Evidence map›Paper›PMID 20718489›Full record

ArticleJournal of proteome research2010

Proteomic characterization of human plasma high density lipoprotein fractionated by gel filtration chromatography.

Scott M Gordon, Jingyuan Deng, L Jason Lu, W Sean Davidson

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02998918 (Effects of Short-term Curcumin and Multi-polyphenol Supplementation on the Anti-inflammatory Properties of HDL), which is not on this map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
10.0field-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.

NCT02998918 nacompletednot on this mapstarted 2016, after this paper: background citation

Effects of Short-term Curcumin and Multi-polyphenol Supplementation on the Anti-inflammatory Properties of HDL

TypeinterventionalSponsorUniversity of South CarolinaRan2016 to 2020Enrolled21ConditionsInflammation, Atherosclerosis, Cardiovascular DiseaseArmsPolyResveratrol Supplementation, Curcumin Supplementation
3 · Its place in the literature

Who cites it

129 citing papers in PubMed, 241 citations in OpenAlex.

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  13. Deciphering Acute Coronary Syndromes Pathobiology Through Proteomics.Journal of cardiovascular development and disease · 2025
    Review
  14. Article
  15. Article
  16. Transport functions of intestinal lymphatic vessels.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  17. Article
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  20. Article

69 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

4 authors at 2 institutions in 1 country.

Scott M GordonCenter for Lipid and Arteriosclerosis Science, University of Cincinnati, Cincinnati, Ohio 45237-0507, USA. Gordonst@mail.uc.edu
Jingyuan Deng
L Jason Lu
W Sean Davidson
Cincinnati Children's Hospital Medical Center · USUniversity of Cincinnati · US

Funding

The molecular basis for high density lipoprotein heterogeneityR21HL104136 · NHLBI · UNIVERSITY OF CINCINNATI · PI DAVIDSON, W SEAN · 2010 to 2011
$440k
NHLBI NIH HHS R21 HL104136
6 · The paper itself

Abstract

Plasma levels of high density lipoprotein cholesterol (HDL-C) are inversely proportional to the incidence of cardiovascular disease. Recent applications of modern proteomic technologies have identified upward of 50 distinct proteins associated with HDL particles with many of these newly discovered proteins implicating HDL in nonlipid transport processes including complement activation, acute phase response and innate immunity. However, almost all MS-based proteomic studies on HDL to date have utilized density gradient ultracentrifugation techniques for HDL isolation prior to analysis. These involve high shear forces and salt concentrations that can disrupt HDL protein interactions and alter particle function. Here, we used high-resolution size exclusion chromatography to fractionate normal human plasma to 17 phospholipid-containing subfractions. Then, using a phospholipid binding resin, we identified proteins that associate with lipoproteins of various sizes by electrospray ionization mass spectrometry. We identified 14 new phospholipid-associated proteins that migrate with traditionally defined HDL, several of which further support roles for HDL in complement regulation and protease inhibition. The increased fractionation inherent to this method allowed us to visualize HDL protein distribution across particle size with unprecedented resolution. The observed heterogeneity across subfractions suggests the presence of HDL particle subpopulations each with distinct protein components that may prove to impart distinct physiological functions.

Indexed as

AdultCentrifugation, Density GradientChemical FractionationChromatography, GelHumansLipoproteins, HDLMaleParticle SizeProteomicsSpectrometry, Mass, Electrospray IonizationYoung AdultLipoproteins, HDL

Identifiers

PMID20718489
PMCPMC3100175
OpenAlexW1964388909

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.