High serum YKL-40 concentration is associated with cardiovascular and all-cause mortality in patients with stable coronary artery disease

Jens Kastrup, Julia S Johansen, Per Winkel, Jørgen Fischer Hansen, Per Hildebrandt, Gorm Boje Jensen, Christian M Jespersen, Erik Kjøller, Hans Jørn Kolmos, Inga Lind, Henrik Nielsen, Christian Gluud, CLARICOR Trial Group, Jens Kastrup, Julia S Johansen, Per Winkel, Jørgen Fischer Hansen, Per Hildebrandt, Gorm Boje Jensen, Christian M JespersenErik Kjøller, Hans Jørn Kolmos, Inga Lind, Henrik Nielsen, Christian Gluud, CLARICOR Trial Group

    127 Citations (Scopus)

    Abstract

    AIMS: Macrophages in atherosclerotic plaques secrete YKL-40. We tested the hypothesis if high serum YKL-40 concentration predicts coronary events and death of patients with stable coronary artery disease (CAD). METHODS AND RESULTS: During the 2.6 years follow-up period (median 2.77 year, interquartile range 0.23 year), 270 patients among the 4298 patients with stable CAD in the CLARICOR trial suffered myocardial infarction (MI) and 377 died (187 classified as cardiovascular death). Serum YKL-40 transformed as Y=log[max(82, serum YKL-40/microg/L)] was significantly associated with cardiovascular death [hazard ratio (HR) = 1.88, 95% confidence interval (CI) = 1.54-2.31, P < 0.001], all-cause mortality (HR = 2.01, 95% CI = 1.75-2.31, P < 0.001), and MI (HR = 1.38, 95% CI = 1.13-1.68, P = 0.002). Following multivariable adjustment for cardiovascular risk factors (age, sex, previous MI, smoking status, hypertension, diabetes mellitus) and selected medical treatments Y contributed significantly to prediction of all-cause mortality (P < 0.001) and cardiovascular mortality (P = 0.001), but not MI (P = 0.25). CONCLUSION: High serum YKL-40 is associated with MI, cardiovascular and all-cause mortality in patients with stable CAD.
    Original languageEnglish
    JournalEuropean Heart Journal
    Volume30
    Issue number9
    Pages (from-to)1066-72
    Number of pages6
    ISSN0195-668X
    DOIs
    Publication statusPublished - 2009

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