS有关。

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