Kline Bryan P, Yochum Gregory S, Brinton David L, Schieffer Kathleen M, Weaver Taelor, Harris Leonard, Deiling Sue, Berg Arthur S, Koltun Walter A
Department of Surgery, Division of Colon and Rectal Surgery, The Pennsylvania State University, College of Medicine, Hershey, Pennsylvania.
Department of Surgery, Division of Colon and Rectal Surgery, The Pennsylvania State University, College of Medicine, Hershey, Pennsylvania; Department of Biochemistry and Molecular Biology, The Pennsylvania State University, College of Medicine, Hershey, Pennsylvania.
J Surg Res. 2021 Nov;267:397-403. doi: 10.1016/j.jss.2021.05.043. Epub 2021 Jul 2.
Diverticular disease is a common but poorly understood disease of the gastrointestinal tract. Recent studies have identified several single nucleotide polymorphisms (SNPs) that are associated with diverticular disease.
The genotypes of three SNPs (rs4662344 in ARHGAP15, rs7609897 in COLQ, and rs67153654 in FAM155A) were identified by Taqman assay in 204 patients with diverticular disease. Clinical characteristics were obtained from the medical record to study association with genotype. To evaluate gene expression in colon tissue, qPCR was performed on 24 patients with diverticulitis, and COLQ was localized using immunohistochemistry.
The ARHGAP15 and COLQ SNPs were significantly associated with both diverticular disease and specifically diverticulitis, while the FAM155A was not associated with either. No association was found with clinical disease characteristics. Heterozygous genotypes at the ARHGAP15 SNP was associated with lower ARHGAP15 expression in colon tissues. COLQ protein localized to the myenteric plexus in the colon.
This study confirmed association of the ARHGAP15 and COLQ SNPs with diverticular disease in our patients but could not confirm FAM155A SNP association. Neither of these SNPs appeared to associate with more severe disease, but genotype at the ARHGAP15 SNP did impact expression of ARHGAP15 in the colon. Additionally, this study is the first to localize COLQ in the colon. Its presence in the myenteric nervous system suggests COLQ SNP variants may contribute to diverticular disease by altering motility.
憩室病是一种常见但了解不足的胃肠道疾病。最近的研究已经鉴定出几种与憩室病相关的单核苷酸多态性(SNP)。
通过Taqman分析法对204例憩室病患者的三个SNP(ARHGAP15中的rs4662344、COLQ中的rs7609897和FAM155A中的rs67153654)进行基因分型。从病历中获取临床特征以研究与基因型的关联。为了评估结肠组织中的基因表达,对24例憩室炎患者进行了qPCR,并使用免疫组织化学法对COLQ进行定位。
ARHGAP15和COLQ的SNP与憩室病以及特定的憩室炎均显著相关,而FAM155A与两者均无关联。未发现与临床疾病特征有关联。ARHGAP15 SNP的杂合基因型与结肠组织中较低的ARHGAP15表达相关。COLQ蛋白定位于结肠的肌间神经丛。
本研究证实了ARHGAP15和COLQ的SNP与我们患者的憩室病相关,但未能证实FAM155A SNP的关联。这些SNP似乎均与更严重的疾病无关,但ARHGAP15 SNP的基因型确实影响结肠中ARHGAP15的表达。此外,本研究首次在结肠中定位了COLQ。它在肌间神经系统中的存在表明COLQ SNP变体可能通过改变蠕动而导致憩室病。