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No relevant midbrain atrophy in Parkinson's disease
被引:5
|作者:
Makinen, E.
[1
,2
]
Joutsa, J.
[1
,2
,3
]
Isotalo, J.
[1
,2
]
Kaasinen, V.
[1
,2
,3
]
机构:
[1] Turku Univ Hosp, Div Clin Neurosci, POB 52, FIN-20521 Turku, Finland
[2] Univ Turku, Turku, Finland
[3] Turku Univ Hosp, Turku PET Ctr, Turku, Finland
来源:
关键词:
dopamine;
midbrain atrophy;
Parkinson's disease;
progressive supranuclear palsy;
PROGRESSIVE SUPRANUCLEAR PALSY;
PONS RATIO;
MRI;
SUBTYPES;
BINDING;
D O I:
10.1111/ane.12551
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Aims of the study - To investigate whether significant midbrain atrophy is present in Parkinson's disease (PD), and if so, whether it can be used as a marker of striatal dopaminergic degeneration. Methods - In total, 150 PD patients and 155 controls were scanned with both brain dopamine transporter (DAT) [I-123]FP-CIT SPECT and 1.5T MRI. Midbrain atrophy was measured from sagittal MRIs using the midbrain-to-pons ratios. Both striatal region-of-interest-based (Brass) and striatal and extrastriatal voxel-by-voxel-based DAT binding (SPM8) were investigated in relation to midbrain atrophy. Results - The midbrain-to-pons ratios in PD patients were slightly lower than those in the controls (mean 0.59 vs 0.61, P < 0.05). The ratios did not significantly correlate with striatal or extrastriatal [I-123] FP-CIT uptake in controls or patients with PD. Conclusions - Mild midbrain atrophy is present in PD and can be detected with MRI. However, the midbrain atrophy in PD is not associated with the level of striatal dopaminergic dysfunction, and midbrain measurements therefore cannot be used as a clinically useful predictor of dopamine function.
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页码:378 / 381
页数:4
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