Retinal microvascular alterations in patients with active rheumatoid arthritis without cardiovascular risk factors:

Silvia Piantoni1, Francesca Regola1, Fabrizio Angeli1

  • 1Rheumatology and Clinical immunology Unit, ASST Spedali Civili, Department of Clinical and Experimental Sciences, University of Brescia, Brescia, Italy.

Frontiers in Medicine
|February 29, 2024
PubMed
Abstract

Insights

Rheumatoid arthritis patients treated with Abatacept (ABA) showed reduced retinal microvascular damage. This immune modulation therapy may reverse early cardiovascular changes in RA patients.

Area of Science:

  • Ophthalmology and Cardiovascular Medicine
  • Rheumatology and Immunology

Background:

  • Rheumatoid arthritis (RA) patients face increased cardiovascular (CV) risk due to early microvascular damage.
  • Retinal arteriole wall-to-lumen ratio (WLR) is a non-invasive marker for early microvascular damage.
  • Abatacept (ABA), a T-cell modulator, is used for RA and hypothesized to offer CV protection.

Purpose of the Study:

  • To investigate non-invasively the morphological characteristics of retinal arterioles in RA patients treated with ABA.
  • To assess the potential of ABA in mitigating microvascular alterations associated with RA.

Main Methods:

  • Seventeen RA patients without prior CV risk factors were evaluated using adaptive optics imaging of retinal arterioles.
  • Measurements were taken at baseline (T0), 6 months (T6), and 12 months (T12) during ABA therapy.
  • Office and 24-h ambulatory blood pressure monitoring, and echocardiography were also performed.

Main Results:

  • A significant progressive reduction in retinal arteriole WLR was observed from T0 to T12 (p=0.009).
  • The reduction in WLR correlated with decreased disease activity (DAS28-CRP) (r=0.789, p=0.005).
  • Diastolic office blood pressure significantly decreased, with a trend for reduction in 24-h ambulatory blood pressure.

Conclusions:

  • Abatacept treatment for 12 months reduced retinal microvascular alterations in RA patients.
  • These improvements occurred in parallel with reduced disease activity, suggesting immune modulation may reverse microvascular damage.