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Nonmotor Symptoms in Patients with PARK2 Mutations

Decreased (123)I-meta-iodobenzylguanidine (MIBG) uptake in MIBG myocardial scintigraphy, olfactory dysfunction, and rapid eye movement (REM) sleep behavior disorder (RBD) are considered useful early indicators of Parkinson disease. We investigated whether patients with PARK2 mutations exhibited myoc...

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Autores principales: Yoritaka, Asako, Shimo, Yumi, Shimo, Yasushi, Inoue, Yuichi, Yoshino, Hiroyo, Hattori, Nobutaka
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3026966/
https://www.ncbi.nlm.nih.gov/pubmed/21317980
http://dx.doi.org/10.4061/2011/473640
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author Yoritaka, Asako
Shimo, Yumi
Shimo, Yasushi
Inoue, Yuichi
Yoshino, Hiroyo
Hattori, Nobutaka
author_facet Yoritaka, Asako
Shimo, Yumi
Shimo, Yasushi
Inoue, Yuichi
Yoshino, Hiroyo
Hattori, Nobutaka
author_sort Yoritaka, Asako
collection PubMed
description Decreased (123)I-meta-iodobenzylguanidine (MIBG) uptake in MIBG myocardial scintigraphy, olfactory dysfunction, and rapid eye movement (REM) sleep behavior disorder (RBD) are considered useful early indicators of Parkinson disease. We investigated whether patients with PARK2 mutations exhibited myocardial sympathetic abnormalities using MIBG scintigraphy, olfactory dysfunction using the Sniffin' Sticks olfactory test, and RBD using polysomnography. None of the examined patients had RBD, and all except 1 patient exhibited an increase in the olfactory threshold. Moreover, one of the oldest patients exhibited impairment in identification and discrimination. Of 12 patients with PARK2 mutations, 4 patients, who were older than patients without abnormal uptake, exhibited decreased MIBG uptake. The results obtained in this study suggest that some patients with PARK2 mutations have increased thresholds of olfactory function and myocardial sympathetic dysfunction as nonmotor symptoms.
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spelling pubmed-30269662011-02-11 Nonmotor Symptoms in Patients with PARK2 Mutations Yoritaka, Asako Shimo, Yumi Shimo, Yasushi Inoue, Yuichi Yoshino, Hiroyo Hattori, Nobutaka Parkinsons Dis Clinical Study Decreased (123)I-meta-iodobenzylguanidine (MIBG) uptake in MIBG myocardial scintigraphy, olfactory dysfunction, and rapid eye movement (REM) sleep behavior disorder (RBD) are considered useful early indicators of Parkinson disease. We investigated whether patients with PARK2 mutations exhibited myocardial sympathetic abnormalities using MIBG scintigraphy, olfactory dysfunction using the Sniffin' Sticks olfactory test, and RBD using polysomnography. None of the examined patients had RBD, and all except 1 patient exhibited an increase in the olfactory threshold. Moreover, one of the oldest patients exhibited impairment in identification and discrimination. Of 12 patients with PARK2 mutations, 4 patients, who were older than patients without abnormal uptake, exhibited decreased MIBG uptake. The results obtained in this study suggest that some patients with PARK2 mutations have increased thresholds of olfactory function and myocardial sympathetic dysfunction as nonmotor symptoms. SAGE-Hindawi Access to Research 2011-01-13 /pmc/articles/PMC3026966/ /pubmed/21317980 http://dx.doi.org/10.4061/2011/473640 Text en Copyright © 2011 Asako Yoritaka et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Yoritaka, Asako
Shimo, Yumi
Shimo, Yasushi
Inoue, Yuichi
Yoshino, Hiroyo
Hattori, Nobutaka
Nonmotor Symptoms in Patients with PARK2 Mutations
title Nonmotor Symptoms in Patients with PARK2 Mutations
title_full Nonmotor Symptoms in Patients with PARK2 Mutations
title_fullStr Nonmotor Symptoms in Patients with PARK2 Mutations
title_full_unstemmed Nonmotor Symptoms in Patients with PARK2 Mutations
title_short Nonmotor Symptoms in Patients with PARK2 Mutations
title_sort nonmotor symptoms in patients with park2 mutations
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3026966/
https://www.ncbi.nlm.nih.gov/pubmed/21317980
http://dx.doi.org/10.4061/2011/473640
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