Evidence map›Paper›PMID 31550181›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2019

CD44 contributes to hyaluronan-mediated insulin resistance in skeletal muscle of high-fat-fed C57BL/6 mice.

Annie Hasib, Chandani K Hennayake, Deanna P Bracy, Aimée R Bugler-Lamb, Louise Lantier, Faisel Khan, Michael L J Ashford, Rory J McCrimmon, David H Wasserman, Li Kang

Open access · bronzeAbstract 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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.6field-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

27 citing papers in PubMed, 58 citations in OpenAlex.

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  17. Inhibition of hyaluronan synthesis prevents β-cell loss in obesity-associated type 2 diabetes.Matrix biology : journal of the International Society for Matrix Biology · 2023
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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 2 institutions in 2 countries.

Annie HasibDivision of Systems Medicine, School of Medicine, University of Dundee, Dundee, Scotland, United Kingdom.
Chandani K HennayakeDivision of Systems Medicine, School of Medicine, University of Dundee, Dundee, Scotland, United Kingdom.
Deanna P BracyDepartment of Molecular Physiology and Biophysics and Mouse Metabolic Phenotyping Centre, Vanderbilt University, Nashville, Tennessee.
Aimée R Bugler-LambDivision of Systems Medicine, School of Medicine, University of Dundee, Dundee, Scotland, United Kingdom.
Louise LantierDepartment of Molecular Physiology and Biophysics and Mouse Metabolic Phenotyping Centre, Vanderbilt University, Nashville, Tennessee.ORCID 0000-0002-6620-4976
Faisel KhanDivision of Systems Medicine, School of Medicine, University of Dundee, Dundee, Scotland, United Kingdom.
Michael L J AshfordDivision of Systems Medicine, School of Medicine, University of Dundee, Dundee, Scotland, United Kingdom.
Rory J McCrimmonDivision of Systems Medicine, School of Medicine, University of Dundee, Dundee, Scotland, United Kingdom.
David H WassermanDepartment of Molecular Physiology and Biophysics and Mouse Metabolic Phenotyping Centre, Vanderbilt University, Nashville, Tennessee.
Li KangDivision of Systems Medicine, School of Medicine, University of Dundee, Dundee, Scotland, United Kingdom.ORCID 0000-0002-6990-1996
University of Dundee · GBVanderbilt University · US

Funding

Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Vanderbilt Mouse Metabolic Phenotyping CenterU2CDK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2016 to 2021
$6.3M
INTEGRATED CONTROL OF MUSCLE GLUCOSE UPTAKE IN VIVOR01DK054902 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 1999 to 2020
$5.9M
Exercise and Fuel MetabolismR37DK050277 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2008 to 2017
$4.2M
British Heart Foundation PG/18/56/33935NIDDK NIH HHS R01 DK054902NIDDK NIH HHS R37 DK050277NIDDK NIH HHS U24 DK059637NIDDK NIH HHS U2C DK059637
6 · The paper itself

Abstract

Extracellular matrix hyaluronan is increased in skeletal muscle of high-fat-fed insulin-resistant mice, and reduction of hyaluronan by PEGPH20 hyaluronidase ameliorates diet-induced insulin resistance (IR). CD44, the main hyaluronan receptor, is positively correlated with type 2 diabetes. This study determines the role of CD44 in skeletal muscle IR. Global CD44-deficient (

Indexed as

Diet, High-FatAnimalsBody WeightGlucoseGlucose Clamp TechniqueHyaluronan ReceptorsHyaluronic AcidHyaluronoglucosaminidaseInsulin ResistanceMiceMice, Inbred C57BLMice, KnockoutMuscle, SkeletalCd44 protein, mouseGlucoseHyaluronan ReceptorsHyaluronic AcidHyaluronoglucosaminidasePEGPH20extracellular matrixhyaluronaninsulin resistance

Identifiers

PMID31550181
PMCPMC6957377
OpenAlexW2975494551

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.