Candidate pharmacogenetic signals at CCL2 and ITPA associated with JAK inhibitor response in Taiwanese rheumatoid arthritis

Our data prioritise CCL2 and ITPA as candidate pharmacogenetic signals for JAKi response. Given the use of a persistence-based effectiveness endpoint and the exploratory nature of secondary EULAR-based outcome assessments, independent replication using standardised ACR/EULAR outcomes is warranted.

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Publication Details

Journal
Clinical and Experimental Rheumatology
Published
2025-09-27
DOI
https://doi.org/10.55563/clinexprheumatol/17yc25
Primary Topic
Myeloproliferative Neoplasms: Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00
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article

Candidate pharmacogenetic signals at CCL2 and ITPA associated with JAK inhibitor response in Taiwanese rheumatoid arthritis

I. C. Chen, Su Hao Lo, T. C. Wu, C Kao et al.
Clinical and Experimental Rheumatology
Myeloproliferative Neoplasms: Diagnosis and Treatment
article

Candidate pharmacogenetic signals at CCL2 and ITPA associated with JAK inhibitor response in Taiwanese rheumatoid arthritis

I. C. Chen, Su Hao Lo, T. C. Wu, C Kao, Yi-Ming Chen, Yen-Ju Chen, Wen-Nan Huang, Feng-Cheng Liu, Ting-Yu Hsieh
article en

Abstract

Our data prioritise CCL2 and ITPA as candidate pharmacogenetic signals for JAKi response. Given the use of a persistence-based effectiveness endpoint and the exploratory nature of secondary EULAR-based outcome assessments, independent replication using standardised ACR/EULAR outcomes is warranted.

Clinical and Experimental Rheumatology
Tri-Service General Hospital (TW), National Yang Ming Chiao Tung University (TW), National Chung Hsing University (TW), Taichung Veterans General Hospital (TW), National Defense Medical Center (TW), Chung Shan Medical University (TW)
Zero hunger
Openalex Percentile: Top 22%
Myeloproliferative Neoplasms: Diagnosis and Treatment
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