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A Free-breathing fMRI Method to Study Human Olfactory Function
Published on: July 30, 2017
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Exploring white matter microstructure and olfaction dysfunction in early parkinson disease: diffusion MRI reveals new
Soheila Sobhani1,2,3, Farzaneh Rahmani4,5, Mohammad Hadi Aarabi1,2,3
1Basir Eye Health Research Center, Tehran, Iran.
Brain Imaging and Behavior
|November 15, 2017
Summary
Olfaction dysfunction is an early Parkinson disease (PD) sign. Diffusion MRI connectometry reveals white matter changes correlating with smell loss, offering potential early PD detection markers.
Area of Science:
- Neuroimaging
- Neuroscience
- Neurology
Background:
- Olfaction dysfunction is a recognized marker of prodromal Parkinson disease (PD).
- Current olfactory screening tests for PD lack specificity and have long lead times.
- Advanced imaging markers are needed for accurate PD prediction and early detection.
Purpose of the Study:
- To investigate white matter microstructural differences in de novo Parkinson disease (PD) patients with varying degrees of olfaction dysfunction using diffusion MRI connectometry.
- To identify correlations between olfactory function (University of Pennsylvania Smell Identification Test - UPSIT score) and specific white matter tract connectivity.
- To explore the potential of diffusion MRI parameters as early diagnostic markers for PD.
Main Methods:
- Diffusion MRI connectometry was performed on 85 de novo PD patients and 36 healthy controls.
- Analysis focused on identifying white matter tracts with significant differences in quantitative anisotropy between PD subgroups and correlating connectivity with UPSIT scores.
- Multiple regression analysis was employed, controlling for age, sex, Geriatric Depression Scale (GDS), and Montreal Cognitive Assessment (MoCA) scores.
Main Results:
- PD patients with anosmia showed decreased connectivity in key white matter tracts including the inferior longitudinal fasciculus, fornix, middle cerebellar peduncle (MCP), cingulum, corticospinal tract (CST), and corpus callosum (CC).
- UPSIT scores significantly correlated negatively with connectivity in the CC and fornix, and positively with connectivity in the cingulum and MCP.
- Olfactory function (UPSIT score) did not predict white matter connectivity in healthy controls.
Conclusions:
- Microstructural changes in specific white matter tracts are associated with the clinical phenotype of olfaction dysfunction in prodromal PD.
- Diffusion MRI parameters in these identified tracts may serve as sensitive and specific signature markers for the early detection of PD.
- This study is the first to demonstrate the discriminative role of the UPSIT score in identifying PD-specific white matter microstructural alterations.
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