Fatty acid binding protein 4, resistin, diastolic dysfunction, and cardiovascular risk in patients with rheumatoid

Mariusz Ciołkiewicz1, Anna Kuryliszyn-Moskal1, Ewa Jabłońska2

  • 1Department of Rehabilitation, Medical University of Bialystok, Bialystok, Poland.

Insights

Fatty acid binding protein 4 (FABP4) is linked to higher cardiovascular risk and diastolic dysfunction in rheumatoid arthritis (RA) patients. Lateral e' velocity is the best echocardiographic measure for assessing this risk in RA.

Area of Science:

  • Cardiology
  • Rheumatology
  • Biomarkers

Background:

  • Rheumatoid arthritis (RA) patients face elevated cardiovascular (CV) risk.
  • Early detection of subclinical cardiac involvement is crucial for timely intervention.
  • Fatty acid binding protein 4 (FABP4) and resistin are potential biomarkers for CV risk in RA.

Purpose of the Study:

  • Evaluate associations between serum FABP4 and resistin levels with CV risk scores in RA patients.
  • Assess relationships between FABP4 and resistin with echocardiographic parameters of left ventricular diastolic dysfunction (LVDD).
  • Identify the most informative LVDD parameter for CV risk stratification in RA.

Main Methods:

  • Fifty-one RA patients were enrolled.
  • Serum FABP4 and resistin levels were measured.
  • Associations with CV risk scores and LVDD parameters were analyzed using regression models.

Main Results:

  • FABP4 showed a significant positive association with the ERS-RA CV risk score.
  • FABP4 was associated with abnormal LVDD parameters, including E/A ratio and left atrial volume index.
  • Lateral e' velocity demonstrated the strongest association with all CV risk scores among LVDD parameters.

Conclusions:

  • Serum FABP4 is a significant biomarker associated with increased CV risk and LVDD in RA patients.
  • Lateral e' velocity is the most informative echocardiographic parameter for CV risk stratification in RA.
  • These findings support FABP4 and specific echocardiographic measures for improved CV risk assessment in RA.
Abstract

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