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MicroRNA expression patterns in indeterminate inflammatory bowel disease

机译:不确定性炎症性肠病中的MicroRNA表达模式

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A diagnosis of idiopathic inflammatory bowel disease requires synthesis of clinical, radiographic, endoscopic, surgical, and histologic data. While most cases of inflammatory bowel disease can be specifically classified as either ulcerative colitis or Crohns disease, 5–10% of patients have equivocal features placing them into the indeterminate colitis category. This study examines whether microRNA biomarkers assist in the classification of classically diagnosed indeterminate inflammatory bowel disease. Fresh frozen colonic mucosa from the distal-most part of the colectomy from 53 patients was used (16 indeterminate colitis, 14 Crohns disease, 12 ulcerative colitis, and 11 diverticular disease controls). Total RNA extraction and quantitative reverse-transcription-PCR was performed using five pairs of microRNA primers (miR-19b, miR-23b, miR-106a, miR-191, and miR-629). Analysis of variance was performed assessing differences among the groups. A significant difference in expressions of miR-19b, miR-106a, and miR-629 was detected between ulcerative colitis and Crohns disease groups (PP<0.05); no significant difference was present between indeterminate and ulcerative colitis groups. Among the 16 indeterminate colitis patients, 15 showed ulcerative colitis-like and one Crohns disease-like microRNA pattern. MicroRNA expression patterns in indeterminate colitis are far more similar to those of ulcerative colitis than Crohns disease. MicroRNA expression patterns of indeterminate colitis provide molecular evidence indicating that most cases are probably ulcerative colitis—similar to the data from long-term clinical follow-up studies. Validation of microRNA results by additional long-term outcome data is needed, but the data presented show promise for improved classification of indeterminate inflammatory bowel disease.
机译:诊断特发性炎症性肠病需要综合临床,影像学,内镜,手术和组织学数据。尽管大多数炎症性肠病可以明确地归类为溃疡性结肠炎或克罗恩氏病,但5-10%的患者具有模棱两可的特征,因此属于不确定的结肠炎类别。这项研究检查了microRNA生物标记物是否有助于经典诊断的不确定性炎症性肠病的分类。使用了来自53例结肠切除术最远端的新鲜冷冻结肠粘膜(16例不确定性结肠炎,14例克罗恩氏病,12例溃疡性结肠炎和11例憩室病对照)。使用五对microRNA引物(miR-19b,miR-23b,miR-106a,miR-191和miR-629)进行总RNA提取和定量逆转录PCR。进行方差分析以评估各组之间的差异。溃疡性结肠炎和克罗恩氏病组之间的miR-19b,miR-106a和miR-629的表达存在显着差异(PP <0.05);不确定性和溃疡性结肠炎组之间没有显着差异。在16名不确定的结肠炎患者中,有15名表现出溃疡性结肠炎样和一种克罗恩病样microRNA模式。与克罗恩氏病相比,不确定性结肠炎中的MicroRNA表达模式与溃疡性结肠炎中的MicroRNA表达模式更为相似。不确定性结肠炎的MicroRNA表达模式提供了分子证据,表明大多数病例可能是溃疡性结肠炎-与长期临床随访研究的数据相似。需要通过其他长期结果数据来验证microRNA结果,但所提供的数据显示有望改善不确定性炎症性肠病的分类。

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