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首页> 外文期刊>Journal of clinical gastroenterology >Cannabinoid receptor 1 gene polymorphism and irritable bowel syndrome in the Korean population: a hypothesis-generating study.
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Cannabinoid receptor 1 gene polymorphism and irritable bowel syndrome in the Korean population: a hypothesis-generating study.

机译:朝鲜族人群中大麻素受体1基因多态性与肠易激综合症:一项假设产生的研究。

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OBJECTIVE: The cannabinoids affect gastrointestinal function and are thought to be involved in the pathogenesis of irritable bowel syndrome (IBS). We hypothesized that genetic variants of the cannabinoid receptor 1 gene (CNR1) might be associated with IBS. METHODS: One hundred sixty-two IBS patients, who met the Rome II criteria, and 423 healthy controls were subjected to genotyping of polymorphic triplet AAT repeats located in the 3-flanking region of the CNR1 gene. RESULTS: Allele frequencies of AAT triplet repeats in the CNR1 gene differed markedly between the controls and IBS patients (P<0.01). Controls had a lower frequency of distribution of 10 alleles or more. We divided the alleles into 2 groups (10), and 3 genotypes 10/>10. The CNR1 having>10/>10 AAT triplet repeats occurred with greater frequency in IBS patients than in the controls (P<0.01). A strong genotype association was observed between the CNR1 >10/>10 genotype and all IBS subtypes compared with controls (P<0.01 for each). The allele frequencies and the CNR1 genotypes did not differ between the 3 IBS subtypes. Symptom scores for abdominal discomfort or pain were higher in patients with the CNR1 >10/>10 genotype than in patients with the other genotypes (P<0.05). CONCLUSIONS: We found a different distribution of allelic frequency of AAT repeats in the CNR1 gene in healthy controls and IBS patients, and a significant association between the CNR1 >10/>10 genotype and IBS. These results suggest that the CNR1 gene is a potential candidate gene involved in IBS in Korea.
机译:目的:大麻素影响肠胃功能,并被认为与肠易激综合征(IBS)的发病机制有关。我们假设大麻素受体1基因(CNR1)的遗传变异可能与IBS相关。方法:对符合Rome II标准的162名IBS患者和423名健康对照者进行了位于CNR1基因3侧翼区域的多态性三联体AAT重复序列的基因分型。结果:CNR1基因AAT三联体重复的等位基因频率在对照组和IBS患者之间有显着差异(P <0.01)。对照组的等位基因分布频率较低,为10个或更多。我们将等位基因分为2个组( 10)和3个基因型 10 /> 10。与对照组相比,IBS患者中具有> 10 /> 10个AAT三重重复的CNR1发生频率更高(P <0.01)。与对照组相比,在CNR1> 10 /> 10基因型与所有IBS亚型之间观察到强烈的基因型关联(每个P <0.01)。 3种IBS亚型之间的等位基因频率和CNR1基因型没有差异。 CNR1> 10 /> 10基因型患者的腹部不适或疼痛症状评分高于其他基因型患者(P <0.05)。结论:我们发现健康对照者和IBS患者CNR1基因中AAT重复的等位基因频率分布不同,且CNR1> 10 /> 10基因型与IBS之间存在显着关联。这些结果表明CNR1基因是韩国IBS中潜在的候选基因。

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