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Using in vivo corneal confocal microscopy to identify diabetic sensorimotor polyneuropathy risk profiles in patients with type 1 diabetes

OBJECTIVE: Diabetic sensorimotor peripheral neuropathy (DSP) is the most prevalent complication in diabetes mellitus. Identifying DSP risk is essential for intervening early in the natural history of the disease. Small nerve fibers are affected earliest in the disease progression and evidence of thi...

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Autores principales: Lewis, Evan J H, Perkins, Bruce A, Lovblom, Lief E, Bazinet, Richard P, Wolever, Thomas M S, Bril, Vera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316911/
https://www.ncbi.nlm.nih.gov/pubmed/28243447
http://dx.doi.org/10.1136/bmjdrc-2016-000251
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author Lewis, Evan J H
Perkins, Bruce A
Lovblom, Lief E
Bazinet, Richard P
Wolever, Thomas M S
Bril, Vera
author_facet Lewis, Evan J H
Perkins, Bruce A
Lovblom, Lief E
Bazinet, Richard P
Wolever, Thomas M S
Bril, Vera
author_sort Lewis, Evan J H
collection PubMed
description OBJECTIVE: Diabetic sensorimotor peripheral neuropathy (DSP) is the most prevalent complication in diabetes mellitus. Identifying DSP risk is essential for intervening early in the natural history of the disease. Small nerve fibers are affected earliest in the disease progression and evidence of this damage can be identified using in vivo corneal confocal microscopy (IVCCM). RESEARCH DESIGN AND METHODS: We applied IVCCM to a cohort of 40 patients with type 1 diabetes to identify their DSP risk profile. We measured standard IVCCM parameters including corneal nerve fiber length (CNFL), and performed nerve conduction studies and quantitative sensory testing. RESULTS: 40 patients (53% female), with a mean age of 48±14, BMI 28.1±5.8, and diabetes duration of 27±18 years were enrolled between March 2014 and June 2015. Mean IVCCM CNFL was 12.0±5.2 mm/mm(2) (normal ≥15 mm/mm(2)). Ten patients (26%) without DSP were identified as being at risk of future DSP with mean CNFL 11.0±2.1 mm/mm(2). Six patients (15%) were at low risk of future DSP with mean CNFL 19.0±4.6 mm/mm(2), while 23 (59%) had established DSP with mean CNFL 10.5±4.5 mm/mm(2). CONCLUSIONS: IVCCM can be used successfully to identify the risk profile for DSP in patients with type 1 diabetes. This methodology may prove useful to classify patients for DSP intervention clinical trials.
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spelling pubmed-53169112017-02-27 Using in vivo corneal confocal microscopy to identify diabetic sensorimotor polyneuropathy risk profiles in patients with type 1 diabetes Lewis, Evan J H Perkins, Bruce A Lovblom, Lief E Bazinet, Richard P Wolever, Thomas M S Bril, Vera BMJ Open Diabetes Res Care Pathophysiology/Complications OBJECTIVE: Diabetic sensorimotor peripheral neuropathy (DSP) is the most prevalent complication in diabetes mellitus. Identifying DSP risk is essential for intervening early in the natural history of the disease. Small nerve fibers are affected earliest in the disease progression and evidence of this damage can be identified using in vivo corneal confocal microscopy (IVCCM). RESEARCH DESIGN AND METHODS: We applied IVCCM to a cohort of 40 patients with type 1 diabetes to identify their DSP risk profile. We measured standard IVCCM parameters including corneal nerve fiber length (CNFL), and performed nerve conduction studies and quantitative sensory testing. RESULTS: 40 patients (53% female), with a mean age of 48±14, BMI 28.1±5.8, and diabetes duration of 27±18 years were enrolled between March 2014 and June 2015. Mean IVCCM CNFL was 12.0±5.2 mm/mm(2) (normal ≥15 mm/mm(2)). Ten patients (26%) without DSP were identified as being at risk of future DSP with mean CNFL 11.0±2.1 mm/mm(2). Six patients (15%) were at low risk of future DSP with mean CNFL 19.0±4.6 mm/mm(2), while 23 (59%) had established DSP with mean CNFL 10.5±4.5 mm/mm(2). CONCLUSIONS: IVCCM can be used successfully to identify the risk profile for DSP in patients with type 1 diabetes. This methodology may prove useful to classify patients for DSP intervention clinical trials. BMJ Publishing Group 2017-02-16 /pmc/articles/PMC5316911/ /pubmed/28243447 http://dx.doi.org/10.1136/bmjdrc-2016-000251 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Pathophysiology/Complications
Lewis, Evan J H
Perkins, Bruce A
Lovblom, Lief E
Bazinet, Richard P
Wolever, Thomas M S
Bril, Vera
Using in vivo corneal confocal microscopy to identify diabetic sensorimotor polyneuropathy risk profiles in patients with type 1 diabetes
title Using in vivo corneal confocal microscopy to identify diabetic sensorimotor polyneuropathy risk profiles in patients with type 1 diabetes
title_full Using in vivo corneal confocal microscopy to identify diabetic sensorimotor polyneuropathy risk profiles in patients with type 1 diabetes
title_fullStr Using in vivo corneal confocal microscopy to identify diabetic sensorimotor polyneuropathy risk profiles in patients with type 1 diabetes
title_full_unstemmed Using in vivo corneal confocal microscopy to identify diabetic sensorimotor polyneuropathy risk profiles in patients with type 1 diabetes
title_short Using in vivo corneal confocal microscopy to identify diabetic sensorimotor polyneuropathy risk profiles in patients with type 1 diabetes
title_sort using in vivo corneal confocal microscopy to identify diabetic sensorimotor polyneuropathy risk profiles in patients with type 1 diabetes
topic Pathophysiology/Complications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316911/
https://www.ncbi.nlm.nih.gov/pubmed/28243447
http://dx.doi.org/10.1136/bmjdrc-2016-000251
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