Journal of Lipid Research (Oct 2010)

Lipoprotein(a) levels and long-term cardiovascular risk in the contemporary era of statin therapy

  • Stephen J. Nicholls,
  • W.H. Wilson Tang,
  • Heather Scoffone,
  • Danielle M. Brennan,
  • Jaana Hartiala,
  • Hooman Allayee,
  • Stanley L. Hazen

Journal volume & issue
Vol. 51, no. 10
pp. 3055 – 3061

Abstract

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Lipoprotein(a) [Lp(a)] has enhanced atherothrombotic properties. The ability of Lp(a) levels to predict adverse cardiovascular outcomes in patients undergoing coronary angiography has not been examined. The relationship between serum Lp(a) levels and both the extent of angiographic disease and 3-year incidence of major adverse cardiovascular events (MACE: death, myocardial infarction, stroke, and coronary revascularization) was investigated in 2,769 patients who underwent coronary angiography [median Lp(a) 16.4 mg/dl, elevated levels (≥30 mg/dl) in 38%]. An elevated Lp(a) was associated with a 2.3-fold [95% confidence interval (CI), 1.7–3.2, P 100 mg/dl (P = 0.02), but not <70 mg/dl (P = 0.77). Polymorphisms of Lp(a) were also associated with both plasma Lp(a) levels and coronary stenosis, but not a greater rate of MACE. Lp(a) levels correlate with the extent of obstructive disease and predict the need for coronary revascularization in subjects with suboptimal LDL-C control. This supports the need to intensify lipid management in patients with elevated Lp(a) levels.

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