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Median neuropathy at the wrist as an early manifestation of diabetic neuropathy
AIMS/INTRODUCTION: To elucidate the clinical significance of median neuropathy at the wrist (MN) in patients with diabetes. MATERIALS AND METHODS: In total, 340 patients with diabetes who were hospitalized for glycemic control were enrolled in the present study. The diagnoses of MN and diabetic poly...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234235/ https://www.ncbi.nlm.nih.gov/pubmed/25422772 http://dx.doi.org/10.1111/jdi.12211 |
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author | Horinouchi, Shuji Deguchi, Takahisa Arimura, Kimiyoshi Arimura, Aiko Dochi, Yukari Uto, Tadashi Nakamura, Tomonori Arimura, Yumiko Nishio, Yoshihiko Takashima, Hiroshi |
author_facet | Horinouchi, Shuji Deguchi, Takahisa Arimura, Kimiyoshi Arimura, Aiko Dochi, Yukari Uto, Tadashi Nakamura, Tomonori Arimura, Yumiko Nishio, Yoshihiko Takashima, Hiroshi |
author_sort | Horinouchi, Shuji |
collection | PubMed |
description | AIMS/INTRODUCTION: To elucidate the clinical significance of median neuropathy at the wrist (MN) in patients with diabetes. MATERIALS AND METHODS: In total, 340 patients with diabetes who were hospitalized for glycemic control were enrolled in the present study. The diagnoses of MN and diabetic polyneuropathy (DPN) were based on electrophysiological criteria. A total of 187 patients were divided into four subgroups: patients without MN or DPN; patients with MN without DPN; patients with MN and DPN; and patients with DPN without MN. Intergroup comparisons of clinical characteristics and results of nerve conduction studies were carried out. RESULTS: A total of 71 patients had neither MN nor DPN; 25 had MN, but no DPN; 55 had MN and DPN; and 36 had DPN, but no MN. In comparison with the MN and DPN group, the MN without DPN group included more patients in the early phase of diabetes (diagnosed within the past 5 years) and fewer patients with diabetic microangiopathy. Comparative median nerve conduction studies showed significantly lower motor and sensory nerve conduction velocities, longer F-wave latencies, and smaller sensory nerve action potentials in patients with MN and DPN than in those without DPN. CONCLUSIONS: MN in patients with diabetes could be attributed to an impairment in axonal function at common entrapment sites, and could be used to identify an early manifestation of diabetic neuropathy. |
format | Online Article Text |
id | pubmed-4234235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42342352014-11-24 Median neuropathy at the wrist as an early manifestation of diabetic neuropathy Horinouchi, Shuji Deguchi, Takahisa Arimura, Kimiyoshi Arimura, Aiko Dochi, Yukari Uto, Tadashi Nakamura, Tomonori Arimura, Yumiko Nishio, Yoshihiko Takashima, Hiroshi J Diabetes Investig Articles AIMS/INTRODUCTION: To elucidate the clinical significance of median neuropathy at the wrist (MN) in patients with diabetes. MATERIALS AND METHODS: In total, 340 patients with diabetes who were hospitalized for glycemic control were enrolled in the present study. The diagnoses of MN and diabetic polyneuropathy (DPN) were based on electrophysiological criteria. A total of 187 patients were divided into four subgroups: patients without MN or DPN; patients with MN without DPN; patients with MN and DPN; and patients with DPN without MN. Intergroup comparisons of clinical characteristics and results of nerve conduction studies were carried out. RESULTS: A total of 71 patients had neither MN nor DPN; 25 had MN, but no DPN; 55 had MN and DPN; and 36 had DPN, but no MN. In comparison with the MN and DPN group, the MN without DPN group included more patients in the early phase of diabetes (diagnosed within the past 5 years) and fewer patients with diabetic microangiopathy. Comparative median nerve conduction studies showed significantly lower motor and sensory nerve conduction velocities, longer F-wave latencies, and smaller sensory nerve action potentials in patients with MN and DPN than in those without DPN. CONCLUSIONS: MN in patients with diabetes could be attributed to an impairment in axonal function at common entrapment sites, and could be used to identify an early manifestation of diabetic neuropathy. BlackWell Publishing Ltd 2014-11 2014-03-28 /pmc/articles/PMC4234235/ /pubmed/25422772 http://dx.doi.org/10.1111/jdi.12211 Text en © 2014 The Authors. Journal of Diabetes Investigation published by Asian Association of the Study of Diabetes (AASD) and Wiley Publishing Asia Pty Ltd http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 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 | Articles Horinouchi, Shuji Deguchi, Takahisa Arimura, Kimiyoshi Arimura, Aiko Dochi, Yukari Uto, Tadashi Nakamura, Tomonori Arimura, Yumiko Nishio, Yoshihiko Takashima, Hiroshi Median neuropathy at the wrist as an early manifestation of diabetic neuropathy |
title | Median neuropathy at the wrist as an early manifestation of diabetic neuropathy |
title_full | Median neuropathy at the wrist as an early manifestation of diabetic neuropathy |
title_fullStr | Median neuropathy at the wrist as an early manifestation of diabetic neuropathy |
title_full_unstemmed | Median neuropathy at the wrist as an early manifestation of diabetic neuropathy |
title_short | Median neuropathy at the wrist as an early manifestation of diabetic neuropathy |
title_sort | median neuropathy at the wrist as an early manifestation of diabetic neuropathy |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4234235/ https://www.ncbi.nlm.nih.gov/pubmed/25422772 http://dx.doi.org/10.1111/jdi.12211 |
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