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      Genetic Polymorphisms of rs9949644 in MAPK4 Are Associated with Clinical Response to Methotrexate in Patients with Psoriasis

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          Abstract

          Background: The study aimed to investigate the relationship of MAPK4 genetic variants with the efficacy of methotrexate (MTX) in psoriasis patients. Methods: Patients treated with MTX were classified as responders or nonresponders if the Psoriasis Area and Severity Index (PASI) at week 12 was reduced to greater than 75% or lower than 75%, respectively. The genotypes of 14 MAPK4 single-nucleotide polymorphisms in 310 patients were analyzed. The expression levels of MAPK4 protein were detected by Western blot. Results: Only rs9949644 polymorphisms were associated with the efficacy after adjusting for the confounding factors. Patients with the rs9949644 AG or GG genotype had a better clinical response compared to patients with the AA genotype. Rs9949644 polymorphisms were significantly associated with the PASI improvement rate. Besides, the protein level of MAPK4, positively associated with the psoriasis severity, was higher in patients. There were no significant differences of MAPK4 protein levels among the three groups. While after treatment, MAPK4 levels in the AG or GG group showed a significantly down-regulated trend. Conclusion: By demonstrating the significant association of MAPK4 with the efficacy of MTX, this study indicates that MAPK4 may be involved in the psoriasis progression and act as a predictor of therapeutic response.

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          Author and article information

          Journal
          DRM
          Dermatology
          10.1159/issn.1018-8665
          Dermatology
          Dermatology
          S. Karger AG
          1018-8665
          1421-9832
          2024
          February 2024
          26 July 2023
          : 240
          : 1
          : 111-118
          Affiliations
          [_a] aDepartment of Dermatology and Department of Transfusion Medicine, Huashan Hospital, Fudan University, Shanghai, China
          [_b] bDepartment of Information, Huashan Hospital, Fudan University, Shanghai, China
          [_c] cDepartment of Dermatology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland
          Author notes
          *Yong Lin, linyong7007@163.com, Zhicheng Wang, ahwzc@126.com, Kexiang Yan, ykx2292002@aliyun.com
          Article
          533260 Dermatology 2024;240:111–118
          10.1159/000533260
          37494889
          2ef0d8fb-7dec-4144-b9f3-7ba6e7ac1e35
          © 2023 S. Karger AG, Basel

          Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.

          History
          : 03 May 2022
          : 20 July 2023
          Page count
          Figures: 1, Tables: 4, Pages: 8
          Funding
          This study was financially supported by the National Natural Science Foundation of China (number 81773322, 81673080, 82173420); the Shanghai Pujiang Program (under Grant No. 2019PJD004); and the Clinical Research Plan of SHDC (number SHDC2020CR6022 and SHDC2020CR1014B and SHDC22022302).
          Categories
          Genetics – Research Article

          Medicine
          MAPK4,Methotrexate,Psoriasis
          Medicine
          MAPK4, Methotrexate, Psoriasis

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