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Left ventricular remodeling in rheumatoid arthritis patients without clinical heart failure. | LitMetric

AI Article Synopsis

  • * In a study involving 158 RA patients without clinical HF, it was found that left ventricular (LV) remodeling prevalence increased from 40% at baseline to 60% over a follow-up period of 4 to 6 years.
  • * Higher interleukin-6 (IL-6) levels were linked to concentric LV remodeling, indicating its potential as a biomarker, while the medication tocilizumab was associated with baseline LV remodeling; future research is needed on IL-6's role in

Article Abstract

Rheumatoid arthritis (RA) patients have a 1.5- to twofold higher risk of developing heart failure (HF) and a twofold increased risk of HF-associated mortality compared to those without RA. HF is preceded subclinically by left ventricular (LV) remodeling in the general population. There is a relative absence of prospective studies following RA patients from pre-clinical to clinical HF as well as prospective studies of LV remodeling in RA without clinical HF. In our study, 158 RA patients without clinical HF were enrolled and underwent transthoracic echocardiography (TTE) at baseline and on follow-up between 4 and 6 years. Extensive characterization of RA disease activity and cardiovascular risk factors were performed. LV remodeling was prevalent at 40% at baseline and increased to 60% over time. Higher levels of interleukin-6 (IL 6) were associated with concentric LV remodeling on follow-up. The use of tocilizumab was also significantly associated with baseline LV remodeling (relative wall thickness). These findings suggest a role for IL-6 as a biomarker for LV remodeling in RA patients without clinical HF. Future research should focus on prospective follow-up of LV remodeling and the effects of IL-6 inhibition on LV remodeling in RA patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10362590PMC
http://dx.doi.org/10.1186/s13075-023-03113-8DOI Listing

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