Evidence map›Paper›PMID 23766259›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2013

2H2O-based high-density lipoprotein turnover method for the assessment of dynamic high-density lipoprotein function in mice.

Takhar Kasumov, Belinda Willard, Ling Li, Min Li, Heather Conger, Jennifer A Buffa, Stephen Previs, Arthur McCullough, Stanley L Hazen, Jonathan D Smith

Open access · bronzeAbstract readValidation Study
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. HDL flux is higher in patients with nonalcoholic fatty liver disease.American journal of physiology. Endocrinology and metabolism · 2019
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Monitoring the synthesis of biomolecules using mass spectrometry.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2016
    Article
  14. Article
  15. Article
  16. ORMDL orosomucoid-like proteins are degraded by free-cholesterol-loading-induced autophagy.Proceedings of the National Academy of Sciences of the United States of America · 2015
    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

10 authors at 1 institution in 1 country.

Takhar KasumovDepartment of Gastroenterology and Hepatology, Case Western Reserve University School of Medicine, Cleveland Clinic, Cleveland, OH 44195, USA.
Belinda Willard
Ling Li
Min Li
Heather Conger
Jennifer A Buffa
Stephen Previs
Arthur McCullough
Stanley L Hazen
Jonathan D Smith
Case Western Reserve University · US

Funding

Regression of Atherosclerosis CoreP01HL098055 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI FISHER, EDWARD A · 2010 to 2014
$12.1M
Enabling studies of proteome dynamicsR21RR025346 · NCRR · CASE WESTERN RESERVE UNIVERSITY · PI KASUMOV, TAKHAR · 2009 to 2011
$583k
NCRR NIH HHS R21 RR025346NHLBI NIH HHS P01 HL098055
6 · The paper itself

Abstract

objectiveHigh-density lipoprotein (HDL) promotes reverse cholesterol transport from peripheral tissues to the liver for clearance. Reduced HDL-cholesterol (HDLc) is associated with atherosclerosis; however, as a predictor of cardiovascular disease, HDLc has limitations because it is not a direct marker of HDL functionality. Our objective was to develop a mass spectrometry-based method for the simultaneous measurement of HDLc and ApoAI kinetics in mice, using a single (2)H2O tracer, and use it to examine genetic and drug perturbations on HDL turnover in vivo. APPROACH AND

resultsMice were given (2)H2O in the drinking water, and serial blood samples were collected at different time points. HDLc and ApoAI gradually incorporated (2)H, allowing experimental measurement of fractional catabolic rates and production rates for HDLc and ApoAI. ApoE(-/-) mice displayed increased fractional catabolic rates (P<0.01) and reduced production rates of both HDLc and ApoAI (P<0.05) compared with controls. In human ApoAI transgenic mice, levels and production rates of HDLc and human ApoAI were strikingly higher than in wild-type mice. Myriocin, an inhibitor of sphingolipid synthesis, significantly increased both HDL flux and macrophage-to-feces reverse cholesterol transport, indicating compatibility of this HDL turnover method with the macrophage-specific reverse cholesterol transport assay.

conclusions(2)H2O-labeling can be used to measure HDLc and ApoAI flux in vivo, and to assess the role of genetic and pharmacological interventions on HDL turnover in mice. Safety, simplicity, and low cost of the (2)H2O-based HDL turnover approach suggest that this assay can be scaled for human use to study effects of HDL targeted therapies on dynamic HDL function.

Indexed as

DeuteriumAnimalsApolipoprotein A-IApolipoproteins EAtherosclerosisCholesterolDrinkingFatty Acids, MonounsaturatedFemaleHumansImmunosuppressive AgentsLipoproteins, HDLLiverMacrophagesMaleMass SpectrometryApolipoprotein A-IApolipoproteins ECholesterolDeuteriumFatty Acids, MonounsaturatedImmunosuppressive AgentsLipoproteins, HDLthermozymocidinWaterapolipoprotein A-Icholesteroldeuterium oxidelipoproteins, HDLmass spectrometryprotein biosynthesis

Identifiers

PMID23766259
PMCPMC3958961
OpenAlexW2111697619

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.