TY - JOUR
T1 - Biomarkers of Clot Activation and Degradation and Risk of Future Major Cardiovascular Events in Acute Exacerbation of COPD
T2 - A Cohort Sub-Study in a Randomized Trial Population
AU - Kamstrup, Peter
AU - Sand, Jannie Marie Bulow
AU - Ulrik, Charlotte Suppli
AU - Janner, Julie
AU - Ronn, Christian Philip
AU - Ronnow, Sarah Rank
AU - Leeming, Diana Julie
AU - Jensen, Sidse Graff
AU - Wilcke, Torgny
AU - Mathioudakis, Alexander G.
AU - Miravitlles, Marc
AU - Lapperre, Therese
AU - Bendstrup, Elisabeth
AU - Frikke-Schmidt, Ruth
AU - Murray, Daniel D.
AU - Itenov, Theis
AU - Bossios, Apostolos
AU - Nielsen, Susanne Dam
AU - Vestbo, Jorgen
AU - Biering-Sorensen, Tor
AU - Karsdal, Morten
AU - Jensen, Jens-Ulrik
AU - Sivapalan, Pradeesh
PY - 2022
Y1 - 2022
N2 - Cardiovascular diseases are common in patients with chronic obstructive pulmonary disease (COPD). Clot formation and resolution secondary to systemic inflammation may be a part of the explanation. The aim was to determine whether biomarkers of clot formation (products of von Willebrand Factor formation and activation) and clot resolution (product of fibrin degeneration) during COPD exacerbation predicted major cardiovascular events (MACE). The cohort was based on clinical data and biobank plasma samples from a trial including patients admitted with an acute exacerbation of COPD (CORTICO-COP). Neo-epitope biomarkers of formation and the activation of von Willebrand factor (VWF-N and V-WFA, respectively) and cross-linked fibrin degradation (X-FIB) were assessed using ELISAs in EDTA plasma at the time of acute admission, and analyzed for time-to-first MACE within 36 months, using multivariable Cox proportional hazards models. In total, 299/318 participants had samples available for analysis. The risk of MACE for patients in the upper quartile of each biomarker versus the lower quartile was: X-FIB: HR 0.98 (95% CI 0.65-1.48), VWF-N: HR 1.56 (95% CI 1.07-2.27), and VWF-A: HR 0.78 (95% CI 0.52-1.16). Thus, in COPD patients with an acute exacerbation, VWF-N was associated with future MACE and warrants further studies in a larger population.
AB - Cardiovascular diseases are common in patients with chronic obstructive pulmonary disease (COPD). Clot formation and resolution secondary to systemic inflammation may be a part of the explanation. The aim was to determine whether biomarkers of clot formation (products of von Willebrand Factor formation and activation) and clot resolution (product of fibrin degeneration) during COPD exacerbation predicted major cardiovascular events (MACE). The cohort was based on clinical data and biobank plasma samples from a trial including patients admitted with an acute exacerbation of COPD (CORTICO-COP). Neo-epitope biomarkers of formation and the activation of von Willebrand factor (VWF-N and V-WFA, respectively) and cross-linked fibrin degradation (X-FIB) were assessed using ELISAs in EDTA plasma at the time of acute admission, and analyzed for time-to-first MACE within 36 months, using multivariable Cox proportional hazards models. In total, 299/318 participants had samples available for analysis. The risk of MACE for patients in the upper quartile of each biomarker versus the lower quartile was: X-FIB: HR 0.98 (95% CI 0.65-1.48), VWF-N: HR 1.56 (95% CI 1.07-2.27), and VWF-A: HR 0.78 (95% CI 0.52-1.16). Thus, in COPD patients with an acute exacerbation, VWF-N was associated with future MACE and warrants further studies in a larger population.
KW - COPD exacerbation
KW - major cardiovascular events
KW - coagulation
KW - biomarkers
KW - von Willebrand factor
KW - cross-linked fibrin degradation
KW - VON-WILLEBRAND-FACTOR
KW - D-DIMER
KW - ADAMTS13 ACTIVITY
KW - FACTOR ANTIGEN
KW - MORTALITY
U2 - 10.3390/biomedicines10082011
DO - 10.3390/biomedicines10082011
M3 - Journal article
C2 - 36009558
VL - 10
JO - Biomedicines
JF - Biomedicines
SN - 2227-9059
IS - 8
M1 - 2011
ER -