Neural substrates of apathy in Parkinson's disease: A systematic review of structural and functional neuroimaging studies
Clinical Snapshot
PICO Framework
| P — Population | Patients with Parkinson's disease with and without apathy, compared to healthy controls |
| I — Intervention | Neuroimaging assessment (structural MRI, functional MRI, DTI, PET/SPECT) |
| C — Comparator | PD patients without apathy and healthy controls |
| O — Outcomes | Neural correlates of apathy including structural, functional, and molecular brain alterations |
Bottom Line
This systematic review identifies consistent involvement of fronto-striatal-limbic networks in apathy among Parkinson's disease patients, with particular alterations in dorsolateral prefrontal cortex, anterior cingulate, and nucleus accumbens. However, significant methodological heterogeneity across the 16 included studies prevents definitive conclusions about a unified neural signature. While the findings advance our understanding of apathy's neurobiological basis in PD, the evidence remains insufficient to guide clinical decision-making or treatment stratification. The review highlights the need for standardized apathy assessment tools and harmonized neuroimaging protocols in future research. Clinicians should continue relying on validated clinical scales for apathy assessment rather than neuroimaging markers, while recognizing that apathy represents a distinct neuropsychiatric syndrome partially dissociable from depression in PD patients.
Key Findings
P Value: Not reported - qualitative synthesis
Effect Size: Not quantified - narrative synthesis only
Primary Outcome: Fronto-striatal-limbic network alterations in apathetic PD patients
Nnt Or Sensitivity: Correlations with apathy severity reported but not quantified across studies
Confidence Interval: Not applicable - no meta-analysis performed
Clinical Application
Limited clinical utility as no unified imaging signature identified for diagnostic or prognostic purposes Relevant for Australian neurologists and psychiatrists managing PD patients, though neuroimaging findings not yet ready for routine clinical application. May inform future research directions in Australian movement disorder centres Parkinson's disease patients presenting with apathy symptoms in movement disorder clinics
Abstract
BACKGROUND: Apathy is a frequent and disabling non-motor symptom in Parkinson's disease (PD), characterized by diminished motivation, reduced goal-directed behavior, and emotional indifference. Growing evidence suggests that apathy in PD represents a distinct neuropsychiatric syndrome that may coexist with depression and global cognitive impairment, while also showing partially dissociable clinical and neural correlates. OBJECTIVE: This systematic review aimed to investigate the neural substrates of apathy in PD by synthesizing evidence from structural and functional neuroimaging studies. METHODS: Following PRISMA guidelines, we searched PubMed, Embase, Web of Science, and Scopus for studies assessing apathy in PD through neuroimaging techniques, including structural MRI, resting-state functional MRI, diffusion tensor imaging, PET/SPECT molecular imaging, and connectivity analyses. Apathy severity was evaluated using validated clinical scales, and findings were compared between PD population with and without apathy, as well as healthy controls. RESULTS: Across 16 heterogeneous studies, recurrent findings implicated structural, functional, and molecular alterations within fronto-striatal-limbic networks. However, differences in apathy measures and neuroimaging modalities limit direct comparability across studies and do not support a single unified imaging signature of apathy in PD. Apathetic PD subjects consistently exhibited reduced gray matter volume and altered spontaneous activity in the dorsolateral, inferior frontal gyri, anterior cingulate cortex (ACC), and nucleus accumbens, alongside disrupted functional and structural connectivity in fronto-limbic tracts. These alterations were significantly correlated with apathy severity and, in several studies, remained detectable after accounting for depressive symptoms or global cognitive status. Furthermore, the available findings suggest that apathy in PD may involve heterogeneous neurobiological mechanisms, including variable involvement of frontal, striatal, and limbic circuits; however, current evidence remains insufficient to support firm transmitter-based subtyping or treatment stratification. CONCLUSIONS: Current evidence suggests that apathy in PD involves partially dissociable neural correlates across prefrontal, striatal, and limbic systems. However, methodological heterogeneity across studies limits strong generalization, and future harmonized longitudinal studies are needed to clarify which findings are robust and clinically meaningful.
References
- 1.Marafioti, G., Culicetto, L., Blundo, C., Susinna, C., Restuccia, G., Di Lorenzo, G., Quartarone, A., & Lo Buono, V. (2026). Neural substrates of apathy in Parkinson's disease: A systematic review of structural and functional neuroimaging studies. Brain Research Bulletin, 111922. https://doi.org/10.1016/j.brainresbull.2026.111922
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