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The diagnostic accuracy of Sudoscan in transthyretin familial amyloid polyneuropathy.

Authors :
Castro, José
Miranda, Bruno
Castro, Isabel
de Carvalho, Mamede
Conceição, Isabel
Source :
Clinical Neurophysiology. May2016, Vol. 127 Issue 5, p2222-2227. 6p.
Publication Year :
2016

Abstract

Objective Transthyretin familial amyloid polyneuropathy (TTR-FAP) is an axonal sensory-motor and autonomic neuropathy. Reliable quantification of sudomotor function could prove essential in the diagnosis and early treatment management. We aim to assess the diagnostic value of a new sudomotor test ( Sudoscan ) in TTR-FAP. Methods One hundred and thirty-three TTR-FAP Val30Met carriers, divided in asymptomatic and symptomatic stage 1, were compared with 37 healthy controls. We analyzed the right sural sensory nerve action potential (SNAP), the plantar sympathetic skin response (SSR) and the electrochemical skin conductance (ESC) measured by Sudoscan in both hands and feet. Results All neurophysiological measures were significantly worse in the symptomatic group. However, feet ESC was the only test distinguishing symptomatic patients with autonomic dysfunction from those without autonomic dysfunction, and both groups from asymptomatic subjects and healthy controls. Feet ESC was a significant independent predictor for the presence of symptoms and autonomic failure, after adjusting for demographic characteristics, sural SNAP and SSR amplitudes ( p < 0.05). Feet ESC showed 76% sensitivity and 85% specificity for detection of dysautonomia. Conclusion Feet ESC is a sensitive test to assess early autonomic dysfunction in TTR-FAP subjects. This investigation should be considered for routine assessment in this population. Significance Abnormal feet responses on Sudoscan support early diagnosis in TTR-FAP. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13882457
Volume :
127
Issue :
5
Database :
Academic Search Index
Journal :
Clinical Neurophysiology
Publication Type :
Academic Journal
Accession number :
114459766
Full Text :
https://doi.org/10.1016/j.clinph.2016.02.013