Jin Seon-Pil, Kim Hosu, Moon Ji Hwan, Kim-Schulze Seunghee, Chun Yookyung Sophie, Nam Hyo Jeong, Bang Yoon Ji, Lee Ji Su, Kim Jung Eun, Park Chung-Gyu, Kim Hyun Je, Lee Dong Hun
Department of Dermatology, Seoul National University Hospital, Republic of Korea.
Department of Dermatology, Seoul National University College of Medicine, Republic of Korea.
World Allergy Organ J. 2024 Aug 8;17(8):100949. doi: 10.1016/j.waojou.2024.100949. eCollection 2024 Aug.
Cardiovascular diseases (CVDs) have been associated with atopic dermatitis (AD), including in Korean patients. Previous studies on AD have primarily focused on patients of European ancestry, while the Asian endotype exhibits distinct characteristics. This study aimed to characterize the blood proteomic signature of Korean patients with moderate-to-severe AD, with an emphasis on proteins related to CVDs.
A total of 78 participants, including 39 patients with moderate-to-severe AD and 39 age- and sex-matched healthy controls, were enrolled. Blood proteomics analysis was performed using the Olink CVD II panel, which measures the expression levels of 92 proteins associated with CVDs.
Unsupervised hierarchical clustering revealed 44 upregulated and 5 downregulated proteins in AD patients compared to healthy controls. Principal component analysis (PCA) effectively distinguished AD patients from healthy subjects based on the complete set of proteins or the subset of upregulated proteins. A multiple linear regression model comprising CCL17 and FGF21 showed a strong correlation with disease severity (R = 0.619). Correlation analysis identified 25 highly correlated proteins, including STK4, ITGB1BP2, and DECR1, which were newly found to be upregulated in Korean AD patients. Pathway analysis highlighted the involvement of these proteins in vascular system, inflammation, and lipid metabolism pathways.
The blood proteomic profile of moderate-to-severe AD patients in Korea differed from healthy controls using the CVD II panel. This study provides potential biomarkers for the AD-CVD association and insights into the pathways contributing to this relationship in the Korean population.
心血管疾病(CVDs)与特应性皮炎(AD)相关,韩国患者亦是如此。既往关于AD的研究主要集中在欧洲血统的患者,而亚洲亚型表现出不同的特征。本研究旨在描绘韩国中重度AD患者的血液蛋白质组学特征,重点关注与CVDs相关的蛋白质。
共纳入78名参与者,包括39例中重度AD患者和39名年龄及性别匹配的健康对照。使用Olink CVD II检测板进行血液蛋白质组学分析,该检测板可测量92种与CVDs相关蛋白质的表达水平。
无监督层次聚类显示,与健康对照相比,AD患者中有44种蛋白质上调,5种蛋白质下调。主成分分析(PCA)基于全套蛋白质或上调蛋白质子集有效地将AD患者与健康受试者区分开来。包含CCL17和FGF21的多元线性回归模型与疾病严重程度呈强相关(R = 0.619)。相关性分析确定了25种高度相关的蛋白质,包括STK4、ITGB1BP2和DECR1,这些蛋白质在韩国AD患者中被新发现上调。通路分析突出了这些蛋白质参与血管系统、炎症和脂质代谢通路。
使用CVD II检测板,韩国中重度AD患者的血液蛋白质组学特征与健康对照不同。本研究为AD-CVD关联提供了潜在的生物标志物,并深入了解了韩国人群中促成这种关系的通路。