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Progression of Neuropsychiatric Symptoms over Time in an Incident Parkinson's Disease Cohort (ICICLE-PD).
Dlay, J K; Duncan, G W; Khoo, T K; Williams-Gray, C H; Breen, D P; Barker, R A; Burn, D J; Lawson, R A; Yarnall, A J.
Afiliação
  • Dlay JK; Institute of Neuroscience, Newcastle University, Newcastle upon Tyne NE4 5PL, UK.
  • Duncan GW; Institute of Neuroscience, Newcastle University, Newcastle upon Tyne NE4 5PL, UK.
  • Khoo TK; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh EH16 4SB, UK.
  • Williams-Gray CH; School of Medicine and Menzies Health Institute Queensland, Griffith University, Gold Coast 4222, Australia.
  • Breen DP; School of Medicine, University of Wollongong, New South Wales 2522, Australia.
  • Barker RA; John van Geest Centre for Brain Repair, University of Cambridge, Cambridge CB2 0PY, UK.
  • Burn DJ; Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh EH16 4SB, UK.
  • Lawson RA; Anne Rowling Regenerative Neurology Clinic, University of Edinburgh, Edinburgh EH16 4SB, UK.
  • Yarnall AJ; Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh EH16 4UX, UK.
Brain Sci ; 10(2)2020 Feb 02.
Article em En | MEDLINE | ID: mdl-32024222
ABSTRACT

BACKGROUND:

Cross-sectional studies have identified that the prevalence of neuropsychiatric symptoms (NPS) in Parkinson's disease (PD) ranges from 70-89%. However, there are few longitudinal studies determining the impact of NPS on quality of life (QoL) in PD patients and their caregivers. We seek to determine the progression of NPS in early PD.

METHODS:

Newly diagnosed idiopathic PD cases (n = 212) and age-matched controls (n = 99) were recruited into a longitudinal study. NPS were assessed using the Neuropsychiatric Inventory with Caregiver Distress scale (NPI-D). Further neuropsychological and clinical assessments were completed by participants, with reassessment at 18 and 36 months. Linear mixed-effects modelling determined factors associated with NPI-D and QoL over 36 months.

RESULTS:

Depression, anxiety, apathy and hallucinations were more frequent in PD than controls at all time points (p < 0.05). Higher motor severity at baseline was associated with worsening NPI-D scores over time (ß = 0.1, p < 0.05), but not cognition. A higher NPI total score was associated with poorer QoL at any time point (ß = 0.3, p < 0.001), but not changed in QoL scores.

CONCLUSION:

NPS are significantly associated with poorer QoL, even in early PD. Screening for NPS from diagnosis may allow efficient delivery of better support and treatment to patients and their families.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article