Evidence map›Paper›PMID 28720429›Full record

ReviewPharmacology & therapeutics2018

Stable isotope-based flux studies in nonalcoholic fatty liver disease.

Arthur McCullough, Stephen Previs, Takhar Kasumov

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Dietary fatty acid oxidation is decreased in non-alcoholic fatty liver disease: A palmitate breath test study.Liver international : official journal of the International Association for the Study of the Liver · 2020
    Article
  11. HDL flux is higher in patients with nonalcoholic fatty liver disease.American journal of physiology. Endocrinology and metabolism · 2019
    Article
  12. 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

3 authors at 3 institutions in 1 country.

Arthur McCulloughDepartment of Gastroenterology & Hepatology, Cleveland Clinic, Cleveland, OH, USA.
Stephen PrevisMerck & Co., Inc., Kenilworth, NJ, USA.
Takhar KasumovDepartment of Gastroenterology & Hepatology, Cleveland Clinic, Cleveland, OH, USA; Department of Pharmaceutical Sciences, College of Pharmacy, Northeast Ohio Medical University, Rootstown, OH, USA. Electronic address: tkasumov@neomed.edu.
Cleveland Clinic · USMerck & Co., Inc., Rahway, NJ, USA (United States) · USNortheast Ohio Medical University · US

Funding

Follistatin-like protein 1 in cardiac and systemic metabolismR01HL129120 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI RECCHIA, FABIO A, WALSH, KENNETH · 2016 to 2019
$2.9M
Novel computational methods for in vivo proteome dynamics estimation using heavy water metabolic labeling and LC-MSR01GM112044 · NIGMS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SADYGOV, ROVSHAN G · 2015 to 2023
$2.7M
Enabling studies of proteome dynamicsR21RR025346 · NCRR · CASE WESTERN RESERVE UNIVERSITY · PI KASUMOV, TAKHAR · 2009 to 2011
$583k
Mitochondrial Proteome Dynamics in Heart Failure Assessed with Heavy WaterR21HL114407 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI KASUMOV, TAKHAR · 2012 to 2013
$394k
NCRR NIH HHS R21 RR025346NHLBI NIH HHS R01 HL129120NHLBI NIH HHS R21 HL114407NIGMS NIH HHS R01 GM112044
6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease and is associated with the worldwide epidemics of obesity, diabetes and cardiovascular diseases. NAFLD ranges from benign fat accumulation in the liver (steatosis) to non-alcoholic steatohepatitis (NASH), and cirrhosis which can progress to hepatocellular carcinoma and liver failure. Mass spectrometry and magnetic resonance spectroscopy-coupled stable isotope-based flux studies provide new insights into the understanding of NAFLD pathogenesis and the disease progression. This review focuses mainly on the utilization of mass spectrometry-based methods for the understanding of metabolic abnormalities in the different stages of NAFLD. For example, stable isotope-based flux studies demonstrated multi-organ insulin resistance, dysregulated glucose, lipids and lipoprotein metabolism in patients with NAFLD. We also review recent developments in the stable isotope-based technologies for the study of mitochondrial dysfunction, oxidative stress and fibrogenesis in NAFLD. We highlight the limitations of current methodologies, discuss the emerging areas of research in this field, and future directions for the applications of stable isotopes to study NAFLD and its complications.

Indexed as

AnimalsHumansIsotopesMass SpectrometryNon-alcoholic Fatty Liver DiseaseIsotopesCitric acid cycleFatty acid oxidationFibrosisNAFLDOxidative stressStable isotopes

Identifiers

PMID28720429
PMCPMC5743607
OpenAlexW2734852894

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.