Evidence map›Paper›PMID 33324081›Full record

ArticleDiabetes, metabolic syndrome and obesity : targets and therapy2020

Maturity-Onset Diabetes of the Young Identified Among Algerian Probands with Early-Onset Diabetes.

Faiza Bouldjennet, Anette P Gjesing, Malha Azzouz, Samir Ait Abderrahman, Amina El Guecier, Said Ali, Brahim Oudjit, Farida Mennadi-Lacete, Lyèce Yargui, Aissa Boudiba and 4 more

Open access · goldAbstract read
In one paragraph

Article in Diabetes, metabolic syndrome and obesity : targets and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 84% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
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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

14 authors at 4 institutions in 2 countries.

Faiza Bouldjennet *Laboratory of Cellular and Molecular Biology, Cytokine and NO Synthase Team, University of Science and Technology, Houari Boumediene (USTHB), Algiers, Algeria.
Anette P Gjesing *The Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-4580-1576
Malha AzzouzDiabetology Department of Mustapha Pacha Hospital, Algiers, Algeria.
Samir Ait AbderrahmanDiabetology Department of Mohamed Seghir Nekkache Hospital, Algiers, Algeria.ORCID 0000-0002-1503-1390
Amina El GuecierInternal Medicine Department of Djillali Bounaâma Hospital, Algiers, Algeria.
Said AliLaboratory of Biochemistry, Mustapha Pacha, Algiers, Algeria.
Brahim OudjitDiabetology Department of Mohamed Seghir Nekkache Hospital, Algiers, Algeria.
Farida Mennadi-LacetePediatric Department of Parnet Hospital, Algiers, Algeria.
Lyèce YarguiLaboratory of Biochemistry, Mustapha Pacha, Algiers, Algeria.ORCID 0000-0003-1239-7159
Aissa BoudibaDiabetology Department of Mustapha Pacha Hospital, Algiers, Algeria.
Ahcène ChibaneInternal Medicine Department of Djillali Bounaâma Hospital, Algiers, Algeria.
Chafia Touil-BoukoffaLaboratory of Cellular and Molecular Biology, Cytokine and NO Synthase Team, University of Science and Technology, Houari Boumediene (USTHB), Algiers, Algeria.
Torben HansenThe Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0001-8748-3831
Rachida RaacheLaboratory of Cellular and Molecular Biology, Cytokine and NO Synthase Team, University of Science and Technology, Houari Boumediene (USTHB), Algiers, Algeria.
Hôpital Mustapha Pacha · DZUniversity of Sciences and Technology Houari Boumediene · DZCentre Hospitalo-Universitaire Bab El Oued · DZUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo investigate the prevalence of variants within selected maturity-onset diabetes of the young (MODY)-genes among Algerian patients initially diagnosed with type 1 diabetes (T1D) or type 2 diabetes (T2D), yet presenting with a MODY-like phenotype.

methodsEight unrelated patients with early-onset diabetes (before 30 years) and six relatives with diabetes were examined by targeted re-sequencing for variants in genes known to be involved in MODY (

resultsA total of 12 variants were identified, of which three were classified as pathogenic and one as a variant of uncertain clinical significance (VUS). Two of the pathogenic variants were found in

conclusionVariants in known MODY-genes can be the cause of early-onset diabetes in Algerians diagnosed with T1D or T2D among patients presenting with a MODY-like phenotype; thus, genetic screening should be considered.

Indexed as

early-onsetgenesMODYmonogenic diabetestype 1 diabetes

Identifiers

PMID33324081
PMCPMC7733395
OpenAlexW3112157527

What OpenQuestion holds

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Registered trials

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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.