Evidence map›Paper›PMID 29712723›Full record

ArticleThe Journal of biological chemistry2018

Modification by isolevuglandins, highly reactive γ-ketoaldehydes, deleteriously alters high-density lipoprotein structure and function.

Linda S May-Zhang, Valery Yermalitsky, Jiansheng Huang, Tiffany Pleasent, Mark S Borja, Michael N Oda, W Gray Jerome, Patricia G Yancey, MacRae F Linton, Sean S Davies

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

31 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Lifestyles, metabolome and diabetic kidney disease: a cohort study.QJM : monthly journal of the Association of Physicians · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Oxidative modification of HDL by lipid aldehydes impacts HDL function.Archives of biochemistry and biophysics · 2022
    Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Mechanisms of Post-critical Illness Cardiovascular Disease.Frontiers in cardiovascular medicine · 2022
    Review
  14. Article
  15. Emerging Anti-Atherosclerotic Therapies.International journal of molecular sciences · 2021
    Review
  16. Article
  17. High-Density Lipoproteins in Kidney Disease.International journal of molecular sciences · 2021
    Review
  18. Article
  19. Article
  20. 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

10 authors at 6 institutions in 2 countries.

Linda S May-ZhangFrom the Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 37232-6602.
Valery YermalitskyFrom the Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 37232-6602.
Jiansheng Huangthe Division of Cardiovascular Medicine, Department of Medicine, and.
Tiffany PleasentMeharry Medical College, Nashville, Tennessee 37208.
Mark S Borjathe Department of Chemistry and Biochemistry, California State University East Bay, Hayward, California 94542, and.
Michael N Odathe Children's Hospital Oakland Research Institute, Oakland, California 94609.
W Gray Jeromethe Department of Pathology, Vanderbilt Medical Center, Nashville, Tennessee 37232.
Patricia G Yanceythe Division of Cardiovascular Medicine, Department of Medicine, and.
MacRae F LintonFrom the Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 37232-6602.
Sean S DaviesFrom the Department of Pharmacology, Vanderbilt University, Nashville, Tennessee 37232-6602, sean.davies@vanderbilt.edu.ORCID 0000-0001-9879-8062
Vanderbilt University · USCardiovascular Research Center · BRCalifornia State University, East Bay · USChildren’s Institute · USMeharry Medical College · USVanderbilt University Medical Center · US

Funding

Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Non-coding RNA & Bioinformatics CoreP01HL116263 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI VICKERS, KASEY C · 2014 to 2025
$24.7M
Effect of isolevuglandin in HDL structure-function in atherosclerosisF32HL138745 · NHLBI · VANDERBILT UNIVERSITY · PI ZHANG, LINDA · 2017 to 2019
$184k
NHLBI NIH HHS F32 HL138745NHLBI NIH HHS P01 HL116263NIDDK NIH HHS P30 DK058404
6 · The paper itself

Abstract

Cardiovascular disease risk depends on high-density lipoprotein (HDL) function, not HDL-cholesterol. Isolevuglandins (IsoLGs) are lipid dicarbonyls that react with lysine residues of proteins and phosphatidylethanolamine. IsoLG adducts are elevated in atherosclerosis. The consequences of IsoLG modification of HDL have not been studied. We hypothesized that IsoLG modification of apoA-I deleteriously alters HDL function. We determined the effect of IsoLG on HDL structure-function and whether pentylpyridoxamine (PPM), a dicarbonyl scavenger, can preserve HDL function. IsoLG adducts in HDL derived from patients with familial hypercholesterolemia (

Indexed as

AldehydesAnimalsApolipoprotein A-IApolipoprotein A-IICells, CulturedCholesterolFemaleHumansHyperlipoproteinemia Type IIKetonesLipid MetabolismLipidsLipoproteins, HDLMacrophagesMaleMiceAldehydesApolipoprotein A-IApolipoprotein A-IICholesterolisolevuglandinKetonesLipidsLipoproteins, HDLphosphatidylethanolaminePhosphatidylethanolaminesaldehydesatherosclerosishigh-density lipoprotein (HDL)inflammationisolevuglandinslipid peroxidationoxidative stressreactive lipid species

Identifiers

PMID29712723
PMCPMC6005447
OpenAlexW2807975858

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.