Evidence map›Paper›PMID 31237448›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2019

Obeticholic acid ameliorates dyslipidemia but not glucose tolerance in mouse model of gestational diabetes.

Saraid McIlvride, Vanya Nikolova, Hei Man Fan, Julie A K McDonald, Annika Wahlström, Elena Bellafante, Eugene Jansen, Luciano Adorini, David Shapiro, Peter Jones and 3 more

Open access · hybridAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
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  10. Nuclear Receptors in Pregnancy and Outcomes: Clinical Perspective.Advances in experimental medicine and biology · 2022
    Article
  11. Review
  12. Review
  13. Obeticholic acid improves fetal bile acid profile in a mouse model of gestational hypercholanemia.American journal of physiology. Gastrointestinal and liver physiology · 2020
    Article
  14. 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

13 authors at 5 institutions in 4 countries.

Saraid McIlvrideSchool of Life Course Sciences, King's College London, London, United Kingdom.
Vanya NikolovaSchool of Life Course Sciences, King's College London, London, United Kingdom.
Hei Man FanSchool of Life Course Sciences, King's College London, London, United Kingdom.
Julie A K McDonaldDepartment of Surgery and Cancer, Imperial College London, London, United Kingdom.
Annika WahlströmDepartment of Molecular and Clinical Medicine, University of Gothenburg, Gothenburg, Sweden.
Elena BellafanteSchool of Life Course Sciences, King's College London, London, United Kingdom.
Eugene JansenNational Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands.
Luciano AdoriniIntercept Pharmaceuticals, San Diego, California.
David ShapiroIntercept Pharmaceuticals, San Diego, California.
Peter JonesSchool of Life Course Sciences, King's College London, London, United Kingdom.ORCID 0000-0003-1201-2335
Julian R MarchesiDepartment of Surgery and Cancer, Imperial College London, London, United Kingdom.
Hanns-Ulrich MarschallDepartment of Molecular and Clinical Medicine, University of Gothenburg, Gothenburg, Sweden.
Catherine WilliamsonSchool of Life Course Sciences, King's College London, London, United Kingdom.
King's College London · GBImperial College London · GBIntercept Pharmaceuticals (United States) · USUniversity of Gothenburg · SENational Institute for Public Health and the Environment · NL

Funding

Wellcome TrustWellcome Trust P30874
6 · The paper itself

Abstract

Metabolism alters markedly with advancing gestation, characterized by progressive insulin resistance, dyslipidemia, and raised serum bile acids. The nuclear receptor farnesoid X receptor (FXR) has an integral role in bile acid homeostasis and modulates glucose and lipid metabolism. FXR is known to be functionally suppressed in pregnancy. The FXR agonist, obeticholic acid (OCA), improves insulin sensitivity in patients with type 2 diabetes with nonalcoholic fatty liver disease. We therefore hypothesized that OCA treatment during pregnancy could improve disease severity in a mouse model of gestational diabetes mellitus (GDM). C57BL/6J mice were fed a high-fat diet (HFD; 60% kcal from fat) for 4 wk before and throughout pregnancy to induce GDM. The impact of the diet supplemented with 0.03% OCA throughout pregnancy was studied. Pregnant HFD-fed mice displayed insulin resistance and dyslipidemia. OCA significantly reduced plasma cholesterol concentrations in nonpregnant and pregnant HFD-fed mice (by 22.4%,

Indexed as

AnimalsBlood GlucoseChenodeoxycholic AcidDiabetes, GestationalDiet, High-FatDisease Models, AnimalDyslipidemiasFemaleGlucose IntoleranceInsulin ResistanceLipid MetabolismMaleMiceMice, Inbred C57BLPregnancyPregnancy ComplicationsBlood GlucoseChenodeoxycholic Acidobeticholic acidbile acidsFXRhigh-fat dietinsulin resistance

Identifiers

PMID31237448
PMCPMC6732461
OpenAlexW2956138079

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.