# Heart Failure in Rheumatoid Arthritis: Epidemiology, Pathogenesis, Diagnosis, Treatment, and Emerging Insights—A Comprehensive Review

**Authors:** Goran Šukara, Josip Tečer, Ivana Jurin, Majda Golob, Marko Barešić, Joško Mitrović

PMC · DOI: 10.3390/medicina62020380 · Medicina · 2026-02-14

## TL;DR

This review explores how rheumatoid arthritis increases heart failure risk and discusses new ways to detect and manage it.

## Contribution

The paper provides a comprehensive review of emerging insights into heart failure in rheumatoid arthritis, including novel diagnostic and therapeutic approaches.

## Key findings

- Heart failure is a significant cause of mortality in rheumatoid arthritis patients.
- Modern RA therapies may impact cardiovascular health, including heart failure outcomes.
- Novel imaging and biomarker approaches are advancing early detection of heart failure in RA.

## Abstract

Rheumatoid arthritis (RA) is a chronic, systemic inflammatory disease associated with an increased risk of cardiovascular complications, including heart failure (HF). HF represents a major cause of morbidity and mortality among patients with RA, contributing substantially to their reduced life expectancy. The early detection and optimal management of both traditional cardiovascular risk factors and RA-related inflammation are crucial to improving outcomes. In this comprehensive narrative review, we synthesize and critically appraise contemporary evidence on the epidemiology, pathophysiology, diagnosis, and management of HF in RA. We further explore emerging insights into the inflammatory and immune-mediated mechanisms driving myocardial dysfunction, advances in the early and preclinical detection of HF through novel imaging and biomarker approaches, and the evolving impact of modern RA therapies on cardiovascular health with a focus on heart failure. These developments highlight the importance of integrated, multidisciplinary strategies to prevent and manage heart failure in patients with rheumatoid arthritis.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252), rheumatoid arthritis (MONDO:0008383)

## Full-text entities

- **Genes:** IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, ADM (adrenomedullin) [NCBI Gene 133] {aka AM, PAMP}, HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123] {aka DRB1, HLA-DR1B, HLA-DRB, SS1}, FGF23 (fibroblast growth factor 23) [NCBI Gene 8074] {aka ADHR, FGFN, HFTC2, HPDR2, HYPF, PHPTC}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, NR3C2 (nuclear receptor subfamily 3 group C member 2) [NCBI Gene 4306] {aka MCR, MLR, MR, NR3C2VIT}
- **Diseases:** metabolic syndrome (MESH:D024821), VA (MESH:C563443), fibrosis (MESH:D005355), cardiomyocyte loss (MESH:D016388), Chronic inflammation (MESH:D007249), myocardial disease (MESH:D004194), cardiomyocyte injury (MESH:D014947), coronary microvascular dysfunction (MESH:D003327), dyslipidemia (MESH:D050171), myocardial alterations (MESH:D004408), myocardial remodeling (MESH:D064752), diabetes (MESH:D003920), ischemic (MESH:D002545), endothelial dysfunction (MESH:D014652), Abnormal ventricular function (MESH:D018754), myocardial edema (MESH:D004487), chronic kidney disease (MESH:D051436), cardiac arrest (MESH:D006323), obesity (MESH:D009765), autoimmune (MESH:D001327), ventricular arrhythmia (MESH:D001145), weight gain (MESH:D015430), LV dysfunction (MESH:D018487), immune-mediated diseases (MESH:C567355), stroke (MESH:D020521), myocardial effects (MESH:D065606), cardiomyopathy (MESH:D009202), ischemia (MESH:D007511), thrombosis (MESH:D013927), microvascular (MESH:D017566), phenotypes (MESH:C537393), RA (MESH:D001172), atherosclerosis (MESH:D050197), death (MESH:D003643), hypertension (MESH:D006973), hypertrophy (MESH:D006984), ischemic complication (MESH:D017202), fibromyalgia (MESH:D005356), CV complications (MESH:D002318), MI (MESH:D009203), insulin resistance (MESH:D007333), myocardial abnormalities (MESH:D006330), diastolic (MESH:D006337), toxicity (MESH:D064420), joint erosions (MESH:D014077), myocardial involvement (MESH:C564676), ATTACH (MESH:D006333), Cardiac involvement (MESH:D006331), coronary artery disease (MESH:D003324), systemic (MESH:D015619), SCA (MESH:C565772), myocardial remodeling and dysfunction (MESH:D020257), impaired exercise capacity (MESH:D000092202), joint destruction (MESH:D008105), HFpEF (MESH:D054144), systolic (MESH:D000092244), HFrEF (MESH:D054143)
- **Chemicals:** tocilizumab (MESH:C502936), upadacitinib (MESH:C000613732), tofacitinib (MESH:C479163), adalimumab (MESH:D000068879), MTX (MESH:D008727), sarilumab (MESH:C000592401), infliximab (MESH:D000069285), nitric oxide (MESH:D009569), sulfasalazine (MESH:D012460), NO (MESH:D009614), prednisolone (MESH:D011239), BioRender (-), sodium (MESH:D012964), HCQ (MESH:D006886), Rituximab (MESH:D000069283), leflunomide (MESH:D000077339), prednisone (MESH:D011241), steroid (MESH:D013256), gadolinium (MESH:D005682), lipid (MESH:D008055), baricitinib (MESH:C000596027), calcium (MESH:D002118), ROS (MESH:D017382)
- **Species:** Homo sapiens (human, species) [taxon 9606], HF [taxon 2008765]

## Full text

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## References

79 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943436/full.md

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Source: https://tomesphere.com/paper/PMC12943436