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Differential myelinated and unmyelinated sensory and autonomic skin nerve fiber involvement in patients with ophthalmic postherpetic neuralgia

Postherpetic neuralgia (PHN) is a common and exceptionally drug-resistant neuropathic pain condition. In this cross-sectional skin biopsy study, seeking information on the responsible pathophysiological mechanisms we assessed how ophthalmic PHN affects sensory and autonomic skin innervation. We took...

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Autores principales: Truini, Andrea, Haanpaa, Maija, Provitera, Vincenzo, Biasiotta, Antonella, Stancanelli, Annamaria, Caporaso, Giuseppe, Santoro, Lucio, Cruccu, Giorgio, Nolano, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4523825/
https://www.ncbi.nlm.nih.gov/pubmed/26300742
http://dx.doi.org/10.3389/fnana.2015.00105
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author Truini, Andrea
Haanpaa, Maija
Provitera, Vincenzo
Biasiotta, Antonella
Stancanelli, Annamaria
Caporaso, Giuseppe
Santoro, Lucio
Cruccu, Giorgio
Nolano, Maria
author_facet Truini, Andrea
Haanpaa, Maija
Provitera, Vincenzo
Biasiotta, Antonella
Stancanelli, Annamaria
Caporaso, Giuseppe
Santoro, Lucio
Cruccu, Giorgio
Nolano, Maria
author_sort Truini, Andrea
collection PubMed
description Postherpetic neuralgia (PHN) is a common and exceptionally drug-resistant neuropathic pain condition. In this cross-sectional skin biopsy study, seeking information on the responsible pathophysiological mechanisms we assessed how ophthalmic PHN affects sensory and autonomic skin innervation. We took 2-mm supraorbital punch skin biopsies from the affected and unaffected sides in 10 patients with ophthalmic PHN. Using indirect immunofluorescence and a large panel of antibodies including protein gene product (PGP) 9.5 we quantified epidermal unmyelinated, dermal myelinated and autonomic nerve fibers. Although skin biopsy showed reduced epidermal and dermal myelinated fiber density in specimens from the affected side, the epidermal/dermal myelinated nerve fiber ratio was lower in the affected than in the unaffected side (p < 0.001), thus suggesting a predominant epidermal unmyelinated nerve fiber loss. Conversely, autonomic skin innervation was spared. Our study showing that ophthalmic PHN predominantly affects unmyelinated nerve fiber and spares autonomic nerve fiber might help to understand the pathophysiological mechanisms underlying this difficult-to-treat condition.
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spelling pubmed-45238252015-08-21 Differential myelinated and unmyelinated sensory and autonomic skin nerve fiber involvement in patients with ophthalmic postherpetic neuralgia Truini, Andrea Haanpaa, Maija Provitera, Vincenzo Biasiotta, Antonella Stancanelli, Annamaria Caporaso, Giuseppe Santoro, Lucio Cruccu, Giorgio Nolano, Maria Front Neuroanat Neuroscience Postherpetic neuralgia (PHN) is a common and exceptionally drug-resistant neuropathic pain condition. In this cross-sectional skin biopsy study, seeking information on the responsible pathophysiological mechanisms we assessed how ophthalmic PHN affects sensory and autonomic skin innervation. We took 2-mm supraorbital punch skin biopsies from the affected and unaffected sides in 10 patients with ophthalmic PHN. Using indirect immunofluorescence and a large panel of antibodies including protein gene product (PGP) 9.5 we quantified epidermal unmyelinated, dermal myelinated and autonomic nerve fibers. Although skin biopsy showed reduced epidermal and dermal myelinated fiber density in specimens from the affected side, the epidermal/dermal myelinated nerve fiber ratio was lower in the affected than in the unaffected side (p < 0.001), thus suggesting a predominant epidermal unmyelinated nerve fiber loss. Conversely, autonomic skin innervation was spared. Our study showing that ophthalmic PHN predominantly affects unmyelinated nerve fiber and spares autonomic nerve fiber might help to understand the pathophysiological mechanisms underlying this difficult-to-treat condition. Frontiers Media S.A. 2015-08-04 /pmc/articles/PMC4523825/ /pubmed/26300742 http://dx.doi.org/10.3389/fnana.2015.00105 Text en Copyright © 2015 Truini, Haanpaa, Provitera, Biasiotta, Stancanelli, Caporaso, Santoro, Cruccu and Nolano. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Truini, Andrea
Haanpaa, Maija
Provitera, Vincenzo
Biasiotta, Antonella
Stancanelli, Annamaria
Caporaso, Giuseppe
Santoro, Lucio
Cruccu, Giorgio
Nolano, Maria
Differential myelinated and unmyelinated sensory and autonomic skin nerve fiber involvement in patients with ophthalmic postherpetic neuralgia
title Differential myelinated and unmyelinated sensory and autonomic skin nerve fiber involvement in patients with ophthalmic postherpetic neuralgia
title_full Differential myelinated and unmyelinated sensory and autonomic skin nerve fiber involvement in patients with ophthalmic postherpetic neuralgia
title_fullStr Differential myelinated and unmyelinated sensory and autonomic skin nerve fiber involvement in patients with ophthalmic postherpetic neuralgia
title_full_unstemmed Differential myelinated and unmyelinated sensory and autonomic skin nerve fiber involvement in patients with ophthalmic postherpetic neuralgia
title_short Differential myelinated and unmyelinated sensory and autonomic skin nerve fiber involvement in patients with ophthalmic postherpetic neuralgia
title_sort differential myelinated and unmyelinated sensory and autonomic skin nerve fiber involvement in patients with ophthalmic postherpetic neuralgia
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4523825/
https://www.ncbi.nlm.nih.gov/pubmed/26300742
http://dx.doi.org/10.3389/fnana.2015.00105
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