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OGTT is recommended for glucose homeostasis assessments in Friedreich ataxia

Diabetes is a common complication of Friedreich ataxia, requiring sensitive diagnostic methods. Here, we compared the performance of different tests that assess glucose tolerance, insulin sensitivity, and β‐cell function in Friedreich ataxia patients, heterozygous FXN mutation carriers and controls....

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Autores principales: Azzi, Anne‐Sophie, Cosentino, Cristina, Kibanda, Jésabelle, Féry, Françoise, Cnop, Miriam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331656/
https://www.ncbi.nlm.nih.gov/pubmed/30656194
http://dx.doi.org/10.1002/acn3.686
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author Azzi, Anne‐Sophie
Cosentino, Cristina
Kibanda, Jésabelle
Féry, Françoise
Cnop, Miriam
author_facet Azzi, Anne‐Sophie
Cosentino, Cristina
Kibanda, Jésabelle
Féry, Françoise
Cnop, Miriam
author_sort Azzi, Anne‐Sophie
collection PubMed
description Diabetes is a common complication of Friedreich ataxia, requiring sensitive diagnostic methods. Here, we compared the performance of different tests that assess glucose tolerance, insulin sensitivity, and β‐cell function in Friedreich ataxia patients, heterozygous FXN mutation carriers and controls. We find that diabetes is underdiagnosed with fasting glucose alone. The oral glucose tolerance test (OGTT) provides 1.2‐ to 3.5‐fold more diagnoses of impaired glucose homeostasis and diabetes, and adequately measures insulin sensitivity, insulin secretion, and β‐cell function. Clinicians in charge of Friedreich ataxia patients and researchers should incorporate the OGTT as an accurate diagnostic and research tool.
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spelling pubmed-63316562019-01-17 OGTT is recommended for glucose homeostasis assessments in Friedreich ataxia Azzi, Anne‐Sophie Cosentino, Cristina Kibanda, Jésabelle Féry, Françoise Cnop, Miriam Ann Clin Transl Neurol Brief Communications Diabetes is a common complication of Friedreich ataxia, requiring sensitive diagnostic methods. Here, we compared the performance of different tests that assess glucose tolerance, insulin sensitivity, and β‐cell function in Friedreich ataxia patients, heterozygous FXN mutation carriers and controls. We find that diabetes is underdiagnosed with fasting glucose alone. The oral glucose tolerance test (OGTT) provides 1.2‐ to 3.5‐fold more diagnoses of impaired glucose homeostasis and diabetes, and adequately measures insulin sensitivity, insulin secretion, and β‐cell function. Clinicians in charge of Friedreich ataxia patients and researchers should incorporate the OGTT as an accurate diagnostic and research tool. John Wiley and Sons Inc. 2018-11-25 /pmc/articles/PMC6331656/ /pubmed/30656194 http://dx.doi.org/10.1002/acn3.686 Text en © 2018 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Brief Communications
Azzi, Anne‐Sophie
Cosentino, Cristina
Kibanda, Jésabelle
Féry, Françoise
Cnop, Miriam
OGTT is recommended for glucose homeostasis assessments in Friedreich ataxia
title OGTT is recommended for glucose homeostasis assessments in Friedreich ataxia
title_full OGTT is recommended for glucose homeostasis assessments in Friedreich ataxia
title_fullStr OGTT is recommended for glucose homeostasis assessments in Friedreich ataxia
title_full_unstemmed OGTT is recommended for glucose homeostasis assessments in Friedreich ataxia
title_short OGTT is recommended for glucose homeostasis assessments in Friedreich ataxia
title_sort ogtt is recommended for glucose homeostasis assessments in friedreich ataxia
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331656/
https://www.ncbi.nlm.nih.gov/pubmed/30656194
http://dx.doi.org/10.1002/acn3.686
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