Glomerular Filtration Rate and Associated Risks of Cardiovascular Events, Mortality, and Severe Hypoglycemia in Patients with Type 2 Diabetes: Secondary Analysis (DEVOTE 11)

Autor: Amod, A, Buse, JB, McGuire, DK, Pieber, TR, Pop-Busui, R, Pratley, RE, Zinman, B, Hansen, MB, Jia, T, Mark, T, Poulter, NR, DEVOTE Study Group
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Insulin degludec
CHRONIC KIDNEY-DISEASE
medicine.medical_specialty
ALBUMINURIA
Endocrinology
Diabetes and Metabolism

medicine.medical_treatment
DEVOTE Study Group
Renal function
030209 endocrinology & metabolism
Type 2 diabetes
030204 cardiovascular system & hematology
ALL-CAUSE
urologic and male genital diseases
03 medical and health sciences
Endocrinology & Metabolism
MELLITUS
DEGLUDEC
0302 clinical medicine
Insulin glargine U100
Diabetes mellitus
Internal medicine
Chronic kidney disease
Internal Medicine
Medicine
Original Research
Severe hypoglycemia
Science & Technology
business.industry
Insulin glargine
Insulin
EMPAGLIFLOZIN
medicine.disease
Cardiovascular disease
female genital diseases and pregnancy complications
3. Good health
RENAL OUTCOMES
LIRAGLUTIDE
Basal insulin analogs
Glomerular filtration rate
business
FOLLOW-UP
Life Sciences & Biomedicine
Mace
medicine.drug
Kidney disease
INSULIN GLARGINE
Zdroj: Diabetes Therapy
Popis: Introduction The associations of chronic kidney disease (CKD) severity, cardiovascular disease (CVD), and insulin with the risks of major adverse cardiovascular events (MACE), mortality, and severe hypoglycemia in patients with type 2 diabetes (T2D) at high cardiovascular (CV) risk are not known. This secondary, pooled analysis of data from the DEVOTE trial examined whether baseline glomerular filtration rate (GFR) categories were associated with a higher risk of these outcomes. Methods DEVOTE was a treat-to-target, double-blind trial involving 7637 patients with T2D at high CV risk who were randomized to once-daily treatment with either insulin degludec (degludec) or insulin glargine 100 units/mL (glargine U100). Patients with estimated GFR data at baseline (n = 7522) were analyzed following stratification into four GFR categories. Results The risks of MACE, CV death, and all-cause mortality increased with worsening baseline GFR category (P
Databáze: OpenAIRE