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Cardiovascular drugs and therapy / sponsored by the International Society of Cardiovascular Pharmacotherapy

Publication date: 1994-01-01
Pages: 509 - 13
Publisher: Springer (part of Springer Nature)

Author:

Lijnen, Paul
Van Hoof, R ; Amery, A

Keywords:

Adult, Aged, Apolipoprotein A-I, Apolipoprotein A-II, Apolipoproteins B, Blood Pressure, Celiprolol, Cholesterol, LDL, Double-Blind Method, Female, Humans, Hypertension, Lipoproteins, Male, Middle Aged, Nifedipine, Phosphatidylcholine-Sterol O-Acyltransferase, Triglycerides, Science & Technology, Life Sciences & Biomedicine, Cardiac & Cardiovascular Systems, Pharmacology & Pharmacy, Cardiovascular System & Cardiology, CELIPROLOL, BETA(1) SELECTIVITY, PLASMA LIPIDS, NIFEDIPINE, BLOCKER-INDUCED CHANGES, BETA-BLOCKER, CHOLESTEROL ACYLTRANSFERASE, LECITHIN, PLASMA, 1115 Pharmacology and Pharmaceutical Sciences, Cardiovascular System & Hematology, 3201 Cardiovascular medicine and haematology, 3214 Pharmacology and pharmaceutical sciences

Abstract:

During a double-blind, randomized study in hypertensive patients, changes in plasma lipid and lipoprotein levels during treatment with celiprolol were compared with those occurring during nifedipine treatment. Fifty-three patients (28 men and 25 women) with mild-to-moderate hypertension, aged 20-64 years, were studied. After a 1-month placebo run-in period, patients were randomly assigned to receive either nifedipine (40 mg daily) or celiprolol (200 mg daily), each time using a double-dummy technique. After 6 weeks, dosages of each drug could be doubled. After 6 weeks, there were no differences in plasma lipids between the two treatment groups. However, the changes after 12 weeks of treatment were different (p < 0.05) between the groups, leading to lower levels of plasma esterified cholesterol, low-density lipoprotein (LDL) cholesterol, and apoprotein AI, AII, and B in the celiprolol group. Plasma lecithin cholesterol acyltransferase activity (LCAT) was not modified. The present study showed that celiprolol was at least equivalent to nifedipine in terms of secondary effects on plasma lipids and lipoprotein.