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Published Online: 1 July 2014

Skin Conductance Levels May Reflect Emotional Blunting in Behavioral Variant Frontotemporal Dementia

Publication: The Journal of Neuropsychiatry and Clinical Neurosciences

Abstract

The authors evaluated skin conductance as a measure of emotional blunting among 10 patients with behavioral variant frontotemporal dementia compared with 10 with Alzheimer’s disease and 14 healthy control subjects. It was concluded that low skin conductance levels in this disorder indicate a low resting sympathetic state and low emotional arousal.

Abstract

Emotional blunting is a core diagnostic feature of behavioral variant frontotemporal dementia (bvFTD). The authors evaluated skin conductance as a measure of emotional blunting among 10 patients with bvFTD compared with 10 with Alzheimer’s disease and 14 healthy control subjects. Despite responses to an auditory startle stimulus, skin conductance levels (SCLs) were lower in the patients with bvFTD compared with the other groups. The low SCLs significantly correlated with ratings of emotional blunting. The authors conclude that low SCLs in bvFTD indicate a low resting sympathetic state and low emotional arousal. The measurement of SCLs may be a useful noninvasive diagnostic test for bvFTD.

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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: 227 - 232
PubMed: 25093763

History

Received: 30 November 2012
Revision received: 7 April 2013
Revision received: 16 July 2013
Accepted: 18 July 2013
Published online: 1 July 2014
Published in print: Summer 2014

Authors

Details

Simantini J. Karve, Ph.D.
From the Dept. of Neurology (SJK, MFM, EJ, MM, JSS) and Dept. of Psychiatry & Biobehavioral Sciences (MFM), David Geffen School of Medicine, University of California, Los Angeles, CA; and Section of Neurology, VA Greater Los Angeles Healthcare Center, Los Angeles, CA (SJK, MFM, NK, EJ, MM, JSS).
Mario F. Mendez, M.D., Ph.D.
From the Dept. of Neurology (SJK, MFM, EJ, MM, JSS) and Dept. of Psychiatry & Biobehavioral Sciences (MFM), David Geffen School of Medicine, University of California, Los Angeles, CA; and Section of Neurology, VA Greater Los Angeles Healthcare Center, Los Angeles, CA (SJK, MFM, NK, EJ, MM, JSS).
Natalie Kaiser, Ph.D.
From the Dept. of Neurology (SJK, MFM, EJ, MM, JSS) and Dept. of Psychiatry & Biobehavioral Sciences (MFM), David Geffen School of Medicine, University of California, Los Angeles, CA; and Section of Neurology, VA Greater Los Angeles Healthcare Center, Los Angeles, CA (SJK, MFM, NK, EJ, MM, JSS).
Elvira Jimenez, M.P.H.
From the Dept. of Neurology (SJK, MFM, EJ, MM, JSS) and Dept. of Psychiatry & Biobehavioral Sciences (MFM), David Geffen School of Medicine, University of California, Los Angeles, CA; and Section of Neurology, VA Greater Los Angeles Healthcare Center, Los Angeles, CA (SJK, MFM, NK, EJ, MM, JSS).
Michelle Mather, B.A.
From the Dept. of Neurology (SJK, MFM, EJ, MM, JSS) and Dept. of Psychiatry & Biobehavioral Sciences (MFM), David Geffen School of Medicine, University of California, Los Angeles, CA; and Section of Neurology, VA Greater Los Angeles Healthcare Center, Los Angeles, CA (SJK, MFM, NK, EJ, MM, JSS).
Jill S. Shapira, R.N., Ph.D.
From the Dept. of Neurology (SJK, MFM, EJ, MM, JSS) and Dept. of Psychiatry & Biobehavioral Sciences (MFM), David Geffen School of Medicine, University of California, Los Angeles, CA; and Section of Neurology, VA Greater Los Angeles Healthcare Center, Los Angeles, CA (SJK, MFM, NK, EJ, MM, JSS).

Notes

Send correspondence to M. F. Mendez, M.D., Ph.D.; e-mail: [email protected]

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