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Target attainment in insulin-naive patients at high risk for hypoglycemia: Results from ACHIEVE Control
Authors:John Anderson  Luigi Meneghini  Debbie Hinnen  Jasvinder Gill  Mathieu Coudert  Pierre Evenou  Medha Munshi
Institution:1. The Frist Clinic, 2400 Patterson Street, Suite 400, Nashville, TN, USA;2. University of Texas Southwestern Medical Center and Parkland Health & Hospital System, 5323 Harry Hines Boulevard, Dallas, TX, USA;3. Memorial Hospital Diabetes Center, University of Colorado Health, 175 S Union Boulevard, Suite 305, Colorado Springs, CO, USA;4. Sanofi, 55 Corporate Drive, Bridgewater, NJ, USA;5. Sanofi, 1 Avenue Pierre Brossolette, Chilly-Mazarin, France;6. Sanofi, 410 Thames Valley Park Drive, Reading, Berkshire, UK;7. Joslin Diabetes Center, 1 Joslin Place, Boston, MA, USA
Abstract:AimsTo better understand outcomes in people with type 2 diabetes at high risk of hypoglycemia, we conducted post hoc analyses in subgroups of participants from the real-world ACHIEVE Control study (NCT02451137) with ≥1 hypoglycemia risk factor.MethodsInsulin-naive adults with type 2 diabetes and A1c ≥8% were randomized 1:1 to insulin glargine 300 U/mL (Gla-300) or standard-of-care basal insulin (SOC-BI). Participants had documented history of ≥1 risk factors for hypoglycemia: chronic kidney disease, cardiovascular disease, dementia or blindness, age ≥65 years, or history of hypoglycemia. Outcomes included individualized A1c target attainment without documented symptomatic hypoglycemia (blood glucose BG] ≤3.9 mmol/L or <3.0 mmol/L) or severe hypoglycemia, A1c target attainment, and absence of documented symptomatic or severe hypoglycemia at 6 and 12 months.ResultsWithin subgroups, odds ratios generally showed trends favoring Gla-300 versus SOC-BI, particularly for hypoglycemia avoidance in participants ≥65 years of age (BG ≤3.9 mmol/L; odds ratio, 1.52; 95% confidence interval, 1.14–2.03) and those with chronic kidney disease (BG ≤3.9 mmol/L; odds ratio, 2.28; 95% confidence interval, 1.26–4.12). Results were consistent with the overall population.ConclusionsThese data suggest potential benefit of Gla-300 versus SOC-BI for avoiding hypoglycemia in participants with ≥1 hypoglycemia risk factor.
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