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Do statins reduce the cardiovascular risk in patients with rheumatoid arthritis?
Kathrin Danninger1, Uta C Hoppe, Herwig Pieringer
1Academic Research Unit, 2nd Department of Medicine, General Hospital Linz, Linz, Austria.
Insights
Statins may reduce cardiovascular risk in rheumatoid arthritis (RA) patients during primary prevention. However, statin discontinuation in RA patients increases cardiovascular event risk, though overall benefits require further investigation.
Area of Science:
- Rheumatology
- Cardiology
- Pharmacology
Background:
- Rheumatoid arthritis (RA) patients face elevated cardiovascular (CV) morbidity and mortality.
- Traditional CV risk factors do not fully account for the excess CV risk in RA.
- The efficacy of statin therapy in RA patients remains uncertain.
Purpose of the Study:
- To systematically review evidence on statin treatment and its impact on CV events in RA patients.
- To evaluate the role of statins in primary and secondary CV prevention in RA.
Main Methods:
- A systematic literature review was conducted using PubMed.
- Search terms included various statins and 'arthritis'.
- Four studies with 4896 RA patients were analyzed for CV event outcomes.
Main Results:
- Statins showed reduced CV events and mortality in RA primary prevention.
- No significant difference in secondary prevention post-myocardial infarction (MI) between RA and non-RA patients.
- Statin discontinuation in RA patients was linked to increased risk of MI or CV mortality.
- Atorvastatin 80 mg reduced overall CV disease risk compared to lower doses.
Conclusions:
- Statin treatment appears to reduce CV risk in RA primary prevention.
- Statin discontinuation increases CV event risk in RA patients.
- Further research is needed to clarify the overall significance and optimal use of statins in RA.
Objective:
Patients with rheumatoid arthritis (RA) are at significantly higher risk of cardiovascular (CV) morbidity and mortality compared with the general population. Traditional CV risk factors cannot explain the total excess of CV morbidity and mortality in RA patients. At present, it is not clear whether treatment with statins might be of benefit in RA patients. The aim of the present systematic literature review is to summarize the published evidence concerning treatment with statins and its impact on CV events in RA patients.
Methods:
A systematic literature review of studies on RA and statins was carried out in the database PubMed. Search terms were 'simvastatin OR atorvastatin OR fluvastatin OR lovastatin OR pravastatin OR rosuvastatin OR statin AND arthritis'. Papers were included in this review when the reported outcome was on CV events in RA patients. After exclusion of the studies not fulfilling our inclusion criteria four studies were finally analyzed. The total number of RA patients included in these studies was 4896.
Results:
Statins were associated with reduced CV events and mortality in RA in primary prevention but not in secondary prevention. In secondary prevention after myocardial infarction (MI) there was no statistically significant difference between RA or non-RA patients either receiving atorvastatin 80 mg or simvastatin 20-40 mg daily. Treatment with atorvastatin 80 mg led to a reduction in overall risk of CV disease in both patients with and without inflammatory joint disease compared to patients receiving the conventional/low-dose statin treatment. Statin discontinuation in RA patients was associated with an increased risk of acute myocardial infarction or CV mortality. Myalgia, diarrhoea, abdominal pain and nausea may be more frequent in RA patients than in controls.
Conclusion:
The published evidence shows that in RA patients statin treatment appears to reduce CV risk in primary prevention and that statin discontinuation is associated with an increased risk for CV events. However, the significance of statin treatment in RA patients still remains unclear as only very little evidence has been published. Whether all RA patients would benefit from treatment with statins still needs to be investigated.
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