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  4. Growth Differentiation Factor 15 Predicts AM-Cause Morbidity and Mortality in Stable Coronary Heart Disease
 
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Growth Differentiation Factor 15 Predicts AM-Cause Morbidity and Mortality in Stable Coronary Heart Disease
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Growth Differentiation Factor 15 at 1 Month After an Acute Coronary Syndrome Is Associated With Increased Risk of Major Bleeding.pdf (1.15 MB)
Published version
Author(s)
Hagstrom, E
Held, C
Stewart, RAH
Aylward, PE
Budaj, A
more
Type
Journal Article
Abstract
Background-—Growth differentiation factor-15 (GDF-15) is related to major bleeding when measured at initial presentation in
patients with acute coronary syndromes (ACSs) treated with dual antiplatelet therapy. It is unknown whether follow-up
measurements provide additional information. The objective of this study was to investigate whether GDF-15 measured 1 month
after an ACS provides additional information beyond the baseline levels with regard to the risk of major bleeding.
Methods and Results-—GDF-15 was measured at baseline and at 1 month after an ACS in 4049 patients included in the PLATelet
inhibition and patient Outcomes (PLATO) trial. The association between 1-month GDF-15 level and non–coronary artery bypass
grafting surgery-related major bleeding was assessed by a multivariable Cox model, adjusting for baseline GDF-15, age, anemia,
impaired renal function, history of gastrointestinal bleeding, and sex. Elevated GDF-15 (>1800 ng/L) at 1 month was associated
with an increased risk of non-coronary artery bypass grafting-related major bleeding (3.9% versus 1.2%; hazard ratio, 3.38; 95% CI,
1.89–6.06), independent of baseline GDF-15. Patients who had elevated GDF-15 levels at baseline and subsequent nonelevated
GDF-15 at 1 month had a similar risk as patients who had nonelevated levels at both measurements.
Conclusions-—GDF-15 at 1 month after an ACS is related to the risk of bleeding during DAPT and provides additional information
on the bleeding risk beyond baseline GDF-15 levels. GDF-15 levels may therefore be useful as part of decision support concerning
long-term antithrombotic treatment in patients post-ACS.
Date Issued
2016-12-30
Date Acceptance
2016-09-13
Citation
Clinical Chemistry, 2016, 63 (1), pp.325-333
URI
http://hdl.handle.net/10044/1/51343
DOI
https://www.dx.doi.org/10.1373/clinchem.2016.260570
ISSN
1530-8561
Publisher
American Association for Clinical Chemistry
Start Page
325
End Page
333
Journal / Book Title
Clinical Chemistry
Volume
63
Issue
1
Copyright Statement
© 2017 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the Creative Commons
Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is noncommercial
and no modifications or adaptations are made.
License URL
http://creativecommons.org/licenses/by-nc-nd/4.0/
Subjects
Science & Technology
Life Sciences & Biomedicine
Medical Laboratory Technology
LONG-TERM RISK
CARDIOVASCULAR EVENTS
PROGNOSTIC VALUE
BIOMARKERS
COMMUNITY
CARDIOMYOCYTES
ASSOCIATION
DYSFUNCTION
DARAPLADIB
STRESS
Publication Status
Published
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