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Fifty years of pancreatic islet pathology in human type 1 diabetes: insights gained and progress made

Type 1 diabetes is increasing in incidence in many parts of the world and it might be imagined that the pathological processes that underlie disease progression are firmly understood. However, this is not the case; rather, our collective understanding is still surprisingly rudimentary. There are var...

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Autores principales: Morgan, Noel G., Richardson, Sarah J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6223849/
https://www.ncbi.nlm.nih.gov/pubmed/30255378
http://dx.doi.org/10.1007/s00125-018-4731-y
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author Morgan, Noel G.
Richardson, Sarah J.
author_facet Morgan, Noel G.
Richardson, Sarah J.
author_sort Morgan, Noel G.
collection PubMed
description Type 1 diabetes is increasing in incidence in many parts of the world and it might be imagined that the pathological processes that underlie disease progression are firmly understood. However, this is not the case; rather, our collective understanding is still surprisingly rudimentary. There are various reasons for this but one of the most important is that the target organ (the pancreas) has been examined at, or soon after, diagnosis in only a small number of cases worldwide over the past half a century. This review provides a summary of some of the insights gained from these studies and highlights areas of ongoing uncertainty. In particular, it considers the process of insulitis (a form of islet inflammation that occurs characteristically in type 1 diabetes) and discusses the factors that may influence the access of immune cells to the beta cells. Attention is also drawn to recent evidence implying that two distinct profiles of insulitis exist, which occur differentially in people who develop type 1 diabetes at increasing ages. Emphasis is also placed on the emerging (and somewhat surprising) consensus that the extent of beta cell loss is variable among people with type 1 diabetes and that many (especially those who are older at onset) retain significant numbers of insulin-producing cells long after diagnosis. We conclude by emphasising the importance of renewed efforts to study the human pancreas at disease onset and consider how the current insights may inform the design of future strategies to slow or halt the rate of beta cell loss. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00125-018-4731-y) contains a slideset of the figures for download, which is available to authorised users.
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spelling pubmed-62238492018-11-19 Fifty years of pancreatic islet pathology in human type 1 diabetes: insights gained and progress made Morgan, Noel G. Richardson, Sarah J. Diabetologia Review Type 1 diabetes is increasing in incidence in many parts of the world and it might be imagined that the pathological processes that underlie disease progression are firmly understood. However, this is not the case; rather, our collective understanding is still surprisingly rudimentary. There are various reasons for this but one of the most important is that the target organ (the pancreas) has been examined at, or soon after, diagnosis in only a small number of cases worldwide over the past half a century. This review provides a summary of some of the insights gained from these studies and highlights areas of ongoing uncertainty. In particular, it considers the process of insulitis (a form of islet inflammation that occurs characteristically in type 1 diabetes) and discusses the factors that may influence the access of immune cells to the beta cells. Attention is also drawn to recent evidence implying that two distinct profiles of insulitis exist, which occur differentially in people who develop type 1 diabetes at increasing ages. Emphasis is also placed on the emerging (and somewhat surprising) consensus that the extent of beta cell loss is variable among people with type 1 diabetes and that many (especially those who are older at onset) retain significant numbers of insulin-producing cells long after diagnosis. We conclude by emphasising the importance of renewed efforts to study the human pancreas at disease onset and consider how the current insights may inform the design of future strategies to slow or halt the rate of beta cell loss. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00125-018-4731-y) contains a slideset of the figures for download, which is available to authorised users. Springer Berlin Heidelberg 2018-09-25 2018 /pmc/articles/PMC6223849/ /pubmed/30255378 http://dx.doi.org/10.1007/s00125-018-4731-y Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Morgan, Noel G.
Richardson, Sarah J.
Fifty years of pancreatic islet pathology in human type 1 diabetes: insights gained and progress made
title Fifty years of pancreatic islet pathology in human type 1 diabetes: insights gained and progress made
title_full Fifty years of pancreatic islet pathology in human type 1 diabetes: insights gained and progress made
title_fullStr Fifty years of pancreatic islet pathology in human type 1 diabetes: insights gained and progress made
title_full_unstemmed Fifty years of pancreatic islet pathology in human type 1 diabetes: insights gained and progress made
title_short Fifty years of pancreatic islet pathology in human type 1 diabetes: insights gained and progress made
title_sort fifty years of pancreatic islet pathology in human type 1 diabetes: insights gained and progress made
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6223849/
https://www.ncbi.nlm.nih.gov/pubmed/30255378
http://dx.doi.org/10.1007/s00125-018-4731-y
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