血清钙保护蛋白和b细胞活化因子是幽门螺杆菌感染的潜在生物标志物

Akam Jasim Mustafa, Hazhar M. Balaky, P. Ismail, Hawdang Othman Abdalla, Khawla Mahruf Muhammed
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引用次数: 0

摘要

人类对幽门螺杆菌引起的细菌感染总是产生强大的免疫反应,幽门螺杆菌引起各种胃肠道感染。钙保护蛋白(CALP)和b细胞活化因子(BAFF)是炎症生物标志物,在细菌感染的胃肠道中性粒细胞反应中起作用。该研究旨在评估血清CALP和BAFF作为幽门螺杆菌感染和消化性溃疡患者的炎症生物标志物。目前的研究包括112人,包括62名幽门螺杆菌感染患者(34名男性和28名女性),他们通过幽门螺杆菌粪便抗原检测阳性被临床诊断为幽门螺杆菌感染;将他们与50名健康人群(34名男性和16名女性)的对照组进行比较,这些健康人群的年龄和性别与幽门螺杆菌感染患者相匹配。采用ELISA法检测血清CALP和BAFF水平。采用未配对Man-Whitney U检验和受试者工作特征(ROC)曲线分析,对两组生化指标进行统计学比较。幽门螺杆菌感染患者血清CALP水平明显高于健康对照组[99.50(115.8)][116.4(120.7),p=0.0132]。同样,与健康对照组相比,幽门螺杆菌感染患者血清BAFF浓度显著升高[485.7(367.1),p=0.0014][444.5(513.0)]。ROC曲线分析显示,血清CALP和BAFF作为幽门螺杆菌感染的合理炎症生物标志物,在(0.6361,0.6748)的ROC曲线下面积分别有统计学意义(p=0.0135, p=0.0015)。CALP和BAFF是参与幽门螺杆菌感染的发展和病因学的有效炎症生物标志物。血清CALP和BAFF水平可作为幽门螺杆菌诱导慢性炎症的生物标志物。CALP和BAFF生物标志物可联合用于幽门螺杆菌感染的诊断和预后预测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum Calprotectin and B-cell activating factor are potential biomarkers for Helicobacter pylori infection
Humans always mount a robust immune response to the bacterial infection caused by Helicobacter pylori, which causes various gastrointestinal tract infections. Calprotectin (CALP) and B-Cell Activating Factor (BAFF) are inflammatory biomarkers having a role in the gastrointestinal neutrophilic response to bacterial infection. The study was designed to assess serum CALP and BAFF as inflammatory biomarkers in H. pylori infection and peptic ulcer patients. The current study comprised 112 people, including 62 H. pylori-infected patients (34 men and 28 women) who were clinically diagnosed with H. pylori infection via testing positive for the H. pylori stool antigen test; they were compared to a control group of 50 healthy people (34 men and 16 women) who were age and gender-matched to H. pylori-infected patients. The serum level of CALP and BAFF were assayed using the ELISA technique. The biochemical parameters were statistically compared between patients and controls by unpaired Man-Whitney U t-test and Receiver Operating Characteristic (ROC) curve analysis. There was a significant elevation of serum CALP in H. pylori-infected patients [116.4(120.7), p=0.0132] in comparison to healthy controls [99.50(115.8)]. Similarly, there was a significant elevation of serum BAFF concentration in H. pylori-infected patients [485.7(367.1), p=0.0014] in comparison to healthy controls [444.5(513.0)]. The ROC curve analysis suggests serum CALP and BAFF as reasonable inflammatory biomarkers for H. pylori infection with statistically significant (p=0.0135, p=0.0015) area under the ROC curve of (0.6361, 0.6748), respectively. CALP and BAFF are potent inflammatory biomarkers involved in the development and etiology of H. pylori infection. Serum CALP and BAFF levels could be used as biomarkers for chronic inflammation induced by H. pylori. CALP and BAFF biomarkers can be combined to diagnose and predict the prognosis of H. pylori infection.
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