The natural history of diabetic peripheral neuropathy determined by a 12 year prospective study using vibration perception thresholds
The development and long term progression of diabetic peripheral neuropathy was studied using vibration perception threshold (VPT) as a validated measure. Three hundred and ninety-two patients had a normal age corrected VPT (12.1±3.7 volts) at baseline, with an age corrected logarithmic VPTscore <...
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Published in: | Journal of clinical neuroscience Vol. 8; no. 6; pp. 520 - 524 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier Ltd
01-11-2001
Elsevier |
Subjects: | |
Online Access: | Get full text |
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Summary: | The development and long term progression of diabetic peripheral neuropathy was studied using vibration perception threshold (VPT) as a validated measure. Three hundred and ninety-two patients had a normal age corrected VPT (12.1±3.7 volts) at baseline, with an age corrected logarithmic VPTscore <12. 19.9% developed an abnormal VPT over a 12 year period, increasing from 14.2±3.7 volts (VPTscore 10.4±0.6) at baseline to 35.9±9.5 volts (VPTscore 12.6±0.45) at follow up (P = 0.0001), and from 10.1±3.7volts (VPTscore 9.4±0.8) to 14.2±4.7 (VPTscore 9.8±0.8) in the rest. Over 80% thus retained a ‘normal’ VPT after a mean diabetes duration of 16 years despite only average glycaemic control, suggesting that non-ideal long term glycaemic control leads to neuropathy in a subset of predisposed patients. VPT was correlated in 123 diabetic patients with definitive criteria for neuropathy and a range of quantitative sensory and autonomic tests. 62/63 patients with abnormal VPT fulfilled neuropathy criteria; of patients with normal VPT who fulfilled neuropathy criteria, all had at least one abnormal thermal threshold test result. We conclude that a combination of log-transformed VPT values (VPTscore >10.1) and thermal thresholds can identify diabetic patients at risk of developing peripheral neuropathy and select patients likely to benefit from prophylaxis in clinical trials. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0967-5868 1532-2653 |
DOI: | 10.1054/jocn.2001.0893 |