TY - JOUR
T1 - Temporal Pattern of Growth Differentiation Factor-15 Protein After Acute Coronary Syndrome (From the BIOMArCS Study)
AU - Buljubasic, Nermina
AU - Vroegindewey, Maxime M.
AU - Oemrawsingh, Rohit M.
AU - Asselbergs, Folkert W.
AU - Cramer, Etienne
AU - Liem, Anho
AU - van der Harst, Pim
AU - Maas, Arthur
AU - Ronner, Eelko
AU - Schotborgh, Carl
AU - Wardeh, Alexander J.
AU - Akkerhuis, K. Martijn
AU - Boersma, Eric
N1 - Funding Information:
Funding: The BIOMArCS study is supported and funded by the Netherlands Heart Foundation (grant number 2007B012 ), the Netherlands Heart Institute (project number 071.01) and the Working Group on Cardiovascular Research Netherlands, all of which are non-commercial funding bodies. The funding sources had no involvement in the study design; collection, analysis and interpretation of data; writing of the manuscript and in the decision to submit the article for publication.
Funding Information:
Funding: The BIOMArCS study is supported and funded by the Netherlands Heart Foundation (grant number 2007B012), the Netherlands Heart Institute (project number 071.01)and the Working Group on Cardiovascular Research Netherlands, all of which are non-commercial funding bodies. The funding sources had no involvement in the study design; collection, analysis and interpretation of data; writing of the manuscript and in the decision to submit the article for publication.
Funding Information:
Funding: The BIOMArCS study is supported and funded by the Netherlands Heart Foundation (grant number 2007B012), the Netherlands Heart Institute (project number 071.01) and the Working Group on Cardiovascular Research Netherlands, all of which are non-commercial funding bodies. The funding sources had no involvement in the study design; collection, analysis and interpretation of data; writing of the manuscript and in the decision to submit the article for publication. Funding: The BIOMArCS study is supported and funded by the Netherlands Heart Foundation (grant number 2007B012), the Netherlands Heart Institute (project number 071.01) and the Working Group on Cardiovascular Research Netherlands, all of which are non-commercial funding bodies. The funding sources had no involvement in the study design; collection, analysis and interpretation of data; writing of the manuscript and in the decision to submit the article for publication.
Publisher Copyright:
© 2019 Elsevier Inc.
PY - 2019/7/1
Y1 - 2019/7/1
N2 - Growth differentiation factor-15 (GDF-15)has appeared as a promising biomarker with strong predictive abilities in acute coronary syndrome (ACS). However, studies are solely based on single measurements in the acute phase of an ACS event. The way GDF-15 patterns in post-ACS patients behave on the long term is largely unknown. We conducted a nested case-control study within our multicenter, prospective, observational biomarker study (BIOMArCS)of 844 ACS patients. Following an index ACS event, high-frequency blood sampling was performed during 1-year of follow-up. GDF-15 was determined batchwise by electrochemiluminescence immunoassays in 37 cases with a recurrent event during 1-year follow-up, and in 74 event-free controls. Cases and controls had a mean ± standard deviation age of 66.9 ± 11.3 years and 81% were men. From 30 days onwards, patients showed stable levels, which were on average 333 (95% confidence interval 68 to 647)pg/mL higher in cases than controls (1704 vs 1371 pg/mL; p value 0.013). Additionally, in the post 30-day period, GDF-15 showed low within-individual variability in both cases and controls. In conclusion, post-ACS patients experiencing a recurrent event had stable and systematically higher GDF-15 levels during 30-day to 1-year follow-up than their event-free counterparts with otherwise similar clinical characteristics. Thus, postdischarge blood sampling might be used throughout the course of 1 year to improve prognostication, whereas, in view of the low within-individual variation, the number of repeated sampling moments might be limited.
AB - Growth differentiation factor-15 (GDF-15)has appeared as a promising biomarker with strong predictive abilities in acute coronary syndrome (ACS). However, studies are solely based on single measurements in the acute phase of an ACS event. The way GDF-15 patterns in post-ACS patients behave on the long term is largely unknown. We conducted a nested case-control study within our multicenter, prospective, observational biomarker study (BIOMArCS)of 844 ACS patients. Following an index ACS event, high-frequency blood sampling was performed during 1-year of follow-up. GDF-15 was determined batchwise by electrochemiluminescence immunoassays in 37 cases with a recurrent event during 1-year follow-up, and in 74 event-free controls. Cases and controls had a mean ± standard deviation age of 66.9 ± 11.3 years and 81% were men. From 30 days onwards, patients showed stable levels, which were on average 333 (95% confidence interval 68 to 647)pg/mL higher in cases than controls (1704 vs 1371 pg/mL; p value 0.013). Additionally, in the post 30-day period, GDF-15 showed low within-individual variability in both cases and controls. In conclusion, post-ACS patients experiencing a recurrent event had stable and systematically higher GDF-15 levels during 30-day to 1-year follow-up than their event-free counterparts with otherwise similar clinical characteristics. Thus, postdischarge blood sampling might be used throughout the course of 1 year to improve prognostication, whereas, in view of the low within-individual variation, the number of repeated sampling moments might be limited.
KW - Acute Coronary Syndrome/blood
KW - Aged
KW - Biomarkers/blood
KW - Case-Control Studies
KW - Female
KW - Follow-Up Studies
KW - Growth Differentiation Factor 15/blood
KW - Humans
KW - Male
KW - Middle Aged
KW - Prospective Studies
KW - Time Factors
UR - http://www.scopus.com/inward/record.url?scp=85064955141&partnerID=8YFLogxK
U2 - 10.1016/j.amjcard.2019.03.049
DO - 10.1016/j.amjcard.2019.03.049
M3 - Article
C2 - 31047655
AN - SCOPUS:85064955141
SN - 0002-9149
VL - 124
SP - 8
EP - 13
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 1
ER -