Evidence map›Paper›PMID 32629758›Full record

ArticleNutrients2020

Reactive Dicarbonyl Scavenging Effectively Reduces MPO-Mediated Oxidation of HDL and Restores PON1 Activity.

Jiansheng Huang, Patricia G Yancey, Huan Tao, Mark S Borja, Loren E Smith, Valentina Kon, Sean S Davies, MacRae F Linton

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Chronic, Environmentally Relevant PMThe Kaohsiung journal of medical sciences · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Oxidative modification of HDL by lipid aldehydes impacts HDL function.Archives of biochemistry and biophysics · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. 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

8 authors at 3 institutions in 1 country.

Jiansheng HuangDepartment of Medicine, Division of Cardiovascular Medicine, Atherosclerosis Research Unit, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Patricia G YanceyDepartment of Medicine, Division of Cardiovascular Medicine, Atherosclerosis Research Unit, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Huan TaoDepartment of Medicine, Division of Cardiovascular Medicine, Atherosclerosis Research Unit, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Mark S BorjaDepartment of Chemistry & Biochemistry, California State University East Bay, Hayward, CA 94542, USA.
Loren E SmithDepartment of Anesthesiology, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Valentina KonDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Sean S DaviesDepartment of Pharmacology, Vanderbilt University, Nashville, TN 37232, USA.
MacRae F LintonDepartment of Medicine, Division of Cardiovascular Medicine, Atherosclerosis Research Unit, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Vanderbilt University Medical Center · USVanderbilt University · USCalifornia State University, East Bay · US

Funding

Non-coding RNA & Bioinformatics CoreP01HL116263 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DAVIES, SEAN STEPHEN · 2014 to 2025
$24.7M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Vanderbilt Mouse Metabolic Phenotyping CenterU2CDK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2016 to 2021
$6.3M
Perioperative high-density lipoproteins and postoperative AKIK23GM134482 · NIGMS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SMITH, LOREN ELISA · 2020 to 2024
$933k
NHLBI NIH HHS HL116263NHLBI NIH HHS P01 HL116263NIDDK NIH HHS U24 DK059637NIDDK NIH HHS U2C DK059637NIGMS NIH HHS K23 GM134482
6 · The paper itself

Abstract

Atheroprotective functions of high-density lipoproteins (HDL) are related to the activity of HDL-associated enzymes such as paraoxonase 1 (PON1). We examined the impact of inhibition of myeloperoxidase (MPO)-mediated HDL oxidation by PON1 on HDL malondialdehyde (MDA) content and HDL function. In the presence of PON1, crosslinking of apoAI in response to MPO-mediated oxidation of HDL was abolished, and MDA-HDL adduct levels were decreased. PON1 prevented the impaired cholesterol efflux capacity of MPO-oxidized HDL from

Indexed as

AnimalsAnti-Inflammatory AgentsApolipoprotein A-IAryldialkylphosphataseATP Binding Cassette Transporter 1BenzylaminesDisease Models, AnimalFree Radical ScavengersHumansHypercholesterolemiaHyperlipoproteinemia Type IILipoproteins, HDLMacrophagesMalondialdehydeMiceMice, Inbred C57BL2-(aminomethyl)phenolAnti-Inflammatory AgentsApolipoprotein A-IAryldialkylphosphataseATP Binding Cassette Transporter 1BenzylaminesFree Radical ScavengersLipoproteins, HDLMalondialdehydePeroxidasePyridoxinecholesterol effluxfamilial hypercholesterolemiahigh-density lipoprotein (HDL), malondialdehyde (MDA), reactive dicarbonyl scavengersinflammationmacrophages

Identifiers

PMID32629758
PMCPMC7400685
OpenAlexW3037159313

What Socratic holds

Textmetadata
LicenceCC BY
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.