Synergistic association of combined glycemic and blood pressure level with risk of complications in US veterans with diabetes.
Ontology highlight
ABSTRACT: Hemoglobin A1c levels less than 7.0% and systolic blood pressure (SBP) less than 140?mmHg are each associated with lower risk of vascular complications in patients with diabetes mellitus. Associations between combined A1c level and SBP categories and risk of mortality and morbidity in diabetic patients are not well characterized.We examined 891?670 US diabetic veterans with baseline estimated glomerular filtration rates more than 60?ml/min per 1.73?m (mean age 67?±?11 years, 97% men, 17% African-Americans). The associations of mutually exclusive combined categories of A1c (<6.5, 6.5-6.9, 7.0-7.9, 8.0-8.9, 9.0-9.9, and ?10%) and SBP (<100, 100-119, 120-139, 140-159, 160-179, and ?180?mmHg) with the risk of all-cause mortality and incident chronic kidney disease (CKD), coronary heart disease, and stroke were examined in Cox models adjusted for baseline characteristics using patients with concomitant A1c 6.5-6.9% and SBP of 120-139?mmHg as the referent group.A total of 221?529 (25%) patients died, and 178?588 (20%), 43?373 (5%) and 36?935 (4%) developed CKD, coronary heart disease and stroke, respectively, during a median follow-up of 7.4 years. SBP displayed a J-shaped association with each outcome except CKD risk that was linearly associated with SBP across all A1c categories. A1c above 7.0% was associated with monotonically worse outcomes for all end points in all SBP categories. Patients with the combined highest A1c and SBP levels experienced the worst outcomes.SBP greater than 120-139?mmHg and A1c greater than 7.0% are associated with higher mortality and vascular complications in diabetic patients, independent of each other. Combined efforts to improve both glycemic and blood pressure control may synergistically improve outcomes in patients with normal kidney function.
SUBMITTER: Gosmanov AR
PROVIDER: S-EPMC5705006 | biostudies-literature | 2016 May
REPOSITORIES: biostudies-literature
ACCESS DATA
