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Published on: October 12, 2017
Meta-analysis of the relationship between non-high-density lipoprotein cholesterol reduction and coronary heart
Jennifer G Robinson1, Songfeng Wang, Brian J Smith
1Lipid Research Clinic, University of Iowa, Iowa City, IA 52242, USA. jennifer-g-robinson@uiowa.edu
Insights
Lowering non-high-density lipoprotein cholesterol (HDL-C) effectively reduces coronary heart disease (CHD) risk. Most lipid-modifying therapies show a 1:1 relationship between non-HDL-C reduction and CHD risk decrease.
Area of Science:
- Cardiology
- Metabolic Disorders
- Pharmacology
Background:
- Non-high-density lipoprotein cholesterol (non-HDL-C) is a key secondary lipid target in cardiovascular therapy.
- Understanding the relationship between non-HDL-C reduction and coronary heart disease (CHD) risk is crucial for optimizing treatment strategies.
Purpose of the Study:
- To investigate the association between lowering non-high-density lipoprotein cholesterol (non-HDL-C) and the reduction in coronary heart disease (CHD) risk.
- To compare this relationship across various lipid-modifying therapies.
Main Methods:
- A meta-analysis of randomized placebo or active-controlled trials was conducted.
- Bayesian random-effects models were used to estimate the effect of mean non-HDL-C reduction on CHD risk, adjusted for study duration.
- Cochrane's Q statistic assessed heterogeneity among trials.
Main Results:
- Data from 14 statin, 7 fibrate, and 6 niacin trials were analyzed, alongside single trials for bile acid sequestrants, diet, and ileal bypass surgery.
- For statins, a 1% decrease in non-HDL-C correlated with a 0.99 relative risk of CHD over 4.5 years.
- Fibrates showed similar results to statins, while niacin monotherapy demonstrated a 1:1 relationship; combination niacin trials lacked consistent findings.
Conclusions:
- Non-HDL-C is a significant therapeutic target for preventing coronary heart disease (CHD).
- Most lipid-modifying drugs, when used as monotherapy, exhibit a direct 1:1 correlation between the percentage of non-HDL-C lowered and the resulting CHD risk reduction.
Objectives:
To determine the relationship between non-high-density lipoprotein cholesterol (HDL-C) lowering and coronary heart disease (CHD) risk reduction for various lipid-modifying therapies.
Background:
Non-HDL-C is the second lipid target of therapy after low-density lipoprotein cholesterol (LDL-C).
Methods:
Randomized placebo or active-controlled trials were evaluated. The effect of mean non-HDL-C reduction on the relative risk of nonfatal myocardial infarction and CHD death was estimated using Bayesian random-effects meta-analysis models adjusted for study duration. Cochrane's Q was used to test for heterogeneity.
Results:
Inclusion criteria were met by 14 statin (n = 100,827), 7 fibrate (n = 21,647), and 6 niacin (n = 4,445) trials, and 1 trial each of a bile acid sequestrant (n = 3,806), diet (n = 458), and ileal bypass surgery (n = 838). For statins, each 1% decrease in non-HDL-C resulted in an estimated 4.5-year CHD relative risk of 0.99 (95% Bayesian confidence interval: 0.98 to 1.00). The fibrate model did not differ from the statin model (Bayes factor K = 0.49) with no evidence of heterogeneity. The niacin model was moderately different from the statin model (K = 7.43), with heterogeneity among the trials (Q = 11.8, 5 df; p = 0.038). The only niacin monotherapy trial (n = 3,908) had a 1:1 relationship between non-HDL-C and risk reduction. No consistent relationships were apparent for the 5 small trials of niacin in combination. The 95% confidence intervals for the single trials of diet, bile acid sequestrants, and surgery also included the 1:1 relationship.
Conclusions:
Non-HDL-C is an important target of therapy for CHD prevention. Most lipid-modifying drugs used as monotherapy have an approximately 1:1 relationship between percent non-HDL-C lowering and CHD reduction.
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