Department of Experimental and Clinical Medicine, University of Firenze, 50134 Firenze, Italy.
Department of Internal Medicine 3-Rheumatology and Immunology, Friedrich Alexander University Erlangen-Nuremberg and Universitätsklinikum Erlangen, 91054 Erlangen, Germany.
Int J Mol Sci. 2023 May 16;24(10):8817. doi: 10.3390/ijms24108817.
Behçet's syndrome (BS) is a rare systemic vasculitis characterized by different clinical manifestations. As no specific laboratory tests exist, the diagnosis relies on clinical criteria, and the differential diagnosis with other inflammatory diseases can be challenging. Indeed, in a relatively small proportion of patients, BS symptoms include only mucocutaneous, articular, gastrointestinal, and non-typical ocular manifestations, which are frequently found also in psoriatic arthritis (PsA). We investigate the ability of serum interleukin (IL)-36α-a pro-inflammatory cytokine involved in cutaneous and articular inflammatory diseases-to differentiate BS from PsA. A cross-sectional study was performed on 90 patients with BS, 80 with PsA and 80 healthy controls. Significantly lower IL-36α concentrations were found in patients with BS as compared to PsA, although in both groups IL-36α was significantly increased compared to healthy controls. An empirical cut-off of 420.6 pg/mL displayed a specificity of 0.93, with a sensitivity of 0.70 (AUC 0.82) in discriminating PsA from BS. This cut-off displayed a good diagnostic performance also in BS patients lacking highly specific BS manifestations. Our results indicate that IL-36α might be involved in the pathogenesis of both BS and PsA, and might be a candidate biomarker to support the differential diagnosis of BS.
贝赫切特综合征(BS)是一种罕见的系统性血管炎,其特征是不同的临床表现。由于没有特定的实验室检查,因此诊断依赖于临床标准,与其他炎症性疾病的鉴别诊断具有挑战性。实际上,在相对较小比例的患者中,BS 症状仅包括黏膜皮肤、关节、胃肠道和非典型眼部表现,这些表现也经常出现在银屑病关节炎(PsA)中。我们研究了血清白细胞介素(IL)-36α(一种参与皮肤和关节炎症性疾病的促炎细胞因子)区分 BS 与 PsA 的能力。对 90 例 BS 患者、80 例 PsA 患者和 80 例健康对照进行了横断面研究。与 PsA 相比,BS 患者的 IL-36α 浓度明显较低,尽管与健康对照组相比,两组的 IL-36α 均显著升高。经验性截值为 420.6 pg/mL 时,区分 PsA 和 BS 的特异性为 0.93,敏感性为 0.70(AUC 为 0.82)。该截值在缺乏高度特异性 BS 表现的 BS 患者中也具有良好的诊断性能。我们的研究结果表明,IL-36α 可能参与了 BS 和 PsA 的发病机制,可能是支持 BS 鉴别诊断的候选生物标志物。