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Maturity-onset diabetes of the young: update and perspectives on diagnosis and treatment

Maturity-onset diabetes of the young (MODY) is a clinically heterogeneous group of monogenic disorders characterized by ß-cell dysfunction. MODY accounts for between 2% and 5% of all diabetes cases, and distinguishing it from type 1 or type 2 diabetes is a diagnostic challenge. Recently, MODY-causin...

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Autor principal: Jang, Kyung Mi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Yeungnam University College of Medicine 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986955/
https://www.ncbi.nlm.nih.gov/pubmed/31914718
http://dx.doi.org/10.12701/yujm.2019.00409
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author Jang, Kyung Mi
author_facet Jang, Kyung Mi
author_sort Jang, Kyung Mi
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description Maturity-onset diabetes of the young (MODY) is a clinically heterogeneous group of monogenic disorders characterized by ß-cell dysfunction. MODY accounts for between 2% and 5% of all diabetes cases, and distinguishing it from type 1 or type 2 diabetes is a diagnostic challenge. Recently, MODY-causing mutations have been identified in 14 different genes. Sanger DNA sequencing is the gold standard for identifying the mutations in MODY-related genes, and may facilitate the diagnosis. Despite the lower frequency among diabetes mellitus cases, a correct genetic diagnosis of MODY is important for optimizing treatment strategies. There is a discrepancy in the disease-causing locus between the Asian and Caucasian patients with MODY. Furthermore, the prevalence of the disease in Asian populations remains to be studied. In this review, the current understanding of MODY is summarized and the Asian studies of MODY are discussed in detail.
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spelling pubmed-69869552020-02-05 Maturity-onset diabetes of the young: update and perspectives on diagnosis and treatment Jang, Kyung Mi Yeungnam Univ J Med Review Article Maturity-onset diabetes of the young (MODY) is a clinically heterogeneous group of monogenic disorders characterized by ß-cell dysfunction. MODY accounts for between 2% and 5% of all diabetes cases, and distinguishing it from type 1 or type 2 diabetes is a diagnostic challenge. Recently, MODY-causing mutations have been identified in 14 different genes. Sanger DNA sequencing is the gold standard for identifying the mutations in MODY-related genes, and may facilitate the diagnosis. Despite the lower frequency among diabetes mellitus cases, a correct genetic diagnosis of MODY is important for optimizing treatment strategies. There is a discrepancy in the disease-causing locus between the Asian and Caucasian patients with MODY. Furthermore, the prevalence of the disease in Asian populations remains to be studied. In this review, the current understanding of MODY is summarized and the Asian studies of MODY are discussed in detail. Yeungnam University College of Medicine 2020-01-09 /pmc/articles/PMC6986955/ /pubmed/31914718 http://dx.doi.org/10.12701/yujm.2019.00409 Text en Copyright © 2020 Yeungnam University College of Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Jang, Kyung Mi
Maturity-onset diabetes of the young: update and perspectives on diagnosis and treatment
title Maturity-onset diabetes of the young: update and perspectives on diagnosis and treatment
title_full Maturity-onset diabetes of the young: update and perspectives on diagnosis and treatment
title_fullStr Maturity-onset diabetes of the young: update and perspectives on diagnosis and treatment
title_full_unstemmed Maturity-onset diabetes of the young: update and perspectives on diagnosis and treatment
title_short Maturity-onset diabetes of the young: update and perspectives on diagnosis and treatment
title_sort maturity-onset diabetes of the young: update and perspectives on diagnosis and treatment
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986955/
https://www.ncbi.nlm.nih.gov/pubmed/31914718
http://dx.doi.org/10.12701/yujm.2019.00409
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