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Influence of atorvastatin on blood pressure control in treated hypertensive, normolipemic patients - An open, pilot
Agnieszka M Kuklinska1, Barbara Mroczko, Wlodzimierz J Musial
1Department of Cardiology, Medical University, Bialystok, Poland. agnieszka.kuklinska@gmail.com
Insights
High-dose atorvastatin significantly reduced blood pressure (BP) in patients with hypertension, independent of its lipid-lowering effects. This hypotensive effect was linked to increased nitric oxide (NO) and decreased autoantibodies against oxidatively modified low-density lipoprotein (ox-LDL).
Area of Science:
- Cardiology
- Pharmacology
- Hypertension Research
Background:
- Primary arterial hypertension is a significant cardiovascular risk factor.
- Endothelial dysfunction and oxidative stress play roles in hypertension.
- Statins are primarily known for lipid-lowering effects.
Purpose of the Study:
- To investigate the effect of high-dose atorvastatin on blood pressure in hypertensive patients.
- To determine if this effect is linked to changes in endothelial function and oxidative stress biomarkers.
- To assess the impact of atorvastatin on prostacyclin metabolites, nitric oxide (NO), and autoantibodies against oxidatively modified low-density lipoprotein (ox-LDL).
Main Methods:
- An open-label study involving 56 normolipemic patients with controlled primary arterial hypertension.
- Patients were randomized to receive atorvastatin 80 mg daily (n=39) or continue previous therapy (n=17).
- Blood pressure was monitored using 24-h ambulatory BP measurement; biomarker levels were analyzed.
Main Results:
- Atorvastatin treatment led to a significant reduction in systolic BP (-5.7 mmHg) and diastolic BP (-3.9 mmHg).
- The blood pressure reduction was independent of lipid-lowering effects.
- While prostacyclin metabolites and NO levels did not significantly increase, the decrease in BP correlated with an increase in NO and a decrease in autoantibodies against ox-LDL.
Conclusions:
- High-dose atorvastatin effectively reduces blood pressure in hypertensive patients, irrespective of lipid changes.
- The hypotensive effect is associated with increased nitric oxide and decreased autoantibodies against ox-LDL.
- The open-label design necessitates cautious interpretation of these findings.
Aims:
The aim of the study was to determine whether a high dose of atorvastatin lowers blood pressure (BP) in normolipemic patients with well controlled primary arterial hypertension and if this effect is associated with alteration of biomarkers of endothelial function and oxidative stress. In this open-label study, normolipemic patients (n=56) were randomized in the proportion of 2:1 to receive atorvastatin 80 mg daily for 3 months (statin-treated, ST n=39), or to previous therapy (statin-free, SF). BP was measured using a 24-h ambulatory BP measurement device. Plasma levels of 6-keto-PGF(1alpha) (prostacyclin metabolite), serum nitric oxide (NO) and levels of autoantibodies immunoglobulin G against oxidatively modified low-density lipoprotein (ox-LDL) were measured.
Major Findings:
The mean change in systolic BP and diastolic BP for ST was - 5.7 mmHg (95% CI -4.1 to -7.2 mmHg) and -3.9 mmHg (95% CI -2.7 to -5.0 mmHg), respectively. Hypotensive statin effect was independent of lipid lowering. No change of BP in SF patients was observed. In ST, prostacyclin metabolites and NO concentrations were not significantly increased and autoantibodies against ox-LDL concentrations did not change. In ST, the decrease in BP correlated with increase in NO and decrease in autoantibodies against ox-LDL.
Principal Conclusion:
High-dose atorvastatin resulted in reduction of BP independently of lipid-lowering effect, changes in endothelial function and oxidative stress, but it was related to the increase in NO and decrease in autoantibodies against ox-LDL. However, because of the open design of the study, these results should be carefully debated.
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