单位:[1]Department of Dermatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.皮肤病与性病科华中科技大学同济医学院附属同济医院[2]Department of Dermatology, Traditional Chinese and Western Medicine Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Atopic dermatitis (AD) can be classified into intrinsic AD(IAD) and extrinsic AD(EAD). However, the differences in clinical features and pathogenesis between these two subtypes of AD are currently unclear. This study aimed to analyse the differences in clinical features and peripheral blood biomarkers between Chinese patients with severe IAD and EAD in order to elucidate the physiopathogenesis of AD.A total of 316 hospitalised patients definitively diagnosed with severe AD were included in this study. There were 72 cases of severe IAD and 244 cases of severe EAD. The clinical features of the patients were recorded in details. Serum total IgE, IgA, IgG, IgM, complementC3/C4, peripheral blood cell counts, lactate dehydrogenase (LDH), C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), IL-2R, IL-6, IL-8, and TNF-α in AD patients and 60 age-matched healthy controls were analysed. IAD and EAD had similar severity/Scoring Atopic Dermatitis (SCORAD) scores.Compared with healthy controls, IAD patients had significantly higher total IgE, eosinophils, monocytes, LDH, CRP, IL-2R, IL-6, IL-8 and TNF-α, and lower IgM and C4. EAD patients had significantly higher total IgE, IgA, eosinophils, white blood cell (WBC) counts, neutrophils, monocytes, basophils, LDH, CRP, IL-2R, IL-6, IL-8, TNF-α and lower IgM than healthy controls. IAD patients had a higher percentage of rural/urban living and female/male, a shorter course of disease and lower total IgE, eosinophils, WBC counts, neutrophils, monocytes, basophils, LDH, IgG and C4 than EAD patients. SCORAD scores, eosinophils, LDH expression levels increased with total IgE uniquely in patients with EAD.IAD and EAD exhibit specific clinical features and molecular changes. IAD has a more complex physiopathogenesis, and deserves further investigation.
基金:
The Knowledge Innovation Project of the Wuhan Science and Technology
Bureau, Grant/Award Number: 2022020801020528. Project of the Beijing
Science and Innovation Foundation for Medical Development, Grant/
Award Number: KC2022-JX-0165.
第一作者单位:[1]Department of Dermatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.[2]Department of Dermatology, Traditional Chinese and Western Medicine Hospital of Wuhan, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
通讯作者:
通讯机构:[1]Department of Dermatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.[*1]Department of Dermatology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan 430030, China.
推荐引用方式(GB/T 7714):
Liu Zhong,Shi Zeqi,Deng Yunhua.Clinical features and biomarker differences of severe intrinsic and extrinsic atopic dermatitis[J].CUTANEOUS AND OCULAR TOXICOLOGY.2024,43(1):97-103.doi:10.1080/15569527.2023.2300782.
APA:
Liu Zhong,Shi Zeqi&Deng Yunhua.(2024).Clinical features and biomarker differences of severe intrinsic and extrinsic atopic dermatitis.CUTANEOUS AND OCULAR TOXICOLOGY,43,(1)
MLA:
Liu Zhong,et al."Clinical features and biomarker differences of severe intrinsic and extrinsic atopic dermatitis".CUTANEOUS AND OCULAR TOXICOLOGY 43..1(2024):97-103