Evidence map›Paper›PMID 33263263›Full record

Trial reportJournal of the American Heart Association2020

Effect of Anacetrapib on Cholesterol Efflux Capacity: A Substudy of the DEFINE Trial.

Mark P Metzinger, Suzanne Saldanha, Jaskeerat Gulati, Kershaw V Patel, Ayea El-Ghazali, Sneha Deodhar, Parag H Joshi, Colby Ayers, Anand Rohatgi

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of the American Heart Association, 2020. 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
2.6field-weighted citation impact, top 9% 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

9 authors at 1 institution in 1 country.

Mark P MetzingerDivision of Cardiology Department of Internal Medicine UT Southwestern Medical Center Dallas TX.
Suzanne SaldanhaDivision of Cardiology Department of Internal Medicine UT Southwestern Medical Center Dallas TX.
Jaskeerat GulatiDivision of Cardiology Department of Internal Medicine UT Southwestern Medical Center Dallas TX.
Kershaw V PatelDivision of Cardiology Department of Internal Medicine UT Southwestern Medical Center Dallas TX.
Ayea El-GhazaliDivision of Cardiology Department of Internal Medicine UT Southwestern Medical Center Dallas TX.
Sneha DeodharDivision of Cardiology Department of Internal Medicine UT Southwestern Medical Center Dallas TX.
Parag H JoshiDivision of Cardiology Department of Internal Medicine UT Southwestern Medical Center Dallas TX.
Colby AyersDivision of Cardiology Department of Internal Medicine UT Southwestern Medical Center Dallas TX.
Anand RohatgiDivision of Cardiology Department of Internal Medicine UT Southwestern Medical Center Dallas TX.
Southwestern Medical Center · US

Funding

The Genetic and Molecular Basis of Cholesterol EffluxR01HL136724 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI ROHATGI, ANAND KUMAR · 2018 to 2022
$3.8M
Mentoring Patient-Oriented Research in Deep Lipid Phenotyping for Cardiovascular DiseaseK24HL146838 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI Anand Kumar Rohatgi · 2019 to 2026
$945k
NHLBI NIH HHS K24 HL146838NHLBI NIH HHS R01 HL136724
6 · The paper itself

Abstract

Background Anacetrapib is the only cholesteryl ester transfer protein inhibitor proven to reduce coronary heart disease (CHD). However, its effects on reverse cholesterol transport have not been fully elucidated. Macrophage cholesterol efflux (CEC), the initial step of reverse cholesterol transport, is inversely associated with CHD and may be affected by sex as well as haptoglobin copy number variants among patients with diabetes mellitus. We investigated the effect of anacetrapib on CEC and whether this effect is modified by sex, diabetes mellitus, and haptoglobin polymorphism. Methods and Results A total of 574 participants with CHD were included from the DEFINE (Determining the Efficacy and Tolerability of CETP Inhibition With Anacetrapib) trial. CEC was measured at baseline and 24-week follow-up using J774 macrophages, boron dipyrromethene difluoride-labeled cholesterol, and apolipoprotein B-depleted plasma. Haptoglobin copy number variant was determined using an ELISA assay. Anacetrapib increased CEC, adjusted for baseline CEC, risk factors, and changes in lipids/apolipoproteins (standard β, 0.23; 95% CI, 0.05-0.41). This CEC-raising effect was seen only in men (

Indexed as

AgedAnticholesteremic AgentsApolipoproteinsCase-Control StudiesCholesterolCholesterol Ester Transfer ProteinsCholesterol, HDLCoronary DiseaseDiabetes MellitusDouble-Blind MethodFemaleGenotypeHaptoglobinsHumansMacrophagesMaleanacetrapibAnticholesteremic AgentsApolipoproteinsCholesterolCholesterol Ester Transfer ProteinsCholesterol, HDLHaptoglobinsOxazolidinonesPlaceboscholesteryl ester transfer proteincoronary heart diseasediabetes mellitushaptoglobin genotypesex

Identifiers

PMID33263263
PMCPMC7955402
OpenAlexW3108048195

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.