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Morphological And Functional Research In Parkinson Disease By Magnetic Resonance Imaging
Shuaiwen Wang1, Junqiang Lei1, and Shunlin Guo1

1Department of Radiology, the First Hospital of Lanzhou University, Lanzhou, People's Republic of China

Synopsis

Parkinson's disease (PD) is the second most common neurodegenerative disease after AD, and the most frequent subcortical degenerative disease.We hope to found morphological and functional characteristic change in PD

abstract

Purpose: Parkinson disease(PD) is accompanied by degeneration of the nigrostriatal dopaminergic system,with neuronal loss and reactive gliosis in the substantia nigra found at autopsy. Whereas PD are characterized by the general neuronal loss of the dopaminergic system,a high percentage of surviving neurons contain intracellular inclusions in the form of Lewy body,similar to other neurodegenerative disorders1-3.

Method: PD and normal control group(NC) study to evaluate nigrosome-1 from substantia nigra ,underwent susceptibility weighted imaging(SWI) at 3T MRI scanner (MAGNETOM Skyra, Siemens Healthcare)in 16 PD patients and 12 NC were scanned(Sequence:3D GRE-SWI,TR:27ms,TE:20ms,Flip angle:15deg,Matrix size:256×256).The bilateral substantia nigra was evaluated by two neuroradiologists for the presence,absence or indecisive presence of nigrosome-14-13. In the meantime,we using blood oxygen level dependent(BOLD) (Slice:40,Slice thickness:3mm,TR:3200ms,TE:30ms,Flip angle:90deg,Matrix size:64×64)to investigate differences in high function area within the DMN14-16 in patients with PD and NC by regional homogeneity,we base on cluster size and morphometry to test differences in these two group by functional MRI,try to discover an result to answer what kind of relationship between structural abnormalities and function disoder17,18.

Results: We identified nigrosome-1 in NC and it was not identified in the PD,the swallow-tail sign was discriminated.Meanwhile,our findings persent a functional disorder of the DMN in PD patients,there were not significant change in inferior parietal cortex(IPC) and middle temporal lobe(MTL) by the two groups,but posterior cingulate cortex(PCC) and medial prefrontal cortex(mPFC) were obviously increased(p<0.05) by one-sample t-test and gaussian random field(GRF) correction(voxel-level p and cluster-level p<0.05).

Discussion: Parkinson's disease is based on the degeneration of the dopaminergic neurons in substantia nigra, because of reduce the secretion of inhibitory neurotransmitter,the balance of excitement and inhibition in substantia nigra-striatum pathways is upset, extrapyramidal reactions is caused by hyperexcitability and transmit to the motor cortex by nerve pathways and the corresponding clinical symptoms19-26. Conclusion: In the absence of significant differences between PD and NC group.Interosculation morphology and function research maybe could explain the clinic term a disorder with prominent bradykinesia and mutple extrapyramidal symptoms.

Acknowledgements

The authors thank Siemens Healthcare for technical assistance

References

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Figures

Figure1.The pathways of nerve fiber go through cerebellum and brain stein,some of them pass bilateral substantia nigra the dopaminergic neuron,and crossed the thalamus and arrive in striatum, cerebral cortex ultimately.

Figure2.A demonstrates the structure of nigrosome-1(yellow area presented);B shows the normal structure of substantia nigra and nigrosome-1;C shows nigrosome-1 disappear from substantia nigra in PD.

Figure3.A-C present high funcion aera of regional homogeneity in DMN by normal control in resting-state, D-E present high funcion aera of regional homogeneity in DMN by PD in resting-state.

Demographic data of the prospective study group.

The absence, presence and indecisive presence of nigrosome-1 in Parkinson’s disease and normal controls.

The relatively high function of voxel size in IPC, MTL, PCC, mPFC from DMN between PD and NC;IPC=inferior parietal cortex and,MTL=middle temporal lobe,PCC=posterior cingulate cortex, mPFC=medial prefrontal cortex.

Proc. Intl. Soc. Mag. Reson. Med. 25 (2017)
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