Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.
J Clin Gastroenterol. 2011 Jan;45(1):45-9. doi: 10.1097/MCG.0b013e3181dd1573.
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 >10), and 3 genotypes ≤ 10/≤ 10, heterozygote, and >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.
目的:大麻素会影响胃肠道功能,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 有关。
方法:162 名符合罗马 II 标准的 IBS 患者和 423 名健康对照者接受了位于 CNR1 基因 3'侧翼区的多态性三核苷酸 AAT 重复序列的基因分型。
结果:CNR1 基因中的 AAT 三核苷酸重复等位基因频率在对照组和 IBS 患者之间差异显著(P<0.01)。对照组的 10 个或更多等位基因的分布频率较低。我们将等位基因分为 2 组(≤10 和>10),并将 3 种基因型分为≤10/≤10、杂合子和>10/>10。与对照组相比,IBS 患者中 CNR1 携带>10/>10 AAT 三核苷酸重复的频率更高(P<0.01)。与对照组相比,CNR1>10/>10 基因型与所有 IBS 亚型之间存在强烈的基因型关联(P<0.01)。3 种 IBS 亚型的等位基因频率和 CNR1 基因型没有差异。与其他基因型相比,CNR1>10/>10 基因型患者的腹部不适或疼痛症状评分更高(P<0.05)。
结论:我们发现健康对照组和 IBS 患者 CNR1 基因中 AAT 重复等位基因频率分布不同,CNR1>10/>10 基因型与 IBS 显著相关。这些结果表明,CNR1 基因是韩国 IBS 的一个潜在候选基因。
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