Evidence map›Paper›PMID 34547140›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2021

Androgen-induced insulin resistance is ameliorated by deletion of hepatic androgen receptor in females.

Stanley Andrisse, Mingxiao Feng, Zhiqiang Wang, Olubusayo Awe, Lexiang Yu, Haiying Zhang, Sheng Bi, Hongbing Wang, Linhao Li, Serene Joseph and 8 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2021. 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
3.1field-weighted citation impact, top 7% 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, 34 citations in OpenAlex.

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  17. Androgen signalling in the ovaries and endometrium.Molecular human reproduction · 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

18 authors at 6 institutions in 1 country.

Stanley AndrisseDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Mingxiao FengDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Zhiqiang WangDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Olubusayo AweDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Lexiang YuDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Haiying ZhangDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Sheng BiDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Hongbing WangDepartment of Pharmaceutical Sciences, University of Maryland, Baltimore, Maryland, USA.
Linhao LiDepartment of Pharmaceutical Sciences, University of Maryland, Baltimore, Maryland, USA.
Serene JosephDepartment of Cardiovascular Sciences/Center for Metabolic Disease Research, Temple University School of Medicine, Philadelphia, Pennsylvania, USA.
Nicola HellerDepartment of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Franck Mauvais-JarvisDepartment of Medicine, Tulane University Health Sciences Center, New Orleans, Louisiana, USA.
Guang William WongDepartment of Cellular and Molecular Physiology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
James SegarsDepartment of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Andrew WolfeDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Sara DivallDepartment of Pediatrics, Seattle's Children's Hospital, University of Washington, Seattle, Washington, USA.
Rexford AhimaDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Sheng WuDepartment of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Johns Hopkins Medicine · USJohns Hopkins University · USTemple University · USUniversity of Maryland, Baltimore · USSeattle Children's Hospital · USTulane University · US

Funding

JHU-UMD Diabetes Research CenterP30DK079637 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI AHIMA, REXFORD S. · 2013 to 2017
$9.7M
Targeting the estrogen receptor-α to protect functional β-cell mass in womenR01DK074970 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI Franck Mauvais-Jarvis · 2007 to 2026
$6.0M
Understanding the pathogenesis of elevated androgen induced metabolic dysfunction in femalesR01HD095512 · NICHD · TEMPLE UNIV OF THE COMMONWEALTH · PI WU, SHENG · 2018 to 2022
$2.8M
Sex differences in macrophage differentiation in allergic lung inflammationR01HL124477 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI HELLER, NICOLA M · 2014 to 2018
$2.0M
Repurposing estrogens to improve pancreatic islet transplantationR01DK107444 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI MAUVAIS-JARVIS, FRANCK · 2016 to 2019
$1.5M
Hypothalamic Regulation of Hepatic Glucose Production and Glucose HomeostasisR01DK103710 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI BI, SHENG · 2015 to 2018
$1.5M
Insulin and Androgen Interactions in the Infertility of ObesityR00HD068130 · NICHD · JOHNS HOPKINS UNIVERSITY · PI WU, SHENG · 2014 to 2016
$712k
BLRD VA I01 BX003725NHLBI NIH HHS R01 HL124477NICHD NIH HHS R00 HD068130NICHD NIH HHS R01 HD095512NIDDK NIH HHS P30 DK079637NIDDK NIH HHS R01 DK074970NIDDK NIH HHS R01 DK103710NIDDK NIH HHS R01 DK107444
6 · The paper itself

Abstract

Androgen excess is one of the most common endocrine disorders of reproductive-aged women, affecting up to 20% of this population. Women with elevated androgens often exhibit hyperinsulinemia and insulin resistance. The mechanisms of how elevated androgens affect metabolic function are not clear. Hyperandrogenemia in a dihydrotestosterone (DHT)-treated female mouse model induces whole body insulin resistance possibly through activation of the hepatic androgen receptor (AR). We investigated the role of hepatocyte AR in hyperandrogenemia-induced metabolic dysfunction by using several approaches to delete hepatic AR via animal-, cell-, and clinical-based methodologies. We conditionally disrupted hepatocyte AR in female mice developmentally (LivARKO) or acutely by tail vein injection of an adeno-associated virus with a liver-specific promoter for Cre expression in AR

Indexed as

Insulin ResistanceAndrogensAnimalsDihydrotestosteroneFemaleGluconeogenesisGlucoseHepatocytesHomeostasisInsulinLiverMiceMice, Inbred C57BLPyruvic AcidReceptors, AndrogenAndrogensDihydrotestosteroneGlucoseInsulinPyruvic AcidReceptors, Androgenandrogenandrogen receptorglucoseinsulin signalingliverPCOS

Identifiers

PMID34547140
PMCPMC9097557
OpenAlexW3201117601

What OpenQuestion holds

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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.