Evidence mapPaperPMID 34097448Full record

ArticleCirculation2021

HDL in the 21st Century: A Multifunctional Roadmap for Future HDL Research.

Anand Rohatgi, Marit Westerterp, Arnold von Eckardstein, Alan Remaley, Kerry-Anne Rye

Open access · bronzeAbstract readHistorical Article
In one paragraph

Article in Circulation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 192 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
192citing papers in PubMed, 4 pooled it
30.4field-weighted citation impact, top 1% 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

192 citing papers in PubMed, 4 syntheses or guidelines pooled it, 316 citations in OpenAlex.

  1. Pooled it
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  9. Biologics for cardiovascular diseases: from bench to bedside.Signal transduction and targeted therapy · 2026
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132 more citing papers are in PubMed but not listed here.

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

5 authors at 5 institutions in 4 countries.

Anand RohatgiDepartment of Internal Medicine, Division of Cardiology, University of Texas Southwestern Medical Center, Dallas (A. Rohatgi).
Marit WesterterpDepartment of Pediatrics, Section Molecular Genetics, University Medical Center Groningen, University of Groningen, The Netherlands (M.W.).
Arnold von EckardsteinInstitute of Clinical Chemistry, University Hospital Zurich and University of Zurich, Switzerland (A.v.E.).
Alan RemaleyLipoprotein Metabolism Laboratory, Translational Vascular Medicine Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD (A. Remaley).
Kerry-Anne RyeSchool of Medical Sciences, Faculty of Medicine, University of New South Wales, Sydney, Australia (K.-A.R.).
National Heart Lung and Blood Institute · USThe University of Sydney · AUThe University of Texas Southwestern Medical Center · USUniversity Hospital of Zurich · CHUniversity Medical Center Groningen · NL

Funding

Development of Apo Mimetic Peptides for the Treatment Cardiovascular DiseaseZIAHL006095 · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · 2025 to 2025
$1.6M
The Genetic and Molecular Basis of Cholesterol EffluxR01HL136724 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI Anand Kumar Rohatgi · 2022 to 2022
$697k
Mentoring Patient-Oriented Research in Deep Lipid Phenotyping for Cardiovascular DiseaseK24HL146838 · UT SOUTHWESTERN MEDICAL CENTER · 2025 to 2025
$123k
NHLBI NIH HHS K24 HL146838NHLBI NIH HHS R01 HL136724
6 · The paper itself

Abstract

Low high-density lipoprotein cholesterol (HDL-C) characterizes an atherogenic dyslipidemia that reflects adverse lifestyle choices, impaired metabolism, and increased cardiovascular risk. Low HDL-C is also associated with increased risk of inflammatory disorders, malignancy, diabetes, and other diseases. This epidemiologic evidence has not translated to raising HDL-C as a viable therapeutic target, partly because HDL-C does not reflect high-density lipoprotein (HDL) function. Mendelian randomization analyses that have found no evidence of a causal relationship between HDL-C levels and cardiovascular risk have decreased interest in increasing HDL-C levels as a therapeutic target. HDLs comprise distinct subpopulations of particles of varying size, charge, and composition that have several dynamic and context-dependent functions, especially with respect to acute and chronic inflammatory states. These functions include reverse cholesterol transport, inhibition of inflammation and oxidation, and antidiabetic properties. HDLs can be anti-inflammatory (which may protect against atherosclerosis and diabetes) and proinflammatory (which may help clear pathogens in sepsis). The molecular regulation of HDLs is complex, as evidenced by their association with multiple proteins, as well as bioactive lipids and noncoding RNAs. Clinical investigations of HDL biomarkers (HDL-C, HDL particle number, and apolipoprotein A through I) have revealed nonlinear relationships with cardiovascular outcomes, differential relationships by sex and ethnicity, and differential patterns with coronary versus noncoronary events. Novel HDL markers may also have relevance for heart failure, cancer, and diabetes. HDL function markers (namely, cholesterol efflux capacity) are associated with coronary disease, but they remain research tools. Therapeutics that manipulate aspects of HDL metabolism remain the holy grail. None has proven to be successful, but most have targeted HDL-C, not metrics of HDL function. Future therapeutic strategies should focus on optimizing HDL function in the right patients at the optimal time in their disease course. We provide a framework to help the research and clinical communities, as well as funding agencies and stakeholders, obtain insights into current thinking on these topics, and what we predict will be an exciting future for research and development on HDLs.

Indexed as

AtherosclerosisCholesterolHistory, 21st CenturyHumansInflammasomesLipoproteins, HDLOxidative StressProteomicsResearchRisk FactorsCholesterolInflammasomesLipoproteins, HDLatherosclerosisbiomarkersinflammationlipoproteinslipoproteins, HDL

Identifiers

PMID34097448
PMCPMC8189312
OpenAlexW3168827864

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.