Evidence map›Paper›PMID 38484336›Full record

ArticleDiabetes care2024

Haptoglobin Phenotype and Intensive Glycemic Control for Coronary Artery Disease Risk Reduction in People With Type 2 Diabetes: The ADVANCE Study.

Leah E Cahill, Rachel A Warren, Allie S Carew, Andrew P Levy, John Sapp, Michelle Samuel, Elizabeth Selvin, Samantha K Lavallée, Neil Poulter, Michel Marre and 6 more

Open access · greenAbstract read
In one paragraph

Article in Diabetes care, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Relationship between time-varying achieved HbABMJ open diabetes research & care · 2025
    Article
  4. Article
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

16 authors at 9 institutions in 7 countries.

Leah E CahillDepartment of Medicine, Dalhousie University, Halifax, Canada.ORCID 0000-0003-3584-2227
Rachel A WarrenDepartment of Medicine, Dalhousie University, Halifax, Canada.
Allie S CarewDepartment of Medicine, Dalhousie University, Halifax, Canada.
Andrew P LevyRappaport Faculty of Medicine, Technion Israel Institute of Technology, Haifa, Israel.
John SappDepartment of Medicine, Dalhousie University, Halifax, Canada.
Michelle SamuelDepartment of Medicine, Dalhousie University, Halifax, Canada.
Elizabeth SelvinDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.ORCID 0000-0001-6923-7151
Samantha K LavalléeQEII Health Sciences Centre, Nova Scotia Health Authority, Halifax, Canada.
Neil PoulterSchool of Public Health, Imperial College London, London, U.K.
Michel MarreClinique Ambroise Paré, Neuilly-sur-Seine, France.ORCID 0000-0002-3071-1837
Stephen HarrapDepartment of Anatomy and Physiology, University of Melbourne and Royal Melbourne Hospital, Parkville, Australia.
Giuseppe ManciaUniversity of Milano-Bicocca, Milan, Italy.
Katie HarrisThe George Institute for Global Health, University of New South Wales, Sydney, Australia.ORCID 0000-0003-2444-2869
John ChalmersThe George Institute for Global Health, University of New South Wales, Sydney, Australia.ORCID 0000-0002-9931-0580
Mark WoodwardSchool of Public Health, Imperial College London, London, U.K.ORCID 0000-0001-9800-5296
Eric B RimmDepartment of Nutrition, Harvard T. H. Chan School of Public Health, Boston, MA.
Dalhousie University · CAUNSW Sydney · AUHarvard University · USImperial College London · GBInserm · FRJohns Hopkins University · USTechnion – Israel Institute of Technology · ILThe Royal Melbourne Hospital · AUUniversity of Milano-Bicocca · IT

Funding

Research and Mentoring in the Clinical Epidemiology of Type 2 DiabetesK24DK106414 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI SELVIN, ELIZABETH · 2015 to 2019
$654k
Research and Mentoring in the Clinical Epidemiology of Cardiovascular Disease and Type 2 DiabetesK24HL152440 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SELVIN, ELIZABETH · 2020 to 2024
$612k
CIHR PJT173471NHLBI NIH HHS K24 HL152440NIDDK NIH HHS K24 DK106414
6 · The paper itself

Abstract

objectiveIntensive glycemic control reduced coronary artery disease (CAD) events among the Action to Control Cardiovascular Risk in Diabetes (ACCORD) study participants with the haptoglobin (Hp)2-2 phenotype but not in participants without the Hp2-2 phenotype. It is unknown whether and how these results translate across different demographic/clinical characteristics and treatment strategies. RESEARCH DESIGN AND

methodsHaptoglobin phenotype was measured in available samples from the Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation (ADVANCE) biomarker case-cohort study. Weighted multivariable-adjusted Cox regression models were used to evaluate the association between intensive glycemic control (HbA1c target of ≤6.5%) versus standard therapy (based on local guidelines) and major CAD events among participants with (n = 1,327) and without (n = 2,077) the Hp2-2 phenotype separately and within prespecified stratifications by sex, race, previous cardiovascular disease (CVD), diabetes duration, and HDL-cholesterol.

resultsWhile the hazard ratios (HRs) were in the hypothesized differing directions, compared with standard therapy, intensive glycemic control was not significantly associated with risk of CAD events among participants without (1.04, 95% CI 0.82-1.32) or with (0.84, 0.63-1.14, Pinteraction = 0.27) the Hp2-2 phenotype overall. Intensive therapy was associated with lower CAD risk among participants with the Hp2-2 phenotype who had no previous CVD (0.47, 0.29-0.76, Pinteraction = 0.01).

conclusionsOur findings suggest that intensive glycemic control contributes to the prevention of major CAD events among ADVANCE participants with the Hp2-2 phenotype and no previous CVD and are in alignment with our hypothesis that intensive glycemic control may be beneficial in a subset of people with the Hp2-2 phenotype.

Indexed as

Cardiovascular DiseasesCoronary Artery DiseaseDiabetes Mellitus, Type 2Cohort StudiesGlycemic ControlHaptoglobinsHumansPhenotypeRisk FactorsRisk Reduction BehaviorHaptoglobins

Identifiers

PMID38484336
PMCPMC11835605
OpenAlexW4392793298

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.