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探讨家族性地中海热中的 S100A8/A9、新蝶呤和 MMP3。

Exploring S100A8/A9, neopterin, and MMP3 in familial Mediterranean fever.

机构信息

Division of Rheumatology, Department of Internal Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

Department of Emergency Medicine, Istanbul University-Cerrahpasa, Istanbul, Turkey.

出版信息

Clin Exp Immunol. 2024 Sep 16;218(1):93-100. doi: 10.1093/cei/uxae049.

Abstract

Familial Mediterranean fever (FMF) is characterized by inflammatory attacks due to overactivation of pyrin inflammasome. This study aimed to investigate the reliability of S100A8/A9, neopterin, and matrix metalloproteinase 3 (MMP3) at monitoring subclinical inflammation and disease activity, and at differentiating FMF attacks from appendicitis, the most common misdiagnosis among FMF patients. Blood samples (n = 75), comprising from FMF patients during an attack (n = 20), the same FMF patients during the attack-free period (n = 14), patients with appendicitis (n = 24), and healthy volunteers (n = 17) were obtained. Duplicate determinations of S100A8/A9, neopterin, and MMP-3 levels were conducted using the enzyme-linked immunosorbent assay (ELISA). FMF patients with and without attack and patients with appendicitis had significantly elevated S100A8/A9 levels compared to healthy volunteers (P-values: < 0.001, 0.036, 0.002, respectively). Patients with appendicitis and FMF patients with and without attack had significantly increased serum neopterin levels compared to healthy volunteers (P-value: < 0.001). MMP3 levels were significantly higher among patients with appendicitis and FMF patients during attack compared to healthy controls (P-values: < 0.001, 0.001). Serum levels of S100A8/A9, neopterin, and MMP3 were increased significantly during attacks compared to attack-free periods among FMF patients (P-values: 0.03, 0.047, 0.007). S100A8/A9 emerges as a valuable marker for monitoring disease activity. Neopterin and S100A8/A9 might help physicians to monitor subclinical inflammation during the attack-free periods of FMF patients. MMP3 might aid in diagnosing FMF attacks when distinguishing between attack and attack-free periods is challenging.

摘要

家族性地中海热(FMF)的特征是由于 pyrin 炎性小体过度激活而导致的炎症发作。本研究旨在探讨 S100A8/A9、新蝶呤和基质金属蛋白酶 3(MMP3)在监测亚临床炎症和疾病活动方面的可靠性,以及在区分 FMF 发作和最常见的 FMF 患者误诊阑尾炎方面的可靠性。采集了 75 份血液样本,包括 FMF 发作期患者(n=20)、同一 FMF 发作间期患者(n=14)、阑尾炎患者(n=24)和健康志愿者(n=17)。使用酶联免疫吸附试验(ELISA)重复测定 S100A8/A9、新蝶呤和 MMP-3 水平。与健康志愿者相比,FMF 发作期和无发作期患者以及阑尾炎患者的 S100A8/A9 水平显著升高(P 值:<0.001、0.036、0.002)。与健康志愿者相比,阑尾炎患者和 FMF 发作期和无发作期患者的血清新蝶呤水平显著升高(P 值:<0.001)。与健康对照组相比,阑尾炎患者和 FMF 发作期患者的 MMP3 水平显著升高(P 值:<0.001、0.001)。与无发作期相比,FMF 患者发作期血清 S100A8/A9、新蝶呤和 MMP3 水平显著升高(P 值:0.03、0.047、0.007)。S100A8/A9 是监测疾病活动的有价值的标志物。新蝶呤和 S100A8/A9 可能有助于医生监测 FMF 患者无发作期的亚临床炎症。MMP3 可能有助于在区分发作期和无发作期时诊断 FMF 发作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f6c/11404116/7f8840f99ca4/uxae049_fig2.jpg

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