Lipoprotein‐Associated Phospholipase A2 Activity Is a Marker of Risk But Not a Useful Target for Treatment in Patients With Stable Coronary Heart Disease

نویسندگان

  • Lars Wallentin
  • Claes Held
  • Paul W. Armstrong
  • Christopher P. Cannon
  • Richard Y. Davies
  • Christopher B. Granger
  • Emil Hagström
  • Robert A. Harrington
  • Judith S. Hochman
  • Wolfgang Koenig
  • Sue Krug‐Gourley
  • Emile R. Mohler
  • Agneta Siegbahn
  • Elizabeth Tarka
  • Philippe Gabriel Steg
  • Ralph A. H. Stewart
  • Robert Weiss
  • Ollie Östlund
  • Harvey D. White
  • Andrzej Budaj
  • Diego Ardissino
  • Alvaro Avezum
  • Philip E. Aylward
  • Alfonso Bryce
  • Hong Chen
  • Ming‐Fong Chen
  • Ramon Corbalan
  • Anthony J. Dalby
  • Nicolas Danchin
  • Robbert J. De Winter
  • Stefan Denchev
  • Rafael Diaz
  • Moses Elisaf
  • Marcus D. Flather
  • Assen R. Goudev
  • Liliana Grinfeld
  • Steen Husted
  • Hyo‐Soo Kim
  • Ales Linhart
  • Eva Lonn
  • José López‐Sendón
  • Athanasios J. Manolis
  • José C. Nicolau
  • Prem Pais
  • Alexander Parkhomenko
  • Terje R. Pedersen
  • Daniel Pella
  • Marco A. Ramos‐Corrales
  • Mikhail Ruda
  • Mátyás Sereg
  • Saulat Siddique
  • Peter Sinnaeve
  • Piyamitr Sritara
  • Henk P. Swart
  • Rody G. Sy
  • Tamio Teramoto
  • Hung‐Fat Tse
  • W. Douglas Weaver
  • Margus Viigimaa
  • Dragos Vinereanu
  • Junren Zhu
چکیده

BACKGROUND We evaluated lipoprotein-associated phospholipase A2 (Lp-PLA2) activity in patients with stable coronary heart disease before and during treatment with darapladib, a selective Lp-PLA2 inhibitor, in relation to outcomes and the effects of darapladib in the STABILITY trial. METHODS AND RESULTS Plasma Lp-PLA2 activity was determined at baseline (n=14 500); at 1 month (n=13 709); serially (n=100) at 3, 6, and 18 months; and at the end of treatment. Adjusted Cox regression models evaluated associations between Lp-PLA2 activity levels and outcomes. At baseline, the median Lp-PLA2 level was 172.4 μmol/min per liter (interquartile range 143.1-204.2 μmol/min per liter). Comparing the highest and lowest Lp-PLA2 quartile groups, the hazard ratios were 1.50 (95% CI 1.23-1.82) for the primary composite end point (cardiovascular death, myocardial infarction, or stroke), 1.95 (95% CI 1.29-2.93) for hospitalization for heart failure, 1.42 (1.07-1.89) for cardiovascular death, and 1.37 (1.03-1.81) for myocardial infarction after adjustment for baseline characteristics, standard laboratory variables, and other prognostic biomarkers. Treatment with darapladib led to a ≈65% persistent reduction in median Lp-PLA2 activity. There were no associations between on-treatment Lp-PLA2 activity or changes of Lp-PLA2 activity and outcomes, and there were no significant interactions between baseline and on-treatment Lp-PLA2 activity or changes in Lp-PLA2 activity levels and the effects of darapladib on outcomes. CONCLUSIONS Although high Lp-PLA2 activity was associated with increased risk of cardiovascular events, pharmacological lowering of Lp-PLA2 activity by ≈65% did not significantly reduce cardiovascular events in patients with stable coronary heart disease, regardless of the baseline level or the magnitude of change of Lp-PLA2 activity. CLINICAL TRIAL REGISTRATION URL: https://www.clinicaltrials.gov. Unique identifier: NCT00799903.

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Lipoprotein-associated phospholipase A2 predicts future cardiovascular events in patients with coronary heart disease independently of traditional risk factors, markers of inflammation, renal function, and hemodynamic stress.

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عنوان ژورنال:

دوره 5  شماره 

صفحات  -

تاریخ انتشار 2016