# The neurobiology of apathy in depression and neurocognitive impairment in older adults: a review of epidemiological, clinical, neuropsychological and biological research

**Authors:** David C. Steffens, Mario Fahed, Kevin J. Manning, Lihong Wang

PMC · DOI: 10.1038/s41398-022-02292-3 · Translational Psychiatry · 2022-12-26

## TL;DR

Apathy is a common and harmful condition in older adults with depression and cognitive disorders, linked to brain dysfunction and poor health outcomes.

## Contribution

This paper synthesizes current knowledge on apathy's neurobiology and highlights the need for better classification and targeted interventions.

## Key findings

- Apathy is associated with dysfunction in prefrontal brain circuits and executive function impairment.
- Neuroimaging and biomarker studies suggest potential targets for understanding apathy.
- Inconsistent findings may stem from symptom heterogeneity and comorbidities.

## Abstract

Apathy is a common condition that involves diminished initiative, diminished interest and diminished emotional expression or responsiveness. It is highly prevalent in the context of a variety of neuropsychiatric disorders and is related to poor health outcomes. Presence of apathy is associated with cognitive and functional decline in dementia. Despite its negative impact on health, there is no definitive treatment for apathy, a clinical reality that may be due in part to lack of knowledge about assessment, neuropsychological features and neurobiological underpinnings. Here, we review and synthesize evidence from clinical, epidemiological, neuropsychological, peripheral biomarker and neuroimaging research. Apathy is a common feature of depression and cognitive disorders and is associated with impairment in executive function. Neuropsychological and neuroimaging studies point to dysfunction of brain circuitry involving the prefrontal cortex, especially the dorsolateral prefrontal cortex circuit, the dorsomedial prefrontal cortex circuit, and the ventromedial prefrontal cortex circuit. However, inconsistent findings, particularly in neuroimaging may be due to heterogeneity of apathy symptoms (with a need to better elucidate subtypes), neuropsychiatric comorbidities, the severity of cognitive impairment and other factors. These factors need to be accounted for in future studies so that biomarker research can make progress. On the whole, the literature on apathy has identified likely neurocognitive, peripheral biomarker and neuroimaging targets for understanding apathy, but also points to the need to address methodological issues that will better inform future studies. In turn, as we learn more about the underpinning of apathy and its subtypes, subsequent research can focus on new neurally based interventions that will strengthen the clinical management of apathy in the context of its comorbidities.

## Linked entities

- **Diseases:** depression (MONDO:0002050), dementia (MONDO:0001627)

## Full-text entities

- **Genes:** IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, HTR2C (5-hydroxytryptamine receptor 2C) [NCBI Gene 3358] {aka 5-HT1C, 5-HT2C, 5-HTR2C, 5HTR2C, HTR1C}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, BCHE (butyrylcholinesterase) [NCBI Gene 590] {aka BCHED, CHE1, CHE2, E1}, GFAP (glial fibrillary acidic protein) [NCBI Gene 2670] {aka ALXDRD}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}
- **Diseases:** Depressed (MESH:D003866), uncinate fasciculus (MESH:D004833), diminished emotional expression (MESH:D001039), Atrophy (MESH:D001284), executive dysfunction (MESH:D006331), anxiety (MESH:D001007), post-stroke apathy (MESH:D020521), Neurocognitive Disorders (MESH:D019965), hyperlipidemia (MESH:D006949), agitation (MESH:D011595), brain injury (MESH:D001930), impaired concentration and libido (MESH:C567712), Deficit (MESH:D009461), parkinsonism (MESH:D010302), cognitive and functional decline (MESH:D003072), Hyperactivity (MESH:D006948), diminished interest (MESH:D015354), Hypertension (MESH:D006973), Alzheimer's (MESH:D000544), ACC hypoperfusion (MESH:D017034), MCI (MESH:D060825), HIV infection (MESH:D015658), frontostriatal degeneration (MESH:D009410), amnestic (MESH:D000425), Damage (MESH:D020263), leukoaraiosis (MESH:D049292), emotional-affective apathy (MESH:D019964), SOCIAL INTERACTIONLoss (OMIM:300082), subcortical ischemic vascular disease (MESH:D015140), physical disabilities (MESH:D059445), gyrus (MESH:C564353), dopaminergic dysfunction (MESH:D009422), progressive supranuclear palsy (MESH:D013494), neuropsychiatric comorbidities (MESH:C000631768), -C (OMIM:211750), OFC (MESH:D000303), fatigue (MESH:D005221), hallucinations (MESH:D006212), damage to the corpus callosum and (MESH:D061085), VMPFC (MESH:C536329), neurodegenerative diseases (MESH:D019636), intellectual disability (MESH:D008607), blindness (MESH:D001766), major depression (MESH:D003865), PD (MESH:D010300), apathy syndrome (MESH:D013577), cerebrovascular disease (MESH:D002561), emotional blunting (MESH:D014949), frontotemporal lobar degeneration (MESH:D057174), Dementia of Lewy Body (MESH:D020961), decreased interest (MESH:D009123), social isolation (MESH:C565377), thalamic (MESH:D013786), structural damages (MESH:D020914), Behavioral variant-FTD (MESH:D057180), impairments in attention and working memory (MESH:D008569), Diabetes mellitus (MESH:D003920), psychosis (MESH:D011618), Parkinson Disease Dementia (MESH:C537240), grey matter atrophy (MESH:D055652)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

140 references — full list in the complete paper: https://tomesphere.com/paper/PMC9792580/full.md

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Source: https://tomesphere.com/paper/PMC9792580