TY - JOUR
T1 - Impact of age, age at diagnosis and duration of diabetes on the risk of macrovascular and microvascular complications and death in type 2 diabetes
AU - Zoungas, Sophia
AU - Woodward, Mark
AU - Li, Qiang
AU - Cooper, Mark E.
AU - Hamet, Pavel
AU - Harrap, Stephen
AU - Heller, Simon
AU - Marre, Michel
AU - Patel, Anushka
AU - Poulter, Neil
AU - Williams, Bryan
AU - Chalmers, John
N1 - Funding Information:
JC holds a research grant from Servier as principal investigator for ADVANCE. SZ was supported by a Heart Foundation of Australia Career Development Award. MW was supported by an NHMRC Senior Research Fellowship. SZ, JC, MC, MM and MW have received lecturing fees from Servier. All other authors declare that there is no duality of interest associated with their contribution to this manuscript.
Funding Information:
ADVANCE was funded by grants from Servier and the National Health and Medical Research Council (NHMRC) of Australia (project grant ID 211086 and programme grant IDs 358395 and 571281). The sponsors had no role in data collection, data interpretation or the writing of the manuscript.
Publisher Copyright:
© Springer-Verlag Berlin Heidelberg 2014.
PY - 2014/12
Y1 - 2014/12
N2 - Aims/hypothesis Data are inconsistent regarding the associations between age, age at diagnosis of diabetes, diabetes duration and subsequent vascular complications. Methods The associations between age (or age at diagnosis), diabetes duration and major macrovascular events, all-cause death and major microvascular events were examined in 11,140 patients with type 2 diabetes randomly allocated to intensive or standard glucose control in the Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified Release Controlled Evaluation (ADVANCE) trial. Rates were calculated by 5 year baseline age (or age at diagnosis) and diabetes duration strata. Risks were estimated using Cox models adjusted for treatment assignment and HbA1c. Results The mean age (±SD) was 65.8±6.4 years, age at diagnosis was 57.8±8.7 years and diabetes duration was 7.9±6.4 years. Diabetes duration was associated with the risk of macrovascular events (HR 1.13 [95% CI 1.08, 1.17]), microvascular events (1.28 [1.23, 1.33]) and death (1.15 [1.10, 1.20]) whereas age (or age at diagnosis) was only associated with the risk of macrovascular events (1.33 [1.27, 1.39]) and death (1.56 [1.48, 1.64]). No interaction was observed between diabetes duration, age and the risk of macrovascular events or death (both p>0.4). However, an interaction was observed between diabetes duration, age and the risk of microvascular events (p=0.002), such that the effects of increasing diabetes duration were greatest at younger rather than older age. Conclusions/interpretation In patients with type 2 diabetes, age or age at diagnosis and diabetes duration are independently associated with macrovascular events and death whereas only diabetes duration is independently associated with microvascular events and this effect is greater in the youngest patients.
AB - Aims/hypothesis Data are inconsistent regarding the associations between age, age at diagnosis of diabetes, diabetes duration and subsequent vascular complications. Methods The associations between age (or age at diagnosis), diabetes duration and major macrovascular events, all-cause death and major microvascular events were examined in 11,140 patients with type 2 diabetes randomly allocated to intensive or standard glucose control in the Action in Diabetes and Vascular Disease: Preterax and Diamicron Modified Release Controlled Evaluation (ADVANCE) trial. Rates were calculated by 5 year baseline age (or age at diagnosis) and diabetes duration strata. Risks were estimated using Cox models adjusted for treatment assignment and HbA1c. Results The mean age (±SD) was 65.8±6.4 years, age at diagnosis was 57.8±8.7 years and diabetes duration was 7.9±6.4 years. Diabetes duration was associated with the risk of macrovascular events (HR 1.13 [95% CI 1.08, 1.17]), microvascular events (1.28 [1.23, 1.33]) and death (1.15 [1.10, 1.20]) whereas age (or age at diagnosis) was only associated with the risk of macrovascular events (1.33 [1.27, 1.39]) and death (1.56 [1.48, 1.64]). No interaction was observed between diabetes duration, age and the risk of macrovascular events or death (both p>0.4). However, an interaction was observed between diabetes duration, age and the risk of microvascular events (p=0.002), such that the effects of increasing diabetes duration were greatest at younger rather than older age. Conclusions/interpretation In patients with type 2 diabetes, age or age at diagnosis and diabetes duration are independently associated with macrovascular events and death whereas only diabetes duration is independently associated with microvascular events and this effect is greater in the youngest patients.
KW - Age
KW - Age at diagnosis of diabetes
KW - Duration of diabetes
KW - Macrovascular complications
KW - Microvascular complications
KW - Mortality
KW - Type 2 diabetes
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U2 - 10.1007/s00125-014-3369-7
DO - 10.1007/s00125-014-3369-7
M3 - Article
C2 - 25226881
AN - SCOPUS:84926666142
SN - 0012-186X
VL - 57
SP - 2465
EP - 2474
JO - Diabetologia
JF - Diabetologia
IS - 12
ER -