Correlation between dopaminergic and metabolic asymmetry in Lewy body disease - A dual-imaging study

被引:1
作者
Horsager, Jacob [1 ]
Andersen, Katrine B.
Okkels, Niels [1 ]
Knudsen, Karoline
Skjaerbaek, Casper [1 ]
Van den Berge, Nathalie [1 ]
Pavese, Nicola [1 ,3 ]
Gottrup, Hanne [2 ]
Borghammer, Per [1 ,3 ]
机构
[1] Aarhus Univ Hosp, Dept Nucl Med & PET, Palle Juul Jensens Blvd 165,J220, DK-8200 Aarhus N, Denmark
[2] Aarhus Univ Hosp, Dept Neurol, Aarhus, Denmark
[3] Aarhus Univ, Dept Clin Med, Aarhus, Denmark
关键词
Lewy body disease; Parkinson's disease; Lewy body dementia; Imaging; Asymmetry; PARKINSONS-DISEASE; BLOOD-FLOW; RAT MODEL; TRANSPORTER; PROGRESSION; DIAGNOSIS; DEMENTIA; LESIONS; BODIES;
D O I
10.1016/j.parkreldis.2024.107117
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: The a-Synuclein Origin and Connectome (SOC) model of Lewy body diseases postulates that a-syuclein will be asymmetrically distributed in some patients with Lewy body diseases, potentially leading to asymmetric neuronal dysfunction and symptoms. Methods: We included two patient groups: 19 non-demented Parkinson's disease (nPD) patients with [18F]FDG PET and motor symptoms assessed by UPDRS-III, and 65 Lewy body dementia (LBD) patients with [18F]FDG PET and dopamine radioisotope imaging. Asymmetry indices were calculated for [18F]FDG PET by including the cortex for each hemisphere, for dopamine radioisotope imaging by including the putamen and caudate separately, and for motor symptoms by using the difference between right-left UPDRS-III score. Correlations between these asymmetry indices were explored to test the predictions of the SOC model. To identify cases with a more typical LBD imaging profile, we calculated a Cingulate Island Sign (CIS) index on the [18F]FDG PET image. Results: We found a significant correlation between cortical interhemispheric [18F]FDG asymmetry and motorsymptom asymmetry in nPD patients (r = 0.62, P = 0.004). In patients with LBD, we found a significant correlation between cortical interhemispheric [18F]FDG asymmetry and dopamine transporter asymmetry in the caudate (r = 0.37, P = 0.0019), but not in the putamen (r = 0.15, P = 0.22). We observed that the correlation in the caudate was stronger in LBD subjects with the highest CIS index, i.e., with more typical LBD imaging profiles. Conclusion: Our study partly supports the SOC model, but further investigations are needed - ideally of de novo, non-demented PD patients.
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