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Targeting β‐cell functions in therapy for type 2 diabetes

Recently, Leahy et al. issued a “consensus statement” in regard to targeting β‐cell function in therapy for type 2 diabetes that recommends continued multidisciplinary efforts to realign treatment of type 2 diabetes to preserve β‐cell function by early intervention. This might be applicable not only...

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Detalles Bibliográficos
Autores principales: Fujimoto, Shimpei, Inagaki, Nobuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014915/
https://www.ncbi.nlm.nih.gov/pubmed/24843480
http://dx.doi.org/10.1111/j.2040-1124.2011.00117.x
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author Fujimoto, Shimpei
Inagaki, Nobuya
author_facet Fujimoto, Shimpei
Inagaki, Nobuya
author_sort Fujimoto, Shimpei
collection PubMed
description Recently, Leahy et al. issued a “consensus statement” in regard to targeting β‐cell function in therapy for type 2 diabetes that recommends continued multidisciplinary efforts to realign treatment of type 2 diabetes to preserve β‐cell function by early intervention. This might be applicable not only for obese type 2 diabetes in Europe and America, but also for lean type 2 diabetes in Asia. To establish evidence, development of non‐invasive measurements of β‐cell mass for longitudinal observation during long duration of diabetes is critical. In addition, studies that clarify the development of β‐cell dysfunction with regard to both mass reduction and functional impairment are required for the development of novel strategies to preserve β‐cell function by treatment of type 2 diabetes. (J Diabetes Invest, doi: 10.1111/j.2040‐1124.2011.00117.x, 2011)
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spelling pubmed-40149152014-05-19 Targeting β‐cell functions in therapy for type 2 diabetes Fujimoto, Shimpei Inagaki, Nobuya J Diabetes Investig Commentaries Recently, Leahy et al. issued a “consensus statement” in regard to targeting β‐cell function in therapy for type 2 diabetes that recommends continued multidisciplinary efforts to realign treatment of type 2 diabetes to preserve β‐cell function by early intervention. This might be applicable not only for obese type 2 diabetes in Europe and America, but also for lean type 2 diabetes in Asia. To establish evidence, development of non‐invasive measurements of β‐cell mass for longitudinal observation during long duration of diabetes is critical. In addition, studies that clarify the development of β‐cell dysfunction with regard to both mass reduction and functional impairment are required for the development of novel strategies to preserve β‐cell function by treatment of type 2 diabetes. (J Diabetes Invest, doi: 10.1111/j.2040‐1124.2011.00117.x, 2011) Blackwell Publishing Ltd 2011-04-18 2011-06-05 /pmc/articles/PMC4014915/ /pubmed/24843480 http://dx.doi.org/10.1111/j.2040-1124.2011.00117.x Text en © 2011 Asian Association for the Study of Diabetes and Blackwell Publishing Asia Pty Ltd
spellingShingle Commentaries
Fujimoto, Shimpei
Inagaki, Nobuya
Targeting β‐cell functions in therapy for type 2 diabetes
title Targeting β‐cell functions in therapy for type 2 diabetes
title_full Targeting β‐cell functions in therapy for type 2 diabetes
title_fullStr Targeting β‐cell functions in therapy for type 2 diabetes
title_full_unstemmed Targeting β‐cell functions in therapy for type 2 diabetes
title_short Targeting β‐cell functions in therapy for type 2 diabetes
title_sort targeting β‐cell functions in therapy for type 2 diabetes
topic Commentaries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014915/
https://www.ncbi.nlm.nih.gov/pubmed/24843480
http://dx.doi.org/10.1111/j.2040-1124.2011.00117.x
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