TY - JOUR
T1 - Plasma neutrophil gelatinase-associated lipocalin and risk of cardiovascular disease
T2 - Findings from the PREVEND prospective cohort study
AU - Kunutsor, Setor K.
AU - Flores-Guerrero, José L.
AU - Kieneker, Lyanne M.
AU - Nilsen, Tom
AU - Hidden, Clara
AU - Sundrehagen, Erling
AU - Seidu, Samuel
AU - Dullaart, Robin P.F.
AU - Bakker, Stephan J.L.
PY - 2018/11/1
Y1 - 2018/11/1
N2 - Background: Neutrophil gelatinase-associated lipocalin (NGAL), a novel biomarker of acute kidney injury, might play a role in the development of atherosclerotic cardiovascular disease (CVD). We aimed to assess the association of circulating NGAL with CVD risk. Materials and methods: Plasma NGAL concentrations were measured at baseline in 5275 participants in the PREVEND prospective study. Hazard ratios (95% confidence intervals [CI]) for CVD were estimated. Results: After a median follow-up of 8.3 years, 338 participants developed first CVD events. Plasma NGAL was weakly to moderately correlated with several CVD risk markers. There was a non-linear relationship between NGAL and CVD risk. In analyses adjusted for established risk factors, the hazard ratio (95% CI) for CVD in a comparison of the top quartile versus bottom quartiles 1–2 of NGAL values was 1.35 (1.05–1.75; P = 0.022), which was abrogated after additional adjustment for other potential confounders (mainly attributed to high sensitivity C-reactive protein) 1.20 (0.92–1.57; P = 0.176). The association was considerably attenuated following further adjustment for renal function 1.05 (0.79–1.40; P = 0.745). The association between NGAL and CVD risk did not vary importantly in relevant clinical subgroups. Conclusion: Evidence suggests a non-linear association between NGAL and CVD risk, which is dependent on inflammation and renal function.
AB - Background: Neutrophil gelatinase-associated lipocalin (NGAL), a novel biomarker of acute kidney injury, might play a role in the development of atherosclerotic cardiovascular disease (CVD). We aimed to assess the association of circulating NGAL with CVD risk. Materials and methods: Plasma NGAL concentrations were measured at baseline in 5275 participants in the PREVEND prospective study. Hazard ratios (95% confidence intervals [CI]) for CVD were estimated. Results: After a median follow-up of 8.3 years, 338 participants developed first CVD events. Plasma NGAL was weakly to moderately correlated with several CVD risk markers. There was a non-linear relationship between NGAL and CVD risk. In analyses adjusted for established risk factors, the hazard ratio (95% CI) for CVD in a comparison of the top quartile versus bottom quartiles 1–2 of NGAL values was 1.35 (1.05–1.75; P = 0.022), which was abrogated after additional adjustment for other potential confounders (mainly attributed to high sensitivity C-reactive protein) 1.20 (0.92–1.57; P = 0.176). The association was considerably attenuated following further adjustment for renal function 1.05 (0.79–1.40; P = 0.745). The association between NGAL and CVD risk did not vary importantly in relevant clinical subgroups. Conclusion: Evidence suggests a non-linear association between NGAL and CVD risk, which is dependent on inflammation and renal function.
KW - Cardiovascular disease
KW - Cohort study
KW - Neutrophil gelatinase-associated lipocalin
KW - Risk factor
UR - http://www.scopus.com/inward/record.url?scp=85050288786&partnerID=8YFLogxK
U2 - 10.1016/j.cca.2018.07.034
DO - 10.1016/j.cca.2018.07.034
M3 - Article (Academic Journal)
C2 - 30036522
AN - SCOPUS:85050288786
SN - 0009-8981
VL - 486
SP - 66
EP - 75
JO - Clinica Chimica Acta
JF - Clinica Chimica Acta
ER -