Hippocampal Perfusion Affects Motor and Cognitive Functions in Parkinson Disease: An Early Phase 18F‐FP‐CIT Positron Emission Tomography Study

Author:

Chun Min Young123ORCID,Chung Seok Jong123ORCID,Kim Su Hong456,Park Chan Wook17,Jeong Seong Ho18ORCID,Lee Hye Sun9,Lee Phil Hyu1ORCID,Sohn Young H.1,Jeong Yong451011ORCID,Kim Yun Joong123

Affiliation:

1. Department of Neurology Yonsei University College of Medicine Seoul South Korea

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

3. Yonsei Beyond Lab Yongin South Korea

4. Graduate School of Medical Science and Engineering Korea Advanced Institute of Science and Technology Daejeon South Korea

5. Institute for Health Science Technology Korea Advanced Institute of Science and Technology Daejeon South Korea

6. Department of Radiology Yeungnam University College of Medicine Daegu South Korea

7. Department of Physiology Yonsei University College of Medicine Seoul South Korea

8. Department of Neurology Inje University Sanggye Paik Hospital Seoul South Korea

9. Biostatistics Collaboration Unit Yonsei University College of Medicine Seoul South Korea

10. Program of Brain and Cognitive Engineering Korea Advanced Institute of Science and Technology Daejeon South Korea

11. Department of Bio and Brain Engineering Korea Advanced Institute of Science and Technology Daejeon South Korea

Abstract

ObjectiveWe investigated whether hippocampal perfusion changes are associated with cognitive decline, motor deficits, and the risk of dementia conversion in patients with Parkinson disease (PD).MethodsWe recruited patients with newly diagnosed and nonmedicated PD and healthy participants who underwent dual phase 18F‐N‐(3‐fluoropropyl)‐2β‐carboxymethoxy‐3β‐(4‐iodophenyl) nortropane positron emission tomography scans. Patients were classified into 3 groups according to hippocampal perfusion measured by standard uptake value ratios (SUVRs): (1) PD hippocampal hypoperfusion group (1 standard deviation [SD] below the mean hippocampal SUVR of healthy controls; PD‐hippo‐hypo), (2) PD hippocampal hyperperfusion group (1 SD above the mean; PD‐hippo‐hyper), and (3) the remaining patients (PD‐hippo‐normal). We compared the baseline cognitive performance, severity of motor deficits, hippocampal volume, striatal dopamine transporter (DAT) availability, and risk of dementia conversion among the groups.ResultsWe included 235 patients (PD‐hippo‐hypo, n = 21; PD‐hippo‐normal, n = 157; PD‐hippo‐hyper, n = 57) and 48 healthy participants. Patients in the PD‐hippo‐hypo group were older and had smaller hippocampal volumes than those in the other PD groups. The PD‐hippo‐hypo group showed less severely decreased DAT availability in the putamen than the other groups despite similar severities of motor deficit. The PD‐hippo‐hypo group had a higher risk of dementia conversion compared to the PD‐hippo‐normal (hazard ratio = 2.59, p = 0.013) and PD‐hippo‐hyper (hazard ratio = 3.73, p = 0.006) groups, despite similar cognitive performance at initial assessment between groups.InterpretationHippocampal hypoperfusion may indicate a reduced capacity to cope with neurodegenerative processes in terms of the development of motor deficits and cognitive decline in patients with PD. ANN NEUROL 2024;95:388–399

Funder

Korea Health Industry Development Institute

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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