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Extreme Lp(a) predicts a 3- to 4-fold higher heart attack risk, with absolute 10-year risk up to 35% in high-risk men, the Copenhagen City Heart Study of 9330 people (Circulation 2008)

Original title: Extreme lipoprotein(a) levels and risk of myocardial infarction in the general population: the Copenhagen City Heart Study

Circulation · · 8

Kamstrup PR, Benn M, Tybjaerg-Hansen A, Nordestgaard BG

This study examined 9330 men and women from the Copenhagen City Heart Study, measuring Lp(a) shortly after sampling and correcting for regression dilution bias, to test whether extreme Lp(a) levels predict myocardial infarction (MI) in the general population. Over 10 years, 498 participants developed MI. In women, adjusted hazard ratios for MI rose stepwise with Lp(a): 1.1 for 5-29 mg/dL, 1.7 for 30-84 mg/dL, 2.6 for 85-119 mg/dL, and 3.6 for 120 mg/dL or above, compared with below 5 mg/dL; equivalent hazard ratios in men were 1.5, 1.6, 2.6, and 3.7. Absolute 10-year MI risk in smoking, hypertensive women over 60 was 10% at Lp(a) below 5 mg/dL versus 20% at 120 mg/dL or above; equivalent risks in men were 19% and 35%. The findings show a stepwise increase in MI risk with rising Lp(a), with no threshold effect, and extreme Lp(a) levels predicting a 3- to 4-fold increase in MI risk and absolute 10-year risks up to 35% in high-risk men.

Read the paper (DOI)PubMed

Original abstract

Background: Elevated lipoprotein(a) levels are associated with myocardial infarction (MI) in some but not all studies. Limitations of previous studies include lack of risk estimates for extreme lipoprotein(a) levels, measurements in long-term frozen samples, no correction for regression dilution bias, and lack of absolute risk estimates in the general population. We tested the hypothesis that extreme lipoprotein(a) levels predict MI in the general population, measuring levels shortly after sampling, correcting for regression dilution bias, and calculating hazard ratios and absolute risk estimates.

Methods And Results: We examined 9330 men and women from the general population in the Copenhagen City Heart Study. During 10 years of follow-up, 498 participants developed MI. In women, multifactorially adjusted hazard ratios for MI for elevated lipoprotein(a) levels were 1.1 (95% CI, 0.6 to 1.9) for 5 to 29 mg/dL (22nd to 66th percentile), 1.7 (1.0 to 3.1) for 30 to 84 mg/dL (67th to 89th percentile), 2.6 (1.2 to 5.9) for 85 to 119 mg/dL (90th to 95th percentile), and 3.6 (1.7 to 7.7) for > or =120 mg/dL (>95th percentile) versus levels <5 mg/dL (<22nd percentile). Equivalent values in men were 1.5 (0.9 to 2.3), 1.6 (1.0 to 2.6), 2.6 (1.2 to 5.5), and 3.7 (1.7 to 8.0). Absolute 10-year risks of MI were 10% and 20% in smoking, hypertensive women aged >60 years with lipoprotein(a) levels of <5 and > or =120 mg/dL, respectively. Equivalent values in men were 19% and 35%.

Conclusions: We observed a stepwise increase in risk of MI with increasing levels of lipoprotein(a), with no evidence of a threshold effect. Extreme lipoprotein(a) levels predict a 3- to 4-fold increase in risk of MI in the general population and absolute 10-year risks of 20% and 35% in high-risk women and men.

geneticsrisk prediction

Summary written by lp-a.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.