Nuclear Imaging Data‐Driven Classification of Parkinson's Disease

Author:

Totsune Tomoko12,Baba Toru1,Sugimura Yoko13,Oizumi Hideki1,Tanaka Hiroyasu1,Takahashi Toshiaki1,Yoshioka Masaru1,Nagamatsu Ken‐ichi4,Takeda Atsushi13ORCID

Affiliation:

1. Department of Neurology National Hospital Organization Sendai‐Nishitaga Hospital Sendai Japan

2. Department of Aging Research and Geriatric Medicine, Institute of Development, Aging and Cancer Tohoku University Sendai Japan

3. Department of Cognitive & Motor Aging Tohoku University Graduate School of Medicine Sendai Japan

4. Department of Neurosurgery National Hospital Organization Sendai‐Nishitaga Hospital Sendai Japan

Abstract

ABSTRACTBACKGROUNDParkinson's disease (PD) is a heterogeneous neurodegenerative disorder characterized by motor and nonmotor symptoms. Several features have prognostic importance and have been used as key indicators for identifying clinical subtypes. However, the symptom‐based classification approach has limitations with respect to the stability of the obtained subtypes.OBJECTIVESThe purpose of this study was to identify subtypes of PD using nuclear imaging biomarkers targeting the cardiac sympathetic nervous and nigro‐striatal systems and to compare patterns of cortical morphological change among obtained subtypes.METHODSWe performed unbiased hierarchical cluster analysis using 123I‐metaiodobenzylguanidine cardiac scintigraphy and 123I‐N‐(3‐fluoropropyl)‐2β‐carbomethoxy‐3β‐(4‐iodophenyl) nortropane single photon emission computed tomography data for 56 patients with PD. We compared clinical characteristics and the patterns of cortical atrophy in the obtained clusters.RESULTSThree clusters were identified and showed distinct characteristics in onset ages and dopamine‐replacement therapy and deep brain stimulation requirements. According to the characteristics, clusters were classified into two subtypes, namely, “cardio‐cortical impairment (CC)” and “dopaminergic‐dominant dysfunction (DD)” subtype. The three clusters were named according to subtype and time since onset in which 14 patients were classified as “early DD,” 25 as “advanced DD,” and 17 as “early CC.” Compared with the early DD subtype, the early CC subtype showed parietal‐dominant diffuse cortical atrophy and the advanced DD subtype showed left‐side predominant mild cortical atrophy.CONCLUSIONSNuclear imaging biomarker–based classification can be used to identify clinically and pathologically relevant PD subtypes with distinct disease trajectories. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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