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Updated: Apr 12, 2026

Olfactory Assays for Mouse Models of Neurodegenerative Disease
Published on: August 25, 2014
Olfactory function combined with morphology distinguishes Parkinson's disease
Renpei Sengoku1, Satoshi Matsushima2, Keiko Bono3
1Department of Neurology, The Jikei University School of Medicine, Tokyo, Japan; Department of Neurology, Tokyo Metropolitan Geriatric Hospital, Tokyo, Japan.
Reduced olfactory bulb and tract volume on MRI, combined with olfactory tests and cardiovascular assessments, can help differentiate Parkinson's disease (PD) from related disorders.
Area of Science:
- Neurology
- Radiology
- Neuroimaging
Background:
- Parkinson's disease (PD) and related disorders share overlapping symptoms, complicating differential diagnosis.
- Olfactory dysfunction and cardiovascular autonomic neuropathy are common in PD.
Purpose of the Study:
- To assess the utility of olfactory bulb and tract (OB & T) volume on MRI for differentiating PD from PD-related disorders.
- To correlate OB & T volume with olfactory function and cardiovascular dysautonomia.
Main Methods:
- Compared MRI-derived OB & T volumes in patients with PD, multiple system atrophy (MSA), and progressive supranuclear palsy/corticobasal degeneration (PSP/CBD).
- Utilized odor stick identification test for Japanese (OSIT-J) and (123)I-meta-iodobenzylguanidine (MIBG) scintigraphy.
- Defined cut-off values for OSIT-J, MIBG uptake, and OB & T volume to discriminate PD.
Main Results:
- OB & T volume was significantly smaller in PD patients compared to MSA and PSP/CBD groups (p < 0.05).
- A combination of OSIT-J score <8, heart/mediastinum ratio <1.6, and OB & T volume <270 mm(3) identified PD with 91% accuracy.
- Decreasing OSIT-J scores and OB & T volumes correlated with an increased likelihood of PD (p < 0.001).
Conclusions:
- Combined morphological (OB & T volume) and functional (olfactory, cardiovascular) assessments show promise for differentiating PD.
- These preliminary findings suggest MRI-based OB & T volume is a valuable biomarker in PD diagnosis.
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