Evidence map›Paper›PMID 27992493›Full record

Trial reportPloS one2016

Clinical and Metabolic Characteristics among Mexican Children with Different Types of Diabetes Mellitus.

María Lola Evia-Viscarra, Rodolfo Guardado-Mendoza, Edel Rafael Rodea-Montero

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02722655 (Characteristics and Evolution of Diabetes Mellitus in Mexican Children), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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.

NCT02722655 recruitingnot on this map

Characteristics and Evolution of Diabetes Mellitus in Mexican Children: Cohort Study

TypeobservationalSponsorHospital Regional de Alta Especialidad del BajioRan2008 to 2030Enrolled500ConditionsDiabetes Mellitus
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

3 authors.

María Lola Evia-ViscarraDepartment of Pediatric Endocrinology, Hospital Regional de Alta Especialidad del Bajío, León, Guanajuato, México.
Rodolfo Guardado-MendozaDepartment of Research, Hospital Regional de Alta Especialidad del Bajío, León, Guanajuato, México.
Edel Rafael Rodea-MonteroDepartment of Research, Hospital Regional de Alta Especialidad del Bajío, León, Guanajuato, México.ORCID http://orcid.org/0000-0003-4287-9626

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCurrent classification of diabetes mellitus (DM) is based on etiology and includes type 1 (T1DM), type 2 (T2DM), gestational, and other. Clinical and pathophysiological characteristics of T1DM and T2DM in the same patient have been designated as type 1.5 DM (T1.5DM).

objectivesThe aim of this study was to classify pediatric patients with DM based on pancreatic autoimmunity and the presence or absence of overweight/obesity, and to compare the clinical, anthropometric, and biochemical characteristics between children in the different classes of DM.

methodsA sample of 185 patients, recruited (March 2008-April 2015) as part of the Cohort of Mexican Children with DM (CMC-DM); ClinicalTrials.gov, identifier: NCT02722655. The DM classification was made considering pancreatic autoimmunity (via antibodies GAD-65, IAA, and AICA) and the presence or absence of overweight/obesity. Clinical, anthropometric and biochemical variables, grouped by type of DM were compared (Kruskal-Wallis or chi-squared test).

resultsThe final analysis included 140 children; 18.57% T1ADM, 46.43% T1BDM, 12.14% T1.5DM, and 22.86% T2DM. Fasting C-Peptide (FCP), and hs-CRP levels were higher in T1.5DM and T2DM, and the greatest levels were observed in T1.5DM (p<0.001 and 0.024 respectively).

conclusionsWe clearly identified that the etiologic mechanisms of T1DM and T2DM are not mutually exclusive, and we detailed why FCP levels are not critical for the classification system of DM in children. The findings of this study suggest that T1.5DM should be considered during the classification of pediatric DM and might facilitate more tailored approaches to treatment, clinical care and follow-up.

Indexed as

AdolescentAutoantibodiesChildChild, PreschoolC-PeptideC-Reactive ProteinCross-Sectional StudiesDiabetes MellitusFemaleHumansInfantMaleMexicoPancreasAutoantibodiesC-PeptideC-Reactive Protein

Identifiers

PMID27992493
PMCPMC5161364

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.