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Timolol maleate and HDL cholesterol after myocardial infarction
Insights
Long-term timolol treatment reduced high-density lipoprotein (HDL) cholesterol but did not negate its heart-protective benefits. Mortality was reduced in both low and high HDL cholesterol groups with timolol use.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Cardiovascular disease remains a leading cause of mortality worldwide.
- Beta-blockers like timolol are commonly prescribed post-myocardial infarction.
- The impact of beta-blockers on lipid profiles requires further investigation.
Purpose of the Study:
- To analyze the effect of long-term timolol treatment on plasma lipids.
- To assess the prognostic significance of high-density lipoprotein (HDL) cholesterol levels after myocardial infarction.
- To determine if lipid changes influence timolol's cardioprotective effects.
Main Methods:
- Analysis of plasma lipid levels in patients from the Norwegian timolol multicentre study.
- Comparison of HDL cholesterol levels between timolol and placebo groups over one year.
- Evaluation of total mortality rates in relation to HDL cholesterol levels and timolol treatment.
Main Results:
- One-year timolol treatment significantly reduced HDL cholesterol levels (1.32 to 1.26 mmol/l).
- Timolol-treated patients had lower HDL cholesterol than placebo patients after one year (1.26 vs 1.32 mmol/l).
- HDL cholesterol levels post-myocardial infarction showed no prognostic importance for mortality.
- Timolol reduced mortality in both low (24%) and high (43%) HDL cholesterol groups.
Conclusions:
- Timolol treatment leads to a decrease in HDL cholesterol levels.
- The reduction in HDL cholesterol by timolol does not diminish its beneficial effect on reducing mortality after myocardial infarction.
- Timolol's cardioprotective effects are maintained despite alterations in lipid profiles.
Abstract:
The influence of long-term timolol treatment on plasma lipids was analysed in cohorts of the Norwegian timolol multicentre study. The prognostic importance of high-density lipoprotein (HDL) cholesterol concentration after myocardial infarction was also examined. One year timolol treatment was related to a significant reduction in HDL cholesterol levels, from 1.32 mmol l-1 to 1.26 mmol l-1 (P less than 0.05). After one year the HDL cholesterol levels were significantly lower in the timolol treated patients (1.26 mmol l-1) than in the placebo treated patients (1.32 mmol l-1, P less than 0.01). However, the HDL cholesterol values after myocardial infarction had no prognostic importance, and in the placebo group total mortality was the same in patients with low HDL cholesterol (less than 1.25 mmol l-1) and high HDL cholesterol (greater than or equal to 1.25 mmol l-1), respectively 15.0% and 14.8%. Timolol treatment was related to a reduction in mortality both in patients with low (24%, NS) and with high (43%, P less than 0.05) HDL cholesterol levels. Thus, any deleterious effects of timolol on serum lipids did not attenuate its protective effect on the damaged myocardium.
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