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Traditional Framingham risk factors fail to fully account for accelerated atherosclerosis in systemic lupus
J M Esdaile1, M Abrahamowicz, T Grodzicky
1University of British Columbia, Vancouver, Canada. jesdaile@bc.arthritis.ca
Insights
Systemic lupus erythematosus (SLE) patients face significantly higher risks of coronary heart disease (CHD) and stroke. These cardiovascular risks persist even after accounting for traditional risk factors, indicating unique disease-related factors.
Area of Science:
- Cardiology
- Rheumatology
- Epidemiology
Background:
- Systemic lupus erythematosus (SLE) is associated with increased cardiovascular disease risk.
- The precise extent to which traditional risk factors explain this increased risk in SLE is not fully understood.
Purpose of the Study:
- To quantify the excess risk of coronary heart disease (CHD) and stroke in SLE patients.
- To determine if this excess risk can be explained by common cardiovascular risk factors.
Main Methods:
- Retrospective analysis of 263 SLE patients from two registries.
- Assessment of Framingham risk factors and vascular outcomes (MI, CHD death, stroke).
- Logistic regression modeling to estimate relative risks, adjusted for baseline risk factors.
Main Results:
- SLE patients exhibited significantly elevated relative risks: 10.1 for nonfatal MI, 17.0 for CHD death, 7.5 for overall CHD, and 7.9 for stroke.
- These elevated risks remained substantial after controlling for traditional Framingham risk factors.
Conclusions:
- There is a significant and substantial increase in CHD and stroke incidence in SLE patients.
- Traditional risk factors alone do not fully account for the heightened cardiovascular risk in SLE.
Objective:
The frequency of coronary heart disease (CHD) and stroke are increased in systemic lupus erythematosus (SLE), but the extent of the increase is uncertain. We sought to determine to what extent the increase could not be explained by common risk factors.
Methods:
The participants at two SLE registries were assessed retrospectively for the baseline level of the Framingham study risk factors and for the presence of vascular outcomes: nonfatal myocardial infarction (MI), death due to CHD, overall CHD (nonfatal MI, death due to CHD, angina pectoris, and congestive heart failure due to CHD), and stroke. For each patient, the probability of the given outcome was estimated based on the individual's risk profile and the Framingham multiple logistic regression model, corrected for observed followup. Ninety-five percent confidence intervals (95% CIs) were estimated by bootstrap techniques.
Results:
Of 296 SLE patients, 33 with a vascular event prior to baseline were excluded. Of the 263 remaining patients, 34 had CHD events (17 nonfatal MIs, 12 CHD deaths) and 16 had strokes over a mean followup period of 8.6 years. After controlling for common risk factors at baseline, the increase in relative risk for these outcomes was 10.1 for nonfatal MI (95% CI 5.8-15.6), 17.0 for death due to CHD (95% CI 8.1-29.7), 7.5 for overall CHD (95% CI 5.1-10.4), and 7.9 for stroke (95% CI 4.0-13.6).
Conclusion:
There is a substantial and statistically significant increase in CHD and stroke in SLE that cannot be fully explained by traditional Framingham risk factors alone.
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