Effects of Different Forms of Statins on Lipid Profile in Hyperlipidemic Patients
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Date
2023
Authors
Topaloğlu, Caner
Tengiz, İstemihan
Journal Title
Journal ISSN
Volume Title
Publisher
Asian Network Scientific Information-Ansinet
Open Access Color
Green Open Access
No
OpenAIRE Downloads
OpenAIRE Views
Publicly Funded
No
Abstract
Background and Objective: Statins are the cornerstone of dyslipidemia treatment. This class of drugs decreases all lipids, particularly LDL-C and non-HDL-C and consequently the risk of cardiovascular events. Different trials have, frequently, compared the effect of two statins, while very few studies have directly compared three statins in the same study. The aim of this trial was to evaluate the lipid-slowering effect of atorvastatin, rosuvastatin and pitavastatin, at moderate doses, in a head-to-head comparison, in patients with dyslipidemia. Materials and Methods: The current study was a prospective, randomized, open-label, parallel-group study with blinded endpoints (PROBE design) involving 221 patients. After clinical examination, patients were randomized to atorvastatin (20 mg dLG1), rosuvastatin (10 mg dLG1) or pitavastatin (2 mg dLG1) and followed for 6 months. The primary endpoint of this trial was the change of lipids from baseline. Secondary endpoints included: The rate of subjects with LDL-C reduction >30% and 50% and the lowering effect on non-HDL-C. Results: At the end of this study atorvastatin, rosuvastatin and pitavastatin significantly (p<0.001) decreased plasma levels of lipids, compared with baseline values: (TC -30.1, - 39.1 and -26.8%), LDL-C (-39.1, -40.7 and -38.2%), TG (- 20.5, -17.6 and -13.4%), non-HDL-C (-36.4, -37.1 and -33.4%). No statistically significant difference was obtained between statins at the end of treatment. Differently from atorvastatin and rosuvastatin, pitavastatin increased the level of HDL (1.9%). Conclusion: The lipid-lowering efficacy of atorvastatin, rosuvastatin and pitavastatin is not statistically different, except for the HDL-C.
Description
Keywords
Dyslipidemia, statins, atorvastatin, rosuvastatin, pitavastatin, Parallel-Group, Open-Label, Cardiovascular-Disease, High-Risk, Atorvastatin, Pitavastatin, Rosuvastatin, Hypercholesterolemia, Multicenter, Cholesterol, Rosuvastatin, lipid, statin, Dyslipidemia, Statins, Atorvastatin, Pitavastatin
Fields of Science
03 medical and health sciences, 0302 clinical medicine, 0202 electrical engineering, electronic engineering, information engineering, 02 engineering and technology
Citation
WoS Q
Q4
Scopus Q
N/A

OpenCitations Citation Count
N/A
Source
International Journal of Pharmacology
Volume
19
Issue
5
Start Page
708
End Page
713
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