Decoupling of Global Brain Activity and Cerebrospinal Fluid Flow in Parkinson's Disease Cognitive Decline

ABSTRACT Background Deposition and spreading of misfolded proteins (α‐synuclein and tau) have been linked to Parkinson's disease cognitive dysfunction. The glymphatic system may play an important role in the clearance of these toxic proteins via cerebrospinal fluid (CSF) flow through perivascul...

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Published inMovement disorders Vol. 36; no. 9; pp. 2066 - 2076
Main Authors Han, Feng, Brown, Gregory L., Zhu, Yalin, Belkin‐Rosen, Aaron E., Lewis, Mechelle M., Du, Guangwei, Gu, Yameng, Eslinger, Paul J., Mailman, Richard B., Huang, Xuemei, Liu, Xiao
Format Journal Article
LanguageEnglish
Published Hoboken, USA John Wiley & Sons, Inc 01.09.2021
Wiley Subscription Services, Inc
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ISSN0885-3185
1531-8257
1531-8257
DOI10.1002/mds.28643

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Summary:ABSTRACT Background Deposition and spreading of misfolded proteins (α‐synuclein and tau) have been linked to Parkinson's disease cognitive dysfunction. The glymphatic system may play an important role in the clearance of these toxic proteins via cerebrospinal fluid (CSF) flow through perivascular and interstitial spaces. Recent studies discovered that sleep‐dependent global brain activity is coupled to CSF flow, which may reflect glymphatic function. Objective The objective of this current study was to determine if the decoupling of brain activity–CSF flow is linked to Parkinson's disease cognitive dysfunction. Methods Functional and structural MRI data, clinical motor (Unified Parkinson's Disease Rating Scale), and cognitive (Montreal Cognitive Assessment [MoCA]) scores were collected from 60 Parkinson's disease and 58 control subjects. Parkinson's disease patients were subgrouped into those with mild cognitive impairment (MoCA < 26), n = 31, and those without mild cognitive impairment (MoCA ≥ 26), n = 29. The coupling strength between the resting‐state global blood‐oxygen‐level‐dependent signal and associated CSF flow was quantified, compared among groups, and associated with clinical and structural measurements. Results Global blood‐oxygen‐level‐dependent signal–CSF coupling decreased significantly (P < 0.006) in Parkinson's disease patients showing mild cognitive impairment, compared with those without mild cognitive impairment and controls. Reduced global blood‐oxygen‐level‐dependent signal–CSF coupling was associated with decreased MoCA scores present in Parkinson's disease patients (P = 0.005) but not in controls (P = 0.65). Weaker global blood‐oxygen‐level‐dependent signal–CSF coupling in Parkinson's disease patients also was associated with a thinner right entorhinal cortex (Spearman's correlation, −0.36; P = 0.012), an early structural change often seen in Alzheimer's disease. Conclusions The decoupling between global brain activity and associated CSF flow is related to Parkinson's disease cognitive impairment. © 2021 International Parkinson and Movement Disorder Society
Bibliography:The authors report no financial interests or potential conflicts of interest.
Relevant conflicts of interest/financial disclosures
Funding agencies
This work was supported by the National Institutes of Health (NIH) Pathway to Independence Award (K99/R00 5R00NS092996–03), the Brain Initiative award (1RF1MH123247–01), and the NIH R01 award (1R01NS113889‐01A1). This work was also supported by the National Institute of Neurological Disorders and Stroke Parkinson's Disease Biomarker Program (NS06722 and NS112008 to X.H), the National Institute of Aging (AG067651 to G.B), the Hershey Medical Center General Clinical Research Center (National Center for Research Resources, grant UL1 RR033184, which is now at the National Center for Advancing Translational Sciences, grant UL1 TR000127), the PA Department of Health Tobacco CURE Funds, and the Penn State Translational Brain Research Center.
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Statistical Analysis: A. Design, B. Execution, C. Review and Critique
GLB: 1C, 2C, 3A, 3B
XL: 1A, 1B, 2A, 2C, 3A, 3B.
FH: 1A, 1B, 1C, 2B, 2C, 3A
Research project: A. Conception, B. Organization, C. Execution
Manuscript Preparation: A. Writing of the first draft, B. Review and Critique
XH: 1A, 1B, 2A, 2C, 3B
MML: 2C, 3A, 3B
AEBR: 1C, 2B
Author Roles
YZ: 1C, 2B
GD: 2C, 3B
PJR: 3B
YG: 1C, 2C
RBM: 2C, 3B
ISSN:0885-3185
1531-8257
1531-8257
DOI:10.1002/mds.28643