Towards prevention of diabetic peripheral neuropathy: clinical presentation, pathogenesis, and new treatments
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| Názov: | Towards prevention of diabetic peripheral neuropathy: clinical presentation, pathogenesis, and new treatments |
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| Autori: | Melissa A Elafros, Henning Andersen, David L Bennett, Masha G Savelieff, Vijay Viswanathan, Brian C Callaghan, Eva L Feldman |
| Zdroj: | Elafros, M A, Andersen, H, Bennett, D L, Savelieff, M G, Viswanathan, V, Callaghan, B C & Feldman, E L 2022, 'Towards prevention of diabetic peripheral neuropathy : clinical presentation, pathogenesis, and new treatments', The Lancet Neurology, vol. 21, no. 10, pp. 922-936. https://doi.org/10.1016/S1474-4422(22)00188-0 |
| Informácie o vydavateľovi: | Elsevier BV, 2022. |
| Rok vydania: | 2022 |
| Predmety: | Metabolic Syndrome, 03 medical and health sciences, 0302 clinical medicine, Diabetes Mellitus, Type 2, Diabetic Neuropathies, Diabetic Neuropathies/diagnosis, Diabetes Mellitus, Type 2/complications, Quality of Life, Humans, Pain, Pain/etiology, Metabolic Syndrome/complications, 3. Good health |
| Popis: | Diabetic peripheral neuropathy (DPN) occurs in up to half of individuals with type 1 or type 2 diabetes. DPN results from the distal-to-proximal loss of peripheral nerve function, leading to physical disability and sometimes pain, with the consequent lowering of quality of life. Early diagnosis improves clinical outcomes, but many patients still develop neuropathy. Hyperglycaemia is a risk factor and glycaemic control prevents DPN development in type 1 diabetes. However, glycaemic control has modest or no benefit in individuals with type 2 diabetes, probably because they usually have comorbidities. Among them, the metabolic syndrome is a major risk factor for DPN. The pathophysiology of DPN is complex, but mechanisms converge on a unifying theme of bioenergetic failure in the peripheral nerves due to their unique anatomy. Current clinical management focuses on controlling diabetes, the metabolic syndrome, and pain, but remains suboptimal for most patients. Thus, research is ongoing to improve early diagnosis and prognosis, to identify molecular mechanisms that could lead to therapeutic targets, and to investigate lifestyle interventions to improve clinical outcomes. |
| Druh dokumentu: | Article |
| Jazyk: | English |
| ISSN: | 1474-4422 |
| DOI: | 10.1016/s1474-4422(22)00188-0 |
| Prístupová URL adresa: | https://pubmed.ncbi.nlm.nih.gov/36115364 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10112836/pdf/nihms-1884395.pdf http://www.scopus.com/inward/record.url?scp=85138043741&partnerID=8YFLogxK https://doi.org/10.1016/S1474-4422(22)00188-0 https://pure.au.dk/portal/en/publications/0002fac9-88ff-4965-96fd-621459688a18 |
| Rights: | Elsevier TDM |
| Prístupové číslo: | edsair.doi.dedup.....d40bd5d9dbcaf2d71435827d17c60fb9 |
| Databáza: | OpenAIRE |
| Abstrakt: | Diabetic peripheral neuropathy (DPN) occurs in up to half of individuals with type 1 or type 2 diabetes. DPN results from the distal-to-proximal loss of peripheral nerve function, leading to physical disability and sometimes pain, with the consequent lowering of quality of life. Early diagnosis improves clinical outcomes, but many patients still develop neuropathy. Hyperglycaemia is a risk factor and glycaemic control prevents DPN development in type 1 diabetes. However, glycaemic control has modest or no benefit in individuals with type 2 diabetes, probably because they usually have comorbidities. Among them, the metabolic syndrome is a major risk factor for DPN. The pathophysiology of DPN is complex, but mechanisms converge on a unifying theme of bioenergetic failure in the peripheral nerves due to their unique anatomy. Current clinical management focuses on controlling diabetes, the metabolic syndrome, and pain, but remains suboptimal for most patients. Thus, research is ongoing to improve early diagnosis and prognosis, to identify molecular mechanisms that could lead to therapeutic targets, and to investigate lifestyle interventions to improve clinical outcomes. |
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| ISSN: | 14744422 |
| DOI: | 10.1016/s1474-4422(22)00188-0 |
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