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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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. |
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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 > 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. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2020 Altamirano-Bustamante et al 2020 Altamirano-Bustamante et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-41406ebb48c16f6ff0c3e5b045e158a16bbb1387f6eca80ab76e2d7dfcbb1fc33</citedby><cites>FETCH-LOGICAL-c503t-41406ebb48c16f6ff0c3e5b045e158a16bbb1387f6eca80ab76e2d7dfcbb1fc33</cites><orcidid>0000-0001-7297-4689</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7446879/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7446879/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793</link.rule.ids></links><search><contributor>Zheng, Jie</contributor><creatorcontrib>Altamirano-Bustamante, Nelly F.</creatorcontrib><creatorcontrib>Garrido-Magaña, Eulalia</creatorcontrib><creatorcontrib>Morán, Eugenia</creatorcontrib><creatorcontrib>Calderón, Aurora</creatorcontrib><creatorcontrib>Pasten-Hidalgo, Karina</creatorcontrib><creatorcontrib>Castillo-Rodríguez, Rosa Angélica</creatorcontrib><creatorcontrib>Rojas, Gerardo</creatorcontrib><creatorcontrib>Lara-Martínez, Reyna</creatorcontrib><creatorcontrib>Leyva-García, Edgar</creatorcontrib><creatorcontrib>Larralde-Laborde, Mateo</creatorcontrib><creatorcontrib>Domíguez, Guadalupe</creatorcontrib><creatorcontrib>Murata, Chiharu</creatorcontrib><creatorcontrib>Margarita-Vazquez, Yolanda</creatorcontrib><creatorcontrib>Payro, Rafael</creatorcontrib><creatorcontrib>Barbosa, Manuel</creatorcontrib><creatorcontrib>Valderrama, Alejandro</creatorcontrib><creatorcontrib>Montesinos, Hortencia</creatorcontrib><creatorcontrib>Domínguez-Camacho, Alejandra</creatorcontrib><creatorcontrib>García-Olmos, Víctor H.</creatorcontrib><creatorcontrib>Ferrer, Regina</creatorcontrib><creatorcontrib>Medina-Bravo, Patricia G.</creatorcontrib><creatorcontrib>Santoscoy, Fernanda</creatorcontrib><creatorcontrib>Revilla-Monsalve, Cristina</creatorcontrib><creatorcontrib>Jiménez-García, Luis Felipe</creatorcontrib><creatorcontrib>Morán, Julio</creatorcontrib><creatorcontrib>Villalobos-Alva, Jalil</creatorcontrib><creatorcontrib>Villalobos, Mario Javier</creatorcontrib><creatorcontrib>Calzada-León, Raúl</creatorcontrib><creatorcontrib>Altamirano, Perla</creatorcontrib><creatorcontrib>Altamirano-Bustamante, Myriam M.</creatorcontrib><title>Protein-conformational diseases in childhood: Naturally-occurring hIAPP amyloid-oligomers and early β-cell damage in obesity and diabetes</title><title>PloS one</title><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.</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 Sciences</subject><subject>Methods</subject><subject>Morphology</subject><subject>Obesity</subject><subject>Oligomers</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Physical Sciences</subject><subject>Polyclonal antibodies</subject><subject>Polypeptides</subject><subject>Proteins</subject><subject>Research and Analysis Methods</subject><subject>Transmission electron 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Nelly F.</creator><creator>Garrido-Magaña, Eulalia</creator><creator>Morán, Eugenia</creator><creator>Calderón, Aurora</creator><creator>Pasten-Hidalgo, Karina</creator><creator>Castillo-Rodríguez, Rosa Angélica</creator><creator>Rojas, Gerardo</creator><creator>Lara-Martínez, Reyna</creator><creator>Leyva-García, Edgar</creator><creator>Larralde-Laborde, Mateo</creator><creator>Domíguez, Guadalupe</creator><creator>Murata, Chiharu</creator><creator>Margarita-Vazquez, Yolanda</creator><creator>Payro, Rafael</creator><creator>Barbosa, Manuel</creator><creator>Valderrama, Alejandro</creator><creator>Montesinos, Hortencia</creator><creator>Domínguez-Camacho, Alejandra</creator><creator>García-Olmos, Víctor H.</creator><creator>Ferrer, Regina</creator><creator>Medina-Bravo, Patricia G.</creator><creator>Santoscoy, Fernanda</creator><creator>Revilla-Monsalve, Cristina</creator><creator>Jiménez-García, Luis Felipe</creator><creator>Morán, Julio</creator><creator>Villalobos-Alva, 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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 M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-41406ebb48c16f6ff0c3e5b045e158a16bbb1387f6eca80ab76e2d7dfcbb1fc33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Amylin</topic><topic>Amyloid</topic><topic>Antibodies</topic><topic>Beta cells</topic><topic>Biology and Life Sciences</topic><topic>Biomarkers</topic><topic>Biomedical materials</topic><topic>Cell viability</topic><topic>Childhood</topic><topic>Children</topic><topic>Clinical decision making</topic><topic>Complications</topic><topic>Cytotoxicity</topic><topic>Damage</topic><topic>Decision making</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Electron microscopy</topic><topic>Health risks</topic><topic>Hospitals</topic><topic>Medicine</topic><topic>Medicine and Health 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Raúl</creatorcontrib><creatorcontrib>Altamirano, Perla</creatorcontrib><creatorcontrib>Altamirano-Bustamante, Myriam M.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni 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Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One 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 > 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> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2020-08, Vol.15 (8), p.e0237667 |
issn | 1932-6203 1932-6203 |
language | eng |
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source | DOAJ Directory of Open Access Journals; Public Library of Science (PLoS) Journals Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
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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