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Published on: July 29, 2019
Diffusion along perivascular spaces provides evidence interlinking compromised glymphatic function with aging in
Xin Cai1,2,3, Zhenzhen Chen1,4, Chentao He1
1Department of Neurology, Guangdong Neuroscience Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Glymphatic function, measured by the diffusion tensor image analysis along the perivascular space (DTI-ALPS) index, is reduced in Parkinson's disease (PD) patients, particularly in older individuals and those with sleep issues.
Area of Science:
- Neuroscience
- Radiology
- Biomedical Engineering
Background:
- Parkinson's disease (PD) is a neurodegenerative disorder affecting motor function.
- Glymphatic system dysfunction is increasingly implicated in neurodegenerative diseases.
- Noninvasive imaging biomarkers are needed to assess glymphatic function in PD.
Purpose of the Study:
- To evaluate glymphatic function in Parkinson's disease patients using DTI-ALPS.
- To identify factors related to glymphatic function in PD, considering age differences.
Main Methods:
- Retrospective analysis of 93 idiopathic PD patients and 42 healthy controls (HCs).
- Utilized diffusion tensor imaging (DTI) to calculate the analysis along the perivascular space (ALPS) index.
- Correlated ALPS index with clinical data, including age, onset age, sleep scale scores, diabetes history, and motor symptom severity.
Main Results:
- PD patients showed a significantly reduced ALPS index compared to HCs.
- In PD patients, the ALPS index negatively correlated with age, onset age, PDSS-2 scores, and diabetes history.
- A negative correlation between ALPS index and motor symptom severity was observed in PD patients aged 65 and above, but not in younger patients.
Conclusions:
- Reduced ALPS index, indicating compromised glymphatic activity, is associated with Parkinson's disease pathophysiology.
- Glymphatic dysfunction is particularly evident in older PD patients and those with sleep disorders.
- DTI-ALPS serves as a potential noninvasive biomarker for assessing glymphatic function in PD.
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