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Impact of Lipid-Lowering Therapy on Mortality According to the Baseline Non-HDL Cholesterol Level: A Meta-Analysis
Walter Masson1,2,3, Martín Lobo4, Daniel Siniawski4,5,6
1Council of Epidemiology and Cardiovascular Prevention, Argentine Society of Cardiology, Azcuenaga 980, C1115AAD, Buenos Aires, Argentina. walter.masson@hospitalitaliano.org.ar.
Insights
Lipid-lowering therapy significantly reduces cardiovascular and all-cause mortality in individuals with baseline non-HDL cholesterol above 130 mg/dL. This finding highlights the importance of targeting non-HDL cholesterol for better patient outcomes.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Epidemiology
Background:
- Previous research indicated that intensive lipid-lowering therapy reduced mortality for baseline LDL-C > 100 mg/dL.
- Non-high-density lipoprotein cholesterol (non-HDL-C) is a superior predictor of cardiovascular risk compared to LDL-C.
Purpose of the Study:
- To conduct a meta-analysis evaluating the impact of lipid-lowering therapy on total and cardiovascular mortality.
- To assess this impact across various baseline non-HDL-C levels.
Main Methods:
- Systematic meta-analysis of randomized controlled trials with a minimum 6-month follow-up.
- Searched PubMed/Medline, EMBASE, and Cochrane Clinical Trials databases.
- Employed random-effects modeling and meta-regression analyses.
Main Results:
- Analyzed 29 trials involving 233,027 patients.
- Cardiovascular mortality odds ratios (OR) by baseline non-HDL-C: <130 mg/dL (OR 0.95), 130-159 mg/dL (OR 0.71), 160-189 mg/dL (OR 0.82), ≥190 mg/dL (OR 0.63).
- All-cause mortality ORs showed similar trends, with significant reductions for non-HDL-C ≥130 mg/dL.
- Meta-regression confirmed a significant association between baseline non-HDL-C and mortality.
Conclusions:
- Lipid-lowering therapy is associated with reduced all-cause and cardiovascular mortality.
- This benefit is evident when baseline non-HDL-C levels exceed 130 mg/dL.
Introduction:
Previous report showed that more intensive lipid-lowering therapy was associated with less mortality when baseline LDL-C levels were > 100 mg/dL. Non-HDL-C is a better predictor of cardiovascular risk than simpler LDL-C.
Aim:
The objective of this meta-analysis was to define the impact of lipid-lowering therapy on the reduction of total and cardiovascular mortality by different baseline levels of non-HDL-C.
Methods:
We performed a meta-analysis including randomized, controlled clinical trials of lipid-lowering therapy, reporting mortality with a minimum of 6 months of follow-up, searching in PubMed/Medline, EMBASE and Cochrane Clinical Trials databases. The random-effects model and meta-regression were performed.
Results:
Twenty nine trials of lipid-lowering drugs, including 233,027 patients, were considered eligible for the analyses. According to the baseline non-HDL-C level, the results on cardiovascular mortality were: (1) ≥ 190 mg/dL: OR 0.63 (95% CI 0.53-0.76); (2) 160-189 mg/dL: OR 0.82 (95% CI 0.75-0.89); (3) 130-159 mg/dL: OR 0.71 (95% CI 0.52-0.98); (4) < 130 mg/dL: OR 0.95 (95% CI 0.87-1.05). When evaluating mortality from any cause, the results were the following: (1) ≥ 190 mg/dL: OR 0.70 (95% CI 0.61-0.82); (2) 160-189 mg/dL: OR 0.91 (95% CI 0.83-0.98); (3) 130-159 mg/dL; OR 0.88 (95% CI 0.77-1.00); (4) < 130 mg/dL: OR 0.98 (95% CI 0.91-1.06). The meta-regression analysis showed a significant association between baseline non-HDL-C and mortality.
Conclusions:
In these meta-analyses, lipid-lowering therapy was associated with reduction in the risk of all-cause and cardiovascular mortality when baseline non-HDL-C levels were above than 130 mg/dL.
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