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Published on: October 12, 2017
A prospective study of lipoprotein(a) and the risk of myocardial infarction
P M Ridker1, C H Hennekens, M J Stampfer
1Department of Medicine, Brigham and Women's Hospital, Boston, MA 02215-1204.
Insights
Elevated lipoprotein(a) [Lp(a)] levels did not increase myocardial infarction risk in middle-aged men. This study suggests Lp(a) is not a reliable screening tool for cardiovascular risk in this population.
Area of Science:
- Cardiovascular Medicine
- Lipidology
- Preventive Cardiology
Background:
- Lipoprotein(a) [Lp(a)] is an emerging cardiovascular risk factor.
- Previous studies have yielded conflicting results regarding the association between Lp(a) and myocardial infarction (MI).
Purpose of the Study:
- To prospectively evaluate the association between elevated lipoprotein(a) levels and the risk of developing myocardial infarction (MI).
Main Methods:
- A nested case-control study was conducted within the Physicians' Health Study.
- 14,916 male physicians without prior MI or stroke provided baseline plasma samples.
- Follow-up averaged 60.2 months, with Lp(a) levels analyzed in 296 MI cases and matched controls.
Main Results:
- No significant difference in Lp(a) levels was observed between MI cases and controls (median 103.0 mg/L vs 102.5 mg/L, P = .73).
- Analyses controlling for age, smoking, and other cardiovascular risk factors showed no association between Lp(a) levels and MI risk (P for trend = .93).
- No threshold effect was identified at various Lp(a) cutoff levels.
Conclusions:
- This prospective study found no evidence linking lipoprotein(a) levels to an increased risk of future myocardial infarction in predominantly middle-aged white men.
- The findings do not support the use of Lp(a) as a screening tool for cardiovascular risk assessment in this demographic.
Objective:
To assess prospectively the risk of myocardial infarction (MI) associated with elevated levels of lipoprotein(a) (Lp[a]).
Design:
Nested case-control study using prospectively collected plasma samples.
Setting:
Participants in the Physicians' Health Study.
Participants:
A total of 14,916 male physicians aged 40 to 84 years with no prior history of MI or stroke provided plasma samples at baseline and were followed up prospectively for an average period of 60.2 months. Samples from 296 physicians who subsequently developed MI were analyzed for Lp(a) level together with paired controls, matched for smoking status and age.
Main Outcome Measure:
Fatal or nonfatal acute MI.
Results:
The distribution of Lp(a) level among cases was virtually identical to that of controls (P = .88), and there was no significant difference between groups for median Lp(a) levels (103.0 mg/L vs 102.5 mg/L; P = .73). In analyses controlling for age and smoking status, we found no evidence of association between increasing level of Lp(a) and risk of MI (relative risks from lowest to highest quintiles of Lp(a): 1.00, 0.97, 0.83, 0.88, and 1.07; P for trend = .93) or a threshold effect at any prespecified cutoff of Lp(a) level (relative risks associated with Lp[a] levels above the 25th, 50th, 75th, 90th, and 95th percentiles of the control distribution, respectively: 1.04, 1.00, 1.19, 1.00, and 1.07; all P values nonsignificant). Further adjustment for both lipid and nonlipid cardiovascular risk factors had no material impact.
Conclusions:
In this prospective study of predominantly middle-aged white men, we found no evidence of association between Lp(a) level and risk of future MI. These data do not support the use of Lp(a) level as a screening tool to define cardiovascular risk among this population.
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