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Current concepts in the management of diabetic polyneuropathy
Diabetic sensorimotor polyneuropathy (DSPN) is encountered in approximately one‐third of people with diabetes. This, in turn, might markedly impoverish their quality of life, mainly owing to neuropathic pain and foot ulcerations. Painful DSPN might be as frequent as 25% in diabetes patients. Symptom...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015839/ https://www.ncbi.nlm.nih.gov/pubmed/32918837 http://dx.doi.org/10.1111/jdi.13401 |
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author | Ziegler, Dan Papanas, Nikolaos Schnell, Oliver Nguyen, Bich Dao Thi Nguyen, Khue Thy Kulkantrakorn, Kongkiat Deerochanawong, Chaicharn |
author_facet | Ziegler, Dan Papanas, Nikolaos Schnell, Oliver Nguyen, Bich Dao Thi Nguyen, Khue Thy Kulkantrakorn, Kongkiat Deerochanawong, Chaicharn |
author_sort | Ziegler, Dan |
collection | PubMed |
description | Diabetic sensorimotor polyneuropathy (DSPN) is encountered in approximately one‐third of people with diabetes. This, in turn, might markedly impoverish their quality of life, mainly owing to neuropathic pain and foot ulcerations. Painful DSPN might be as frequent as 25% in diabetes patients. Symptoms as a result of DSPN typically comprise pain, paresthesia and numbness in the distal lower limbs. Asymptomatic DSPN might reach 50% among patients with this condition. Unfortunately, DSPN is still not adequately diagnosed and treated. Its management has three priorities: (i) lifestyle improvement, near‐normoglycemia and multifactorial cardiovascular risk intervention; (ii) pathogenesis‐oriented pharmacotherapy; and (iii) symptomatic alleviation of pain. Intensive diabetes therapy showed evidence for favorable effects on the incidence and deterioration of DSPN in type 1 diabetes, but not type 2 diabetes. Among pathogenesis‐oriented treatments, α‐lipoic acid, actovegin, benfotiamine and epalrestat are currently authorized to treat DSPN in several countries. Symptomatic therapy uses analgesics, notably antidepressants, opioids and anticonvulsants, reducing pain by ≥50% in approximately 50% of individuals, but might be limited, particularly by central nervous system‐related adverse events. Local treatment with the capsaicin 8% patch might offer an alternative. In addition to pain relief, therapy should improve sleep, mobility and quality of life. In conclusion, multimodal treatment of DSPN should consider the individual risk profile, pathogenetic treatment and pain management using pharmacotherapy (combinations, if required), as well as non‐pharmacological options. |
format | Online Article Text |
id | pubmed-8015839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80158392021-04-02 Current concepts in the management of diabetic polyneuropathy Ziegler, Dan Papanas, Nikolaos Schnell, Oliver Nguyen, Bich Dao Thi Nguyen, Khue Thy Kulkantrakorn, Kongkiat Deerochanawong, Chaicharn J Diabetes Investig Review Article Diabetic sensorimotor polyneuropathy (DSPN) is encountered in approximately one‐third of people with diabetes. This, in turn, might markedly impoverish their quality of life, mainly owing to neuropathic pain and foot ulcerations. Painful DSPN might be as frequent as 25% in diabetes patients. Symptoms as a result of DSPN typically comprise pain, paresthesia and numbness in the distal lower limbs. Asymptomatic DSPN might reach 50% among patients with this condition. Unfortunately, DSPN is still not adequately diagnosed and treated. Its management has three priorities: (i) lifestyle improvement, near‐normoglycemia and multifactorial cardiovascular risk intervention; (ii) pathogenesis‐oriented pharmacotherapy; and (iii) symptomatic alleviation of pain. Intensive diabetes therapy showed evidence for favorable effects on the incidence and deterioration of DSPN in type 1 diabetes, but not type 2 diabetes. Among pathogenesis‐oriented treatments, α‐lipoic acid, actovegin, benfotiamine and epalrestat are currently authorized to treat DSPN in several countries. Symptomatic therapy uses analgesics, notably antidepressants, opioids and anticonvulsants, reducing pain by ≥50% in approximately 50% of individuals, but might be limited, particularly by central nervous system‐related adverse events. Local treatment with the capsaicin 8% patch might offer an alternative. In addition to pain relief, therapy should improve sleep, mobility and quality of life. In conclusion, multimodal treatment of DSPN should consider the individual risk profile, pathogenetic treatment and pain management using pharmacotherapy (combinations, if required), as well as non‐pharmacological options. John Wiley and Sons Inc. 2020-10-11 2021-04 /pmc/articles/PMC8015839/ /pubmed/32918837 http://dx.doi.org/10.1111/jdi.13401 Text en © 2020 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Review Article Ziegler, Dan Papanas, Nikolaos Schnell, Oliver Nguyen, Bich Dao Thi Nguyen, Khue Thy Kulkantrakorn, Kongkiat Deerochanawong, Chaicharn Current concepts in the management of diabetic polyneuropathy |
title | Current concepts in the management of diabetic polyneuropathy |
title_full | Current concepts in the management of diabetic polyneuropathy |
title_fullStr | Current concepts in the management of diabetic polyneuropathy |
title_full_unstemmed | Current concepts in the management of diabetic polyneuropathy |
title_short | Current concepts in the management of diabetic polyneuropathy |
title_sort | current concepts in the management of diabetic polyneuropathy |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015839/ https://www.ncbi.nlm.nih.gov/pubmed/32918837 http://dx.doi.org/10.1111/jdi.13401 |
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