Evidence map›Paper›PMID 30531230›Full record

ReviewCurrent opinion in lipidology2019

HDL modification: recent developments and their relevance to atherosclerotic cardiovascular disease.

John T Wilkins, Henrique S Seckler

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in lipidology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. ANGPTL3 is a novel HDL component that regulates HDL function.Journal of translational medicine · 2024
    Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. A Modern Approach to Dyslipidemia.Endocrine reviews · 2022
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. 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

2 authors at 1 institution in 1 country.

John T WilkinsDepartment of Medicine (Cardiology).
Henrique S SecklerDepartments of Chemistry and Molecular Biosciences and the Proteomics Center of Excellence.
Northwestern University · US

Funding

TR&D 7: Cell Specific ProteomicsP41GM108569 · NIGMS · NORTHWESTERN UNIVERSITY · PI KELLEHER, NEIL L · 2015 to 2024
$13.6M
Chemistry of Life Processes Predoctoral Training ProgramT32GM105538 · NIGMS · NORTHWESTERN UNIVERSITY · PI KELLEHER, NEIL L · 2013 to 2022
$2.7M
Associations Among Apolipoprotein A1 Structural Variants and High-Density Lipoprotein FunctionK23HL133601 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI WILKINS, JOHN THOMAS · 2016 to 2019
$663k
NHLBI NIH HHS K23 HL133601NIGMS NIH HHS P41 GM108569NIGMS NIH HHS T32 GM105538
6 · The paper itself

Abstract

purpose of reviewIn the last 2 years, significant advances in the understanding of HDL particle structure and the associations between particle structure, function, and atherosclerosis have been made. We will review and provide clinical and epidemiological context to these recent advances. RECENT

findingsSeveral recent studies have analyzed the associations between HDL particle size distribution, number, and particle function and specific environmental, behavioral, and pharmacologic exposures. Detailed phenotyping of HDL-associated protein complements, particularly apolipoproteins, strongly suggests structural subspecies of HDL exist with differential associations with HDL function and ASCVD risk. SUMMARY: The recent data on biological and structural variation in HDL suggests the existence of relatively discrete particle species, which share a similar structure and function. We propose that the classical taxonomy that clusters HDL particles by cholesterol content is incomplete. Detailed phenotyping of HDL subspecies in clinical and epidemiological research may yield insights into new risk markers and biochemical pathways that could provide targets for atherosclerotic cardiovascular disease (ASCVD) therapy and prevention in the future.

Indexed as

AnimalsAtherosclerosisHumansLipoproteins, HDLParticle SizeRisk FactorsLipoproteins, HDL

Identifiers

PMID30531230
PMCPMC6439474
OpenAlexW2903690871

What OpenQuestion holds

Textmetadata
LicenceTDM
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.