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Published Online: 6 April 2018

Skin Conduction Levels Differentiate Frontotemporal Dementia From Alzheimer’s Disease

Publication: The Journal of Neuropsychiatry and Clinical Neurosciences

Abstract

Patients with behavioral variant frontotemporal dementia (bvFTD) and Alzheimer’s disease (AD) differ in basic emotional tone. Skin conduction levels (SCLs), a measure of sympathetic tone, may be a sensitive test for discriminating these two dementias early in their course. Previous research has shown differences in resting SCLs between patients with bvFTD and AD, but no study has evaluated the discriminability of SCLs during different environmental conditions. The authors compared bvFTD patients (N=8), AD patients (N=10), and healthy control subjects (N=9) on SCL measures pertaining to real-life vignettes or scenarios differing in valence and emotional intensity. The SCLs among the bvFTD patients were decreased across all conditions, whereas the SCLs among the AD patients were increased compared with control participants. On analysis, the SCLs in response to emotional stimuli differentiated bvFTD from AD with an area under the receiver operator characteristic curve of 95.3%. At a cutoff ≤0.77 μS, emotional vignettes distinguished bvFTD from AD with a sensitivity of 86% and a specificity of 96%. These preliminary results indicate the potential utility of SCLs for differentiating bvFTD from AD early in their course, regardless of environmental condition.

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Information

Published In

Go to The Journal of Neuropsychiatry and Clinical Neurosciences
Go to The Journal of Neuropsychiatry and Clinical Neurosciences
The Journal of Neuropsychiatry and Clinical Neurosciences
Pages: 208 - 213
PubMed: 29621927

History

Received: 24 August 2017
Revision received: 6 November 2017
Accepted: 20 November 2017
Published online: 6 April 2018
Published in print: Summer 2018

Keywords

  1. Cognitive Disorders
  2. Dementia
  3. Diagnosis and Classification in Neuropsychiatry
  4. Alzheimer-s Disease

Authors

Details

Mario F. Mendez, M.D., Ph.D. [email protected]
From the Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles (MFM, SSF, MMA, EEJ, ARC); and the Neurobehavior Unit, VA Greater Los Angeles Healthcare System, Los Angeles (MFM, EEJ).
Sylvia S. Fong, M.A.
From the Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles (MFM, SSF, MMA, EEJ, ARC); and the Neurobehavior Unit, VA Greater Los Angeles Healthcare System, Los Angeles (MFM, EEJ).
Mark M. Ashla, B.A.
From the Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles (MFM, SSF, MMA, EEJ, ARC); and the Neurobehavior Unit, VA Greater Los Angeles Healthcare System, Los Angeles (MFM, EEJ).
Elvira E. Jimenez, M.P.H.
From the Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles (MFM, SSF, MMA, EEJ, ARC); and the Neurobehavior Unit, VA Greater Los Angeles Healthcare System, Los Angeles (MFM, EEJ).
Andrew R. Carr, Ph.D.
From the Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles (MFM, SSF, MMA, EEJ, ARC); and the Neurobehavior Unit, VA Greater Los Angeles Healthcare System, Los Angeles (MFM, EEJ).

Notes

Send correspondence to Dr. Mendez; e-mail: [email protected]

Funding Information

NIA: R01AG034499 and R01AG050967
Supported by an NIH grant (R01AG034499-03) to Dr. Mendez.The authors report no financial relationships with commercial interests.

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