评估作为伊拉克克罗恩病和溃疡性结肠炎患者诊断标志物的血清钙黏蛋白和血清 Oncostatin M 水平。研究

Yahya G. Karwi, Inam S. Arif, S. A. Abdulameer
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摘要

摘要 简介:炎症性肠病(IBD)包括克罗恩病(CD)和溃疡性结肠炎(UC),表现为慢性胃肠道炎症。及时诊断和有效监测对改善预后至关重要。本研究旨在探索血清钙蛋白和oncostatin M作为诊断和监测CD和UC的潜在生物标记物的可能性。钙蛋白在炎症过程中释放,而oncostatin M是一种免疫反应细胞因子,这两种生物标记物已显示出应用前景,但它们在IBD中的确切作用仍不清楚。研究方法本研究采用横断面观察设计,纳入了巴格达教学医院 93 名接受生物治疗的 IBD 患者(50 名 CD 患者,43 名 UC 患者)。研究人员通过访谈收集了患者的人口统计学数据和疾病特征,并使用特异性 ELISA 试剂盒分析了血液样本中的钙粘蛋白和oncostatin M水平。结果显示结果表明,IBD 患者血清中这两种生物标记物的水平明显升高,并随着疾病活动而增加。在 UC 和 CD 患者的不同疾病状态中观察到了明显的区别。结论这些研究结果表明,血清钙蛋白和oncostatin M有可能成为诊断和监测IBD的实用、非侵入性生物标记物。然而,要验证它们的临床实用性并优化 IBD 管理,还需要进一步的研究。
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Evaluating Serum Calprotectin and Serum Oncostatin M Levels as Diagnostic Markers in Crohn's Disease and Ulcerative Colitis Iraqi Patients. Research
Abstract Introduction: Inflammatory bowel disease (IBD), comprising Crohn's disease (CD) and ulcerative colitis (UC), presents as chronic gastrointestinal inflammation. Timely diagnosis and effective monitoring are crucial for better outcomes. This study aims to explore serum calprotectin and oncostatin M as potential biomarkers for diagnosing and monitoring CD and UC. Calprotectin, released during inflammation, and oncostatin M, an immune-response cytokine, have shown promise, but their precise role in IBD remains unclear. Methodology: Using a cross-sectional observational design, the study included 93 IBD patients on biological treatment (50 CD, 43 UC) at Baghdad Teaching Hospital. Demographic data and disease characteristics were collected via interviews, and blood samples were analyzed using specific ELISA kits for calprotectin and oncostatin M levels. Results: The results demonstrated significantly elevated serum levels of both biomarkers in IBD patients, increasing with disease activity. Significant distinctions were observed among different disease statuses in UC and CD patients. Conclusion: These findings suggest that serum calprotectin and oncostatin M have potential as practical and non-invasive biomarkers for diagnosing and monitoring IBD. However, further research is required to validate their clinical utility and optimize IBD management.
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