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. 2022;269(1):93-111.
doi: 10.1016/bs.pbr.2022.01.003. Epub 2022 Feb 9.

Cognition in prodromal Parkinson's disease

Affiliations

Cognition in prodromal Parkinson's disease

Inga Liepelt-Scarfone et al. Prog Brain Res. 2022.

Abstract

One characteristic of Parkinson's disease (PD) is a prodromal phase, lasting many years during which both pre-clinical motor and non-motor symptoms occur. Around one-fifth of patients with PD manifest mild cognitive impairment at time of clinical diagnosis. Thus, important challenges are to define the time of onset of cognitive dysfunction in the prodromal phase of PD, and to define its co-occurrence with other specific characteristics. Evidence for cognitive change in prodromal PD comes from various study designs, including both longitudinal and cross-sectional approaches with different target groups. These studies support the concept that changes in global cognitive function and alterations in executive functions occur, and that these changes may be present up to 6 years before clinical PD diagnosis. Notably, this evidence led to including global cognitive impairment as an independent prodromal marker in the recently updated research criteria of the Movement Disorder Society for prodromal PD. Knowledge in this field, however, is still at its beginning, and evidence is sparse about many aspects of this topic. Further longitudinal studies including standardized assessments of global and domain-specific cognitive functions are needed to gain further knowledge about the first appearance, the course, and the interaction of cognitive deficits with other non-motor symptoms in prodromal stage PD. Treatment approaches, including non-pharmacological interventions, in individuals with prodromal PD might help to prevent or delay cognitive dysfunction in early PD.

Keywords: Cognition; Early detection; Executive function; Memory; Neuropsychological assessment; Parkinson's disease; Prodromal.

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Conflict of interest statement

Disclosures ILS reports unrestricted research grant from Janssen Research and Development, a division of Janssen Pharmaceutica N·V unrelated to the present work. AO has no conflicts of interest to declare; EK received grants from the German Ministry of Education and Research, Parkinson Fonds Deutschland gGmbH, the German Parkinson Society; honoraria from: Oticon GmbH, Hamburg, Germany; Lilly Pharma GmbH, Bad Homburg, Germany; Bernafon AG, Bern, Switzerland; Desitin GmbH, Hamburg, Germany; unrelated to the present work.

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