Department of Medicine II, Saarland University Medical Center, Homburg, Germany.
Department of Gastroenterology and Institute for Digestive Research, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Dis Colon Rectum. 2018 May;61(5):604-611. doi: 10.1097/DCR.0000000000001001.
Colonic diverticulosis is one of the most common gastroenterological disorders. Although diverticulosis is typically benign, many individuals develop diverticulitis or other aspects of diverticular disease. Diverticulosis is thought to stem from a complex interaction of environmental, dietary, and genetic factors; however, the contributing genetic factors remain unknown.
The aim of our present study was to determine the role of genetic variants within genes encoding for collagens of the connective tissue in diverticulosis.
This was a transsectional genetic association study.
This study was conducted at three tertiary referral centers in Germany and Lithuania.
Single-nucleotide polymorphisms in COL3A1 (rs3134646, rs1800255) and COL1A1 (rs1800012) were genotyped in 422 patients with diverticulosis and 285 controls of white descent by using TaqMan assays.
The association of colonoscopy-proven diverticulosis with genetic polymorphisms with herniations was assessed in multivariate models.
The rs3134646, rs1800255, and rs1800012 variants were significantly associated with the risk of developing diverticulosis in the univariate model; however, these associations were not significant in the multivariate logistic regression analysis including additional nongenetic variables. When selectively analyzing sexes, the genotype AA (AA) in rs3134646 remained significantly associated with diverticulosis in men (OR, 1.82; 95% CI, 1.04-3.20; p = 0.04).
Because a candidate approach was used, additional relevant variants could be missed. Within our cohort of patients with diverticulosis, only a small proportion had diverticular disease and thus, we could not examine the variants in these subgroups. Functional studies, including the analysis of the involved collagens, are also warranted.
Our study shows that a variant of COL3A1 (rs3134646) is associated with the risk of developing colonic diverticulosis in white men, whereas rs1800255 (COL3A1) and rs1800012 (COL1A1) were not associated with this condition after adjusting for confounding factors. Our data provide novel valuable insights in the genetic susceptibility to diverticulosis. See Video Abstract at http://links.lww.com/DCR/A504.
结肠憩室病是最常见的肠胃疾病之一。虽然憩室病通常是良性的,但许多人会发展为憩室炎或其他憩室疾病。憩室病被认为源于环境、饮食和遗传因素的复杂相互作用;然而,致病的遗传因素仍不清楚。
本研究旨在确定编码结缔组织胶原的基因中的遗传变异在憩室病中的作用。
这是一项横断面遗传关联研究。
这项研究在德国和立陶宛的三个三级转诊中心进行。
通过 TaqMan 分析,对 422 例经结肠镜证实的憩室病患者和 285 名白种人对照组的 COL3A1(rs3134646、rs1800255)和 COL1A1(rs1800012)中的单核苷酸多态性进行基因分型。
多变量模型评估结肠镜证实的憩室病与疝相关的遗传多态性的关联。
在单变量模型中,rs3134646、rs1800255 和 rs1800012 变异与憩室病的发病风险显著相关;然而,在包括其他非遗传变量的多变量逻辑回归分析中,这些关联并不显著。当选择性分析性别时,rs3134646 中的基因型 AA(AA)在男性中仍与憩室病显著相关(OR,1.82;95%CI,1.04-3.20;p=0.04)。
由于采用了候选方法,可能会错过其他相关的变异。在我们的憩室病患者队列中,只有一小部分患有憩室疾病,因此我们无法在这些亚组中检查这些变异。还需要进行功能研究,包括对涉及的胶原蛋白的分析。
我们的研究表明,COL3A1(rs3134646)的一个变体与白人男性结肠憩室病的发病风险相关,而 rs1800255(COL3A1)和 rs1800012(COL1A1)在调整混杂因素后与该疾病无关。我们的数据为憩室病的遗传易感性提供了新的有价值的见解。