Evidence map›Paper›PMID 37776200›Full record

Observational studyJournal of the American Heart Association2023

Relationship Between Time-Varying Achieved High-Density Lipoprotein Cholesterol and Risk of Coronary Events Depends on Haptoglobin Phenotype Within the ACCORD Lipid Study.

Rachel A Warren, Allie S Carew, Pantelis Andreou, Andrew P Levy, John Sapp, Orit Lache, Henry N Ginsberg, Eric B Rimm, Christine Herman, Susan Kirkland and 1 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Journal of the American Heart Association, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Observational
  3. 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

11 authors at 4 institutions in 3 countries.

Rachel A WarrenDepartment of Medicine Dalhousie University Halifax NS Canada.
Allie S CarewDepartment of Medicine Dalhousie University Halifax NS Canada.
Pantelis AndreouDepartment of Community Health and Epidemiology Dalhousie University Halifax NS Canada.
Andrew P LevyRappaport Faculty of Medicine Technion Israel Institute of Technology Haifa Israel.
John SappDepartment of Medicine Dalhousie University Halifax NS Canada.ORCID 0000-0002-9602-2751
Orit LacheRappaport Faculty of Medicine Technion Israel Institute of Technology Haifa Israel.
Henry N GinsbergDepartment of Medicine Columbia University New York NY.ORCID 0000-0002-4103-3592
Eric B RimmDepartment of Nutrition Harvard T. H. Chan School of Public Health Boston MA.ORCID 0000-0002-1402-7250
Christine HermanQEII Health Sciences Centre Nova Scotia Health Authority Halifax NS Canada.ORCID 0000-0001-6242-5985
Susan KirklandDepartment of Medicine Dalhousie University Halifax NS Canada.
Leah E CahillDepartment of Medicine Dalhousie University Halifax NS Canada.ORCID 0000-0003-3584-2227
Dalhousie University · CATechnion – Israel Institute of Technology · ILColumbia University · USHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background The Hp (haptoglobin)2-2 phenotype (~40% of people) is associated with dysfunctional high-density lipoprotein (HDL) that is heavily oxidized in hyperglycemia, which may explain why raising HDL-cholesterol (HDL-C) does not reliably prevent coronary artery disease (CAD) in diabetes. Methods and Results In this observational study using longitudinal data from the ACCORD (Action to Control Cardiovascular Risk in Diabetes) lipid trial, time-varying (achieved) HDL-C updated at 4, 8, and 12 months, and annually thereafter over a mean of 4.7 years, was analyzed in relation to risk of CAD and secondary outcomes using Cox proportional hazards regression with time-varying covariables among participants with (n=1781) and without (n=3191) the Hp2-2 phenotype. HDL-C did not differ between the phenotypes throughout the study. Having low HDL-C (<40 mg/dL for male participants and <50 mg/dL for female participants) was associated with a greater risk of CAD compared with non-low HDL-C among participants with the non-Hp2-2 phenotype (hazard ratio [HR], 1.48 [95% CI, 1.18-1.87]) but not among the Hp2-2 phenotype (HR, 0.97 [95% CI, 0.70-1.35];

Indexed as

Coronary Artery DiseaseDiabetes MellitusCholesterol, HDLFemaleHaptoglobinsHumansMalePhenotypeRisk FactorsCholesterol, HDLHaptoglobinscoronary artery diseaseepidemiologygenetic associationHDL‐cholesteroltype 2 diabetes

Identifiers

PMID37776200
PMCPMC10727244
OpenAlexW4387218592

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.