TY - JOUR
T1 - Alkaline phosphatase and prognosis in patients with coronary artery disease
AU - Ndrepepa, Gjin
AU - Xhepa, Erion
AU - Braun, Siegmund
AU - Cassese, Salvatore
AU - Fusaro, Massimiliano
AU - Schunkert, Heribert
AU - Kastrati, Adnan
N1 - Publisher Copyright:
© 2017 Stichting European Society for Clinical Investigation Journal Foundation
PY - 2017/5
Y1 - 2017/5
N2 - Background: The evidence on the association between alkaline phosphatase (ALP) and prognosis of patients with coronary artery disease (CAD) is limited. The aim of this study was to assess the association of ALP with the risk of mortality or coronary events in patients with CAD. Materials and methods: The study included 5540 patients with angiography-proven CAD treated with catheter-based coronary revascularization. Baseline ALP measurements were available for analysis in all patients. Patients were divided into three groups: a group with an ALP activity in the 1st tertile (ALP ≤ 65·5 U/L; n = 1855), a group with an ALP activity in the 2nd tertile (ALP > 65·5 to 85·7 U/L; n = 1839) and a group with an ALP in the 3rd tertile (ALP > 85·7 U/L; n = 1846). The primary outcome was all-cause mortality at 3-year follow-up. Results: All-cause deaths (number [Kaplan–Meier estimates]) occurred in 443 patients: 117 (7·2%), 130 (8·1%) and 196 deaths (11·8%) among patients of the 1st, 2nd and 3rd ALP tertiles (unadjusted hazard ratio [HR] = 1·33, 95% confidence interval [CI]: 1·19 to 1·50; P < 0·001, calculated per tertile increment in the ALP activity). After adjustment in multivariable Cox proportional hazards model, ALP was independently associated with the risk of all-cause mortality (adjusted HR = 1·33 [1·18–1·51], P < 0·001, calculated per unit increment in log ALP). The multivariable model for all-cause mortality with baseline variables without ALP had a C statistic of 0·820 [0·797–0·843] which increased to 0·825 [0·804–0·849] after ALP inclusion; delta C statistic 0·005 [0·001–0·011]; P < 0·001. Conclusions: In patients with CAD, elevated ALP activity was independently associated with the risk of 3-year all-cause mortality.
AB - Background: The evidence on the association between alkaline phosphatase (ALP) and prognosis of patients with coronary artery disease (CAD) is limited. The aim of this study was to assess the association of ALP with the risk of mortality or coronary events in patients with CAD. Materials and methods: The study included 5540 patients with angiography-proven CAD treated with catheter-based coronary revascularization. Baseline ALP measurements were available for analysis in all patients. Patients were divided into three groups: a group with an ALP activity in the 1st tertile (ALP ≤ 65·5 U/L; n = 1855), a group with an ALP activity in the 2nd tertile (ALP > 65·5 to 85·7 U/L; n = 1839) and a group with an ALP in the 3rd tertile (ALP > 85·7 U/L; n = 1846). The primary outcome was all-cause mortality at 3-year follow-up. Results: All-cause deaths (number [Kaplan–Meier estimates]) occurred in 443 patients: 117 (7·2%), 130 (8·1%) and 196 deaths (11·8%) among patients of the 1st, 2nd and 3rd ALP tertiles (unadjusted hazard ratio [HR] = 1·33, 95% confidence interval [CI]: 1·19 to 1·50; P < 0·001, calculated per tertile increment in the ALP activity). After adjustment in multivariable Cox proportional hazards model, ALP was independently associated with the risk of all-cause mortality (adjusted HR = 1·33 [1·18–1·51], P < 0·001, calculated per unit increment in log ALP). The multivariable model for all-cause mortality with baseline variables without ALP had a C statistic of 0·820 [0·797–0·843] which increased to 0·825 [0·804–0·849] after ALP inclusion; delta C statistic 0·005 [0·001–0·011]; P < 0·001. Conclusions: In patients with CAD, elevated ALP activity was independently associated with the risk of 3-year all-cause mortality.
KW - Alkaline phosphatase
KW - coronary artery disease
KW - mortality
KW - prognosis
UR - http://www.scopus.com/inward/record.url?scp=85018906772&partnerID=8YFLogxK
U2 - 10.1111/eci.12752
DO - 10.1111/eci.12752
M3 - Article
C2 - 28369867
AN - SCOPUS:85018906772
SN - 0014-2972
VL - 47
SP - 378
EP - 387
JO - European Journal of Clinical Investigation
JF - European Journal of Clinical Investigation
IS - 5
ER -