Evidence map›Paper›PMID 34396783›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2021

Chronic high-fat feeding and prolonged fasting in liver-specific ANGPTL4 knockout mice.

Kathryn M Spitler, Shwetha K Shetty, Emily M Cushing, Kelli L Sylvers-Davie, Brandon S J Davies

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  7. Causal inference in health and disease: a review of the principles and applications of Mendelian randomization.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Review
  8. Obesity-Associated Hyperuricemia in Female Mice: A Reevaluation.Gout, urate, and crystal deposition disease · 2024
    Article
  9. A unified model for regulating lipoprotein lipase activity.Trends in endocrinology and metabolism: TEM · 2024
    Review
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  11. Article
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  14. Non-alcoholic fatty liver disease and liver secretome.Archives of pharmacal research · 2022
    Review
  15. 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

5 authors at 1 institution in 1 country.

Kathryn M SpitlerDepartment of Biochemistry, Fraternal Order of Eagles Diabetes Research Center, and Obesity Research and Education Initiative, University of Iowa, Iowa City, Iowa.ORCID 0000-0002-0062-9613
Shwetha K ShettyDepartment of Biochemistry, Fraternal Order of Eagles Diabetes Research Center, and Obesity Research and Education Initiative, University of Iowa, Iowa City, Iowa.
Emily M CushingDepartment of Biochemistry, Fraternal Order of Eagles Diabetes Research Center, and Obesity Research and Education Initiative, University of Iowa, Iowa City, Iowa.
Kelli L Sylvers-DavieDepartment of Biochemistry, Fraternal Order of Eagles Diabetes Research Center, and Obesity Research and Education Initiative, University of Iowa, Iowa City, Iowa.
Brandon S J DaviesDepartment of Biochemistry, Fraternal Order of Eagles Diabetes Research Center, and Obesity Research and Education Initiative, University of Iowa, Iowa City, Iowa.ORCID 0000-0002-7168-8522
University of Iowa · US

Funding

Regulation of GPIHBP1-dependent and independent triglyceride clearanceR01HL130146 · NHLBI · UNIVERSITY OF IOWA · PI DAVIES, BRANDON SCOTT JOSEPH · 2016 to 2020
$1.9M
NHLBI NIH HHS R01 HL130146
6 · The paper itself

Abstract

Obesity is associated with dyslipidemia, ectopic lipid deposition, and insulin resistance. In mice, the global or adipose-specific loss of function of the protein angiopoietin-like 4 (ANGPTL4) leads to decreased plasma triglyceride levels, enhanced adipose triglyceride uptake, and protection from high-fat diet (HFD)-induced glucose intolerance. ANGPTL4 is also expressed highly in the liver, but the role of liver-derived ANGPTL4 is unclear. The goal of this study was to determine the contribution of hepatocyte ANGPTL4 to triglyceride and glucose homeostasis in mice during a high-fat diet challenge. We generated hepatocyte-specific ANGPTL4 deficient (

Indexed as

Diet, High-FatInsulin ResistanceAngiopoietin-Like Protein 4AnimalsFastingFemaleGlucose IntoleranceLipid MetabolismLiverMaleMiceMice, Inbred C57BLMice, KnockoutTriglyceridesAngiopoietin-Like Protein 4Angptl4 protein, mouseTriglyceridesfastinghigh-fat dietlipoprotein lipaselipoprotein metabolismtriglyceride

Identifiers

PMID34396783
PMCPMC8560380
OpenAlexW3196057122

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.