Volume 18, Issue 3 pp. 425-429

Differences in odor identification among clinical subtypes of Parkinson’s disease

M. Iijima

M. Iijima

Department of Neurology, Tokyo Women’s Medical University School of Medicine, Tokyo

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T. Kobayakawa

T. Kobayakawa

Institute for Human Science and Biomedical Engineering, National Institute of Advanced Industrial Science and Technology, Tsukuba

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S. Saito

S. Saito

Saito Sachiko Taste and Smell Institute, Tsukuba

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M. Osawa

M. Osawa

Department of Neurology, Tokyo Women’s Medical University School of Medicine, Tokyo

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Y. Tsutsumi

Y. Tsutsumi

Department of Neurology, Tokyo Women’s Medical University School of Medicine, Tokyo

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S. Hashimoto

S. Hashimoto

Medical Research Institute, Tokyo Women’s Medical University School of Medicine, Tokyo, Japan

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S. Uchiyama

S. Uchiyama

Department of Neurology, Tokyo Women’s Medical University School of Medicine, Tokyo

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First published: 17 February 2011
Citations: 35
M. Iijima, Department of Neurology, Tokyo Women’s Medical University School of Medicine, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan (tel.: +81 3 3353 8111; fax: +81 3 5269 7324; e-mail: [email protected]).

Abstract

Objective: Olfactory dysfunction is a non-motor symptom in idiopathic Parkinson’s disease (PD). We investigated whether this dysfunction differs among clinical subtypes of PD.

Methods: Participants comprised of 90 patients with idiopathic PD and without dementia. Olfactory function was evaluated using the odor stick identification test for Japanese, which evaluated the detection of 12 odorants familiar to Japanese participants. Patients were divided into tremor-dominant type (TDT), akinetic-rigid type (ART), and mixed type (MXT) PD subgroups using part III of the Unified Parkinson’s Disease Rating Scale.

Results: Fifty-five patients were classified as ART, 21 as MXT, and 14 as TDT. There were no differences in age, sex, or duration of illness among the subtypes. Subjective symptoms of impaired sense of smell were significantly higher (P < 0.05) in the ART than in the TDT. Mean odor identification score was 4.3 in the ART, 5.2 in MXT, and 6.6 in TDT. It was significantly lower in the ART than in the TDT (P < 0.01).

Conclusion: Olfactory dysfunction differed among the clinical subtypes of PD. This suggests that olfactory function might relate to prognosis of patients with PD.

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