Key result
High fasting triglycerides linked to ~61% increased CV risk in statin-treated ACS patients.
Why the study?
It is uncertain whether fasting triglycerides predict cardiovascular risk after ACS in patients treated with statins.
Do elevated fasting triglycerides predict recurrent ischemic events in patients with acute coronary syndrome treated with statins?
RCT (n=17,318)
randomly assigned
Do elevated fasting triglycerides predict recurrent ischemic events in patients with acute coronary syndrome treated with statins?
Answers are grounded in this paper and cite their sources.
Elevated fasting triglycerides independently predict both short- and long-term recurrent cardiovascular events in patients with acute coronary syndrome despite effective statin therapy.
BACKGROUND: Most patients with acute coronary syndrome (ACS) are treated with statins, which reduce atherogenic triglyceride-rich lipoproteins. It is uncertain whether triglycerides predict risk after ACS on a background of statin treatment. OBJECTIVES: This study examined the relationship of fasting triglyceride levels to outcomes after ACS in patients treated with statins. METHODS: Long-term and short-term relationships of triglycerides to risk after ACS were examined in the dal-OUTCOMES trial and atorvastatin arm of the MIRACL (Myocardial Ischemia Reduction with Acute Cholesterol Lowering) trial, respectively. Analysis of dal-OUTCOMES included 15,817 patients (97% statin-treated) randomly assigned 4 to 12 weeks after ACS to treatment with dalcetrapib (a cholesteryl ester transfer protein inhibitor) or placebo and followed for a median 31 months. Analysis of MIRACL included 1,501 patients treated with atorvastatin 80 mg daily beginning 1 to 4 days after ACS and followed for 16 weeks. Fasting triglycerides at initial random assignment were related to risk of coronary heart disease death, nonfatal myocardial infarction, stroke, and unstable angina in models adjusted for age, sex, hypertension, smoking, diabetes, high-density lipoprotein cholesterol, and body mass index. RESULTS: Fasting triglyceride levels were associated with both long-term and short-term risk after ACS. In dal-OUTCOMES, long-term risk increased across quintiles of baseline triglycerides (p<0.001). The hazard ratio in the highest/lowest quintile (>175/≤80 mg/dl) was 1.61 (95% confidence interval: 1.34 to 1.94). There was no interaction of triglycerides and treatment assignment on the primary outcome. In the atorvastatin group of MIRACL, short-term risk increased across tertiles of baseline triglycerides (p=0.03), with a hazard ratio of 1.50 [corrected] (95% confidence interval: 1.05 to 2.15) in highest/lowest tertiles (>195/≤135 mg/dl). The relationship of triglycerides to risk was independent of low-density lipoprotein cholesterol in both studies. CONCLUSIONS: Among patients with ACS treated effectively with statins, fasting triglycerides predict long-term and short-term cardiovascular risk. Triglyceride-rich lipoproteins may be an important additional target for therapy. (A Study of RO4607381 in Stable Coronary Heart Disease Patients With Recent Acute Coronary Syndrome; NCT00658515).
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Schwartz et al. (2015) conducted an RCT in Acute Coronary Syndrome (n=17,318). Highest quintile of fasting triglycerides (>175 mg/dl) vs. Lowest quintile of fasting triglycerides (≤80 mg/dl) was evaluated on Coronary heart disease death, nonfatal myocardial infarction, stroke, and unstable angina (HR 1.61, 95% CI 1.34-1.94, p=<0.001). Among statin-treated patients with acute coronary syndrome, the highest quintile of fasting triglycerides predicted increased long-term cardiovascular risk.
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