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

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 β-cell damage is evident. Here we wanted to investigate the level of naturally-ocurring or real (not sy...

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Veröffentlicht in:PloS one 2020-08, Vol.15 (8), p.e0237667
Hauptverfasser: Altamirano-Bustamante, Nelly F., Garrido-Magaña, Eulalia, Morán, Eugenia, Calderón, Aurora, Pasten-Hidalgo, Karina, Castillo-Rodríguez, Rosa Angélica, Rojas, Gerardo, Lara-Martínez, Reyna, Leyva-García, Edgar, Larralde-Laborde, Mateo, Domíguez, Guadalupe, Murata, Chiharu, Margarita-Vazquez, Yolanda, Payro, Rafael, Barbosa, Manuel, Valderrama, Alejandro, Montesinos, Hortencia, Domínguez-Camacho, Alejandra, García-Olmos, Víctor H., Ferrer, Regina, Medina-Bravo, Patricia G., Santoscoy, Fernanda, Revilla-Monsalve, Cristina, Jiménez-García, Luis Felipe, Morán, Julio, Villalobos-Alva, Jalil, Villalobos, Mario Javier, Calzada-León, Raúl, Altamirano, Perla, Altamirano-Bustamante, Myriam M.
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container_issue 8
container_start_page e0237667
container_title PloS one
container_volume 15
creator Altamirano-Bustamante, Nelly F.
Garrido-Magaña, Eulalia
Morán, Eugenia
Calderón, Aurora
Pasten-Hidalgo, Karina
Castillo-Rodríguez, Rosa Angélica
Rojas, Gerardo
Lara-Martínez, Reyna
Leyva-García, Edgar
Larralde-Laborde, Mateo
Domíguez, Guadalupe
Murata, Chiharu
Margarita-Vazquez, Yolanda
Payro, Rafael
Barbosa, Manuel
Valderrama, Alejandro
Montesinos, Hortencia
Domínguez-Camacho, Alejandra
García-Olmos, Víctor H.
Ferrer, Regina
Medina-Bravo, Patricia G.
Santoscoy, Fernanda
Revilla-Monsalve, Cristina
Jiménez-García, Luis Felipe
Morán, Julio
Villalobos-Alva, Jalil
Villalobos, Mario Javier
Calzada-León, Raúl
Altamirano, Perla
Altamirano-Bustamante, Myriam M.
description 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 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 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 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. Conclusions RIAO 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.
doi_str_mv 10.1371/journal.pone.0237667
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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 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 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. Conclusions RIAO level increases as the number of complications rises; RIAOs &gt; 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.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0237667</identifier><identifier>PMID: 32833960</identifier><language>eng</language><publisher>San Francisco: Public Library of Science</publisher><subject>Amylin ; Amyloid ; Antibodies ; Beta cells ; Biology and Life Sciences ; Biomarkers ; Biomedical materials ; Cell viability ; Childhood ; Children ; Clinical decision making ; Complications ; Cytotoxicity ; Damage ; Decision making ; Diabetes ; Diabetes mellitus ; Electron microscopy ; Health risks ; Hospitals ; Medicine ; Medicine and Health Sciences ; Methods ; Morphology ; Obesity ; Oligomers ; Patients ; Pediatrics ; Physical Sciences ; Polyclonal antibodies ; Polypeptides ; Proteins ; Research and Analysis Methods ; Transmission electron microscopy</subject><ispartof>PloS one, 2020-08, Vol.15 (8), p.e0237667</ispartof><rights>2020 Altamirano-Bustamante et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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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 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 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. Conclusions RIAO level increases as the number of complications rises; RIAOs &gt; 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.</description><subject>Amylin</subject><subject>Amyloid</subject><subject>Antibodies</subject><subject>Beta cells</subject><subject>Biology and Life Sciences</subject><subject>Biomarkers</subject><subject>Biomedical materials</subject><subject>Cell viability</subject><subject>Childhood</subject><subject>Children</subject><subject>Clinical decision making</subject><subject>Complications</subject><subject>Cytotoxicity</subject><subject>Damage</subject><subject>Decision making</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Electron microscopy</subject><subject>Health risks</subject><subject>Hospitals</subject><subject>Medicine</subject><subject>Medicine and Health 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diseases in childhood: Naturally-occurring hIAPP amyloid-oligomers and early β-cell damage in obesity and diabetes</title><author>Altamirano-Bustamante, Nelly F. ; Garrido-Magaña, Eulalia ; Morán, Eugenia ; Calderón, Aurora ; Pasten-Hidalgo, Karina ; Castillo-Rodríguez, Rosa Angélica ; Rojas, Gerardo ; Lara-Martínez, Reyna ; Leyva-García, Edgar ; Larralde-Laborde, Mateo ; Domíguez, Guadalupe ; Murata, Chiharu ; Margarita-Vazquez, Yolanda ; Payro, Rafael ; Barbosa, Manuel ; Valderrama, Alejandro ; Montesinos, Hortencia ; Domínguez-Camacho, Alejandra ; García-Olmos, Víctor H. ; Ferrer, Regina ; Medina-Bravo, Patricia G. ; Santoscoy, Fernanda ; Revilla-Monsalve, Cristina ; Jiménez-García, Luis Felipe ; Morán, Julio ; Villalobos-Alva, Jalil ; Villalobos, Mario Javier ; Calzada-León, Raúl ; Altamirano, Perla ; Altamirano-Bustamante, Myriam 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Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Altamirano-Bustamante, Nelly F.</au><au>Garrido-Magaña, Eulalia</au><au>Morán, Eugenia</au><au>Calderón, Aurora</au><au>Pasten-Hidalgo, Karina</au><au>Castillo-Rodríguez, Rosa Angélica</au><au>Rojas, Gerardo</au><au>Lara-Martínez, Reyna</au><au>Leyva-García, Edgar</au><au>Larralde-Laborde, Mateo</au><au>Domíguez, Guadalupe</au><au>Murata, Chiharu</au><au>Margarita-Vazquez, Yolanda</au><au>Payro, Rafael</au><au>Barbosa, Manuel</au><au>Valderrama, Alejandro</au><au>Montesinos, Hortencia</au><au>Domínguez-Camacho, Alejandra</au><au>García-Olmos, Víctor H.</au><au>Ferrer, Regina</au><au>Medina-Bravo, Patricia G.</au><au>Santoscoy, Fernanda</au><au>Revilla-Monsalve, Cristina</au><au>Jiménez-García, Luis Felipe</au><au>Morán, Julio</au><au>Villalobos-Alva, Jalil</au><au>Villalobos, Mario Javier</au><au>Calzada-León, Raúl</au><au>Altamirano, Perla</au><au>Altamirano-Bustamante, Myriam M.</au><au>Zheng, Jie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protein-conformational diseases in childhood: Naturally-occurring hIAPP amyloid-oligomers and early β-cell damage in obesity and diabetes</atitle><jtitle>PloS one</jtitle><date>2020-08-24</date><risdate>2020</risdate><volume>15</volume><issue>8</issue><spage>e0237667</spage><pages>e0237667-</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><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 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 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 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. Conclusions RIAO level increases as the number of complications rises; RIAOs &gt; 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.</abstract><cop>San Francisco</cop><pub>Public Library of Science</pub><pmid>32833960</pmid><doi>10.1371/journal.pone.0237667</doi><orcidid>https://orcid.org/0000-0001-7297-4689</orcidid><oa>free_for_read</oa></addata></record>
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subjects Amylin
Amyloid
Antibodies
Beta cells
Biology and Life Sciences
Biomarkers
Biomedical materials
Cell viability
Childhood
Children
Clinical decision making
Complications
Cytotoxicity
Damage
Decision making
Diabetes
Diabetes mellitus
Electron microscopy
Health risks
Hospitals
Medicine
Medicine and Health Sciences
Methods
Morphology
Obesity
Oligomers
Patients
Pediatrics
Physical Sciences
Polyclonal antibodies
Polypeptides
Proteins
Research and Analysis Methods
Transmission electron microscopy
title Protein-conformational diseases in childhood: Naturally-occurring hIAPP amyloid-oligomers and early β-cell damage in obesity and diabetes
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