贝赫切特氏病与tenascin-C之间关系的研究。

IF 1.1 Q4 RHEUMATOLOGY Archives of rheumatology Pub Date : 2024-01-15 eCollection Date: 2024-03-01 DOI:10.46497/ArchRheumatol.2024.10163
Haydar Kaplan, Demet Yalcin Kehribar, Muhammed Okuyucu, Metin Ozgen
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摘要

研究目的该研究旨在探讨血清腱鞘蛋白-C水平及其与伴有炎症过程的白塞氏病(BD)发病机制的关系:这项前瞻性分析研究纳入了34名符合2014年国际白塞氏病标准且无合并症的白塞氏病患者(19名男性,15名女性;平均年龄为(31.5±8.2)岁;年龄范围为18至48岁)和37名健康志愿者(21名女性,16名男性;平均年龄为(29.6±5.3)岁;年龄范围为21至45岁)。研究人员记录了参与者的性别、年龄、确诊年龄、临床和实验室数据、用药情况和吸烟史。使用市售的tenascin-C酶联免疫吸附测定试剂盒测定血清tenascin-C水平:结果:两组在年龄(P=0.262)和性别(P=0.287)方面无明显差异。与对照组(27,574±14,533 pg/mL,p)相比,BD 组血清 Tenascin-C 水平明显较低(10,824±7,612 pg/mL):与其他慢性炎症性疾病相比,在 BD 患者中观察到的腱鞘蛋白-C 水平低于健康人,这可能是由于 BD 患者没有长期的慢性炎症病程。腱鞘蛋白-C水平在其他风湿性炎症疾病中较高,而在BD中较低,这一事实可能有助于BD的鉴别诊断。
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An investigation of the relationship between Behçet's disease and tenascin-C.

Objectives: The study aimed to investigate serum tenascin-C levels and its relationship with pathogenesis of Behçet's disease (BD) with inflammatory processes.

Patients and methods: This prospective and analytical study included 34 BD patients (19 males, 15 females; mean age: 31.5±8.2 years; range, 18 to 48 years) who met the 2014 International Criteria for Behçet's Disease and had no comorbidities and 37 healthy volunteers (21 females, 16 males; mean age: 29.6±5.3 years; range, 21 to 45 years). Sex, age, age at diagnosis, clinical and laboratory data, medication use, and smoking history of the participants were recorded. Serum tenascin-C levels were measured using a commercially available tenascin-C enzyme-linked immunosorbent assay kit.

Results: There was no significant difference between the groups in terms of age (p=0.262) and sex (p=0.287). Serum tenascin-C levels were significantly lower in the BD group (10,824±7,612 pg/mL) compared to the control group (27,574±14,533 pg/mL, p<0.001). In the receiver operating characteristic analysis performed for the diagnostic value of tenascin-C level in BD, the sensitivity was determined as 79.4% and the specificity as 82.5% (p<0.001). No statistically significant difference was observed in tenascin-C levels in correlation with clinical characteristics, laboratory values, medication use, and smoking in the BD group.

Conclusion: In contrast to other chronic inflammatory diseases, lower levels of tenascin-C were observed in patients with BD than in the healthy individuals, which can be attributed to the absence of prolonged chronic inflammatory course in BD. The fact that tenascin-C levels are high in other rheumatic inflammatory diseases but low in BD may be useful in the differential diagnosis of BD.

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