Journal
PARKINSONISM & RELATED DISORDERS
Volume 101, Issue -, Pages 119-128Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.parkreldis.2022.06.004
Keywords
Lewy body; Dementia; Parkinson's disease; Blood-brain barrier; Blood biomarker; Neurofilament light chain
Categories
Funding
- Canadian Institutes of Health Research
- Natural Sciences and Engineering Research Council of Canada [RGPIN-2017-06962]
- Michael J Fox Foundation
- Alzheimer's Association
- Brain Canada [AARG501466]
- Michael J. Fox Foundation
- Weston Brain Institute
- Alzheimer's Research UK
- Canada Research Chairs Program
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This study provides evidence of blood-brain barrier dysfunction in Lewy body spectrum diseases. Patients with idiopathic Parkinson's disease (PD) and PD dementia (PDD) and/or dementia with Lewy bodies (DLB) have higher levels of cerebrospinal fluid to blood albumin ratio and blood neurofilament light chain, indicating BBB disruption and neurodegenerative co-pathology involvement. The severity of BBB breakdown is greater in Lewy body diseases with cognitive impairment.
Background: Mixed evidence supports blood-brain barrier (BBB) dysfunction in Lewy body spectrum diseases. Methods: We compare biofluid markers in people with idiopathic Parkinson's disease (PD) and people with PD dementia (PDD) and/or dementia with Lewy bodies (DLB), compared with healthy controls (HC). Seven databases were searched up to May 10, 2021. Outcomes included cerebrospinal fluid to blood albumin ratio (Qalb), and concentrations of 7 blood protein markers that also reflect BBB disruption and/or neurodegenerative copathology. We further explore differences between PD patients with and without evidence of dementia. Random-effects models were used to obtain standardized mean differences (SMD) with 95% confidence interval. Results: Of 13,949 unique records, 51 studies were meta-analyzed. Compared to HC, Q(alb) was higher in PD (N-PD/ N-HC = 224/563; SMD = 0.960 [0.227-1.694], p = 0.010; I-2 = 92.2%) and in PDD/DLB (N-PDD/DLB/N-HC = 265/ 670; SMD = 1.126 [0.358-1.893], p < 0.001; I-2 = 78.2%). Blood neurofilament light chain (NfL) was higher in PD (N-PD/N-HC = 1848/1130; SMD = 0.747 [0.442-1.052], p < 0.001; I-2 = 91.9%) and PDD/DLB (N-PDD/DLB/N-HC = 183/469; SMD = 1.051 [0.678-1.423], p = 0.004; I-2 = 92.7%) than in HC. p-tau 181 (N-PD/N-HC = 276/164; SMD = 0.698 [0.149-1.247], p = 0.013; I-2 = 82.7%) was also higher in PD compared to HC. In exploratory analyses, blood NfL was higher in PD without dementia (N-PDND/N-HC = 1005/740; SMD = 0.252 [0.042-0.462], p = 0.018; I-2 = 71.8%) and higher in PDD (N-PDD/N-HC = 100/111; SMD = 0.780 [0.347-1.214], p < 0.001; I2 = 46.7%) compared to HC. Qalb (N-PDD/N-PDND = 63/191; SMD = 0.482 [0.189-0.774], p = 0.010; I-2 <0.001%) and NfL (N-PDD/N-PDND = 100/223; SMD = 0.595 [0.346-0.844], p < 0.001; I-2 = 3.4%) were higher in PDD than in PD without dementia. Conclusions: Biofluid markers suggest BBB disruption and neurodegenerative co-pathology involvement in common Lewy body diseases. Greater evidence of BBB breakdown was seen in Lewy body disease with cognitive impairment.
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