Effects of Pharmaceutical Intervention on Cardiovascular Risk

Special Issue Editors


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Guest Editor
Cardiology Rehabilitation Unit, IRCCS San Raffaele, 00163 Rome, Italy
Interests: hypercholesterolemia; cardiovascular prevention; cardiac rehabilitation; heart failure

E-Mail Website
Guest Editor
1. Department of Human Science and Promotion of Quality of Life, San Raffaele Open University, 00163 Rome, Italy
2. Cardiovascular Unit, San Raffaele IRCCS, 00163 Rome, Italy
Interests: hypertension; chronic heart failure; atrial fibrillation; exercise training; sport medicine
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Special Issue Information

Dear Colleagues,

Cardiovascular diseases are the leading cause of death worldwide, being responsible for about 30% of total mortality. Considering that cardiovascular diseases are largely preventable, prioritizing preventative measures is fundamentally important to reduce their impact on public health. The current approach to the prevention of cardiovascular diseases includes the promotion a healthy and physically active lifestyle as well as the administration of drugs for treating cardiovascular risk factors such as hypertension, hypercholesterolemia, or diabetes. Although effective and safe risk factor treatments have been developed in the last few decades, there is still much work to be conducted in this area. Risk factors are often poorly treated and therapeutic goals are often disregarded, even in patients considered to be at high cardiovascular risk. There is, therefore, a need to develop new drugs and optimize the use of medications currently available. At the same time, it is necessary to develop therapeutic strategies suited to the patient's risk profile, with the aim of pursuing an increasingly personalized approach, avoiding overtreatments, and minimizing drug-related side effects.

This Special Issue welcomes manuscripts focused on (1) investigating the effects of new drugs and new treatment strategies on cardiovascular risk factors; (2) optimizing the pharmacological management of patients belonging to different risk categories; and (3) assessing patients' adherence to primary prevention drugs and studying strategies for improving adherence to treatments.

Dr. Giuseppe Marazzi
Prof. Dr. Giuseppe Caminiti
Guest Editors

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Keywords

  • cardiovascular risk factors
  • primary prevention
  • hypercholesterolemia
  • diabetes
  • hypertension

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Published Papers (1 paper)

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Research

9 pages, 555 KiB  
Article
Addition of Bempedoic Acid to Statin–Ezetimibe versus Statin Titration in Patients with High Cardiovascular Risk: A Single-Centre Prospective Study
by Giuseppe Marazzi, Giuseppe Caminiti, Marco Alfonso Perrone, Giuseppe Campolongo, Luca Cacciotti, Domenico Mario Giamundo, Ferdinando Iellamo, Paolo Severino, Maurizio Volterrani and Giuseppe Rosano
J. Cardiovasc. Dev. Dis. 2024, 11(9), 286; https://doi.org/10.3390/jcdd11090286 - 14 Sep 2024
Viewed by 1096
Abstract
Reducing levels of low-density lipoprotein cholesterol (LDL-C) below recommended thresholds is a core component of cardiovascular prevention strategies. We hypothesized that the addition of bempedoic acid to patients already on statin–ezetimibe therapy was more effective than titrating the statin dose in reducing LDL-C. [...] Read more.
Reducing levels of low-density lipoprotein cholesterol (LDL-C) below recommended thresholds is a core component of cardiovascular prevention strategies. We hypothesized that the addition of bempedoic acid to patients already on statin–ezetimibe therapy was more effective than titrating the statin dose in reducing LDL-C. The study enrolled 120 patients at high cardiovascular risk and with LDL-C above 70 mg/dL. They were randomly divided into two groups: the bempedoic acid (BA) group, taking bempedoic acid in addition to statin plus ezitimibe, and the statin titration (ST) group, including patients who doubled the dose of statin. At 12 weeks, the BA group presented a more significant decrease in LDL-C compared to the ST group (−22.9% vs. 7.5% p 0.002). The total cholesterol decreased significantly in the BA group compared to ST (−14.8% vs.−4.7%; p 0.013) No significant between-group changes in HDL and triglycerides occurred. At 12 weeks, the number of patients who reached LDL-C lower than 70 mg/dL was 38 (63%) in the BA group versus 22 (37%) in the ST group (between groups, p 0.034). In the BA group, the LDL-lowering effect of bempedoic acid was similar between patients taking atorvastatin and rosuvastatin. No side effects occurred during the follow up period. In conclusion, the addition of bempedoic acid to statin–ezetimibe combined treatment was more effective than doubling the dose of statin in reducing LDL-C levels and increased the number of patients reaching the LDL-C goal. Full article
(This article belongs to the Special Issue Effects of Pharmaceutical Intervention on Cardiovascular Risk)
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