The unprecedented expansion of healthcare data—from electronic health records and insurance claims to biobank repositories and patient‑generated outcomes—has ushered in a new era for autoimmune and rheumatic disease research. Chronic inflammatory conditions such as rheumatoid arthritis and systemic lupus erythematosus exhibit marked interpatient variability in disease activity and treatment response. Research has historically depended on small, single‑center cohorts, limiting generalizability across diverse populations. By leveraging large‑scale, multidimensional datasets and advanced analytical methods, researchers can now uncover population‑level trends, identify subphenotypes, and monitor long‑term safety and efficacy outcomes in real‑world settings. The integration of registry data, wearable device measurements, and patient‑reported outcomes further enriches the evidence base, enabling longitudinal monitoring and the discovery of novel biomarkers. This convergence of big data and clinical inquiry promises to overcome traditional barriers, refine therapeutic strategies, and drive personalized care pathways.
This Research Topic seeks to highlight cutting‑edge methodologies and practical applications of big data analytics in autoimmune and rheumatic diseases. We aim to bridge the gap between data generation and clinical translation by inviting studies that demonstrate how electronic health records (EHR), health insurance claims, genomic and biobank data, patient‑reported outcomes (PROs), and emerging artificial intelligence (AI) techniques can collectively inform robust real‑world evidence (RWE). Contributions should articulate innovative strategies for predictive modeling, risk stratification, bias mitigation, and data integration. Particular emphasis is placed on methods that enhance the validity and reliability of observational findings, address confounding factors, and facilitate the development of precision rheumatology tools capable of optimizing individual patient outcomes.
We welcome Original Research Articles, Systematic Reviews and Meta‑Analyses, Methodology Papers, Brief Communications, and Case Studies that harness big data within the context of autoimmune and rheumatic disorders. Topics of interest include, but are not limited to:
● Comparative effectiveness research using real‑world data
● Predictive modeling and risk stratification in rheumatology
● Integration of omics datasets (genomics, proteomics) with clinical registries
● Machine learning approaches for early diagnosis or treatment optimization
● Methodological challenges such as bias, confounding, and data interoperability
● Federated and global collaborations leveraging networks like TriNetX and OHDSI
Article types and fees
This Research Topic accepts the following article types, unless otherwise specified in the Research Topic description:
Brief Research Report
Case Report
Clinical Trial
Community Case Study
Conceptual Analysis
Data Report
Editorial
FAIR² Data
General Commentary
Articles that are accepted for publication by our external editors following rigorous peer review incur a publishing fee charged to Authors, institutions, or funders.
Article types
This Research Topic accepts the following article types, unless otherwise specified in the Research Topic description:
Brief Research Report
Case Report
Clinical Trial
Community Case Study
Conceptual Analysis
Data Report
Editorial
FAIR² Data
General Commentary
Hypothesis and Theory
Methods
Mini Review
Opinion
Original Research
Perspective
Policy and Practice Reviews
Review
Study Protocol
Systematic Review
Technology and Code
Keywords: Big data, Autoimmune diseases, Rheumatology, Real‑world evidence, Electronic health records, Biobank, Genomics, Patient‑reported outcomes, Machine learning, Precision medicine, Data integration, Federated networks
Important note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.