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Autoimmune Inflammation and Insulin Resistance: Hallmarks So Far and Yet So Close to Explain Diabetes Endotypes

PURPOSE OF REVIEW: Diabetes mellitus can be categorized into two major variants, type 1 and type 2. A number of traits such as clinical phenotype, age at disease onset, genetic background, and underlying pathogenesis distinguish the two forms. RECENT FINDINGS: Recent evidence indicates that type 1 d...

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Autores principales: Petrelli, Alessandra, Giovenzana, Anna, Insalaco, Vittoria, Phillips, Brett E., Pietropaolo, Massimo, Giannoukakis, Nick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668851/
https://www.ncbi.nlm.nih.gov/pubmed/34902055
http://dx.doi.org/10.1007/s11892-021-01430-3
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author Petrelli, Alessandra
Giovenzana, Anna
Insalaco, Vittoria
Phillips, Brett E.
Pietropaolo, Massimo
Giannoukakis, Nick
author_facet Petrelli, Alessandra
Giovenzana, Anna
Insalaco, Vittoria
Phillips, Brett E.
Pietropaolo, Massimo
Giannoukakis, Nick
author_sort Petrelli, Alessandra
collection PubMed
description PURPOSE OF REVIEW: Diabetes mellitus can be categorized into two major variants, type 1 and type 2. A number of traits such as clinical phenotype, age at disease onset, genetic background, and underlying pathogenesis distinguish the two forms. RECENT FINDINGS: Recent evidence indicates that type 1 diabetes can be accompanied by insulin resistance and type 2 diabetes exhibits self-reactivity. These two previously unknown conditions can influence the progression and outcome of the disease. Unlike most conventional considerations, diabetes appears to consist of a spectrum of intermediate phenotypes that includes monogenic and polygenic loci linked to inflammatory processes including autoimmunity, beta cell impairment, and insulin resistance. SUMMARY: Here we discuss why a shift of the classical bi-modal view of diabetes (autoimmune vs. non-autoimmune) is necessary in favor of a model of an immunological continuum of endotypes lying between the two extreme “insulin-resistant” and “autoimmune beta cell targeting,” shaped by environmental and genetic factors which contribute to determine specific immune-conditioned outcomes.
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spelling pubmed-86688512021-12-28 Autoimmune Inflammation and Insulin Resistance: Hallmarks So Far and Yet So Close to Explain Diabetes Endotypes Petrelli, Alessandra Giovenzana, Anna Insalaco, Vittoria Phillips, Brett E. Pietropaolo, Massimo Giannoukakis, Nick Curr Diab Rep Immunology, Transplantation, and Regenerative Medicine (J Florez, Section Editor) PURPOSE OF REVIEW: Diabetes mellitus can be categorized into two major variants, type 1 and type 2. A number of traits such as clinical phenotype, age at disease onset, genetic background, and underlying pathogenesis distinguish the two forms. RECENT FINDINGS: Recent evidence indicates that type 1 diabetes can be accompanied by insulin resistance and type 2 diabetes exhibits self-reactivity. These two previously unknown conditions can influence the progression and outcome of the disease. Unlike most conventional considerations, diabetes appears to consist of a spectrum of intermediate phenotypes that includes monogenic and polygenic loci linked to inflammatory processes including autoimmunity, beta cell impairment, and insulin resistance. SUMMARY: Here we discuss why a shift of the classical bi-modal view of diabetes (autoimmune vs. non-autoimmune) is necessary in favor of a model of an immunological continuum of endotypes lying between the two extreme “insulin-resistant” and “autoimmune beta cell targeting,” shaped by environmental and genetic factors which contribute to determine specific immune-conditioned outcomes. Springer US 2021-12-13 2021 /pmc/articles/PMC8668851/ /pubmed/34902055 http://dx.doi.org/10.1007/s11892-021-01430-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Immunology, Transplantation, and Regenerative Medicine (J Florez, Section Editor)
Petrelli, Alessandra
Giovenzana, Anna
Insalaco, Vittoria
Phillips, Brett E.
Pietropaolo, Massimo
Giannoukakis, Nick
Autoimmune Inflammation and Insulin Resistance: Hallmarks So Far and Yet So Close to Explain Diabetes Endotypes
title Autoimmune Inflammation and Insulin Resistance: Hallmarks So Far and Yet So Close to Explain Diabetes Endotypes
title_full Autoimmune Inflammation and Insulin Resistance: Hallmarks So Far and Yet So Close to Explain Diabetes Endotypes
title_fullStr Autoimmune Inflammation and Insulin Resistance: Hallmarks So Far and Yet So Close to Explain Diabetes Endotypes
title_full_unstemmed Autoimmune Inflammation and Insulin Resistance: Hallmarks So Far and Yet So Close to Explain Diabetes Endotypes
title_short Autoimmune Inflammation and Insulin Resistance: Hallmarks So Far and Yet So Close to Explain Diabetes Endotypes
title_sort autoimmune inflammation and insulin resistance: hallmarks so far and yet so close to explain diabetes endotypes
topic Immunology, Transplantation, and Regenerative Medicine (J Florez, Section Editor)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8668851/
https://www.ncbi.nlm.nih.gov/pubmed/34902055
http://dx.doi.org/10.1007/s11892-021-01430-3
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