Diabetes

Factors linked to early and long-term blood sugar and weight changes with Tirzepatide treatment

Updated

Abstract

For tirzepatide-treated participants achieving HbA1c ≤48 mmol/mol (6.5%) at 52 weeks, 75-84% sustained this until study end (median 81 weeks).

  • Factors predicting initial glycemic control included higher tirzepatide dose, shorter diabetes duration, lower HbA1c, better β-cell function, metformin use alone, and absence of albuminuria at baseline.
  • Sustained glycemic control was associated with greater weight loss, a smaller decrease in fasting glucose, no use of sulfonylureas, and higher β-cell function at 52 weeks.
  • For participants achieving ≥10% weight loss at 52 weeks, 79-82% maintained their weight loss.
  • Predictors for achieving weight loss included higher tirzepatide dose, female sex, no history of cardiovascular disease, and lower baseline HbA1c, kidney function, and triglycerides.
  • A greater decrease in LDL-cholesterol by 52 weeks was linked to maintained weight loss.

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Funding

Competing interests

Duality of Interest. The SURPASS-4 study and these analyses were supported by Eli Lilly and Company. E.R.P. has received honoraria from Eli Lilly and Company, Illumina, and Novo Nordisk. S.D.P. has served as the president of the European Association for the Study of Diabetes/European Foundation for the Study of Diabetes (2020–2022), has received research grants to their institution from AstraZeneca and Boehringer Ingelheim, has served as an adviser for Abbott, Amarin Corporation, Amplitude, Applied Therapeutics, AstraZeneca, Biomea Fusion, Eli Lilly and Company, EVA Pharma, Menarini Group, Novo Nordisk, Sanofi, and Sun Pharma, and has received fees for speaking from AstraZeneca, Boehringer Ingelheim, Eli Lilly and Company, Laboratori Guidotti, Menarini Group, Merck Sharpe & Dohme, and Novo Nordisk. D.R.F. has served as an adviser to Eli Lilly and Company, Novo Nordisk, Abbott, Medtronic, AstraZeneca, Embecta, has received research support from Eli Lilly and Company and Novo Nordisk, and has received fees for speaking from AstraZeneca, Eli Lilly and Company, Abbott, Medtronic, and Novo Nordisk. S.E.K. has served as an adviser to Abarceo Pharma, AltPep, Amgen, Biomea Fusion, Eli Lilly and Company, Merck, Neurimmune, Novo Nordisk, and Oramed Pharmaceuticals, and has received research support from Corcept Therapeutics. I.P., J.Z., A.H., and R.J.W. are employees and shareholders of Eli Lilly and Company. C.N. was an employee of Eli Lilly and Company when this work took place and is a shareholder. No other potential conflicts of interest relevant to this article were reported.
PubMed

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