Subclinical markers of atherosclerosis and cardiovascular risk factors in early arthritis

Carla Andrea Gobbi1, Patricia Asbert, Paula Beatriz Alba

  • 1Universidad Nacional de Córdoba. carlaandreagobbi@hotmail.com.

Insights

Subclinical atherosclerosis markers were not found in early rheumatoid arthritis patients. This suggests that subclinical atherosclerosis may develop later in the disease process, beyond one year of diagnosis.

Area of Science:

  • Rheumatology
  • Cardiology
  • Vascular Ultrasound

Background:

  • Cardiovascular disease (CVD) mortality is elevated in rheumatoid arthritis (RA), exceeding risks from traditional factors, indicating inflammation's role.
  • Subclinical atherosclerosis (SA), indicated by carotid intima-media thickness (cIMT) and plaque, is linked to CVD and may develop early in inflammatory conditions.

Purpose of the Study:

  • To assess sonographic markers of subclinical atherosclerosis and cardiovascular risk factors in patients with early arthritis (EA).

Main Methods:

  • A case-control study compared 30 EA patients (swollen joints, <1 year symptom duration) with matched healthy controls.
  • Carotid ultrasound measured cIMT and plaque presence in the Common Carotid Artery (CCA) and Carotid Bulb (BC).
  • Laboratory tests assessed lipids, C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), and RA-specific antibodies. Disease activity was measured using DAS 28.

Main Results:

  • No significant differences in cIMT (CCA and BC) or carotid plaque presence were observed between EA patients and controls.
  • Lipid profiles, including total cholesterol, triglycerides, HDL, and LDL, were similar between groups.
  • cIMT CCA and BC showed no association with rheumatoid factor (RF), anti-citrullinated peptide (ACCP), CRP, DAS 28, or smoking status.

Conclusions:

  • This study found no ultrasound evidence of subclinical atherosclerosis in early arthritis patients.
  • The findings suggest that subclinical atherosclerosis markers may not be present within the first year of EA diagnosis.
  • Further longitudinal studies are needed to determine the timeline of atherosclerosis development in RA.
Abstract

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