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Corneal confocal microscopy in patients with distal symmetric polyneuropathy compared to controls

BACKGROUND: Diabetic neuropathy (DN) is a very common clinical condition throughout the world. The diagnostic tests currently recommended have low sensitivity, such as electromyography, or are invasive, such as skin biopsy. New techniques have been developed to identify the early involvement of the...

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Autores principales: Pupe, Camila, Dieckmann, Gabriela, Dornas, Ricardo, Nascimento, Osvaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academia Brasileira de Neurologia - ABNEURO 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9703889/
https://www.ncbi.nlm.nih.gov/pubmed/36252590
http://dx.doi.org/10.1055/s-0042-1755231
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author Pupe, Camila
Dieckmann, Gabriela
Dornas, Ricardo
Nascimento, Osvaldo
author_facet Pupe, Camila
Dieckmann, Gabriela
Dornas, Ricardo
Nascimento, Osvaldo
author_sort Pupe, Camila
collection PubMed
description BACKGROUND: Diabetic neuropathy (DN) is a very common clinical condition throughout the world. The diagnostic tests currently recommended have low sensitivity, such as electromyography, or are invasive, such as skin biopsy. New techniques have been developed to identify the early involvement of the peripheral nerve. With the advent of corneal confocal microscopy (CCM), a reduction in corneal innervation in patients with DN has been observed. OBJECTIVE: To compare, through CCM, diabetic patients with symptomatic distal symmetric polyneuropathy (DSP) and controls. METHODS: In the present study, through CCM, we compared the morphological changes in the sub-basal epithelial corneal plexus of 35 diabetic patients with symptomatic DSP with 55 controls. Moreover, we sought to determine a pattern of change regarding the severity stages of DSP, comparing the clinical, laboratory, and nerve-conduction (NC) variables. RESULTS: Differences between the control and diabetic groups were observed for the following variables, respectively: age (44.9 ± 13.24 years versus 57.02 ± 10.4 years; p< 0.001); fiber density (29.7 ± 10.2 versus 16.6 ± 10.2; p< 0.001); number of fibers (4.76 ± 1.30 versus 3.14 ± 1.63; p< 0.001); number of Langerhans cells (4.64 ± 8.05 versus 7.49 ± 10.3; p= 0.035); tortuosity (p< 0.05); and thickness (p< 0.05). Furthermore, inverse relationships were found regarding fiber density and age (p< 0.01) and fiber density and the severity of the disease (p< 0.05). A positive relationship between the conduction velocity of the fibular nerve and fiber density (p< 0.05) was also observed. CONCLUSION: Corneal confocal microscopy proved to be a fast, noninvasive and reproducible method for the diagnosis, staging, and monitoring of diabetic DSP.
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spelling pubmed-97038892022-12-08 Corneal confocal microscopy in patients with distal symmetric polyneuropathy compared to controls Pupe, Camila Dieckmann, Gabriela Dornas, Ricardo Nascimento, Osvaldo Arq Neuropsiquiatr Original Article BACKGROUND: Diabetic neuropathy (DN) is a very common clinical condition throughout the world. The diagnostic tests currently recommended have low sensitivity, such as electromyography, or are invasive, such as skin biopsy. New techniques have been developed to identify the early involvement of the peripheral nerve. With the advent of corneal confocal microscopy (CCM), a reduction in corneal innervation in patients with DN has been observed. OBJECTIVE: To compare, through CCM, diabetic patients with symptomatic distal symmetric polyneuropathy (DSP) and controls. METHODS: In the present study, through CCM, we compared the morphological changes in the sub-basal epithelial corneal plexus of 35 diabetic patients with symptomatic DSP with 55 controls. Moreover, we sought to determine a pattern of change regarding the severity stages of DSP, comparing the clinical, laboratory, and nerve-conduction (NC) variables. RESULTS: Differences between the control and diabetic groups were observed for the following variables, respectively: age (44.9 ± 13.24 years versus 57.02 ± 10.4 years; p< 0.001); fiber density (29.7 ± 10.2 versus 16.6 ± 10.2; p< 0.001); number of fibers (4.76 ± 1.30 versus 3.14 ± 1.63; p< 0.001); number of Langerhans cells (4.64 ± 8.05 versus 7.49 ± 10.3; p= 0.035); tortuosity (p< 0.05); and thickness (p< 0.05). Furthermore, inverse relationships were found regarding fiber density and age (p< 0.01) and fiber density and the severity of the disease (p< 0.05). A positive relationship between the conduction velocity of the fibular nerve and fiber density (p< 0.05) was also observed. CONCLUSION: Corneal confocal microscopy proved to be a fast, noninvasive and reproducible method for the diagnosis, staging, and monitoring of diabetic DSP. Academia Brasileira de Neurologia - ABNEURO 2022-11-21 /pmc/articles/PMC9703889/ /pubmed/36252590 http://dx.doi.org/10.1055/s-0042-1755231 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons AttributionNoncommercial No Derivative License, which permits unrestricted noncommercial use, distribution, and reproduction in any medium provided the original work is properly cited and the work is not changed in any way.
spellingShingle Original Article
Pupe, Camila
Dieckmann, Gabriela
Dornas, Ricardo
Nascimento, Osvaldo
Corneal confocal microscopy in patients with distal symmetric polyneuropathy compared to controls
title Corneal confocal microscopy in patients with distal symmetric polyneuropathy compared to controls
title_full Corneal confocal microscopy in patients with distal symmetric polyneuropathy compared to controls
title_fullStr Corneal confocal microscopy in patients with distal symmetric polyneuropathy compared to controls
title_full_unstemmed Corneal confocal microscopy in patients with distal symmetric polyneuropathy compared to controls
title_short Corneal confocal microscopy in patients with distal symmetric polyneuropathy compared to controls
title_sort corneal confocal microscopy in patients with distal symmetric polyneuropathy compared to controls
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9703889/
https://www.ncbi.nlm.nih.gov/pubmed/36252590
http://dx.doi.org/10.1055/s-0042-1755231
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