Evidence map›Paper›PMID 32833960›Full record

Observational studyPloS one2020

Protein-conformational diseases in childhood: Naturally-occurring hIAPP amyloid-oligomers and early β-cell damage in obesity and diabetes.

Nelly F Altamirano-Bustamante, Eulalia Garrido-Magaña, Eugenia Morán, Aurora Calderón, Karina Pasten-Hidalgo, Rosa Angélica Castillo-Rodríguez, Gerardo Rojas, Reyna Lara-Martínez, Edgar Leyva-García, Mateo Larralde-Laborde and 20 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 pooled it
0.5field-weighted citation impact, top 36% 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

3 citing papers in PubMed, 2 syntheses or guidelines pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. 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

30 authors at 5 institutions in 1 country.

Nelly F Altamirano-BustamanteInstituto Nacional de Pediatría, Mexico City, Mexico.
Eulalia Garrido-MagañaUMAE Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Eugenia MoránUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Aurora CalderónUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Karina Pasten-HidalgoInstituto Nacional de Pediatría, Mexico City, Mexico.
Rosa Angélica Castillo-RodríguezInstituto Nacional de Pediatría, Mexico City, Mexico.
Gerardo RojasUMAE Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Reyna Lara-MartínezFacultad de Ciencias, UNAM, Mexico City, Mexico.
Edgar Leyva-GarcíaUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Mateo Larralde-LabordeUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Guadalupe DomíguezInstituto de Fisiología Celular, UNAM, Mexico City, Mexico.
Chiharu MurataInstituto Nacional de Pediatría, Mexico City, Mexico.
Yolanda Margarita-VazquezInstituto Nacional de Pediatría, Mexico City, Mexico.
Rafael PayroUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Manuel BarbosaUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Alejandro ValderramaInstituto Nacional de Pediatría, Mexico City, Mexico.
Hortencia MontesinosInstituto Nacional de Pediatría, Mexico City, Mexico.
Alejandra Domínguez-CamachoInstituto Nacional de Pediatría, Mexico City, Mexico.
Víctor H García-OlmosInstituto Nacional de Pediatría, Mexico City, Mexico.
Regina FerrerUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Patricia G Medina-BravoHospital Infantil Federico Gómez, Mexico City, Mexico.
Fernanda SantoscoyUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Cristina Revilla-MonsalveUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Luis Felipe Jiménez-GarcíaFacultad de Ciencias, UNAM, Mexico City, Mexico.
Julio MoránInstituto de Fisiología Celular, UNAM, Mexico City, Mexico.
Jalil Villalobos-AlvaUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Mario Javier VillalobosUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Raúl Calzada-LeónInstituto Nacional de Pediatría, Mexico City, Mexico.
Perla AltamiranoUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
Myriam M Altamirano-BustamanteUnidad de Investigación en Enfermedades Metabólicas, Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social, Mexico City, Mexico.ORCID 0000-0001-7297-4689
Mexican Social Security Institute · MXInstituto Nacional de Pediatria · MXInstituto Nacional de Cardiología · MXUniversidad Nacional Autónoma de México · MXHospital Infantil de México Federico Gómez · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsThis is the first time that obesity and diabetes mellitus (DM) as protein conformational diseases (PCD) are reported in children and they are typically diagnosed too late, when β-cell damage is evident. Here we wanted to investigate the level of naturally-ocurring or real (not synthetic) oligomeric aggregates of the human islet amyloid polypeptide (hIAPP) that we called RIAO in sera of pediatric patients with obesity and diabetes. We aimed to reduce the gap between basic biomedical research, clinical practice-health decision making and to explore whether RIAO work as a potential biomarker of early β-cell damage. MATERIALS AND

methodsWe performed a multicentric collaborative, cross-sectional, analytical, ambispective and blinded study; the RIAO from pretreated samples (PTS) of sera of 146 pediatric patients with obesity or DM and 16 healthy children, were isolated, measured by sound indirect ELISA with novel anti-hIAPP cytotoxic oligomers polyclonal antibody (MEX1). We carried out morphological and functional studied and cluster-clinical data driven analysis.

resultsWe demonstrated by western blot, Transmission Electron Microscopy and cell viability experiments that RIAO circulate in the blood and can be measured by ELISA; are elevated in serum of childhood obesity and diabetes; are neurotoxics and works as biomarkers of early β-cell failure. We explored the range of evidence-based medicine clusters that included the RIAO level, which allowed us to classify and stratify the obesity patients with high cardiometabolic risk.

conclusionsRIAO level increases as the number of complications rises; RIAOs > 3.35 μg/ml is a predictor of changes in the current indicators of β-cell damage. We proposed a novel physio-pathological pathway and shows that PCD affect not only elderly patients but also children. Here we reduced the gap between basic biomedical research, clinical practice and health decision making.

Indexed as

Protein Structure, QuaternaryAdolescentAnimalsCell LineCells, CulturedCell SurvivalChildChild, PreschoolCross-Sectional StudiesDiabetes Mellitus, Type 1Diabetes Mellitus, Type 2HumansInsulin-Secreting CellsIslet Amyloid PolypeptideMicroscopy, Electron, TransmissionNeuronsIslet Amyloid Polypeptide

Identifiers

PMID32833960
PMCPMC7446879
OpenAlexW3080317136

What Socratic 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 Socratic graph.