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Corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy

OBJECTIVE: There is an unmet need for better diagnostic tools to further delineate clinical subsets of heterogeneous chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) and multifocal motor neuropathy (MMN) to facilitate treatment decisions. Corneal confocal microscopy (CCM) is a noninv...

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Autores principales: Stettner, Mark, Hinrichs, Lena, Guthoff, Rainer, Bairov, Silja, Petropoulos, Ioannis N., Warnke, Clemens, Hartung, Hans‐Peter, Malik, Rayaz A., Kieseier, Bernd C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748316/
https://www.ncbi.nlm.nih.gov/pubmed/26900579
http://dx.doi.org/10.1002/acn3.275
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author Stettner, Mark
Hinrichs, Lena
Guthoff, Rainer
Bairov, Silja
Petropoulos, Ioannis N.
Warnke, Clemens
Hartung, Hans‐Peter
Malik, Rayaz A.
Kieseier, Bernd C.
author_facet Stettner, Mark
Hinrichs, Lena
Guthoff, Rainer
Bairov, Silja
Petropoulos, Ioannis N.
Warnke, Clemens
Hartung, Hans‐Peter
Malik, Rayaz A.
Kieseier, Bernd C.
author_sort Stettner, Mark
collection PubMed
description OBJECTIVE: There is an unmet need for better diagnostic tools to further delineate clinical subsets of heterogeneous chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) and multifocal motor neuropathy (MMN) to facilitate treatment decisions. Corneal confocal microscopy (CCM) is a noninvasive and reproducible nerve imaging technique. This study evaluates the potential of CCM as a diagnostic surrogate in CIDP and MMN. METHODS: In a cross‐sectional prospective approach, 182 patients and healthy controls were studied using CCM to quantify corneal nerve damage and immune cell infiltration. RESULTS: Patients with CIDP and MMN had a reduction in corneal nerve fiber (CNF) measures and an increase in corneal immune cell infiltrates. In CIDP, CNF parameters decreased with increasing duration of disease. The number of dendritic cells in proximity to CNFs was increased in patients with early disease and correlated with the degree of motor affection. A further reduction in CNF parameters and an increase in nondendritic cells were observed in patients with painful neuropathy. In CIDP patients with antineuronal antibodies the number of nondendritic cells was increased. INTERPRETATION: Our findings suggest that CNF loss may reflect severity of neuropathy and quantification of distinct cells around the CNF plexus may help in stratifying CIDP subtypes, clinical course, and disease activity. However, further longitudinal studies are required before CCM can be considered as a valid surrogate endpoint for patients with CIDP and MMN.
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spelling pubmed-47483162016-02-19 Corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy Stettner, Mark Hinrichs, Lena Guthoff, Rainer Bairov, Silja Petropoulos, Ioannis N. Warnke, Clemens Hartung, Hans‐Peter Malik, Rayaz A. Kieseier, Bernd C. Ann Clin Transl Neurol Research Articles OBJECTIVE: There is an unmet need for better diagnostic tools to further delineate clinical subsets of heterogeneous chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) and multifocal motor neuropathy (MMN) to facilitate treatment decisions. Corneal confocal microscopy (CCM) is a noninvasive and reproducible nerve imaging technique. This study evaluates the potential of CCM as a diagnostic surrogate in CIDP and MMN. METHODS: In a cross‐sectional prospective approach, 182 patients and healthy controls were studied using CCM to quantify corneal nerve damage and immune cell infiltration. RESULTS: Patients with CIDP and MMN had a reduction in corneal nerve fiber (CNF) measures and an increase in corneal immune cell infiltrates. In CIDP, CNF parameters decreased with increasing duration of disease. The number of dendritic cells in proximity to CNFs was increased in patients with early disease and correlated with the degree of motor affection. A further reduction in CNF parameters and an increase in nondendritic cells were observed in patients with painful neuropathy. In CIDP patients with antineuronal antibodies the number of nondendritic cells was increased. INTERPRETATION: Our findings suggest that CNF loss may reflect severity of neuropathy and quantification of distinct cells around the CNF plexus may help in stratifying CIDP subtypes, clinical course, and disease activity. However, further longitudinal studies are required before CCM can be considered as a valid surrogate endpoint for patients with CIDP and MMN. John Wiley and Sons Inc. 2015-12-28 /pmc/articles/PMC4748316/ /pubmed/26900579 http://dx.doi.org/10.1002/acn3.275 Text en © 2015 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 Creative Commons Attribution‐NonCommercial‐NoDerivs (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 Research Articles
Stettner, Mark
Hinrichs, Lena
Guthoff, Rainer
Bairov, Silja
Petropoulos, Ioannis N.
Warnke, Clemens
Hartung, Hans‐Peter
Malik, Rayaz A.
Kieseier, Bernd C.
Corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy
title Corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy
title_full Corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy
title_fullStr Corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy
title_full_unstemmed Corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy
title_short Corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy
title_sort corneal confocal microscopy in chronic inflammatory demyelinating polyneuropathy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748316/
https://www.ncbi.nlm.nih.gov/pubmed/26900579
http://dx.doi.org/10.1002/acn3.275
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