Different impulse control disorder evolution patterns and white matter microstructural damage in the progression of Parkinson’s disease

Author:

Hu Ling,Lin Changfu,Lin Fabin,Wang Lingling,Li Zhenzhen,Cai Zhijun,Liu Xianghong,Ye Qinyong,Wu Yiwen,Cai Guoen

Abstract

BackgroundThe course of impulse control disorders (ICD) varies in the early stage of Parkinson’s disease (PD).AimWe aimed to delineate the association between the evolution pattern of ICD and the progression of PD.MethodsA total of 321 de novo PD patients from the Parkinson’s Progression Markers Initiative database were included. Patients were followed up for a mean of 6.8 years and were classified into different groups according to the evolution patterns of ICD. Disease progression was compared among groups using survival analysis, in which the endpoint was defined as progression to Hoehn and Yahr stage 3 or higher for motor progression and progression to mild cognitive impairment for cognitive decline. In the fourth year of follow-up, four types of ICD evolution patterns were identified: (1) non-ICD-stable (68.2%), a patient who is consistently free of ICD; (2) late-ICD (14.6%), ICD developed during the follow-up of patients; (3) ICD-stable (11.5%), patients showed persistent ICD; and (4) ICD-reversion (5.6%), baseline ICD disappeared during the follow-up of patients with ICD.ResultsThe ICD-reversion type shows daily life non-motor symptoms [Movement Disorder Society-Unified Parkinson Disease Rating Scale (MDS-UPDRS) part I], daily life motor symptoms (MDS-UPDRS part II), rapid eye movement sleep behavior disorder, and anxiety symptoms has a greater impact. PD patients with different ICD evolution patterns had different changes in white matter microstructure at the onset of the disease. Those relevant brain regions are involved in ICD and non-motor functions.ConclusionFour early ICD evolution patterns are identified in de novo PD, with different prognoses and brain white matter microstructural damage patterns, and they may predict motor progression and cognitive decline in PD patients.

Publisher

Frontiers Media SA

Subject

Cognitive Neuroscience,Aging

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