Evidence mapPaperPMID 40633089Full record

Trial reportDiabetes2025

Predictors of Initial and Sustained Glycemic and Weight Response to Tirzepatide: A Post Hoc Analysis of SURPASS-4.

Ewan R Pearson, Stefano Del Prato, Imre Pavo, Denise R Franco, Junyuan Zheng, Claudia Nicolay, Andrea Hemmingway, Russell J Wiese, Steven E Kahn

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetes, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Ewan R PearsonDivision of Population Health & Genomics, School of Medicine, University of Dundee, Dundee, U.K.ORCID 0000-0001-9237-8585
Stefano Del PratoInterdisciplinary Research Center "Health Science," Sant'Anna School of Advanced Studies, Pisa, Italy.ORCID 0000-0002-5388-0270
Imre PavoEli Lilly and Company, Indianapolis, IN.ORCID 0000-0002-2016-7049
Denise R FrancoCPCLIN/DASA Clinical Research Center, São Paulo, Brazil.ORCID 0000-0003-4961-0638
Junyuan ZhengEli Lilly and Company, Indianapolis, IN.
Claudia NicolayEli Lilly and Company, Indianapolis, IN.
Andrea HemmingwayEli Lilly and Company, Indianapolis, IN.ORCID 0000-0002-5856-5114
Russell J WieseEli Lilly and Company, Indianapolis, IN.ORCID 0009-0007-6705-7545
Steven E KahnDivision of Metabolism, Endocrinology and Nutrition, Department of Medicine, Veterans Affairs Puget Sound Health Care System and University of Washington, Seattle, WA.ORCID 0000-0001-7307-9002

Funding

Eli Lilly and Company
6 · The paper itself

Abstract

This post hoc analysis assessed sustainability of lowered glycated hemoglobin (HbA1c) and weight with tirzepatide in people with type 2 diabetes and increased cardiovascular risk. Participants achieving HbA1c ≤48 mmol/mol (6.5%) or weight loss ≥10% at 52 weeks were evaluated for sustained glycemic or weight control and predictors of initial and sustained efficacy. 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 achievement were higher tirzepatide dose, shorter diabetes duration, and lower HbA1c, higher HOMA of β-cell function (HOMA-B), metformin alone, and absence of albuminuria at baseline. Factors predicting sustained glycemic control were greater weight loss, smaller fasting glucose decrease, no sulfonylurea, and higher HOMA-B at 52 weeks. For participants achieving ≥10% weight loss at 52 weeks, 79-82% maintained weight loss. Factors predicting achievement were higher tirzepatide dose, female sex, no cardiovascular disease history, and lower baseline HbA1c, estimated glomerular filtration rate, and triglycerides. Greater decrease in LDL-cholesterol to 52 weeks predicted maintained weight loss. Greater weight loss and better β-cell function achieved with tirzepatide were the main predictors for sustained glycemic control in this post hoc analysis; no clinically meaningful predictor was identified for sustained weight control. ARTICLE HIGHLIGHTS: We aimed to explore sustainability of lowered glycated hemoglobin (HbA1c) and weight with tirzepatide in a post hoc analysis. The question we wanted to answer was what predicted achieving and sustaining HbA1c and weight reduction in A Study of Tirzepatide (LY3298176) Once a Week Versus Insulin Glargine Once a Day in Participants With Type 2 Diabetes and Increased Cardiovascular Risk (SURPASS-4). We found greater weight loss and improved β-cell function were the main predictors for sustained glycemic control with tirzepatide therapy. No clinically relevant predictor was identified for sustained weight loss. Simple clinical measures may predict initial and sustained glycemic control and initial weight loss with tirzepatide.

Indexed as

Blood GlucoseDiabetes Mellitus, Type 2Hypoglycemic AgentsTirzepatideAgedBody WeightFemaleGlycated HemoglobinGlycemic ControlHumansMaleMiddle AgedWeight LossBlood GlucoseGlycated Hemoglobinhemoglobin A1c protein, humanHypoglycemic AgentsTirzepatide

Identifiers

PMID40633089
PMCPMC12451090

What Socratic holds

Texttitle and abstract
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.