Circulating CD31 and resistin levels reflect different stages of coronary atherosclerosis in patients with psoriasis.

Trang Nguyen-Mai Huynh, Fumikazu Yamazaki, Robert J Konrad, Yumiko Nishikawa, Akihiro Tanaka, Yonsu Son, Yoshio Ozaki, Kazuya Takehana, Hideaki Tanizaki
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Abstract

Psoriasis is a skin disease with a complicated pathophysiology that includes an extensive inflammatory cytokine network. Nevertheless, the relationship between psoriasis severity, cytokine levels, and coronary artery atherosclerosis remains poorly understood. Our aim was to find serum markers as potential candidates for cardiovascular disease (CVD) risk monitoring in patients with psoriasis. Therefore, we examined coronary artery atherosclerosis via coronary computed tomography angiography (CCTA), serum cytokine levels via multiple immunoassays, and the patients' psoriasis state. Our findings reveal for the first time that the mainstream psoriasis cytokines interleukin 17A (IL-17A), IL-19, and IL-36 in the sera of Japanese patients with psoriasis showed a linear regression association with the Psoriasis Area and Severity Index score. Furthermore, the serum level of IL-19 was remarkably correlated to Th2-related serum cytokines such as IL-4 and IL-17E. When we investigated potential markers to monitor CVD in patients with psoriasis, circulating cluster of differentiation 31 (CD31) and resistin, but not psoriasis-related cytokines, were expressed differently at each stage of coronary atherosclerosis by CCTA. CD31 and resistin levels rose dramatically in individuals with psoriasis vulgaris (PV) and noncalcified atherosclerosis. In contrast, CD31 was negatively correlated with the coronary artery calcification score (CACS) in patients with PV, whereas resistin was inversely correlated with CACS in patients with psoriatic arthritis. In conclusion, the axis of IL-17A, IL-19, and IL-36 remains associated with the severity of psoriasis during the chronic phase of the disease, regardless of the application of topical or systemic treatment. Monitoring the levels of these cytokines can accurately determine the severity of skin inflammation. Resistin and CD31 are linked to coronary artery lesions and might be good candidates for tracking the progression of coronary atherosclerosis in patients with psoriasis.

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循环 CD31 和抵抗素水平反映了银屑病患者冠状动脉粥样硬化的不同阶段。
银屑病是一种病理生理学复杂的皮肤病,包括广泛的炎症细胞因子网络。然而,人们对牛皮癣严重程度、细胞因子水平和冠状动脉粥样硬化之间的关系仍然知之甚少。我们的目的是寻找血清标志物,作为监测银屑病患者心血管疾病(CVD)风险的潜在候选指标。因此,我们通过冠状动脉计算机断层扫描血管造影术(CCTA)检查了冠状动脉粥样硬化,通过多种免疫测定方法检查了血清细胞因子水平以及患者的银屑病状态。我们的研究结果首次发现,日本银屑病患者血清中的主流银屑病细胞因子白细胞介素 17A(IL-17A)、IL-19 和 IL-36 与银屑病面积和严重程度指数评分呈线性回归关系。此外,血清中 IL-19 的水平与 Th2 相关的血清细胞因子(如 IL-4 和 IL-17E)有明显的相关性。当我们研究监测银屑病患者心血管疾病的潜在标记物时,发现循环中的分化簇 31(CD31)和抵抗素(而非银屑病相关细胞因子)在冠状动脉粥样硬化的每个阶段都有不同的表达。在寻常型银屑病(PV)和非钙化性动脉粥样硬化患者中,CD31 和抵抗素水平急剧上升。相反,在寻常型银屑病患者中,CD31 与冠状动脉钙化评分(CACS)呈负相关,而在银屑病关节炎患者中,抵抗素与 CACS 呈反相关。总之,无论采用局部治疗还是全身治疗,IL-17A、IL-19 和 IL-36 轴都与银屑病慢性期的严重程度有关。监测这些细胞因子的水平可以准确判断皮肤炎症的严重程度。Resistin 和 CD31 与冠状动脉病变有关,可能是跟踪银屑病患者冠状动脉粥样硬化进展情况的良好候选指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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