Evidence mapPaperPMID 33918571Full record

ReviewCells2021

High Density Lipoproteins and Diabetes.

Blake J Cochran, Kwok-Leung Ong, Bikash Manandhar, Kerry-Anne Rye

Abstract readReview
In one paragraph

Review in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
field-weighted citation impact
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

24 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. New Player in an Old Field? Ecto-FArteriosclerosis, thrombosis, and vascular biology · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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.

Blake J CochranLipid Research Group, School of Medical Sciences, Faculty of Medicine, University of New South Wales Sydney, Sydney, NSW 2052, Australia.ORCID 0000-0002-9615-7939
Kwok-Leung OngLipid Research Group, School of Medical Sciences, Faculty of Medicine, University of New South Wales Sydney, Sydney, NSW 2052, Australia.ORCID 0000-0001-7229-7614
Bikash ManandharLipid Research Group, School of Medical Sciences, Faculty of Medicine, University of New South Wales Sydney, Sydney, NSW 2052, Australia.
Kerry-Anne RyeLipid Research Group, School of Medical Sciences, Faculty of Medicine, University of New South Wales Sydney, Sydney, NSW 2052, Australia.ORCID 0000-0002-9751-917X

Funding

National Health and Medical Research Council 1148468National Health and Medical Research Council 2004064
6 · The paper itself

Abstract

Epidemiological studies have established that a high plasma high density lipoprotein cholesterol (HDL-C) level is associated with reduced cardiovascular risk. However, recent randomised clinical trials of interventions that increase HDL-C levels have failed to establish a causal basis for this relationship. This has led to a shift in HDL research efforts towards developing strategies that improve the cardioprotective functions of HDLs, rather than simply increasing HDL-C levels. These efforts are also leading to the discovery of novel HDL functions that are unrelated to cardiovascular disease. One of the most recently identified functions of HDLs is their potent antidiabetic properties. The antidiabetic functions of HDLs, and recent key advances in this area are the subject of this review. Given that all forms of diabetes are increasing at an alarming rate globally, there is a clear unmet need to identify and develop new approaches that will complement existing therapies and reduce disease progression as well as reverse established disease. Exploration of a potential role for HDLs and their constituent lipids and apolipoproteins in this area is clearly warranted. This review highlights focus areas that have yet to be investigated and potential strategies for exploiting the antidiabetic functions of HDLs.

Indexed as

AnimalsApolipoproteinsDiabetes MellitusEndoplasmic Reticulum StressHumansLipoproteins, HDLOxidative StressApolipoproteinsLipoproteins, HDLapoA-IdiabetesHDLskeletal muscleβ-cells

Identifiers

PMID33918571
PMCPMC8069617

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.