Abstract
Apathy is a highly prevalent and disabling neuropsychiatric syndrome, but its multi-dimensional structure is a challenge for progress towards better identification and treatment. A crucial unresolved question is whether social disengagement reflects a distinct deficit in social motivation or a by-product of diminished initiative or emotional blunting. Previous studies have been constrained by modest sample sizes and limited use of apathy-specific instruments or phenotypically narrow cohorts. Here, we analysed item-level data from 11,243 individuals recruited across multiple centres, including 1154 neurological patients with Alzheimer’s disease, Parkinson’s disease, frontotemporal dementia, autoimmune encephalitis and small vessel disease, alongside people with depression and healthy adults. Across exploratory and confirmatory factor analyses, symptom-level network modelling, and lifespan analyses, social apathy consistently emerged as a coherent and separable dimension. This pattern was preserved across health, psychiatric, and neurocognitive cohorts, from adolescence through late life. Recognising social apathy as an independent domain reframes a central aspect of mental health—the motivation to connect, care, and act for others—and provides a foundation for more precise assessment and for interventions targeting both social and neurobiological mechanisms.
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Acknowledgements
This work was supported by the Wellcome Trust and the National Institute for Health Research (NIHR) Oxford Health Biomedical Research Centre. S.Z., S.T., M.J.B., and M.H. are funded by the Wellcome Trust [226645/Z/22/Z]. S.T., S.G.M. and M.H. are funded by and the NIHR Oxford Health BRC. S.G.M. is also supported by the NIHR Oxford BRC. J.B.R. is supported by the Medical Research Council [MC_UU_00030/14; SUAG/092 G116768], the Wellcome Trust [220258], the NIHR Cambridge Biomedical Research Centre [NIHR203312], and the Holt Fellowship. S.R.I. is supported by a Senior Clinical Fellowship from the Medical Research Council [MR/V007173/1], a Wellcome Trust Fellowship [104079/Z/14/Z], the Kogod Centre on Aging (Mayo Clinic), and the NIHR Oxford Biomedical Research Centre. R.Y. is supported by the National Natural Science Foundation of China [82171917, 82471271, U23A20424], the Anhui Provincial Natural Science Foundation [2408085Y047], and the Natural Science Research Project of Anhui Educational Committee [2023AH050592]. Q.Y.T. was funded by Guangdong and Hong Kong Universities “1 + 1 + 1” Joint Research Collaboration Scheme (2025A0505000011). C.L.H. is supported by a grant from the Canterbury Medical Research Foundation [02/2019]. B.A. is supported by an NIHR Academic Clinical Lectureship. We gratefully acknowledge all the participants, their families, and the staff at the Cognitive Disorders Clinic and the Autoimmune Neurology Clinic at John Radcliffe Hospital, Addenbrooke’s Hospital, St George’s Hospital, the New Zealand Brain Research Institute and the China Parkinson’s Disease Advanced Center for their dedication to this programme. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR, or the Department of Health and Social Care.
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SZ conceptualised and designed the study. MH supervised the project and acquired the funding. Patient recruitment and clinical data collection were carried out by SZ, RY, BA, STo, YS, MAR, PG, MJB, STh, SGM, SRI, YSA, PL, MAJA, PH, KW, JBR, CLH, and MH. SZ performed the formal data analysis and visualisation. QYT contributed proprietary software and analytical tools, and reviewed the analysis scripts. SZ and MH wrote the first draft of the manuscript. All authors reviewed and edited the manuscript, and approved the final submitted version.
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S.R.I. has received honoraria and/or research support from Amgen, Argenx, UCB, Roche, Janssen, IQVIA, Clarivate, Slingshot Insights, Cerebral Therapeutics, BioHaven Therapeutics, CSL Behring, and ONO Pharma. S.R.I. also receives licensed royalties on patent application WO/2010/046716 entitled Neurological Autoimmune Disorders, and has filed two other patents entitled Diagnostic Method and Therapy (WO2019211633; US App 17/051,930; PCT application WO202189788A1) and Biomarkers (WO202189788A1; US App 18/279,624; PCT/GB2022/050614). All other authors declare no competing interests.
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Zhao, S., Ye, R., Tang, QY. et al. The social dimension of apathy: evidence for a distinct domain from 11,243 individuals across health and neurocognitive disorders. Transl Psychiatry (2026). https://doi.org/10.1038/s41398-026-04023-4
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DOI: https://doi.org/10.1038/s41398-026-04023-4