CoChat
Sign Up
Cited by 380Neural and Behavioral Psychology StudiesNeurotransmitter Receptor Influence on BehaviorDementia and Cognitive Impairment Research

The DOI matches its Crossref record; 163 of the 168 references it cites were found in a registry or an index.

The anatomy of apathy: A neurocognitive framework for amotivated behaviour

Open access
Le Heron, C., Apps., M.A.J., Husain, M.·2018·Neuropsychologia
DOI 10.1016/j.neuropsychologia.2017.07.003PMC PMC6200857
Open this paper in CoChat — free accountOpen PDF

Abstract

Apathy is a debilitating syndrome associated with many neurological disorders, including several common neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease, and focal lesion syndromes such as stroke. Here, we review neuroimaging studies to identify anatomical correlates of apathy, across brain disorders. Our analysis reveals that apathy is strongly associated with disruption particularly of dorsal anterior cingulate cortex (dACC), ventral striatum (VS) and connected brain regions. Remarkably, these changes are consistent across clinical disorders and imaging modalities. Review of the neuroimaging findings allows us to develop a neurocognitive framework to consider potential mechanisms underlying apathy. According to this perspective, an interconnected group of brain regions - with dACC and VS at its core - plays a crucial role in normal motivated behaviour. Specifically we argue that motivated behaviour requires a willingness to work, to keep working, and to learn what is worth working for. We propose that deficits in any one or more of these processes can lead to the clinical syndrome of apathy, and outline specific approaches to test this hypothesis. A richer neurobiological understanding of the mechanisms underlying apathy should ultimately facilitate development of effective therapies for this disabling condition.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1016/j.neuropsychologia.2017.07.003

Cites

163 of 163 references verified0 citation errors · 0 not checkable

Statistics

Figures

Fig. 1 A reciprocally connected network of brain regions for normal motivated behaviour. A network of medial frontal and striatal regions has been strongly implicated in the generation of motivated behaviour in healthy people. Disruption of components of – or connections between – this network is strongly associated with apathy across brain disorders. The dorsal anterior cingulate cortex (dACC) encompasses the anterior cingulate sulcus (Brodmann area 24c & 32). Here medial prefrontal cortex refers to ventromedial prefrontal and orbitofrontal cortex, two anatomically overlapping regions (particularly Brodmann areas 10, 11 and 47) – see Neubert et al. (2015) for a detailed anatomical description.
Fig. 1 A reciprocally connected network of brain regions for normal motivated behaviour. A network of medial frontal and striatal regions has been strongly implicated in the generation of motivated behaviour in healthy people. Disruption of components of – or connections between – this network is strongly associated with apathy across brain disorders. The dorsal anterior cingulate cortex (dACC) encompasses the anterior cingulate sulcus (Brodmann area 24c & 32). Here medial prefrontal cortex refers to ventromedial prefrontal and orbitofrontal cortex, two anatomically overlapping regions (particularly Brodmann areas 10, 11 and 47) – see Neubert et al. (2015) for a detailed anatomical description.CC BY · PubMed Central
Fig. 2 Decreased metabolism within right ventral striatum is associated with greater increase in apathy scores following deep brain stimulation surgery.
Fig. 2 Decreased metabolism within right ventral striatum is associated with greater increase in apathy scores following deep brain stimulation surgery.CC BY · PubMed Central
Fig. 3 Brain regions in which reduced metabolism was associated with apathy, in a mixed group of patients with dementia (a). A disjunction analysis (controlling for other behavioural disturbances associated with altered metabolism) revealed apathy was specifically associated with hypometabolism in the region of the VTA (b).
Fig. 3 Brain regions in which reduced metabolism was associated with apathy, in a mixed group of patients with dementia (a). A disjunction analysis (controlling for other behavioural disturbances associated with altered metabolism) revealed apathy was specifically associated with hypometabolism in the region of the VTA (b).CC BY · PubMed Central
Fig. 4 Consistent anatomical associations with apathy across imaging modalities and underlying disorders. Changes affecting dorsal anterior cingulate cortex and ventral striatum are particularly prominent (a). A connected system of brain areas consistently associated with apathy, which form an interconnected network within the medial forebrain (b). dACC – dorsal anterior cingulate cortex; mPFC – medial prefrontal cortex; VTA – ventral tegmental area; VS – ventral striatum; VP – ventral pallidum. Images (from top left) adapted with permissions from: (Huang et al., 2013, Robert et al., 2014, Schroeter et al., 2011; Migneco et al., 2001, Remy et al., 2005, Stanton et al., 2013; Baggio et al., 2015, Bruen et al., 2008, Carriere et al., 2014; Hollocks et al., 2015, Marshall et al., 2007, Ota et al., 2012).
Fig. 4 Consistent anatomical associations with apathy across imaging modalities and underlying disorders. Changes affecting dorsal anterior cingulate cortex and ventral striatum are particularly prominent (a). A connected system of brain areas consistently associated with apathy, which form an interconnected network within the medial forebrain (b). dACC – dorsal anterior cingulate cortex; mPFC – medial prefrontal cortex; VTA – ventral tegmental area; VS – ventral striatum; VP – ventral pallidum. Images (from top left) adapted with permissions from: (Huang et al., 2013, Robert et al., 2014, Schroeter et al., 2011; Migneco et al., 2001, Remy et al., 2005, Stanton et al., 2013; Baggio et al., 2015, Bruen et al., 2008, Carriere et al., 2014; Hollocks et al., 2015, Marshall et al., 2007, Ota et al., 2012).CC BY · PubMed Central
Fig. 5 Importance of ACC and VS for motivated behaviour. Effort based decision making. Lesions to ACC, VS or crossed ACC/VS disconnection lesions (pictured) cause rodents to choose more low effort/low reward options, without altering their preference for high rewards options if effort costs are equal (a) (from Hauber and Sommer, 2009). Single neurons within macaque ACC modulate firing rates to the net value of a choice (reward – effort) (b) (from Kennerley et al., 2009). BOLD activity within human ACC signals the subjective value of a choice (reward – effort), whether the cost is physical or cognitive (c) (from Chong et al., 2017) Modulating behavior to foreground and background environment characteristics. BOLD activity correlates with the value of foraging (switching from current option), rather than the value of the actual chosen option (d – left panel) (from Kolling et al., 2012). Single neuronal recordings from the ACC of macaques performing a patch leaving foraging task show earlier increases in firing rate on trials where the animal leaves the patch faster (d – right panel) (from Hayden et al., 2011b) Sustaining behavior towards a goal. Recordings from rodent VS show ramping dopamine signals as the animal approaches a rewarding outcome, thought to drive persistence of behaviour towards the goal (e) (from Howe et al., 2013) Monitoring outcomes of actions. ACC and VS activity encodes information on both reward and effort magnitudes during the outcome phase of an action (f) (from Scholl et al., 2015) (all figures reproduced with permissions).
Fig. 5 Importance of ACC and VS for motivated behaviour. Effort based decision making. Lesions to ACC, VS or crossed ACC/VS disconnection lesions (pictured) cause rodents to choose more low effort/low reward options, without altering their preference for high rewards options if effort costs are equal (a) (from Hauber and Sommer, 2009). Single neurons within macaque ACC modulate firing rates to the net value of a choice (reward – effort) (b) (from Kennerley et al., 2009). BOLD activity within human ACC signals the subjective value of a choice (reward – effort), whether the cost is physical or cognitive (c) (from Chong et al., 2017) Modulating behavior to foreground and background environment characteristics. BOLD activity correlates with the value of foraging (switching from current option), rather than the value of the actual chosen option (d – left panel) (from Kolling et al., 2012). Single neuronal recordings from the ACC of macaques performing a patch leaving foraging task show earlier increases in firing rate on trials where the animal leaves the patch faster (d – right panel) (from Hayden et al., 2011b) Sustaining behavior towards a goal. Recordings from rodent VS show ramping dopamine signals as the animal approaches a rewarding outcome, thought to drive persistence of behaviour towards the goal (e) (from Howe et al., 2013) Monitoring outcomes of actions. ACC and VS activity encodes information on both reward and effort magnitudes during the outcome phase of an action (f) (from Scholl et al., 2015) (all figures reproduced with permissions).CC BY · PubMed Central
Fig. 6 Level of functional connectivity between dorsal ACC (yellow-orange) and supplementary motor area (purple) predicts behavioural apathy scores in healthy subjects (higher score corresponds to greater apathy traits) (fromBonnelle et al., 2016with permission).
Fig. 6 Level of functional connectivity between dorsal ACC (yellow-orange) and supplementary motor area (purple) predicts behavioural apathy scores in healthy subjects (higher score corresponds to greater apathy traits) (fromBonnelle et al., 2016with permission).CC BY · PubMed Central

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 168 references

Research works printed but not linked: 1

  1. Mori, 2006, Principles of diffusion tensor imaging and its applications to basic neuroscience research, Neuron, 51, 527, 10.1016/j.neuron.2006.08.012 · DOI · Paper page

Cited by

Sorted by citations

Items 101–200 of 351

Metadata

Authors
Le Heron, C., Apps., M. A. J., & Husain, M.
Venue
Neuropsychologia
Publisher
Elsevier BV
Published
2018-09
Volume
118
Issue
Pt B
Pages
54-67
ISSN
0028-3932 (ISSN-L)
DOI
10.1016/j.neuropsychologia.2017.07.003
PMC
PMC6200857
OpenAlex
W2726746745
Cited by
380
References
168
Citations by year
2026: 44 · 2025: 43 · 2024: 55 · 2023: 48 · 2022: 55 · 2021: 50 · 2020: 38 · 2019: 20 · 2018: 21
FWCI
13.34
Type
journal article
Language
en
Open access
Licence
Locations
  • Neuropsychologia (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • University of Birmingham Research Portal (University of Birmingham) (submittedVersion)
Funders
  • University of Oxford Christopher Welch Scholarship in Biological Sciences
  • University of Oxford Clarendon Scholarship
  • Green Templeton College Partnership award (GAF1415_CB2_ MSD_758342)
  • Biotechnology and Biological Sciences Research Council AFL Fellowship (BB/M013596/1)
  • Wellcome Trust (098282)
Topics
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
Keywords
apathy, motivated behavior, dorsal anterior cingulate cortex, ventral striatum, neurodegenerative diseases, Parkinson's disease, Alzheimer's disease, stroke, neuroimaging correlates, willingness to work
MeSH terms
Brain, Brain Mapping, Humans, Motivation, Apathy, Neuroimaging

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review