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FAM155A 常见变异与憩室炎有关,但与憩室病无关。

Common variation in FAM155A is associated with diverticulitis but not diverticulosis.

机构信息

Department of Medicine II, Saarland University Medical Center, Saarland University, Homburg, Germany.

Department of Gastroenterology and Institute for Digestive Research, Lithuanian University of Health Sciences, Kaunas, Lithuania.

出版信息

Sci Rep. 2020 Feb 3;10(1):1658. doi: 10.1038/s41598-020-58437-1.

Abstract

Colonic diverticulosis is a very common condition. Many patients develop diverticulitis or other complications of diverticular disease. Recent genome-wide association studies (GWAS) consistently identified three major genetic susceptibility factors for both conditions, but did not discriminate diverticulititis and diverticulosis in particular due the limitations of registry-based approaches. Here, we aimed to confirm the role of the identified variants for diverticulosis and diverticulitis, respectively, within a well-phenotyped cohort of patients who underwent colonoscopy. Risk variants rs4662344 in Rho GTPase-activating protein 15 (ARHGAP15), rs7609897 in collagen-like tail subunit of asymmetric acetylcholinesterase (COLQ) and rs67153654 in family with sequence similarity 155 A (FAM155A) were genotyped in 1,332 patients. Diverticulosis was assessed by colonoscopy, and diverticulitis by imaging, clinical symptoms and inflammatory markers. Risk of diverticulosis and diverticulitis was analyzed in regression models adjusted for cofactors. Overall, the variant in FAM155A was associated with diverticulitis, but not diverticulosis, when controlling for age, BMI, alcohol consumption, and smoking status (OR 0.49 [95% CI 0.27-0.89], p = 0.002). Our results contribute to the assessment specific genetic variants identified in GWAS in the predisposition to the development of diverticulitis in patients with diverticulosis.

摘要

结肠憩室病是一种非常常见的病症。许多患者会出现憩室炎或其他憩室疾病并发症。最近的全基因组关联研究(GWAS)一致确定了这两种疾病的三个主要遗传易感性因素,但由于基于登记的方法的局限性,无法特别区分憩室炎和憩室病。在这里,我们旨在通过对接受结肠镜检查的患者进行良好表型队列研究,分别确认已鉴定的变体在憩室病和憩室炎中的作用。 Rho GTPase-activating protein 15(ARHGAP15)中的 rs4662344、不对称乙酰胆碱酯酶胶原样尾部亚基(COLQ)中的 rs7609897 和家族序列相似性 155A(FAM155A)中的 rs67153654 风险变体在 1332 名患者中进行了基因分型。通过结肠镜检查评估憩室病,通过影像学、临床症状和炎症标志物评估憩室炎。在调整协变量的回归模型中分析憩室病和憩室炎的风险。总体而言,在控制年龄、BMI、饮酒和吸烟状况后,FAM155A 中的变体与憩室炎相关,但与憩室病无关(OR 0.49 [95%CI 0.27-0.89],p=0.002)。我们的结果有助于评估在憩室病患者中发生憩室炎的 GWAS 中鉴定的特定遗传变异。

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