Evidence map›Paper›PMID 31817798›Full record

ReviewInternational journal of molecular sciences2019

Molecular Modelling of Islet β-Cell Adaptation to Inflammation in Pregnancy and Gestational Diabetes Mellitus.

Petra I Lorenzo, Alejandro Martín-Montalvo, Nadia Cobo Vuilleumier, Benoit R Gauthier

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 3 pooled it
3.4field-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

23 citing papers in PubMed, 3 syntheses or guidelines pooled it, 36 citations in OpenAlex.

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  15. Novel Biomolecules in the Pathogenesis of Gestational Diabetes Mellitus 2.0.International journal of molecular sciences · 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

4 authors at 2 institutions in 1 country.

Petra I LorenzoAndalusian Center for Molecular Biology and Regenerative Medicine, CABIMER (Junta de Andalucía-CSIC-Universidad de Sevilla-Universidad Pablo de Olavide), Calle Américo Vespucio, 24, 41092 Sevilla, Spain.
Alejandro Martín-MontalvoAndalusian Center for Molecular Biology and Regenerative Medicine, CABIMER (Junta de Andalucía-CSIC-Universidad de Sevilla-Universidad Pablo de Olavide), Calle Américo Vespucio, 24, 41092 Sevilla, Spain.
Nadia Cobo VuilleumierAndalusian Center for Molecular Biology and Regenerative Medicine, CABIMER (Junta de Andalucía-CSIC-Universidad de Sevilla-Universidad Pablo de Olavide), Calle Américo Vespucio, 24, 41092 Sevilla, Spain.
Benoit R GauthierAndalusian Center for Molecular Biology and Regenerative Medicine, CABIMER (Junta de Andalucía-CSIC-Universidad de Sevilla-Universidad Pablo de Olavide), Calle Américo Vespucio, 24, 41092 Sevilla, Spain.ORCID 0000-0001-8146-7486
Centro Andaluz de Biología Molecular y Medicina Regenerativa · ESInstituto de Salud Carlos III · ES

Funding

Consejería de Economía, Innovación, Ciencia y Empleo, Junta de Andalucía P10.CTS.6359Consejería de Salud, Junta de Andalucía PI-0727-2010, PI-0085-2013Instituto de Salud Carlos III CP14/00105, PI18/01590, PI15/00134Ministerio de Economía y Competitividad PI10/00871, PI13/00593
6 · The paper itself

Abstract

Gestational diabetes mellitus (GDM), a metabolic disease that develops with the increase in insulin resistance during late pregnancy, is currently one of the most common complications affecting pregnancy. The polygenic nature of GDM, together with the interplay between different genetic variants with nutritional and environmental factors has hindered the full understanding of the etiology of this disease. However, an important genetic overlap has been found with type 2 diabetes mellitus (T2DM) and, as in the case of T2DM, most of the identified loci are associated with β-cell function. Early detection of GDM and adequate interventions to control the maternal glycemia are necessary to avoid the adverse outcomes for both the mother and the offspring. The in utero exposure to the diabetic milieu predispose these children for future diseases, among them T2DM, originating a vicious circle implicated in the increased prevalence of both GDM and T2DM. The involvement of inflammatory processes in the development of GDM highlights the importance of pancreatic β-cell factors able to favor the adaptation processes required during gestation, concomitantly with the protection of the islets from an inflammatory milieu. In this regard, two members of the Pax family of transcription factors, PAX4 and PAX8, together with the chromatin remodeler factor HMG20A, have gained great relevance due to their involvement in β-cell mass adaptation together with their anti-inflammatory properties. Mutations in these factors have been associated with GDM, highlighting these as novel candidates for genetic screening analysis in the identification of women at risk of developing GDM.

Indexed as

Blood GlucoseDiabetes, GestationalDiabetes Mellitus, Type 2FemaleHigh Mobility Group ProteinsHomeodomain ProteinsHumansIslets of LangerhansPaired Box Transcription FactorsPAX8 Transcription FactorPregnancyBlood GlucoseHigh Mobility Group ProteinsHMG20A protein, humanHomeodomain ProteinsPaired Box Transcription FactorsPAX4 protein, humanPAX8 protein, humanPAX8 Transcription Factorfetal growth alterationgestational diabetesgestational hypertensionHMG20AinflammationPAX4PAX8pregnancy

Identifiers

PMID31817798
PMCPMC6941051
OpenAlexW2992112108

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.