在不确定性结肠炎队列中,普遍存在的结肠Ileal变性与克罗恩结肠炎的诊断一致。

Medical research archives Pub Date : 2023-08-01 Epub Date: 2023-07-27 DOI:10.18103/mra.v11i8.4188
William A Breaux, Maya A Bragg, Amosy E M'Koma
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引用次数: 0

摘要

背景:以结肠炎症性肠病为主的疾病,即溃疡性结肠炎和克罗恩氏结肠炎的鉴别诊断特征不足,可能导致“不确定结肠炎”的诊断不准确。大约15%的不确定结肠炎患者在结肠镜检查、结肠活检和/或结肠切除术中被诊断。鉴于其不可预测的临床表现,不确定结肠炎的治疗结果取决于未来对结肠炎、克罗恩氏结肠炎或溃疡性结肠炎的诊断。目的:综述异位结肠回肠化生和人α-防御素5(DEFA5别名HD5)在准确区分不确定结肠炎为真正的克罗恩氏结肠炎和/或溃疡性结肠炎方面的诊断效果。设计:我们描述了一种靶向蛋白,用于潜在地将不确定的结肠炎区分为炎症性肠病(即溃疡性结肠炎和克罗恩氏结肠炎)的准确临床亚型诊断。患者:对21例临床诊断不准确的不确定结肠炎患者进行随访、重新评估和数据分析。主要结果指标:我们观察到(i)一些患者的原始诊断从不确定性结肠炎变为溃疡性结肠炎或克罗恩氏结肠炎;和(ii)人α-防御素5在克罗恩结肠炎中异常过表达。结果:21例不确定型结肠炎患者中,15例(71.4%)的不确定诊断发生了变化;9例为溃疡性结肠炎,6例为克罗恩氏结肠炎。在人类结肠手术样本中,人类α-防御素-5在克罗恩结肠炎中显著上调。此外,与人类α-防御素5相比,人类α-国防素5加工酶基质金属蛋白酶-7表达相反。限制:由于α-防御蛋白类蛋白质的序列同源性,先前针对DEFA5产生抗体(Abs)的努力在产生足够的特异性方面存在限制。先前测定中使用的Abs识别α-防御素、活性α-防御蛋白5和非活性前α-防御肽5。单克隆抗体(mAbs)确定α-防御素5的特异性和敏感性是需要克服的局限性,α-防御蛋白5是CC疾病的诊断,而不是其他α-防御肽。结论:用人α-防御素5作为分子生物学标记物,在诊断不确定结肠炎的患者中区分溃疡性结肠炎和克罗恩氏结肠炎是可行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ubiquitous Colonic Ileal Metaplasia Consistent with the Diagnosis of Crohn's Colitis among Indeterminate Colitis Cohorts.

Ubiquitous Colonic Ileal Metaplasia Consistent with the Diagnosis of Crohn's Colitis among Indeterminate Colitis Cohorts.

Ubiquitous Colonic Ileal Metaplasia Consistent with the Diagnosis of Crohn's Colitis among Indeterminate Colitis Cohorts.

Background: Inadequate differentiated diagnostic features of predominantly colonic inflammatory bowel diseases i.e., ulcerative colitis and Crohn's colitis, may lead to inexact diagnosis of "indeterminate colitis". About 15% of indeterminate colitis patients are diagnosed at colonoscopy, in colonic biopsies, and/or at colectomy. Managing outcomes of indeterminate colitis, given its unpredictable clinical presentation, depends on future diagnosis of colitis, Crohn's colitis or ulcerative colitis.

Objective: Overview the diagnostic efficacy of ectopic colonic ileal metaplasia and human α-defens 5 (DEFA5 alias HD5) for accurate delineation of indeterminate colitis into authentic Crohn's colitis and/ or ulcerative colitis.

Design: We describe a targeted protein for potentially differentiating indeterminate colitis into an accurate clinical subtype diagnosis of inflammatory bowel diseases i.e., ulcerative colitis and Crohn's colitis.

Patients: Twenty-one patients with the clinically inexact diagnosis of indeterminate colitis were followed, reassessed and data analyzed.

Main outcome measures: We observed that (i) some patients had their original diagnosis changed from indeterminate colitis to either ulcerative colitis or Crohn's colitis; and (ii) human α-defensin 5 is aberrantly overexpressed in Crohn's colitis.

Results: Fifteen of the twenty-one (71.4%) patients with indeterminate colitis had their inconclusive diagnosis changed; nine patients changed to ulcerative colitis and six to Crohn's colitis. In human colon surgical samples, Human α-defensin-5 was significantly upregulated in Crohn's colitis. In addition, Human α-defensin 5 processing enzyme, matrix metalloptotease-7 was inversely expressed compared to Human α- Defensin 5.

Limitation: Due to the sequence homology of the α-defensin class of proteins, preceding efforts to raise antibodies (Abs) against DEFA5 have limitations to produce adequate specificity. The Abs used in previous assays recognizes the α-defensins, active α-defensins 5 and inactive pro- α-defensins 5. Monoclonal antibodies (mAbs) to determine specificity and sensitivity of α-defensins 5, which is diagnostic of CC disease, and NOT other α-defensins is the limitation to overcome.

Conclusion: It is feasible to differentiate ulcerative colitis from Crohn's colitis among patients with inexact diagnosis of indeterminate colitis using Human α-defensin 5 as a molecular biosignature delineator.

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