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Renin-Angiotensin System-Modifying Antihypertensive Drugs Can Reduce the Risk of Cardiovascular Complications in
Chelsie Hurst1, Maira Soto1, Ernest R Vina2
1Department of Pharmacology, Center for Innovation in Brain Science, College of Medicine, University of Arizona, Tucson.
Insights
Renin-angiotensin system (RAS) drugs significantly lower cardiovascular disease risk in patients with systemic lupus erythematosus. These findings support RAS-modifying therapies for hypertension management in lupus patients.
Area of Science:
- Cardiology
- Rheumatology
- Pharmacology
Background:
- Patients with systemic lupus erythematosus (SLE) face a higher risk of cardiovascular disease (CVD) compared to the general population.
- Antihypertensive drugs targeting the renin-angiotensin system (RAS) are crucial for managing lupus nephritis and may offer additional cardiovascular benefits through anti-inflammatory effects.
- This study investigates the comparative impact of RAS-modifying versus non-RAS antihypertensive drugs on CVD incidence in SLE patients.
Purpose of the Study:
- To compare the incidence of cardiovascular disease in patients with systemic lupus erythematosus treated with renin-angiotensin system (RAS) modifying drugs versus non-RAS drugs.
- To evaluate the potential of RAS-modifying therapies to mitigate cardiovascular risk in SLE patients, considering their renal and extrarenal effects.
Main Methods:
- A large medical insurance claims dataset was utilized, identifying 220,168 patients with lupus.
- A cohort of 31,647 eligible patients (4,018 on RAS drugs, 27,629 on non-RAS drugs) was selected, with propensity score matching applied to balance demographic data, risk factors, and comorbidities.
- The mean age of patients was 46.1 years, with 93.0% being female and 96.9% having a Charlson Comorbidity Index score of 0-4, indicating a generally healthy cohort.
Main Results:
- RAS-modifying drugs were associated with a reduced relative risk (RR) of cardiovascular disease diagnosis (RR 0.80; 95% CI, 0.74-0.87), with a more pronounced effect after propensity score matching (RR 0.62; 95% CI, 0.57-0.68).
- This risk reduction was consistent across patients with and without lupus nephritis.
- RAS-modifying therapies significantly improved 5-year cardiovascular disease-free survival probability (86.0% vs 78.3%).
Conclusions:
- Renin-angiotensin system (RAS)-modifying drugs demonstrate a significant reduction in cardiovascular disease risk among patients with systemic lupus erythematosus.
- These findings suggest that RAS-modifying therapies are a valuable option for hypertension management in SLE patients, potentially impacting clinical decision-making.
- The study highlights the dual benefit of RAS-modifying drugs in managing both renal and cardiovascular complications in SLE.
Background:
Patients with systemic lupus erythematosus have a higher incidence of cardiovascular disease than the general population. Antihypertensive drugs that modify the renin-angiotensin system (RAS) are used to protect renal function in lupus nephritis and may also have extrarenal effects that lower cardiovascular disease risk due to their anti-inflammatory properties. In this study, we compared the effects of RAS vs non-RAS antihypertensive drugs on cardiovascular disease incidence in patients with lupus.
Methods:
Using a medical insurance claims dataset, 220,168 patients with lupus were identified, of which 31,647 patients (4018 patients prescribed RAS drugs, 27,629 patients prescribed non-RAS drugs) were eligible for the study. Patients had a mean age of 46.1 years, were 93.0% female, and healthy (96.9% Charlson Comorbidity Index score 0-4). Patients in the 2 drug groups were propensity score matched using demographic data, risk factors, and comorbidities.
Results:
Use of RAS vs non-RAS drugs lowered the relative risk (RR) of diagnosis of cardiovascular disease (RR 0.80; 95% confidence interval [CI], 0.74-0.87), which was more pronounced after propensity score matching (RR 0.62; 95% CI, 0.57-0.68). The decreased risk in cardiovascular disease occurred regardless of lupus nephritis status (with lupus nephritis: RR 0.51; 95% CI, 0.39-0.65; without lupus nephritis: RR 0.65; 95% CI, 0.59-0.72). RAS-modifying therapies significantly increased cardiovascular disease-free survival probability over a 5-year period (86.0% vs 78.3% probability).
Conclusions:
RAS-modifying drugs reduced the risk of cardiovascular disease in patients with systemic lupus erythematosus in this dataset. These findings have the potential to impact clinical decision-making with regards to hypertension management in patients with lupus.
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