Evidence map›Paper›PMID 33863751›Full record

Trial reportDiabetes care2021

A Type 2 Diabetes Subtype Responsive to ACCORD Intensive Glycemia Treatment.

Arshiya Mariam, Galen Miller-Atkins, Kevin M Pantalone, Robert S Zimmerman, John Barnard, Michael W Kattan, Hetal Shah, Howard L McLeod, Alessandro Doria, Michael J Wagner and 3 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetes care, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Diabetic neuropathy: cutting-edge research and future directions.Signal transduction and targeted therapy · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 1 country.

Arshiya MariamDepartment of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH.
Galen Miller-AtkinsDepartment of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH.
Kevin M PantaloneEndocrinology and Metabolism Institute, Cleveland Clinic, Cleveland, OH.
Robert S ZimmermanEndocrinology and Metabolism Institute, Cleveland Clinic, Cleveland, OH.
John BarnardDepartment of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH.
Michael W KattanDepartment of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH.
Hetal ShahJoslin Diabetes Center and Harvard Medical School, Boston, MA.ORCID 0000-0002-3685-4572
Howard L McLeodTaneja College of Pharmacy, University of South Florida, Tampa, FL.
Alessandro DoriaJoslin Diabetes Center and Harvard Medical School, Boston, MA.ORCID 0000-0002-3830-4304
Michael J WagnerCenter for Pharmacogenomics and Individualized Therapy, University of North Carolina at Chapel Hill, Chapel Hill, NC.
John B BuseDivision of Endocrinology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Alison A Motsinger-ReifBiostatistics and Computational Biology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC.
Daniel M RotroffDepartment of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH rotrofd@ccf.org.ORCID 0000-0003-0553-3220
Cleveland Clinic Lerner College of Medicine · USCleveland Clinic · USJoslin Diabetes Center · USUniversity of North Carolina at Chapel Hill · USNational Institute of Environmental Health Sciences · USUniversity of South Florida · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI Alessandro Doria · 1986 to 2026
$50.5M
Pilot & Feasibility ProgramP30DK124723 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI P Darrell Neufer · 2020 to 2026
$11.0M
Institutional Career Development CoreKL2TR002547 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI DWEIK, RAED A. · 2018 to 2022
$7.7M
Genetic modifiers of the effect of intensive glycemic control on CVD riskR01HL110400 · NHLBI · JOSLIN DIABETES CENTER · PI DORIA, ALESSANDRO · 2011 to 2014
$3.8M
Statistical Genetics of Outcomes and Drug Response in Patients with Type 2 Diabetes.ZIAES103338 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI MOTSINGER-REIF, ALISON · 2019 to 2025
$2.5M
An Exome-Focused Approach to Pharmacogenetic Analysis of the ACCORD TrialR01HL110380 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BUSE, JOHN BERNARD, WAGNER, MICHAEL JAY · 2012 to 2015
$2.4M
NCATS NIH HHS KL2 TR002547NHLBI NIH HHS R01 HL110380NHLBI NIH HHS R01 HL110400NIDDK NIH HHS P30 DK036836NIDDK NIH HHS P30 DK124723
6 · The paper itself

Abstract

objectiveCurrent type 2 diabetes (T2D) management contraindicates intensive glycemia treatment in patients with high cardiovascular disease (CVD) risk and is partially motivated by evidence of harms in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial. Heterogeneity in response to intensive glycemia treatment has been observed, suggesting potential benefit for some individuals. RESEARCH DESIGN AND

methodsACCORD was a randomized controlled trial that investigated whether intensively treating glycemia in individuals with T2D would reduce CVD outcomes. Using a novel approach to cluster HbA

resultsWe identified four clinical groupings in the intensive glycemia arm, and clinical group 4 (C4) displayed fewer CVD (hazard ratio [HR] 0.34;

conclusionsWe found evidence of a T2D clinical group in ACCORD that benefited from intensive glycemia treatment, and membership in this group could be predicted using genetic variants. This study generates new hypotheses with implications for precision medicine in T2D and represents an important development in this landmark clinical trial warranting further investigation.

Indexed as

Cardiovascular DiseasesDiabetes Mellitus, Type 2Blood GlucoseHealth BehaviorHumansProportional Hazards ModelsProto-Oncogene MasRisk FactorsBlood GlucoseMAS1 protein, humanProto-Oncogene Mas

Identifiers

PMID33863751
PMCPMC8247498
OpenAlexW3156979981

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.