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 in | Movement disorders Vol. 36; no. 9; pp. 2066 - 2076 | 
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| Main Authors | , , , , , , , , , , | 
| Format | Journal Article | 
| Language | English | 
| Published | 
        Hoboken, USA
          John Wiley & Sons, Inc
    
        01.09.2021
     Wiley Subscription Services, Inc  | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 0885-3185 1531-8257 1531-8257  | 
| DOI | 10.1002/mds.28643 | 
Cover
| 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 | 
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| 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. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 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 |