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Cardiovascular risk factors and outcomes in early rheumatoid arthritis: a population-based study
Elena Nikiphorou1,2, Simon de Lusignan3,4, Christian D Mallen5
1Centre for Rheumatic Diseases, King's College London, London, UK.
Insights
Cardiovascular disease (CVD) is more common in rheumatoid arthritis (RA) patients before and after diagnosis. Early RA diagnosis may help manage subsequent CVD risk.
Area of Science:
- Rheumatology
- Cardiology
- Epidemiology
Background:
- Rheumatoid arthritis (RA) is a chronic inflammatory disease.
- Cardiovascular disease (CVD) is a significant comorbidity in RA patients.
- Understanding CVD burden in early RA is crucial for patient management.
Purpose of the Study:
- To assess the prevalence of cardiovascular disease (CVD) at and prior to the diagnosis of rheumatoid arthritis (RA).
- To evaluate the subsequent risk of CVD in patients with early RA.
- To determine the impact of traditional and RA-related risk factors on incident CVD.
Main Methods:
- Retrospective case-control study utilizing a large English primary care database.
- Identified 6591 RA patients diagnosed between 2004-2016, matched 1:1 with controls without RA.
- Followed patients for a median of 5.4 years, assessing CVD events (MI, stroke, heart failure) and risk factors.
Main Results:
- CVD, particularly stroke and heart failure, was more prevalent in RA patients at cohort entry.
- An excess of CVD events occurred in the 5 years preceding RA diagnosis.
- RA was associated with a 33% increased risk of post-diagnosis CVD, even after adjusting for risk factors.
Conclusions:
- Patients with early rheumatoid arthritis experience a higher burden of cardiovascular disease prior to diagnosis.
- There is an elevated risk of subsequent cardiovascular events post-RA diagnosis, independent of traditional and RA-specific risk factors.
Objective:
To assess the burden of cardiovascular disease (CVD) at and prior to diagnosis in people with early rheumatoid arthritis (RA) and subsequent CVD in these patients.
Methods:
A retrospective case-control study using a large English primary care database. People with RA (n=6591) diagnosed between 2004 and 2016 (inclusive) were identified using a validated algorithm, matched 1:1 by age and gender to those without RA (n=6591) and followed for a median of 5.4 years. We assessed differences in CVD at, before and after diagnosis, and the impact of traditional and RA-related risk factors (C reactive protein, RA-related autoantibodies and medication use) on incident CVD (a composite of myocardial infarction (MI), stroke or heart failure).
Results:
RA cases and their matched controls were both of mean age 58.7 (SD 15.5) at cohort entry, and 67.5% were female. Some CVD risk factors were more common at RA diagnosis including smoking and diabetes; however, total and low-density lipoprotein cholesterol were lower in patients with RA. CVD was more common in RA at cohort entry; stroke (3.9% vs 2.7%, p<0.001), heart failure (1.6% vs 1.0%, p=0.001), and non-significantly MI (3.1% vs 2.8%, p=0.092). Excess CVD developed in the 5 years preceding diagnosis. After adjustment for traditional and RA-related risk factors, RA was associated with greater risk of post-diagnosis CVD (HR 1.33, 95% CI 1.07 to 1.65, p=0.010).
Conclusions:
An excess of stroke and heart failure occurs before diagnosis of RA. There is excess risk for further cardiovascular events after diagnosis, which is not explained by differences in traditional CVD or RA-related risk factors at diagnosis.
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