Evidence map›Paper›PMID 40164470›Full record

ArticleBMJ mental health2025

Decline in striatal binding ratio associated with accelerated decline in performance on symbol digit modality but not MoCA in Parkinson's Disease Psychosis.

Sara Pisani, Latha Velayudhan, Dag Aarsland, Kallol Ray Chaudhuri, Clive Ballard, Dominic Ffytche, Sagnik Bhattacharyya

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Article in BMJ mental health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Sara PisaniPsychosis Studies, King's College London Institute of Psychiatry Psychology & Neuroscience, London, UK.ORCID 0000-0001-8532-4650
Latha VelayudhanPsychological Medicine, Centre for Healthy Brain Ageing, King's College London Institute of Psychiatry Psychology and Neuroscience, London, UK.
Dag AarslandPsychological Medicine, Centre for Healthy Brain Ageing, King's College London Institute of Psychiatry Psychology and Neuroscience, London, UK.
Kallol Ray ChaudhuriParkinson's Centre of Excellence, Department of Neurology, King's College Hospital NHS Foundation Trust, London, UK.
Clive BallardMedical School, University of Exeter Faculty of Health and Life Sciences, Exeter, UK.
Dominic FfytchePsychological Medicine, Centre for Healthy Brain Ageing, King's College London Institute of Psychiatry Psychology and Neuroscience, London, UK.ORCID 0000-0002-4214-9642
Sagnik BhattacharyyaPsychosis Studies, King's College London Institute of Psychiatry Psychology & Neuroscience, London, UK sagnik.2.bhattacharyya@kcl.ac.uk.

Funding

the National Institute of Health Research (NIHR)
6 · The paper itself

Abstract

backgroundCognitive deficits and reduced dopamine transporter (DAT) binding ratio have been reported in Parkinson's disease psychosis (PDP). However, it remains unclear whether DAT striatal binding ratio (SBR) may contribute to worsening cognitive performance in PDP.

objectivesWe examined this using data from the Parkinson's Progression Markers Initiative.

methodsWe analysed data from 392 PD patients, from baseline to year 4 follow-up, and classified patients into PD with psychosis (PDP) and without psychosis (PDnP). DAT SBR was available from

findingsPDP patients had lower DAT SBR compared with PDnP patients (b=-0.092, p=0.035) over all time points, which remained significant after controlling for age, sex and ethnicity. PDP patients also reported worse trajectory of task performance on the Montreal Cognitive Assessment (MoCA) (b=-0.238, p=0.001) and symbol digit modality (b=-0.534, p=0.016) compared with PDnP patients. Declining performance in symbol digit modality (Group×Time×DAT SBR interaction, b=0.683, p=0.028) but not MoCA was differentially associated with the decline in DAT SBR over time. MoCA scores declined more in PDP compared with PDnP patients over all timepoints (Group×Time interaction, b=-0.284, p=0.016).

conclusionsDecline in striatal presynaptic dopamine function may specifically underlie longitudinal decline in performance in the symbol digit modality task that engages processing speed, associative learning and working memory in PD psychosis. Whether striatal presynaptic dopamine changes explain accelerated longitudinal decline in other cognitive domains in people with PDP remains to be tested.

Indexed as

Cognitive DysfunctionCorpus StriatumDopamine Plasma Membrane Transport ProteinsParkinson DiseasePsychotic DisordersAgedDisease ProgressionFemaleHumansMaleMiddle AgedNeuropsychological TestsTomography, Emission-Computed, Single-PhotonTropanes2-carbomethoxy-8-(3-fluoropropyl)-3-(4-iodophenyl)tropaneDopamine Plasma Membrane Transport ProteinsTropanes

Identifiers

PMID40164470
PMCPMC11962800

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.