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September 11, 2012; 79 (11) Articles

Psychiatric disorders in rapid-onset dystonia-parkinsonism

Allison Brashear, Jared F. Cook, Deborah F. Hill, Alethea Amponsah, Beverly M. Snively, Laney Light, Niki Boggs, Cynthia K. Suerken, Mark Stacy, Laurie Ozelius, Kathleen J. Sweadner, W. Vaughn McCall
First published August 29, 2012, DOI: https://doi.org/10.1212/WNL.0b013e3182698d6c
Allison Brashear
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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Jared F. Cook
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
MA
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Deborah F. Hill
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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Alethea Amponsah
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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Beverly M. Snively
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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Laney Light
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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Niki Boggs
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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Cynthia K. Suerken
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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Mark Stacy
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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Laurie Ozelius
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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Kathleen J. Sweadner
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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W. Vaughn McCall
From the Departments of Neurology (A.B., J.F.C., D.F.H., A.A.), Biostatistical Sciences (B.M.S., L.L., C.K.S.), and Psychiatry and Behavioral Medicine (N.B., W.V.M.), Wake Forest School of Medicine, Wake Forest Baptist Health, Winston-Salem, NC; Department of Neurology (M.S.), Duke University School of Medicine, Duke Health, Durham, NC; Department of Genetics and Genomic Sciences (L.O.), Mount Sinai School of Medicine, New York, NY; and Neurosurgery (K.J.S.), Massachusetts General Hospital, Harvard Medical School, Boston.
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Full PDF
Citation
Psychiatric disorders in rapid-onset dystonia-parkinsonism
Allison Brashear, Jared F. Cook, Deborah F. Hill, Alethea Amponsah, Beverly M. Snively, Laney Light, Niki Boggs, Cynthia K. Suerken, Mark Stacy, Laurie Ozelius, Kathleen J. Sweadner, W. Vaughn McCall
Neurology Sep 2012, 79 (11) 1168-1173; DOI: 10.1212/WNL.0b013e3182698d6c

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Abstract

Objective: Rapid-onset dystonia-parkinsonism (RDP) is caused by a variety of missense mutations in the ATP1A3 gene. Psychiatric comorbidity has been reported, although systematic examination of psychiatric disease in individuals with RDP is lacking. This study examines psychiatric morbidity for 23 patients with RDP in 10 families with family member control subjects and in 3 unrelated patients with RDP, totaling 56 individuals.

Methods: Twenty-nine ATP1A3 mutation–positive individuals were examined; 26 exhibited motor symptoms (motor manifesting carrier [MMC]) and 3 did not (nonmotor manifesting carriers [NMC]). Twenty-seven ATP1A3 mutation-negative participants (noncarriers [NC]) were included. Rates of psychiatric illness for patients with RDP and related asymptomatic gene mutation carriers were compared with those for related nonmutation carriers. Outcome measures included the Unified Parkinson's Disease Rating Scale, Burke-Fahn-Marsden Dystonia Rating Scale, Instrumental Activities of Daily Living, Composite International Diagnostic Interview, Structured Clinical Interview for DSM-IV, Hamilton Depression Scale, Hamilton Anxiety Scale, and Yale-Brown Obsessive-Compulsive Scale.

Results: NMC participants did not report any history of psychiatric disorder. Findings in MMC and NC groups included anxiety (MMC 48, NC 41%), mood (MMC 50%, NC 22%), psychotic (MMC 19%, NC 0%), and substance abuse/dependence (MMC 38%, NC 27%).

Conclusions: ATP1A3 mutations cause a wide spectrum of motor and nonmotor features. Psychotic symptoms tended to emerge before or concurrent with motor symptom onset, suggesting that this could be another expression of the ATP1A3 gene mutation.

GLOSSARY

BFMS=
Burke-Fahn-Marsden Dystonia Rating Scale;
CIDI=
Composite International Diagnostic Interview;
DSM=
Diagnostic and Statistical Manual of Mental Disorders;
HAM-A=
Hamilton Anxiety Scale;
HAM-D=
Hamilton Depression Scale;
MMC=
motor manifesting carrier;
NC=
noncarrier;
NMC=
nonmotor manifesting carrier;
NOS=
not otherwise specified;
RPD=
rapid-onset dystonia-parkinsonism;
UPDRS=
Unified Parkinson's Disease Rating Scale;
Y-BOCS=
Yale-Brown Obsessive-Compulsive Scale

Footnotes

  • Study funding: Supported by the NINDS (grant 5R01-NS058949-04 to A.B.).

  • Received February 10, 2012.
  • Accepted April 19, 2012.
  • Copyright © 2012 by AAN Enterprises, Inc.
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