Evidence map›Paper›PMID 29066462›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2018

Genetic ablation of Cyp8b1 preserves host metabolic function by repressing steatohepatitis and altering gut microbiota composition.

Jay V Patankar, Chi K Wong, Vijay Morampudi, William T Gibson, Bruce Vallance, George N Ioannou, Michael R Hayden

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2018. 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
1.9field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  8. The role of bile acids in human aging.Medical review (2021) · 2024
    Article
  9. Article
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  11. In vivo mouse models to study bile acid synthesis and signaling.Hepatobiliary & pancreatic diseases international : HBPD INT · 2023
    Review
  12. Article
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  15. Article
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  18. Article
  19. Bile acid receptors FXR and TGR5 signaling in fatty liver diseases and therapy.American journal of physiology. Gastrointestinal and liver physiology · 2020
    Review
  20. Macrophage miR-34a Is a Key Regulator of Cholesterol Efflux and Atherosclerosis.Molecular therapy : the journal of the American Society of Gene Therapy · 2020
    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

7 authors at 3 institutions in 2 countries.

Jay V PatankarCentre for Molecular Medicine and Therapeutics, University of British Columbia , Vancouver, British Columbia , Canada.
Chi K WongChild and Family Research Institute, Department of Medical Genetics, University of British Columbia , Vancouver, British Columbia , Canada.
Vijay MorampudiDivision of Gastroenterology, Department of Pediatrics, Child and Family Research Institute, University of British Columbia , Vancouver, British Columbia , Canada.
William T GibsonChild and Family Research Institute, Department of Medical Genetics, University of British Columbia , Vancouver, British Columbia , Canada.
Bruce VallanceDivision of Gastroenterology, Department of Pediatrics, Child and Family Research Institute, University of British Columbia , Vancouver, British Columbia , Canada.
George N IoannouDivision of Gastroenterology, Department of Medicine, Veterans Affairs Puget Sound Health Care System and University of Washington , Seattle, Washington.
Michael R HaydenCentre for Molecular Medicine and Therapeutics, University of British Columbia , Vancouver, British Columbia , Canada.
University of British Columbia · CAChild and Family Research Institute · CAVA Puget Sound Health Care System · US

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Karin E Bornfeldt · 1986 to 2026
$41.4M
CIHR MOP106684NIDDK NIH HHS P30 DK017047
6 · The paper itself

Abstract

Both type 2 diabetes (T2D) and nonalcoholic steatohepatitis (NASH) are associated with reduced hepatic mitochondrial respiratory capacity. Cholic acid (CA) is the predominant 12α-hydroxylated bile acid that regulates hepatic lipid metabolism, and its circulating levels are negatively correlated with insulin resistance. Abolishing CA synthesis via the genetic disruption of the enzyme sterol 12α-hydroxylase ( Cyp8b1

Indexed as

AnimalsBile Acids and SaltsCells, CulturedEnergy MetabolismFemaleGastrointestinal MicrobiomeGene DeletionHost Microbial InteractionsInsulin ResistanceLipid MetabolismLiverMaleMiceMice, Inbred C57BLMice, KnockoutNon-alcoholic Fatty Liver DiseaseBile Acids and SaltsSteroid 12-alpha-Hydroxylase12α-hydroxylated bile acidsCyp8b1FXRgut microbiotanonalcoholic hepatic steatosis

Identifiers

PMID29066462
PMCPMC6008057
OpenAlexW2766644732

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.