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Clinical neuropathy scales in neuropathy associated with impaired glucose tolerance

Authors :
Sujal Singh
Sandra K. Ruby
Lindsay A. Zilliox
Min Zhan
James W. Russell
Source :
Journal of Diabetes and its Complications. 29:372-377
Publication Year :
2015
Publisher :
Elsevier BV, 2015.

Abstract

Disagreement exists on effective and sensitive outcome measures in neuropathy associated with impaired glucose tolerance (IGT). Nerve conduction studies and skin biopsies are costly, invasive and may have their problems with reproducibility and clinical applicability. A clinical measure of neuropathy that has sufficient sensitivity and correlates to invasive measures would enable significant future research.Data was collected prospectively on patients with IGT and symptomatic early neuropathy (neuropathy symptoms2years) and normal controls. The seven scales that were examined were the Neuropathy Impairment Score of the Lower Limb (NIS-LL), Michigan Diabetic Neuropathy Score (MNDS), modified Toronto Clinical Neuropathy Scale (mTCNS), Total Neuropathy Score (Clinical) (TNSc), The Utah Early Neuropathy Scale (UENS), the Early Neuropathy Score (ENS), and the Neuropathy Disability Score (NDS).All seven clinical scales were determined to be excellent in discriminating between patients with neuropathy from controls without neuropathy. The strongest discrimination was seen with the mTCNS. The best sensitivity and specificity for the range of scores obtained, as determined by using receiver operating characteristic curves, was seen for the mTCNS followed by the TNSc. Most scales show a stronger correlation with measures of large rather than small fiber neuropathy.All seven scales identify patients with neuropathy. For the purpose of screening potential patients for a clinical study, the mTCNS followed by the TNSc would be most helpful to select patients with neuropathy.

Details

ISSN :
10568727
Volume :
29
Database :
OpenAIRE
Journal :
Journal of Diabetes and its Complications
Accession number :
edsair.doi.dedup.....4c118f0bbfa516f6051fc054a70f723c
Full Text :
https://doi.org/10.1016/j.jdiacomp.2015.01.011