Evidence map›Paper›PMID 20667817›Full record

ArticleJournal of lipid research2010

Impact of serum amyloid A on high density lipoprotein composition and levels.

Maria C de Beer, Nancy R Webb, Joanne M Wroblewski, Victoria P Noffsinger, Debra L Rateri, Ailing Ji, Deneys R van der Westhuyzen, Frederick C de Beer

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Serum Amyloid A-Mediated Inflammasome Activation of Microglial Cells in Cerebral Ischemia.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  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

8 authors at 2 institutions in 1 country.

Maria C de BeerGraduate Center for Nutritional Science, University of Kentucky Medical Center, Lexington, KY 40536, USA. mdebeer@uky.edu
Nancy R Webb
Joanne M Wroblewski
Victoria P Noffsinger
Debra L Rateri
Ailing Ji
Deneys R van der Westhuyzen
Frederick C de Beer
University of Kentucky · USLexington VA Health Care System · US

Funding

THROMBOSPONDIN1 MEDIATES MACROPHAGE INFILTRATION INTO ADIPOSE TISSUE AND PROMOTEP20RR021954 · NCRR · UNIVERSITY OF KENTUCKY · PI CASSIS, LISA A · 2008 to 2011
$8.3M
Mouse CoreP01HL086670 · NHLBI · UNIVERSITY OF KENTUCKY · PI WEBB, NANCY R · 2007 to 2011
$7.1M
NCRR NIH HHS P20 RR-021954NCRR NIH HHS P20 RR021954NHLBI NIH HHS P01 HL086670NHLBI NIH HHS P01HL-086670
6 · The paper itself

Abstract

Serum amyloid A (SAA) is an acute-phase protein mainly associated with HDL. To study the role of SAA in mediating changes in HDL composition and metabolism during inflammation, we generated mice in which the two major acute-phase SAA isoforms, SAA1.1 and SAA2.1, were deleted [SAA knockout (SAAKO) mice], and induced an acute phase to compare lipid and apolipoprotein parameters between wild-type (WT) and SAAKO mice. Our data indicate that SAA does not affect apolipoprotein A-I (apoA-I) levels or clearance under steady-state conditions. HDL and plasma triglyceride levels following lipopolysaccharide administration, as well as the decline in liver expression of apoA-I and apoA-II, did not differ between both groups of mice. The expected size increase of WT acute-phase HDL was surprisingly also seen in SAAKO acute-phase HDL despite the absence of SAA. HDLs from both mice showed increased phospholipid and unesterified cholesterol content during the acute phase. We therefore conclude that in the mouse, SAA does not impact HDL levels, apoA-I clearance, or HDL size during the acute phase and that the increased size of acute-phase HDL in mice is associated with an increased content of surface lipids, particularly phospholipids, and not surface proteins. These data need to be transferred to humans with caution due to differences in apoA-I structure and remodeling functions.

Indexed as

AnimalsApolipoprotein A-IFemaleGene Expression RegulationGene Knockout TechniquesLipoproteins, HDLLiverMaleMiceSerum Amyloid A ProteinApolipoprotein A-ILipoproteins, HDLSerum Amyloid A Protein

Identifiers

PMID20667817
PMCPMC2952552
OpenAlexW2072232323

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.