Association between choroid plexus volume and cognition in Parkinson disease

Author:

Jeong Seong Ho12ORCID,Jeong Hyun‐Jae3,Sunwoo Mun Kyung4,Ahn Sung Soo5,Lee Seung‐Koo5,Lee Phil Hyu2,Kim Yun Joong267,Sohn Young H.2,Park Chae Jung8,Chung Seok Jong267ORCID

Affiliation:

1. Department of Neurology Inje University Sanggye Paik Hospital Seoul Korea

2. Department of Neurology Yonsei University College of Medicine Seoul Korea

3. Research Institute of Center for Clinical Imaging Data Science Yonsei University College of Medicine Seoul Korea

4. Department of Neurology Bundang Jesaeng General Hospital Seongnam‐si Korea

5. Department of Radiology, Severance Hospital, Research Institute of Radiological Science and Centre for Clinical Imaging Data Science Yonsei University College of Medicine Seoul Korea

6. Department of Neurology, Yongin Severance Hospital Yonsei University Health System Yongin Korea

7. YONSEI BEYOND LAB Yongin Korea

8. Department of Radiology, Yongin Severance Hospital Yonsei University Health System Yongin Korea

Abstract

AbstractBackground and purposeThe choroid plexus (CP) clears harmful metabolites from the central nervous system as part of the glymphatic system. We investigated the association of CP volume (CPV) with baseline and longitudinal cognitive decline in patients with Parkinson disease (PD).MethodsWe retrospectively reviewed the medical records of 240 patients with newly diagnosed PD who had undergone detailed neuropsychological tests and high‐resolution T1‐weighted structural magnetic resonance imaging during the initial assessment. The CPV of each patient was automatically segmented, and the intracranial volume ratio was used in subsequent analyses. The relationship between CPV and baseline composite scores of each cognitive domain was assessed using multivariate linear regression analyses. A Cox proportional hazards model was used to compare the risk of dementia conversion with CPV.ResultsCPV negatively correlated with composite scores of the frontal/executive function domain (β = −0.375, p = 0.002) after adjusting for age, sex, years of education, and parkinsonian symptom duration. The Cox regression model revealed that a larger CPV was associated with a higher risk of dementia conversion (hazard ratio [HR] = 1.509, p = 0.038), which was no longer significant after adjusting for the composite scores of the frontal/executive function domain. A mediation analysis demonstrated that the effect of CPV on the risk of dementia conversion was completely mediated by frontal/executive function (direct effect: HR = 1.203, p = 0.396; indirect effect: HR = 1.400, p = 0.015).ConclusionsBaseline CPV is associated with baseline frontal/executive function, which subsequently influences dementia conversion risk in patients with PD.

Funder

Korea Health Industry Development Institute

National Research Foundation of Korea

Yonsei University College of Medicine

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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