Unknown

Dataset Information

0

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


ABSTRACT: BACKGROUND AND AIMS:This 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 ?-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 ?-cell damage. MATERIALS AND METHODS:We 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. RESULTS:We 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 ?-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. CONCLUSIONS:RIAO level increases as the number of complications rises; RIAOs > 3.35 ?g/ml is a predictor of changes in the current indicators of ?-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.

SUBMITTER: Altamirano-Bustamante NF 

PROVIDER: S-EPMC7446879 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

altmetric image

Publications

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

Altamirano-Bustamante Nelly F NF   Garrido-Magaña Eulalia E   Morán Eugenia E   Calderón Aurora A   Pasten-Hidalgo Karina K   Castillo-Rodríguez Rosa Angélica RA   Rojas Gerardo G   Lara-Martínez Reyna R   Leyva-García Edgar E   Larralde-Laborde Mateo M   Domíguez Guadalupe G   Murata Chiharu C   Margarita-Vazquez Yolanda Y   Payro Rafael R   Barbosa Manuel M   Valderrama Alejandro A   Montesinos Hortencia H   Domínguez-Camacho Alejandra A   García-Olmos Víctor H VH   Ferrer Regina R   Medina-Bravo Patricia G PG   Santoscoy Fernanda F   Revilla-Monsalve Cristina C   Jiménez-García Luis Felipe LF   Morán Julio J   Villalobos-Alva Jalil J   Villalobos Mario Javier MJ   Calzada-León Raúl R   Altamirano Perla P   Altamirano-Bustamante Myriam M MM  

PloS one 20200824 8


<h4>Background and aims</h4>This 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 ba  ...[more]

Similar Datasets

| S-EPMC6895187 | biostudies-literature
| S-EPMC6149893 | biostudies-other
| S-EPMC5486015 | biostudies-literature
| S-EPMC5970100 | biostudies-literature
| S-EPMC3158298 | biostudies-literature
| S-EPMC9055351 | biostudies-literature
| S-EPMC8199700 | biostudies-literature
| S-EPMC4004235 | biostudies-literature
| S-EPMC6263551 | biostudies-literature
| S-EPMC4258429 | biostudies-literature