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Prediction of protective sensory loss, neuropathy and foot ulceration in type 2 diabetes

OBJECTIVES: To prospectively determine clinical and biochemical characteristics associated with the development of peripheral neuropathy, loss of protective sensation, and foot ulceration in persons with type 2 diabetes mellitus (DM) over 7 years. RESEARCH DESIGN AND METHODS: Graded monofilament (MF...

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Autores principales: Paisey, R B, Darby, T, George, A M, Waterson, M, Hewson, P, Paisey, C F, Thomson, M P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873950/
https://www.ncbi.nlm.nih.gov/pubmed/27239314
http://dx.doi.org/10.1136/bmjdrc-2015-000163
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author Paisey, R B
Darby, T
George, A M
Waterson, M
Hewson, P
Paisey, C F
Thomson, M P
author_facet Paisey, R B
Darby, T
George, A M
Waterson, M
Hewson, P
Paisey, C F
Thomson, M P
author_sort Paisey, R B
collection PubMed
description OBJECTIVES: To prospectively determine clinical and biochemical characteristics associated with the development of peripheral neuropathy, loss of protective sensation, and foot ulceration in persons with type 2 diabetes mellitus (DM) over 7 years. RESEARCH DESIGN AND METHODS: Graded monofilament (MF) testing, vibration perception threshold, and neuropathy symptom questionnaires were undertaken in 206 participants with type 2 DM without peripheral vascular disease or history of foot ulceration and 71 healthy participants without DM at baseline and after 7 years. 6 monthly glycosylated hemoglobin (HbA1c) levels and annual serum lipid profiles were measured during follow-up of those with DM. Incident foot ulceration was recorded at follow-up. RESULTS: Taller stature and higher quartiles of serum triglyceride and HbA1c levels were associated with neuropathy at follow-up (p=0.008). Remission of baseline neuropathy was observed in 7 participants at follow-up. 9 participants with type 2 DM developed foot ulcers by the end of the study, only 1 at low risk. Mean HbA1c levels were higher in those who developed foot ulceration (p<0.0001). 1 participant with neuropathy throughout developed a Charcot foot. Failure to perceive 2 or more 2, 4 and 6 g MF stimuli at baseline predicted loss of protective sensation at follow-up. CONCLUSIONS: Tall stature and worse metabolic control were associated with progression to neuropathy. Mean HbA1c levels were higher in those who developed foot ulcers. Graded MF testing may enrich recruitment to clinical trials and assignation of high risk for foot ulceration.
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spelling pubmed-48739502016-05-27 Prediction of protective sensory loss, neuropathy and foot ulceration in type 2 diabetes Paisey, R B Darby, T George, A M Waterson, M Hewson, P Paisey, C F Thomson, M P BMJ Open Diabetes Res Care Pathophysiology/Complications OBJECTIVES: To prospectively determine clinical and biochemical characteristics associated with the development of peripheral neuropathy, loss of protective sensation, and foot ulceration in persons with type 2 diabetes mellitus (DM) over 7 years. RESEARCH DESIGN AND METHODS: Graded monofilament (MF) testing, vibration perception threshold, and neuropathy symptom questionnaires were undertaken in 206 participants with type 2 DM without peripheral vascular disease or history of foot ulceration and 71 healthy participants without DM at baseline and after 7 years. 6 monthly glycosylated hemoglobin (HbA1c) levels and annual serum lipid profiles were measured during follow-up of those with DM. Incident foot ulceration was recorded at follow-up. RESULTS: Taller stature and higher quartiles of serum triglyceride and HbA1c levels were associated with neuropathy at follow-up (p=0.008). Remission of baseline neuropathy was observed in 7 participants at follow-up. 9 participants with type 2 DM developed foot ulcers by the end of the study, only 1 at low risk. Mean HbA1c levels were higher in those who developed foot ulceration (p<0.0001). 1 participant with neuropathy throughout developed a Charcot foot. Failure to perceive 2 or more 2, 4 and 6 g MF stimuli at baseline predicted loss of protective sensation at follow-up. CONCLUSIONS: Tall stature and worse metabolic control were associated with progression to neuropathy. Mean HbA1c levels were higher in those who developed foot ulcers. Graded MF testing may enrich recruitment to clinical trials and assignation of high risk for foot ulceration. BMJ Publishing Group 2016-05-05 /pmc/articles/PMC4873950/ /pubmed/27239314 http://dx.doi.org/10.1136/bmjdrc-2015-000163 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
Paisey, R B
Darby, T
George, A M
Waterson, M
Hewson, P
Paisey, C F
Thomson, M P
Prediction of protective sensory loss, neuropathy and foot ulceration in type 2 diabetes
title Prediction of protective sensory loss, neuropathy and foot ulceration in type 2 diabetes
title_full Prediction of protective sensory loss, neuropathy and foot ulceration in type 2 diabetes
title_fullStr Prediction of protective sensory loss, neuropathy and foot ulceration in type 2 diabetes
title_full_unstemmed Prediction of protective sensory loss, neuropathy and foot ulceration in type 2 diabetes
title_short Prediction of protective sensory loss, neuropathy and foot ulceration in type 2 diabetes
title_sort prediction of protective sensory loss, neuropathy and foot ulceration in type 2 diabetes
topic Pathophysiology/Complications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4873950/
https://www.ncbi.nlm.nih.gov/pubmed/27239314
http://dx.doi.org/10.1136/bmjdrc-2015-000163
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