Evidence mapPaperPMID 35477454Full record

ArticleCardiovascular diabetology2022

Heterogeneous treatment effects of intensive glycemic control on major adverse cardiovascular events in the ACCORD and VADT trials: a machine-learning analysis.

Justin A Edward, Kevin Josey, Gideon Bahn, Liron Caplan, Jane E B Reusch, Peter Reaven, Debashis Ghosh, Sridharan Raghavan

Open access · goldAbstract read
In one paragraph

Article in Cardiovascular diabetology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

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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

8 authors at 5 institutions in 1 country.

Justin A EdwardDivision of Cardiology, University of Colorado School of Medicine, Aurora, CO, USA.
Kevin JoseyDepartment of Veterans Affairs Eastern Colorado Healthcare System, Rocky Mountain, Regional VA Medical Center, Medicine Service (111), 1700 North Wheeling Street, Aurora, CO, 80045, USA.
Gideon BahnDepartment of Veterans Affairs, Hines VA Hospital, Hines, IL, USA.
Liron CaplanDepartment of Veterans Affairs Eastern Colorado Healthcare System, Rocky Mountain, Regional VA Medical Center, Medicine Service (111), 1700 North Wheeling Street, Aurora, CO, 80045, USA.
Jane E B ReuschDepartment of Veterans Affairs Eastern Colorado Healthcare System, Rocky Mountain, Regional VA Medical Center, Medicine Service (111), 1700 North Wheeling Street, Aurora, CO, 80045, USA.
Peter ReavenDepartment of Veterans Affairs Phoenix VA Medical Center, Phoenix, AZ, USA.
Debashis GhoshDepartment of Biostatistics and Informatics, Colorado School of Public Health, Aurora, CO, USA.
Sridharan RaghavanDepartment of Veterans Affairs Eastern Colorado Healthcare System, Rocky Mountain, Regional VA Medical Center, Medicine Service (111), 1700 North Wheeling Street, Aurora, CO, 80045, USA. Sridharan.raghavan@cuanschutz.edu.
Colorado School of Public Health · USUniversity of Colorado Denver · USVA Eastern Colorado Health Care System · USEdward Hines, Jr. VA Hospital · USPhoenix VA Health Care System · US

Funding

CSRD VA IK2 CX001907NCI NIH HHS R01 CA129102
6 · The paper itself

Abstract

backgroundEvidence to guide type 2 diabetes treatment individualization is limited. We evaluated heterogeneous treatment effects (HTE) of intensive glycemic control in type 2 diabetes patients on major adverse cardiovascular events (MACE) in the Action to Control Cardiovascular Risk in Diabetes Study (ACCORD) and the Veterans Affairs Diabetes Trial (VADT).

methodsCausal forests machine learning analysis was performed using pooled individual data from two randomized trials (n = 12,042) to identify HTE of intensive versus standard glycemic control on MACE in patients with type 2 diabetes. We used variable prioritization from causal forests to build a summary decision tree and examined the risk difference of MACE between treatment arms in the resulting subgroups.

resultsA summary decision tree used five variables (hemoglobin glycation index, estimated glomerular filtration rate, fasting glucose, age, and body mass index) to define eight subgroups in which risk differences of MACE ranged from - 5.1% (95% CI - 8.7, - 1.5) to 3.1% (95% CI 0.2, 6.0) (negative values represent lower MACE associated with intensive glycemic control). Intensive glycemic control was associated with lower MACE in pooled study data in subgroups with low (- 4.2% [95% CI - 8.1, - 1.0]), intermediate (- 5.1% [95% CI - 8.7, - 1.5]), and high (- 4.3% [95% CI - 7.7, - 1.0]) MACE rates with consistent directions of effect in ACCORD and VADT alone.

conclusionsThis data-driven analysis provides evidence supporting the diabetes treatment guideline recommendation of intensive glucose lowering in diabetes patients with low cardiovascular risk and additionally suggests potential benefits of intensive glycemic control in some individuals at higher cardiovascular risk.

Indexed as

Cardiovascular DiseasesDiabetes Mellitus, Type 2Glycemic ControlBlood GlucoseClinical Trials as TopicHumansMachine LearningRisk FactorsBlood GlucoseGlycemic controlHeterogeneityMachine learningSubgroup effectsType 2 diabetes

Identifiers

PMID35477454
PMCPMC9047276
OpenAlexW4225265596

What Socratic holds

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LicenceCC BY
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Registered trials

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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.