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Published on: October 12, 2017
Lipoprotein(a) as a risk predictor for cardiac mortality in patients with acute coronary syndromes
Insights
Elevated lipoprotein(a) levels in acute coronary syndrome patients predict cardiac death. A concentration of >= 30 mg/dL indicates higher risk in myocardial infarction, while >= 7.9 mg/dL is significant for unstable angina.
Area of Science:
- Cardiology
- Atherosclerosis Research
- Clinical Risk Stratification
Background:
- Elevated lipoprotein(a) [Lp(a)] is a recognized risk factor for atherothrombotic diseases.
- The prognostic value of baseline Lp(a) in acute coronary syndromes (ACS) requires further elucidation.
Purpose of the Study:
- To investigate whether baseline Lp(a) concentrations predict adverse outcomes in patients hospitalized with ACS.
- To determine specific Lp(a) thresholds for risk stratification in myocardial infarction (MI) and unstable angina (UA) patients.
Main Methods:
- Prospective study of 519 patients admitted with suspected ACS.
- Assessment of baseline Lp(a) concentrations and their association with cardiac death over a median 3-year follow-up.
- Utilized univariate and multivariate regression models for prognostic significance analysis.
Main Results:
- In MI patients (n=266), baseline Lp(a) >= 30 mg/dL was linked to a 62% increase in cardiac death (29.8% vs 18.6%, P=0.04).
- A baseline Lp(a) >= 30 mg/dL remained an independent predictor of cardiac death in MI patients (P=0.037).
- In UA patients (n=197), baseline Lp(a) >= 7.9 mg/dL predicted cardiac death in both univariate (P=0.021) and multivariate (P=0.035) analyses.
Conclusions:
- Baseline Lp(a) concentrations are associated with increased cardiac death risk in ACS patients.
- An Lp(a) threshold of >= 30 mg/dL is a relevant risk discriminator for MI.
- Lower Lp(a) concentrations (>= 7.9 mg/dL) are prognostically significant in patients admitted with unstable angina.
Aims:
Raised lipoprotein(a) concentrations are considered to be a risk factor for atherothrombotic diseases. We examined whether baseline concentrations were a risk factor for an adverse outcome in patients admitted with acute coronary syndromes.
Methods And Results:
Five hundred and nineteen patients admitted with suspected acute coronary syndromes were studied and followed prospectively for a median of 3 years. The prognostic significance of a baseline lipoprotein(a) concentration of > or = 30 mg x dl(-1) or lower for subsequent cardiac death was assessed in patients with myocardial infarction (266) and unstable angina (197) and compared with other variables in regression models. In patients with myocardial infarction, a baseline lipoprotein(a) concentration of > or =30 mg x dl(-1) was associated with a 62% increase in subsequent cardiac death compared to the lower concentration group (29.8% vs 18.6%, Log rank P=0.04). In a multivariate regression model a baseline lipoprotein(a) concentration of > or = 30 mg x dl(-1) retained its significance as an independent predictor of cardiac death (P=0.037). In patients with unstable angina, baseline concentrations of > or = 7.9 mg x dl(-1) were found to be significant predictors of cardiac death in univariate (P=0.021) and multivariate (P=0.035) regression models.
Conclusion:
Baseline lipoprotein(a) concentrations in patients admitted with acute coronary syndromes are associated with an increased risk of cardiac death. For patients with myocardial infarction a concentration of > or = 30 mg x dl(-1) appears appropriate as a risk discriminator; for patients admitted with unstable angina, however, much lower concentrations of lipoprotein(a) appear to be prognostically important.
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