Evidence mapPaperPMID 41925680Full record

Trial reportDiabetes care2026

Comparison of the Continuous Glucose Monitoring Profiles of Four Glucose-Lowering Medications in the GRADE Randomized Trial.

Richard M Bergenstal, Jill P Crandall, Samuel P Rosin, Nicole M Butera, Anne Bantle, Cyrus Desouza, Elizabeth Duran-Valdez, Stephanie Hall, William H Herman, Mary L Johnson and 6 more

Abstract readRandomized Controlled TrialComparative Study
In one paragraph

Trial report in Diabetes care, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Richard M BergenstalInternational Diabetes Center, HealthPartners Institute, Minneapolis, MN.ORCID 0000-0002-9050-5584
Jill P CrandallDivision of Endocrinology and Fleischer Institute for Diabetes & Metabolism, Albert Einstein College of Medicine, Bronx, NY.ORCID 0000-0001-5576-4428
Samuel P RosinThe Biostatistics Center, Department of Biostatistics and Bioinformatics, Milken Institute School of Public Health, The George Washington University, Bethesda, MD.
Nicole M ButeraThe Biostatistics Center, Department of Biostatistics and Bioinformatics, Milken Institute School of Public Health, The George Washington University, Bethesda, MD.ORCID 0000-0002-8901-3881
Anne BantleDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Minnesota, Minneapolis, MN.
Cyrus DesouzaDivision of Diabetes, Endocrinology & Metabolism, University of Nebraska Medical Center, Omaha Veterans Affairs Medical Center, Omaha, NE.ORCID 0000-0001-6660-0568
Elizabeth Duran-ValdezUniversity of New Mexico, Albuquerque, NM.
Stephanie HallThe Biostatistics Center, Department of Biostatistics and Bioinformatics, Milken Institute School of Public Health, The George Washington University, Bethesda, MD.
William H HermanDivision of Metabolism, Endocrinology, and Diabetes, Department of Internal Medicine, University of Michigan, Ann Arbor, MI.ORCID 0000-0002-0502-674X
Mary L JohnsonInternational Diabetes Center, HealthPartners Institute, Minneapolis, MN.
Violet LagariMiami Veterans Affairs Healthcare System/University of Miami, Miami, FL.
Mary E LarkinDiabetes Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Lawrence S PhillipsAtlanta Veterans Affairs Medical Center, Decatur, GA.ORCID 0000-0002-6542-8046
Holly J WillisInternational Diabetes Center, HealthPartners Institute, Minneapolis, MN.
Heidi Krause-SteinraufThe Biostatistics Center, Department of Biostatistics and Bioinformatics, Milken Institute School of Public Health, The George Washington University, Bethesda, MD.ORCID 0000-0001-6894-4110
GRADE Research Group*

Funding

Continuation of the Glycemia Reduction Approaches in Diabetes: A Comparative Effectiveness (GRADE) StudyU01DK098246 · NIDDK · GEORGE WASHINGTON UNIVERSITY · PI Heidi Krause-Steinrauf, JOHN M LACHIN · 2021 to 2022
$21.0M
American Diabetes AssociationCDC HHSDivision of Diabetes, Endocrinology, and Metabolic Diseases U01DK098246Division of Diabetes, Endocrinology, and Metabolic Diseases U34DK088043NHLBI NIH HHSNIDDK NIH HHS U01 DK098246
6 · The paper itself

Abstract

objectiveGlycemic management metrics derived from continuous glucose monitoring (CGM) are increasingly recognized as important therapeutic targets. We performed one of the first comparisons of CGM metrics and achievement of CGM targets among four classes of glucose-lowering medications in combination with metformin. RESEARCH DESIGN AND

methodsThe Glycemia Reduction Approaches in Diabetes (GRADE) study randomly assigned participants with type 2 diabetes and taking metformin to add one of four glucose-lowering medications (insulin glargine, glimepiride, liraglutide, or sitagliptin) and followed them for glycemic outcomes for 5 ± 1.3 years. A 2-week masked CGM analysis was conducted midstudy in 1,080 participants to evaluate CGM metrics, 24-h ambulatory glucose profile, and achievement of consensus goals. Treatment effects among the four groups were compared.

resultsThe sitagliptin and liraglutide groups had the highest time in range 70-180 mg/dL (TIR70-180) and the lowest time below range <70 mg/dL (TBR<70) and percentage coefficient of variation (%CV). The glimepiride group had the lowest TIR70-180, and the highest %CV, TBR<70, and number of CGM-derived hypoglycemic events (P < 0.001), and was the only drug showing daytime hypoglycemia. Sitagliptin and liraglutide were best for achieving consensus goals of very low TBR<54 <1% and the combined metric of TIR70-180 >70% and TBR<70 <4% (P < 0.001). When stratified by HbA1c, mean glucose did not differ among treatments, but %CV and TBR<70 were higher with glargine and glimepiride within each HbA1c stratum.

conclusionsIncretin class drugs had the lowest %CV, the least hypoglycemia, and best achievement of CGM-based glycemic targets. CGM metrics and profiles provide clinical insights, beyond HbA1c, to guide diabetes management.

Indexed as

Diabetes Mellitus, Type 2Hypoglycemic AgentsBlood GlucoseContinuous Glucose MonitoringFemaleGlycated HemoglobinHumansInsulin GlargineLiraglutideMaleMetforminMiddle AgedSitagliptin PhosphateSulfonylurea CompoundsBlood GlucoseglimepirideGlycated HemoglobinHypoglycemic AgentsInsulin GlargineLiraglutideMetforminSitagliptin PhosphateSulfonylurea Compounds

Identifiers

PMID41925680
PMCPMC13186179

What Socratic holds

Texttitle and abstract
LicenceTDM
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.