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Objective: To determine the effect of different doses of atorvastatin on the serum soluble intercellular adhesion molecules-1 (sICAM-1) in patients undergoing percutaneous coronary intervention (PCI).
Methods: The study consisted of 38 patients with unstable angina and 10 patients with old infarction who underwent elected PCI for stenotic lesions of the coronary artery. Patients were randomly assigned to either aggressive group or conventional one. After PCI the patients took atorvastatin 20 mg per day or 10 mg per day. Blood lipid profile was examined before, and 3 months after the PCI. SICAM-1 was examined before the PCI, 48 hours and 3 months after the PCI.
Results: The total cholesterol and LDL-Cholesterol 3 months after the PCI in the 2 groups were lower than those before the PCI (P<0.01). The aggressive group showed greater reduction in concentrations of TC and LDL-C than the conventional group (P<0.01). The changes in concentrations of HDL-C between pre-PCI and 3 months after the PCI and TG were not obvious (P>0.05). sICAM-1 in the 2 groups 48 hours after the PCI significantly higher than that before the PCI (P<0.01). But sICAM-1 in the 2 groups 3 months after the PCI significantly lower than that before the PCI (P<0.01 or P<0.05). The aggressive group showed greater reduction than the conventional group (P<0.01). TC and LDL-C were positively correlated with sICAM-1(r=0.2413, r=0.2691, all P<0.05).
Conclusion: Atorvastatin 20 mg per day reduces TC, LDL-C, and sICAM-1 to a greater extent than atorvastatin 10 mg per day. The effect on sICAM-1 is partly related to reduce lipid profile.
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Trials
September 2025
Department of Pharmacology, Faculty of Medicine, University of Kelaniya, Kelaniya, Sri Lanka.
Background: Most guidelines recommend high-intensity statins for the secondary prevention of acute coronary syndrome (ACS). However, several studies from other Asian populations suggest enhanced sensitivity to statins, with effective low-density lipoprotein cholesterol (LDL-C) reduction seen at lower doses and possible higher incidence of adverse effects at higher statin doses. However, there is no published data from Sri Lanka.
View Article and Find Full Text PDFAACE Endocrinol Diabetes
May 2025
Henry Ford Health System, Endocrinology Metabolism, Detroit, Michigan.
Background/objective: This case describes a 70-year-old woman who developed transient proteinuria after starting high-dose rosuvastatin following a non-ST elevation myocardial infarction. The objective of this report is to describe the development of proteinuria in a patient after high-dose rosuvastatin therapy and discuss the subsequent resolution with a medication switch.
Case Report: A 70-year-old woman with a history of type 2 diabetes, primary hypertension, hypothyroidism, and hyperlipidemia, developed proteinuria after receiving high-dose rosuvastatin following an episode of non-ST elevation myocardial infarction.
Am J Cardiovasc Drugs
August 2025
University of Texas Southwestern, Dallas, TX, USA.
Introduction: Transthyretin amyloid cardiomyopathy (ATTR-CM) is an increasingly recognized cause of heart failure (HF), with a higher prevalence in older patients with comorbidities requiring concomitant medical therapy. Acoramidis is a next-generation transthyretin stabilizer with near-complete protein stabilization (≥ 90%) administered orally twice daily (BID) for treatment of ATTR-CM. We report on oral medication use in patients with ATTR-CM using two complementary sources: the ATTRibute-CM trial and real-world claims data.
View Article and Find Full Text PDFAm J Vet Res
July 2025
Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California-Davis, Davis, CA.
Objective: To evaluate the plasma concentrations and determine the pharmacokinetic profile of pravastatin after administration of a single oral dose in cockatiels.
Methods: A pilot study was performed at single oral doses of 20, 40, and 80 mg/kg. Based on the results of the pilot study, 14 adult cockatiels (7 male and 7 female) were administered a 40-mg/kg dose using a compounded oral suspension of pravastatin via oral gavage.
Front Pharmacol
July 2025
Department of Pharmacy, Shengli Clinical Medical College of Fujian Medical University, Fuzhou University Affiliated Provincial Hospital, Fuzhou, China.
Background: Inclisiran is an siRNA-based cholesterol-lowering drug with N-acetylgalactosamine carbohydrate (GalNAc) and is used for the treatment of hypercholesterolemia or dyslipidemia. It reduces LDL-C by 50%, with a convenient dosing schedule and fewer adverse events. Unlike statins, inclisiran has not been associated with an increased risk of muscle or liver adverse events in clinical studies.
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