Chuan Fu Yap,Nisha Nair,Ann W Morgan,John D Isaacs,Anthony G Wilson,Kimme Hyrich,Guillermo Barturen,María Riva-Torrubia,Marta Gut,Ivo Gut,Marta E Alarcón Riquelme,Anne Barton,Darren Plant
{"title":"阿达木单抗治疗的类风湿关节炎患者全血转录组学数据的机器学习分析确定了反应的预测性生物标志物。","authors":"Chuan Fu Yap,Nisha Nair,Ann W Morgan,John D Isaacs,Anthony G Wilson,Kimme Hyrich,Guillermo Barturen,María Riva-Torrubia,Marta Gut,Ivo Gut,Marta E Alarcón Riquelme,Anne Barton,Darren Plant","doi":"10.1002/art.43255","DOIUrl":null,"url":null,"abstract":"OBJECTIVES\r\nTumor necrosis factor inhibitors (TNFi) have significantly improved rheumatoid arthritis (RA) management, yet variability in patient response remains a substantial challenge, with approximately 40% of patients discontinuing TNFi due to non-response or adverse effects. This study aimed to identify biomarkers predictive of adalimumab treatment response using whole blood transcriptomics, leveraging machine learning models for data mining followed by targeted statistical analysis.\r\n\r\nMETHODS\r\nA cohort of RA patients starting TNFi therapy (n=100) was assessed for treatment response at 6 months, with RNA sequencing performed on baseline (pre-treatment) and 3-month follow-up samples. Machine learning classifiers were built to identify predictive biomarkers for treatment outcomes. This was followed by a network analysis on the biomarkers to elucidate the most influential biomarker, which was subsequently confirmed through survival analysis.\r\n\r\nRESULTS\r\nDifferential gene expression analysis in 97 samples passing QC identified 84 genes associated with treatment response. Random Forest classifiers achieved high predictive accuracy with AUCs up to 0.86, identifying genes contributing to treatment outcomes. Network analysis further elucidated gene interactions, highlighting MZB1 as a novel biomarker not captured by machine learning alone. MZB1's role in B cell development and antibody production was associated with anti-drug antibody formation, impacting treatment efficacy.\r\n\r\nCONCLUSION\r\nThis study advances the understanding of transcriptomic alterations in RA treatment and enhancing our understanding of treatment response mechanisms. Whilst the gene signatures identified require independent replication, the study serves as a starting point to pave the way for personalized therapeutic strategies in patients commencing TNFi therapy in RA.","PeriodicalId":129,"journal":{"name":"Arthritis & Rheumatology","volume":"58 1","pages":""},"PeriodicalIF":11.4000,"publicationDate":"2025-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Machine Learning Analysis of Whole-Blood Transcriptomics Data in Rheumatoid Arthritis Patients Treated with Adalimumab Identifies Predictive Biomarkers of Response.\",\"authors\":\"Chuan Fu Yap,Nisha Nair,Ann W Morgan,John D Isaacs,Anthony G Wilson,Kimme Hyrich,Guillermo Barturen,María Riva-Torrubia,Marta Gut,Ivo Gut,Marta E Alarcón Riquelme,Anne Barton,Darren Plant\",\"doi\":\"10.1002/art.43255\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"OBJECTIVES\\r\\nTumor necrosis factor inhibitors (TNFi) have significantly improved rheumatoid arthritis (RA) management, yet variability in patient response remains a substantial challenge, with approximately 40% of patients discontinuing TNFi due to non-response or adverse effects. This study aimed to identify biomarkers predictive of adalimumab treatment response using whole blood transcriptomics, leveraging machine learning models for data mining followed by targeted statistical analysis.\\r\\n\\r\\nMETHODS\\r\\nA cohort of RA patients starting TNFi therapy (n=100) was assessed for treatment response at 6 months, with RNA sequencing performed on baseline (pre-treatment) and 3-month follow-up samples. Machine learning classifiers were built to identify predictive biomarkers for treatment outcomes. This was followed by a network analysis on the biomarkers to elucidate the most influential biomarker, which was subsequently confirmed through survival analysis.\\r\\n\\r\\nRESULTS\\r\\nDifferential gene expression analysis in 97 samples passing QC identified 84 genes associated with treatment response. Random Forest classifiers achieved high predictive accuracy with AUCs up to 0.86, identifying genes contributing to treatment outcomes. Network analysis further elucidated gene interactions, highlighting MZB1 as a novel biomarker not captured by machine learning alone. MZB1's role in B cell development and antibody production was associated with anti-drug antibody formation, impacting treatment efficacy.\\r\\n\\r\\nCONCLUSION\\r\\nThis study advances the understanding of transcriptomic alterations in RA treatment and enhancing our understanding of treatment response mechanisms. Whilst the gene signatures identified require independent replication, the study serves as a starting point to pave the way for personalized therapeutic strategies in patients commencing TNFi therapy in RA.\",\"PeriodicalId\":129,\"journal\":{\"name\":\"Arthritis & Rheumatology\",\"volume\":\"58 1\",\"pages\":\"\"},\"PeriodicalIF\":11.4000,\"publicationDate\":\"2025-05-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Arthritis & Rheumatology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1002/art.43255\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"RHEUMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Arthritis & Rheumatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/art.43255","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RHEUMATOLOGY","Score":null,"Total":0}
Machine Learning Analysis of Whole-Blood Transcriptomics Data in Rheumatoid Arthritis Patients Treated with Adalimumab Identifies Predictive Biomarkers of Response.
OBJECTIVES
Tumor necrosis factor inhibitors (TNFi) have significantly improved rheumatoid arthritis (RA) management, yet variability in patient response remains a substantial challenge, with approximately 40% of patients discontinuing TNFi due to non-response or adverse effects. This study aimed to identify biomarkers predictive of adalimumab treatment response using whole blood transcriptomics, leveraging machine learning models for data mining followed by targeted statistical analysis.
METHODS
A cohort of RA patients starting TNFi therapy (n=100) was assessed for treatment response at 6 months, with RNA sequencing performed on baseline (pre-treatment) and 3-month follow-up samples. Machine learning classifiers were built to identify predictive biomarkers for treatment outcomes. This was followed by a network analysis on the biomarkers to elucidate the most influential biomarker, which was subsequently confirmed through survival analysis.
RESULTS
Differential gene expression analysis in 97 samples passing QC identified 84 genes associated with treatment response. Random Forest classifiers achieved high predictive accuracy with AUCs up to 0.86, identifying genes contributing to treatment outcomes. Network analysis further elucidated gene interactions, highlighting MZB1 as a novel biomarker not captured by machine learning alone. MZB1's role in B cell development and antibody production was associated with anti-drug antibody formation, impacting treatment efficacy.
CONCLUSION
This study advances the understanding of transcriptomic alterations in RA treatment and enhancing our understanding of treatment response mechanisms. Whilst the gene signatures identified require independent replication, the study serves as a starting point to pave the way for personalized therapeutic strategies in patients commencing TNFi therapy in RA.
期刊介绍:
Arthritis & Rheumatology is the official journal of the American College of Rheumatology and focuses on the natural history, pathophysiology, treatment, and outcome of rheumatic diseases. It is a peer-reviewed publication that aims to provide the highest quality basic and clinical research in this field. The journal covers a wide range of investigative areas and also includes review articles, editorials, and educational material for researchers and clinicians. Being recognized as a leading research journal in rheumatology, Arthritis & Rheumatology serves the global community of rheumatology investigators and clinicians.