Evidence map›Paper›PMID 31479304›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2019

Pancreatic β-cell-specific deletion of insulin-degrading enzyme leads to dysregulated insulin secretion and β-cell functional immaturity.

Cristina M Fernández-Díaz, Beatriz Merino, José F López-Acosta, Pilar Cidad, Miguel A de la Fuente, Carmen D Lobatón, Alfredo Moreno, Malcolm A Leissring, Germán Perdomo, Irene Cózar-Castellano

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 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 32 citations in OpenAlex.

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  18. TNF-Oxidative medicine and cellular longevity · 2022
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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 3 institutions in 2 countries.

Cristina M Fernández-DíazInstituto de Biología y Genética Molecular, Universidad de Valladolid-Consejo Superior de Investigaciones Científicas, Valladolid, Spain.
Beatriz MerinoInstituto de Biología y Genética Molecular, Universidad de Valladolid-Consejo Superior de Investigaciones Científicas, Valladolid, Spain.
José F López-AcostaInstituto de Biología y Genética Molecular, Universidad de Valladolid-Consejo Superior de Investigaciones Científicas, Valladolid, Spain.
Pilar CidadInstituto de Biología y Genética Molecular, Universidad de Valladolid-Consejo Superior de Investigaciones Científicas, Valladolid, Spain.
Miguel A de la FuenteInstituto de Biología y Genética Molecular, Universidad de Valladolid-Consejo Superior de Investigaciones Científicas, Valladolid, Spain.
Carmen D LobatónInstituto de Biología y Genética Molecular, Universidad de Valladolid-Consejo Superior de Investigaciones Científicas, Valladolid, Spain.
Alfredo MorenoInstituto de Biología y Genética Molecular, Universidad de Valladolid-Consejo Superior de Investigaciones Científicas, Valladolid, Spain.
Malcolm A LeissringInstitute for Memory Impairments and Neurological Disorders, University of California, Irvine, California.
Germán PerdomoDepartmento de Ciencias de la Salud, Facultad de Ciencias de la Salud, Universidad de Burgos, Burgos, Spain.
Irene Cózar-CastellanoInstituto de Biología y Genética Molecular, Universidad de Valladolid-Consejo Superior de Investigaciones Científicas, Valladolid, Spain.ORCID 0000-0002-6065-5362
Universidad de Valladolid · ESUniversidad de Burgos · ESUniversity of California, Irvine · US

Funding

Zinc-targeting inhibitors of insulin-degrading enzymeR01GM115617 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LEISSRING, MALCOLM A · 2016 to 2020
$1.4M
Transient defects in Abeta catabolism in the etiology of sporadic Alzheimer diseaseR21AG052718 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI LEISSRING, MALCOLM A · 2017 to 2018
$425k
NIA NIH HHS R21 AG052718NIGMS NIH HHS R01 GM115617
6 · The paper itself

Abstract

Inhibition of insulin-degrading enzyme (IDE) has been proposed as a possible therapeutic target for type 2 diabetes treatment. However, many aspects of IDE's role in glucose homeostasis need to be clarified. In light of this, new preclinical models are required to elucidate the specific role of this protease in the main tissues related to insulin handling. To address this, here we generated a novel line of mice with selective deletion of the

Indexed as

AnimalsBlood GlucoseC-PeptideFemaleGlucoseGlucose Tolerance TestGlucose Transporter Type 1HomeostasisHumansInsulin-Secreting CellsInsulin SecretionInsulysinMaleMiceMice, KnockoutRatsBlood GlucoseC-PeptideGlucoseGlucose Transporter Type 1Ide protein, mouseInsulysinRNA, Small InterferingSlc2a1 protein, mousebeta-cell immaturityGKGlut1Glut2insulin-degrading enzymeinsulin secretion

Identifiers

PMID31479304
PMCPMC7132327
OpenAlexW2972131388

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.