Relative contribution of cardiovascular risk factors and rheumatoid arthritis clinical manifestations to atherosclerosis

I Del Rincón, GL Freeman, RW Haas… - Arthritis & …, 2005 - Wiley Online Library
I Del Rincón, GL Freeman, RW Haas, DH O'Leary, A Escalante
Arthritis & Rheumatism, 2005Wiley Online Library
Objective To estimate the contribution of cardiovascular (CV) risk factors and rheumatoid
arthritis (RA) disease manifestations to atherosclerosis in RA. Methods We used high‐
resolution carotid ultrasound to measure the carotid intima‐media thickness (IMT) and
plaque in 631 RA patients. Using R2 measures from multivariable models, we estimated the
contribution of demographic characteristics (age, sex, and ethnic group), CV risk factors
(diabetes mellitus, hypercholesterolemia, cigarette smoking, hypertension, and body mass …
Objective
To estimate the contribution of cardiovascular (CV) risk factors and rheumatoid arthritis (RA) disease manifestations to atherosclerosis in RA.
Methods
We used high‐resolution carotid ultrasound to measure the carotid intima‐media thickness (IMT) and plaque in 631 RA patients. Using R2 measures from multivariable models, we estimated the contribution of demographic characteristics (age, sex, and ethnic group), CV risk factors (diabetes mellitus, hypercholesterolemia, cigarette smoking, hypertension, and body mass index, and RA manifestations (joint tenderness, swelling, and deformity, nodules, erythrocyte sedimentation rate [ESR], C‐reactive protein, rheumatoid factor, the HLA–DRB1 shared epitope, and cumulative glucocorticoid dose) to each of the outcomes. Estimates were obtained in the full sample, and within strata defined by age, sex, and ethnic group. We tested for interaction between CV risk factors and RA manifestations.
Results
The contribution of demographic factors, CV risk factors, and RA manifestations to IMT and plaque R2 varied depending on the patients' age stratum. Demographic features explained 11–16% of IMT variance, CV risk factors explained 4%–12%, and RA manifestations explained 1–6%. The greatest contribution of RA manifestations occurred in the youngest age group, while that of CV risk factors occurred in the older age groups. Results for carotid plaque were similar. There was a significant interaction between the number of CV risk factors present and the ESR, suggesting that the ESR's effect on IMT varied according to the number of CV risk factors.
Conclusion
Both established CV risk factors and manifestations of RA inflammation contribute significantly to carotid atherosclerosis in RA, and may modify one another's effects. These findings may have implications regarding the prevention of atherosclerosis in RA.
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