Cargando…

Corneal Confocal Microscopy Identifies Small-Fiber Neuropathy in Subjects With Impaired Glucose Tolerance Who Develop Type 2 Diabetes

OBJECTIVE: Impaired glucose tolerance (IGT) through to type 2 diabetes is thought to confer a continuum of risk for neuropathy. Identification of subjects at high risk of developing type 2 diabetes and, hence, worsening neuropathy would allow identification and risk stratification for more aggressiv...

Descripción completa

Detalles Bibliográficos
Autores principales: Azmi, Shazli, Ferdousi, Maryam, Petropoulos, Ioannis N., Ponirakis, Georgios, Alam, Uazman, Fadavi, Hassan, Asghar, Omar, Marshall, Andrew, Atkinson, Andrew J., Jones, Wendy, Boulton, Andrew J.M., Tavakoli, Mitra, Jeziorska, Maria, Malik, Rayaz A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4512140/
https://www.ncbi.nlm.nih.gov/pubmed/25877814
http://dx.doi.org/10.2337/dc14-2733
_version_ 1782382455165026304
author Azmi, Shazli
Ferdousi, Maryam
Petropoulos, Ioannis N.
Ponirakis, Georgios
Alam, Uazman
Fadavi, Hassan
Asghar, Omar
Marshall, Andrew
Atkinson, Andrew J.
Jones, Wendy
Boulton, Andrew J.M.
Tavakoli, Mitra
Jeziorska, Maria
Malik, Rayaz A.
author_facet Azmi, Shazli
Ferdousi, Maryam
Petropoulos, Ioannis N.
Ponirakis, Georgios
Alam, Uazman
Fadavi, Hassan
Asghar, Omar
Marshall, Andrew
Atkinson, Andrew J.
Jones, Wendy
Boulton, Andrew J.M.
Tavakoli, Mitra
Jeziorska, Maria
Malik, Rayaz A.
author_sort Azmi, Shazli
collection PubMed
description OBJECTIVE: Impaired glucose tolerance (IGT) through to type 2 diabetes is thought to confer a continuum of risk for neuropathy. Identification of subjects at high risk of developing type 2 diabetes and, hence, worsening neuropathy would allow identification and risk stratification for more aggressive management. RESEARCH DESIGN AND METHODS: Thirty subjects with IGT and 17 age-matched control subjects underwent an oral glucose tolerance test, assessment of neuropathic symptoms and deficits, quantitative sensory testing, neurophysiology, skin biopsy, and corneal confocal microscopy (CCM) to quantify corneal nerve fiber density (CNFD), branch density (CNBD), and fiber length (CNFL) at baseline and annually for 3 years. RESULTS: Ten subjects who developed type 2 diabetes had a significantly lower CNFD (P = 0.003), CNBD (P = 0.04), and CNFL (P = 0.04) compared with control subjects at baseline and a further reduction in CNFL (P = 0.006), intraepidermal nerve fiber density (IENFD) (P = 0.02), and mean dendritic length (MDL) (P = 0.02) over 3 years. Fifteen subjects who remained IGT and 5 subjects who returned to normal glucose tolerance had no significant baseline abnormality on CCM or IENFD but had a lower MDL (P < 0.0001) compared with control subjects. The IGT subjects showed a significant decrease in IENFD (P = 0.02) but no change in MDL or CCM over 3 years. Those who returned to NGT showed an increase in CNFD (P = 0.05), CNBD (P = 0.04), and CNFL (P = 0.05), but a decrease in IENFD (P = 0.02), over 3 years. CONCLUSIONS: CCM and skin biopsy detect a small-fiber neuropathy in subjects with IGT who develop type 2 diabetes and also show a dynamic worsening or improvement in corneal and intraepidermal nerve morphology in relation to change in glucose tolerance status.
format Online
Article
Text
id pubmed-4512140
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher American Diabetes Association
record_format MEDLINE/PubMed
spelling pubmed-45121402016-08-01 Corneal Confocal Microscopy Identifies Small-Fiber Neuropathy in Subjects With Impaired Glucose Tolerance Who Develop Type 2 Diabetes Azmi, Shazli Ferdousi, Maryam Petropoulos, Ioannis N. Ponirakis, Georgios Alam, Uazman Fadavi, Hassan Asghar, Omar Marshall, Andrew Atkinson, Andrew J. Jones, Wendy Boulton, Andrew J.M. Tavakoli, Mitra Jeziorska, Maria Malik, Rayaz A. Diabetes Care Pathophysiology/Complications OBJECTIVE: Impaired glucose tolerance (IGT) through to type 2 diabetes is thought to confer a continuum of risk for neuropathy. Identification of subjects at high risk of developing type 2 diabetes and, hence, worsening neuropathy would allow identification and risk stratification for more aggressive management. RESEARCH DESIGN AND METHODS: Thirty subjects with IGT and 17 age-matched control subjects underwent an oral glucose tolerance test, assessment of neuropathic symptoms and deficits, quantitative sensory testing, neurophysiology, skin biopsy, and corneal confocal microscopy (CCM) to quantify corneal nerve fiber density (CNFD), branch density (CNBD), and fiber length (CNFL) at baseline and annually for 3 years. RESULTS: Ten subjects who developed type 2 diabetes had a significantly lower CNFD (P = 0.003), CNBD (P = 0.04), and CNFL (P = 0.04) compared with control subjects at baseline and a further reduction in CNFL (P = 0.006), intraepidermal nerve fiber density (IENFD) (P = 0.02), and mean dendritic length (MDL) (P = 0.02) over 3 years. Fifteen subjects who remained IGT and 5 subjects who returned to normal glucose tolerance had no significant baseline abnormality on CCM or IENFD but had a lower MDL (P < 0.0001) compared with control subjects. The IGT subjects showed a significant decrease in IENFD (P = 0.02) but no change in MDL or CCM over 3 years. Those who returned to NGT showed an increase in CNFD (P = 0.05), CNBD (P = 0.04), and CNFL (P = 0.05), but a decrease in IENFD (P = 0.02), over 3 years. CONCLUSIONS: CCM and skin biopsy detect a small-fiber neuropathy in subjects with IGT who develop type 2 diabetes and also show a dynamic worsening or improvement in corneal and intraepidermal nerve morphology in relation to change in glucose tolerance status. American Diabetes Association 2015-08 2015-04-15 /pmc/articles/PMC4512140/ /pubmed/25877814 http://dx.doi.org/10.2337/dc14-2733 Text en © 2015 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered.
spellingShingle Pathophysiology/Complications
Azmi, Shazli
Ferdousi, Maryam
Petropoulos, Ioannis N.
Ponirakis, Georgios
Alam, Uazman
Fadavi, Hassan
Asghar, Omar
Marshall, Andrew
Atkinson, Andrew J.
Jones, Wendy
Boulton, Andrew J.M.
Tavakoli, Mitra
Jeziorska, Maria
Malik, Rayaz A.
Corneal Confocal Microscopy Identifies Small-Fiber Neuropathy in Subjects With Impaired Glucose Tolerance Who Develop Type 2 Diabetes
title Corneal Confocal Microscopy Identifies Small-Fiber Neuropathy in Subjects With Impaired Glucose Tolerance Who Develop Type 2 Diabetes
title_full Corneal Confocal Microscopy Identifies Small-Fiber Neuropathy in Subjects With Impaired Glucose Tolerance Who Develop Type 2 Diabetes
title_fullStr Corneal Confocal Microscopy Identifies Small-Fiber Neuropathy in Subjects With Impaired Glucose Tolerance Who Develop Type 2 Diabetes
title_full_unstemmed Corneal Confocal Microscopy Identifies Small-Fiber Neuropathy in Subjects With Impaired Glucose Tolerance Who Develop Type 2 Diabetes
title_short Corneal Confocal Microscopy Identifies Small-Fiber Neuropathy in Subjects With Impaired Glucose Tolerance Who Develop Type 2 Diabetes
title_sort corneal confocal microscopy identifies small-fiber neuropathy in subjects with impaired glucose tolerance who develop type 2 diabetes
topic Pathophysiology/Complications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4512140/
https://www.ncbi.nlm.nih.gov/pubmed/25877814
http://dx.doi.org/10.2337/dc14-2733
work_keys_str_mv AT azmishazli cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT ferdousimaryam cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT petropoulosioannisn cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT ponirakisgeorgios cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT alamuazman cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT fadavihassan cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT asgharomar cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT marshallandrew cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT atkinsonandrewj cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT joneswendy cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT boultonandrewjm cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT tavakolimitra cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT jeziorskamaria cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes
AT malikrayaza cornealconfocalmicroscopyidentifiessmallfiberneuropathyinsubjectswithimpairedglucosetolerancewhodeveloptype2diabetes