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August 15, 2017; 89 (7) Article

Automatic measurement of prosody in behavioral variant FTD

Naomi Nevler, Sharon Ash, Charles Jester, David J. Irwin, Mark Liberman, Murray Grossman
First published July 19, 2017, DOI: https://doi.org/10.1212/WNL.0000000000004236
Naomi Nevler
From the Penn Frontotemporal Degeneration Center, Department of Neurology (N.N., S.A., C.J., D.J.I., M.G.), and Linguistic Data Consortium (M.L.), University of Pennsylvania, Philadelphia.
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Sharon Ash
From the Penn Frontotemporal Degeneration Center, Department of Neurology (N.N., S.A., C.J., D.J.I., M.G.), and Linguistic Data Consortium (M.L.), University of Pennsylvania, Philadelphia.
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Charles Jester
From the Penn Frontotemporal Degeneration Center, Department of Neurology (N.N., S.A., C.J., D.J.I., M.G.), and Linguistic Data Consortium (M.L.), University of Pennsylvania, Philadelphia.
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David J. Irwin
From the Penn Frontotemporal Degeneration Center, Department of Neurology (N.N., S.A., C.J., D.J.I., M.G.), and Linguistic Data Consortium (M.L.), University of Pennsylvania, Philadelphia.
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Mark Liberman
From the Penn Frontotemporal Degeneration Center, Department of Neurology (N.N., S.A., C.J., D.J.I., M.G.), and Linguistic Data Consortium (M.L.), University of Pennsylvania, Philadelphia.
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Murray Grossman
From the Penn Frontotemporal Degeneration Center, Department of Neurology (N.N., S.A., C.J., D.J.I., M.G.), and Linguistic Data Consortium (M.L.), University of Pennsylvania, Philadelphia.
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Automatic measurement of prosody in behavioral variant FTD
Naomi Nevler, Sharon Ash, Charles Jester, David J. Irwin, Mark Liberman, Murray Grossman
Neurology Aug 2017, 89 (7) 650-656; DOI: 10.1212/WNL.0000000000004236

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Abstract

Objective: To help understand speech changes in behavioral variant frontotemporal dementia (bvFTD), we developed and implemented automatic methods of speech analysis for quantification of prosody, and evaluated clinical and anatomical correlations.

Methods: We analyzed semi-structured, digitized speech samples from 32 patients with bvFTD (21 male, mean age 63 ± 8.5, mean disease duration 4 ± 3.1 years) and 17 matched healthy controls (HC). We automatically extracted fundamental frequency (f0, the physical property of sound most closely correlating with perceived pitch) and computed pitch range on a logarithmic scale (semitone) that controls for individual and sex differences. We correlated f0 range with neuropsychiatric tests, and related f0 range to gray matter (GM) atrophy using 3T T1 MRI.

Results: We found significantly reduced f0 range in patients with bvFTD (mean 4.3 ± 1.8 ST) compared to HC (5.8 ± 2.1 ST; p = 0.03). Regression related reduced f0 range in bvFTD to GM atrophy in bilateral inferior and dorsomedial frontal as well as left anterior cingulate and anterior insular regions.

Conclusions: Reduced f0 range reflects impaired prosody in bvFTD. This is associated with neuroanatomic networks implicated in language production and social disorders centered in the frontal lobe. These findings support the feasibility of automated speech analysis in frontotemporal dementia and other disorders.

GLOSSARY

ALS=
amyotrophic lateral sclerosis;
bvFTD=
behavioral variant of frontotemporal dementia;
FTLD=
frontotemporal lobar degeneration;
GM=
gray matter;
HC=
healthy controls;
IFG=
inferior frontal gyrus;
NPI=
Neuropsychiatric Inventory;
SAD=
speech activity detector;
ST=
semitones

Footnotes

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Supplemental data at Neurology.org

  • Editorial, page 644

  • Received January 4, 2017.
  • Accepted in final form April 21, 2017.
  • © 2017 American Academy of Neurology
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