TY - JOUR
T1 - Glycated haemoglobin and the risk of cardiovascular disease, diabetes and all-cause mortality in the Copenhagen City Heart Study
AU - Eskesen, K
AU - Jensen, M T
AU - Galatius, S
AU - Vestergaard, H
AU - Hildebrandt, P
AU - Marott, J L
AU - Jensen, J S
N1 - © 2012 The Association for the Publication of the Journal of Internal Medicine.
PY - 2013/1
Y1 - 2013/1
N2 - Objective: Individuals with diabetes mellitus (DM) have a considerably elevated risk of developing serious health problems including cardiovascular disease (CVD). Long-term elevated levels of blood glucose in nondiabetic individuals may also be associated with increased risk of CVD. The aim of this study was to investigate the relationships between glycated haemoglobin A1c (HbA1c) and CVD, DM and all-cause mortality. Subjects and design: The Copenhagen City Heart Study is a prospective study of individuals from the Danish general population. The cohort was followed for 10 years via national registers with respect to incident CVD, DM and all-cause mortality. Follow-up was 100% complete. Results: A total of 5127 subjects were included, of whom 597 had DM. In the nondiabetic population, HbA1c was significantly associated with incident CVD events in both univariate [hazard ratio (HR) 1.38, 95% CI 1.11-1.71] and multivariate analyses (HR 1.31, 95% CI 1.05-1.64). In the nondiabetic population, increased levels of HbA1c were correlated with developing DM. There was a threefold increase in risk of incident DM per unit increase in HbA1c with a univariate HR of 3.83 (95% CI 1.96-7.51). This relationship was essentially unchanged after multivariate adjustments (HR 4.19, 95% CI 2.01-8.71). Furthermore, we found that net reclassification improvement for diagnosed DM and CVD was significantly improved with the addition of HbA1c in the analyses. Although not statistically significant, we found a strong trend towards an association between HbA1c and all-cause mortality (HR 1.21, 95% CI 0.99-1.47). We did not find the same associations amongst the population with DM. Conclusion: In the Danish general population, HbA1c was strongly associated with CVD in individuals without DM.
AB - Objective: Individuals with diabetes mellitus (DM) have a considerably elevated risk of developing serious health problems including cardiovascular disease (CVD). Long-term elevated levels of blood glucose in nondiabetic individuals may also be associated with increased risk of CVD. The aim of this study was to investigate the relationships between glycated haemoglobin A1c (HbA1c) and CVD, DM and all-cause mortality. Subjects and design: The Copenhagen City Heart Study is a prospective study of individuals from the Danish general population. The cohort was followed for 10 years via national registers with respect to incident CVD, DM and all-cause mortality. Follow-up was 100% complete. Results: A total of 5127 subjects were included, of whom 597 had DM. In the nondiabetic population, HbA1c was significantly associated with incident CVD events in both univariate [hazard ratio (HR) 1.38, 95% CI 1.11-1.71] and multivariate analyses (HR 1.31, 95% CI 1.05-1.64). In the nondiabetic population, increased levels of HbA1c were correlated with developing DM. There was a threefold increase in risk of incident DM per unit increase in HbA1c with a univariate HR of 3.83 (95% CI 1.96-7.51). This relationship was essentially unchanged after multivariate adjustments (HR 4.19, 95% CI 2.01-8.71). Furthermore, we found that net reclassification improvement for diagnosed DM and CVD was significantly improved with the addition of HbA1c in the analyses. Although not statistically significant, we found a strong trend towards an association between HbA1c and all-cause mortality (HR 1.21, 95% CI 0.99-1.47). We did not find the same associations amongst the population with DM. Conclusion: In the Danish general population, HbA1c was strongly associated with CVD in individuals without DM.
U2 - 10.1111/j.1365-2796.2012.02594.x
DO - 10.1111/j.1365-2796.2012.02594.x
M3 - Journal article
C2 - 23009556
SN - 0954-6820
VL - 273
SP - 94
EP - 101
JO - Journal of Internal Medicine
JF - Journal of Internal Medicine
IS - 1
ER -
