4.6 Article

Large-scale plasma-metabolome analysis identifies potential biomarkers of psoriasis and its clinical subtypes

期刊

JOURNAL OF DERMATOLOGICAL SCIENCE
卷 102, 期 2, 页码 78-84

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jdermsci.2021.03.006

关键词

Psoriasis; Psoriatic arthritis; Metabolome; Biomarker

资金

  1. Japan Society for the Promotion of Science (JSPS) KAKENHI [20K21834, 19H01021]
  2. Japan Agency for Medical Research and Development (AMED) [JP20km0405211, JP20ek0109413, JP20ek0410075, JP20gm4010006, JP20km0405217]
  3. Takeda Science Foundation
  4. Bioinformatics Initiative of Osaka University Graduate School of Medicine, Grant Program for Next Generation Principal Investigators at Immunology Frontier Research Center (WPI-IFReC), Osaka University
  5. Grants-in-Aid for Scientific Research [20K21834] Funding Source: KAKEN

向作者/读者索取更多资源

This study conducted metabolome analysis to identify metabolite biomarkers of psoriasis and its subtypes PsA and PsC, revealing significant changes in specific metabolites and differences between PsA and PsC, contributing to the understanding of psoriasis pathophysiology.
Background: Psoriasis is an immune-mediated skin disease for which the crosstalk between genetic and environmental factors is responsible. To date, no definitive diagnostic criteria for psoriasis yet, and specific biomarkers are required. Objective: We performed metabolome analysis to identify metabolite biomarkers of psoriasis and its subtypes such as psoriatic arthritis (PsA) and cutaneous psoriasis (PsC). Methods: We constructed metabolomics profiling of 130 plasma samples (42 PsA patients, 50 PsC patients, and 38 healthy controls) using a nontargeted metabolomics approach. Results: Psoriasis-control association tests showed that one metabolite (ethanolamine phosphate) was significantly increased in psoriasis samples than in the controls, whereas three metabolites decreased (false discovery rate [FDR] < 0.05; XA0019, nicotinic acid, and 20 alpha-hydroxyprogesterone). In the association test between PsA and PsC, tyramine significantly increased in PsA than in PsC, whereas mucic acid decreased (FDR < 0.05). Molecular pathway analysis of the PsA-PsC association test identified enrichment of vitamin digestion and absorption pathway in PsC (P = 1.3 x 10-4). Correlation network analyses elucidated that a subnetwork centered on aspartate was constructed among the psoriasisassociated metabolites; meanwhile, the major subnetwork among metabolites with differences between PsA and PsC was primarily formed from saturated fatty acids. Conclusion: Our large-scale metabolome analysis highlights novel characteristics of plasma metabolites in psoriasis and the differences between PsA and PsC, which could be used as potential biomarkers of psoriasis and its clinical subtypes. These findings contribute to our understanding of psoriasis pathophysiology. (c) 2021 The Authors. Published by Elsevier B.V. on behalf of Japanese Society for Investigative Dermatology. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据