Mapping the brain atrophy mediating increased impatience for reward in frontotemporal dementia

Choices involving trade-offs between larger later (LL) and smaller sooner (SS) rewards-known as intertemporal preferences-are altered in many psychiatric and neurodegenerative conditions, leading to a preference for immediate rewards. Behavioural variant frontotemporal dementia (bvFTD), a neurodegenerative disorder characterised by high impulsivity and atrophies in brain systems relevant for decision-making, provides a neuropathological model to investigate structural networks linked to higher impatience for reward. We studied 22 bvFTD patients and 17 controls, using two intertemporal choice (ITC) tasks involving (1) monetary and (2) food rewards. We compared outcomes of these tasks (discount rate and sensitivity to LL reward amounts) between groups and examined correlations with bvFTD symptoms. We applied whole-brain mediation analysis to participants' structural MRI data to identify neural mediators of higher impatience for reward in bvFTD. BvFTD patients showed higher discount rates and lower sensitivity to LL reward for both money and food. These ITC outcomes for money (but not food) were related to inhibition deficits and lower executive functions among patients. Reduced grey matter density in the medial pulvinar and parahippocampal cortex mediated bvFTD's alteration of ITC outcomes. Lesions of these structures involved in emotional salience and projection may constitute neural markers of impatience for reward.

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Publication Details

Journal
Communications Biology
Published
2026-01-09
DOI
https://doi.org/10.1038/s42003-025-09450-5
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Mapping the brain atrophy mediating increased impatience for reward in frontotemporal dementia

Liane Schmidt, Hilke Plaßmann, Anaïs Durand, Richard Levy et al.
Communications Biology
Dementia and Cognitive Impairment Research
article

Mapping the brain atrophy mediating increased impatience for reward in frontotemporal dementia

Liane Schmidt, Hilke Plaßmann, Anaïs Durand, Richard Levy, Bénédicte Batrancourt, Leonie Koban
article en

Abstract

Choices involving trade-offs between larger later (LL) and smaller sooner (SS) rewards-known as intertemporal preferences-are altered in many psychiatric and neurodegenerative conditions, leading to a preference for immediate rewards. Behavioural variant frontotemporal dementia (bvFTD), a neurodegenerative disorder characterised by high impulsivity and atrophies in brain systems relevant for decision-making, provides a neuropathological model to investigate structural networks linked to higher impatience for reward. We studied 22 bvFTD patients and 17 controls, using two intertemporal choice (ITC) tasks involving (1) monetary and (2) food rewards. We compared outcomes of these tasks (discount rate and sensitivity to LL reward amounts) between groups and examined correlations with bvFTD symptoms. We applied whole-brain mediation analysis to participants' structural MRI data to identify neural mediators of higher impatience for reward in bvFTD. BvFTD patients showed higher discount rates and lower sensitivity to LL reward for both money and food. These ITC outcomes for money (but not food) were related to inhibition deficits and lower executive functions among patients. Reduced grey matter density in the medial pulvinar and parahippocampal cortex mediated bvFTD's alteration of ITC outcomes. Lesions of these structures involved in emotional salience and projection may constitute neural markers of impatience for reward.

Communications BiologyVol. 9(1)
Université Claude Bernard Lyon 1 (FR), INSEAD (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Sorbonne Université (FR), Centre de Recherche en Neurosciences de Lyon (FR), Institut du Cerveau (FR), Centre des Sciences du Goût et de l'Alimentation (FR)
Agence Nationale de la Recherche, Fondation pour la Recherche Médicale
Peace, Justice and strong institutions
Openalex Percentile: Top 91%
Dementia and Cognitive Impairment Research
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