2023 Impact Factor
2023 Impact Factor
Apathy is a common symptom in older, cognitively impaired adults. In its first conceptualizations, apathy was described as a “lack of motivation, later evolving into a syndrome with multiple dimensions [1]. An expert panel recently reported revised criteria for apathy [2], defining it as a quantitative reduction of goal-directed activity in comparison to the patient’s previous level of functioning (criterion A). Symptoms must persist for at least four weeks, and affect at least two of the three apathy dimensions (behavior/cognition; emotion; social interaction; criterion B). Apathy should cause identifiable functional impairments (criterion C), and should not be fully explained by other factors, such as effects of a substance or major changes in the patient’s environment (criterion D).
Consistent with this definition, apathy should be differentiated from other common conditions such as depression and its core symptom of anhedonia. In their excellent review, Chong and Husain [3] emphasize that apathy, although debilitating, is consistently distinct from depression and generalized cognitive dysfunction.
As a symptom, the prevalence of apathy in disorders that directly involve the cortex is 60%, and disorders of subcortical structures developing apathy at a 40% rate [4]. It has been described in multiple disorders including Alzheimer’s disease, frontotemporal dementia, Huntington’s disease, major depressive disorder, Parkinson’s Disease, schizophrenia, cerebrovascular disease, traumatic brain injury, and vascular dementia [5]. Moreover, a large population based study of behavioral and psychological symptoms of cognitive impairment found apathy to be highly prevalent at 31.9%. The same study found it to be persistent and disabling [6].
In fact, apathy has been further been associated with functional decline, caregiver burden, increased cost of care due to early institutionalization, and increased mortality [7] . Apathy has also been described in healthy individuals with an estimated prevalence of 1.45% in young subjects with reduced quality of life and behavioral activation [8] and shows patterns of increasing with age, especially in persons above the age of 65 [9].
This review will focus on neurocognitive, biological and clinical aspects of apathy. We will discuss the neuropsychology and associated neurobiological underpinnings of apathy in various pathological conditions, identifiy methods to assess apathy clinically, and review the literature on managing apathy across various disorders.
Apathy has also been described as a failure to generate options for behavior; a diminished ability to select between options that depend on weighing their potential costs and benefits; and an impaired ability to initiate action and to learn from outcomes [10]. Another conceptualization of apathy details it as a multidimensional syndrome reflecting deficits in executive functioning (lack of motivation to plan, organize or sustain attention), emotional functioning (bunting, indifference) and initiation (impaired generation of thoughts) [11]. Throughout the literature, authors have described similar concepts with terms such as “initiative, enthusiasm, emotion” or “Intellectual curiosity, action initiation, self-awareness”, leading up to the consensus criteria included above [11]. Although definitions of apathy and anhedonia can sometimes be conflated, Apathy presents as an overall lack of motivation based on decreased goal-directed behavior or thoughts, as well as affective flattening or indifference. [1]. Indeed, a lack of desire to pursue a reward or pleasure from a reward is common to both apathy and anhedonia, while emotional blunting/indifference is specific to apathy. An anhedonic individual may still consider social relationships as being important despite a lack of drive to pursue them while an apathetic individual no longer finds social relationships to be a valuable endeavor [12]. Another common concept commonly conflated with Apathy and Anhedonia is Alexithymia, which refers to difficulty identifying and describing feelings often linked to functional somatic disorders [13] (Fig. 1).
From a neuroscience perspective, multiple attempts have been made to describe the underlying mechanisms of apathy. It was originally described as a dysfunction in the dopaminergic system leading to lack of motivation [1]. Across various pathologies, apathy seems associated with disruption of medial frontal cortex (Anterior Cingulate Cortex [ACC] and Orbitofrontal Cortex [OFC]), as well as subcortical structures (ventral striatum, medial thalamus, ventral tegmental area), with dorsal anterior cingulate cortex (dACC), and ventral striatum (VS) being the most consistently identified [14]. Other structures linked to apathy in Alzheimer’s disease (both in decreased volume or decreased metabolism on functional magnetic resonance imaging [fMRI]) are the posterior cingulate cortex, the putamen, and the inferior temporal cortex, with a greater association with right-sided compared to left-sided structures [15].
Other regions implicated less consistently in the goal-directed dimension of apathy are the insula, Dorsolateral Prefrontal Cortex (DLPFC), OFC, which are monosynap-tically connected to each other and to the dACC and VS [14]. The dACC-VS circuit seems to have a role in the 3 components of motivation: willingness to initiate an action, to sustain performance of an action, and to learn whether actions are worth performing. The circuit plays a role in giving actions a value, when making a cost-benefit decision [14]. The value ascribed to performing action (reward anticipation) is independent from its “hedonic impact” or “liking” [16], which is deficient in anhedonia, a symptom of depression. Hedonic impact has been linked to activity in the medial orbitofrontal cortex (mOFC) [17] and the ventral striatum, the latter seems to code for positive prediction errors when reward is unexpected [18]. In fact, in studying patients with schizophrenia, Simon et al. concluded that apathy was observed with deficits in anticipatory reward processing (ventral striatum activity). This contrasts with anhedonia, which seems to be linked to a deficit in response to rewarding outcomes (ventral striatum and mOFC activity) [19].
Apathy in depression is a common finding particularly in depression with late-age onset [20]. Late-life depression (LLD) has been associated with several functional neural changes: an increase in metabolism in ventral limbic structures, including the amygdala, the pregenual anterior cingulate, the posterior orbital cortex, and the posterior cingulate and decreased metabolism in dorsal neocortical areas and basal ganglia, including the lateral and dorsolateral cortex, the dorsal anterior cingulate, and caudate nucleus [21].
Compared with elderly controls, older depressed adults showed increased intrinsic connectivity within the frontal parietal network (increased connectivity between superior parietal lobe [SPL] and DLPFC). The SPL appears to be involved in directing attention to visual and tactile stimuli as well as monitoring of internal body representation [22]. DLPFC on the other hand has been shown to have altered activity in preparation to overcome prepotency learning tasks, showing increased activation with increased preparatory demand [23,24]. Hypotheses about this include that older depressed individuals have increased attentional control for internal body states [22].
For patients with LLD, there is also increased intrinsic activity within the sensorimotor network, that is hypothesized to be linked to compensatory mechanisms counteracting cognitive decline [22] and within the default mode network including left precuneus, the subgenual ACC, and lateral parietal regions, the ventromedial prefrontal cortex (vmPFC) [21]. The latter has also been found to have attenuated intrinsic activity, which was positively associated with depression severity and normalized with treatment [25]. In fact, the vmPFC (which includes the orbitofrontal cortex, the rostral cingulate cortex, and the ventral medial frontal gyrus) has been associated with the evaluation and regulation of emotional events and stimuli and the contextual processing of reward. In LLD, there is a decreased response to negative compared with positive stimuli [25]. Others found decreased functional connec-tivity between the regions within the reward network: right nucleus accumbens and the right medial orbitofrontal cortex (mOFC), and between the regions within the attention network, right rostral ACC and bilateral superior frontal gyrus [23].
Apathy is also seen as a common poststroke symptom [26]. In acute stroke, apathy may be the result of functional changes affecting an area involved in apathy generation. Instances of this include strokes in the ACC, striatum, ventral basal ganglia, thalamus and PFC. A remarkable finding in strokes specifically, is that apathy can result from damages to areas outside of those involved in apathy. This is theorized to be the consequence of diaschisis and transneuronal degeneration. Diaschisis is functional impairment due to distant damage to connected other parts of the brain. An example of this is reduced prefrontal hemodynamic response following subcortical, cerebellar and thalamic infarcts. Transneuronal degeneration are structural changes that follow these functional alterations [27]. Studies by Jang et al. [28] show that when left or right caudate lesions led to apathy by secondary lesions to the white matter tracts joining the caudate and prefrontral cortex. Further evidence of the role of white matter tracts in the genesis of apathy is found in Cerebral small vessel disease. Damage to major white matter tracts such as anterior cingulum has been associated with apathy [29]. Whitespread damage to network efficacy seems to follow damage from small vessel disease [30].
In Mild Cognitive Impairment, Apathy is an early symptom and its presence has been linked to rapid progression of symptoms, and a 7-fold increase in the rate of convert-sion to Alzheimer’s disease (AD) [31].
In Alzheimer’s, Apathy is one of the most frequent symptom found on the neuropsychiatric inventory (NPI), with an overall prevalence of 49% [10,32].
A disconnection syndrome involving microalterations of the anterior cingulum (AC) is a proposed mechanism explaining the onset of apathy in AD [33]. The posterior cingulate cortex, the putamen, and the inferior temporal cortex, with a greater association with right-sided compared to left-sided structures are linked to Alzheimer’s both in decreased volume or decreased metabolism on fMRI [15]. As detailed in Nobis and Husain’s [10] excellent review, there was no consensus between studies about the regional atrophy and apathy in Alzheimer’s. Abnormal white matter integrity on the other hand in AD patients has been reported. These white matter changes were found in the corpus callosum, which was also correlated with severity of apathy. Severity of apathy was correlated with loss of integrity of the right superior longitudinal fasciculus, left anterior and posterior cingulum, and bilateral uncinate fasciculus. On beta Amyloid PET imaging, severity of apathy was correlated with beta Amyloid deposition in medial and orbitofrontal areas, insula, and right ACC [10].
In Frontotemporal Dementia, Apathy is especially prevalent in the behavioral variant with a frequency as high as 90.5%. It is the most common neuropsychiatric symptom and is prevalent throughout the course of the illness [7,34]. Apathy has been correlated with changes in the orbitofrontal cortex and anterior cingulate, particularly on the right, with atrophy noted on morphometry MRI in the right lateral orbitofrontal cortex, anterior cingulate [35]. PET studies have shown correlation between apathy and hypometabolism of orbitofrontal cortex and anterior cingulate [36].
In Parkinson’s Disease and Lewy body dementia, the prevalence of apathy has ranged from 17% to 70% and 35% to 100% [37].
The neuroscientific pathways underlying apathy in Parkinson’s Disease pertain to a dopaminergic deficit in the mesocorticolimbic pathway. PET studies show decreased dopamine binding in the Orbitofrontal cortex, amygdala, dorsolateral prefrontal cortex and striatum. When a ligand that binds to both dopamine and noradrenaline transporters was used, the degree of apathy correlated inversely with binding in the ventral striatum. When executive dysfunction predominates in apathy rather than the emotional blunting, lesions affecting this are dorsolateral and ventrolateral prefrontal cortex or the caudate [38].
To diagnose Apathy, the 2018 expert panel recommends the criteria detailed in Table 1.
Because Apathy tends to be subtle and manifest differently, we recommend the use of scales for its assessment and tracking. Choosing the tool used to assess and track severity can vary based on the pathology, the informant (clinician, patient, caretaker) and the symptoms [2]. The supplement to the above consensus criteria contains an excellent and exhaustive repository of all the developed tools. In our experience, the most used tool is the Apathy Evaluation Scale (AES). It is based on Marin’s conceptualiza-tion of apathy, which described a triad of cognition, behavior and emotion. Alternatively, Levy and Dubois identified three apathetic subtypes: cognitive, emotional-affective and auto-activation. The latter component is what distin-guishes it from Marin’s conceptualization [39]. Another widely used too is the dimensional apathy scale which allows for examination and grading of the subtypes above [39]. Although apathy and depression can present with overlapping symptoms, the emotional-affective subtype is different from depression in that its “emotional neutrality” whereas depression has a negative affect [39].
In Parkinson’s, the Lille apathy rating scale (LARS) is a sensitive screen tool capable of distinguishing between apathy and depression [40]. The Apathy-motivation Index (AMI) was adapted from the LARS to assess apathy in healthy people [41].
Apathy can be a devastating symptom for both the patient and their caregivers. Patients with apathy have a lower quality of life, have increased risk of mortality and early institutionalization [4]. Caregivers may view the loss of motivation as volitional or oppositional behavior, leading to additional caregiver distress [42]. Careful and repeated psychoeducation is necessary.
From a non-pharmacological standpoint, although the quality of the evidence varies, several interventions were found to be effective. In their systematic review, Theleritis et al. [43] found evidence for recreational activities derived from the Need-driven dementia-compromised behavior model, live music, Snoezelen (multi-sensory room), reminiscence therapy, and stimulation-retreat model of care, among others. There is a death of evidence for the treatment of isolated apathy in healthy individuals.
There are multiple reports of Selective Serotonin Reuptake Inhibitors (SSRIs) worsening apathy in depression. Yuen et al. [44] found that apathy is a common feature of late-life depression but is a distinct clinical syndrome that is “insufficiently addressed by SSRI alone”. In fact, they found that individuals with structural abnormalities of the posterior subgenual cingulate cortex which connects via the uncinate fasciculus to limbic structures were more likely to show persistence of apathy in geriatric depres-sion. They also found that improvement of apathy with SSRI was independent of change in depression scores. There were no statistically significant worsening of apathy scores in this study, though this may in part due to its limitations [44].
Given the heterogeneity of the presentation, data lacks as to effective treatments in vascular apathy. A study by Moretti et al. [45], found long-term rivastigmine use in subcortical vascular dementia to be tolerable and correlated with stability of cognitive performance and daily function, with improvements in executive function, planning behavior, neuropsychiatric symptoms and social conduct. Although apathy is not specifically mentioned, the above improvements are all components of apathy [45].
Cholinesterase inhibitors have been used for the treatment of Apathy in AD. Evidence for this is lacking as most reviews have found either no or limited evidence of beneficial benefit [10,46]. Promising preliminary results were found when donepezil was combined with the cholinergic precursor choline alphoscerate (versus donepezil alone). It demonstrated significantly lower ratings of apathy after 1 and 2 years in the combined treatment arm compared to donepezil-only [47]. Methylphenidate has also been studied in mild Alzheimer’s disease and was found to improve apathy over 12-weeks. It also improved cognition, functional status, caregiver burden, CGI scores (improvement and severity), and depression [48]. Subse-quent reviews concluded that methylphenidate’s effect was small but significant, though it should be weighed against its significant side effects including high blood pressure, cough and osteoarticular pain [46]. In the Okayama Depression and Apathy Project, patients receiving escitalopram showed significant improvement in GDS score in Alzheimer’s whereas patients receiving sertraline showed improvement in the Apathy Scale [49].
Repetitive Transcranial Magnetic Stimulation (rTMS) targeting frontal lobe dysfunction (abnormal activity in DLPFC, OFC, medial prefrontal cortices [mPFC], anterior cingulate gyrus, and supplementary motor area [SMA]) with 10 Hz on the left DLPFC produced the best effect size in a crossover study conducted with nine subjects with MCI. Improvements in AES-S compared to sham groups were noticed at 2 weeks. They also saw improvements in cognition. Though the sample size was a limiting factor, this study could open the door to further studies to utilize rTMS for the treatment of apathy in MCI [31].
Pramipexole was found to produce significantly lower total apathy scores, especially when compared with ropinirole and L-dopa [50]. Overvliet et al. [51] recommend, based on an extensive review of literature, rivastigmine as a treatment of apathy in patients with Parkinson’s Disease, and pramipexole or selegiline in Parkinson’s Disease patients with apathy without cognitive disturbance. It bears mentioning however that rivastigmine was not effective in controlling apathy in Parkinson’s Disease dementia on a 1-year follow-up [52]. Pagonabarraga and colleagues recommended determining the predominant subdomain of apathy in PD patients may help guide the choice of therapy: dopamine agonists and other dopaminergic drugs, such as methylphenidate, for emotional-affective deficits; AcetylCholinesterase Inhibitors for cognitive deficits; and dopamine agonists for auto-activation deficit [38].
Depression, a very common comorbidity of Parkinson’s Disease, is often treated with SSRIs. SSRIs have been linked to worsening of apathy in Parkinson’s Disease [53]. Serotonin and Norepinephrine Reputake Inhibitors, quetiapine and clozapine were not associated with apathy worsening, while Selegiline and Rasagiline were associated with lower prevalence of apathy [53].
There is limited evidence for the use of Cholinesterase inhibitors in randomized control trials. Evidence for pramipexole is promising, though lacking studies in which apathy is the primary outcome measure.
A small study where agomelatine, an antidepressant with MT1 and MT2 receptor agonism and 5-HT2C receptor antagonism, was compared to melatonin, agomelatine showed significant reduction of apathy scores in patients with FTD, and associated decrease in caregiver distress. Agomelatine presumably leads to an increase in dopaminergic and noradrenergic tone in the prefrontal cortex [54]. Citalopram was associated with a decrease in apathy in a study by Herrmann et al. [55]. Intranasal oxytocin is currently under investigation in a phase 2 trial by Finger et al. [56].
Apathy is a prevalent and debilitating symptom that can occur in several degenerative and non-degenerative pathologies. Its neuroscientific underpinnings involve the dopaminergic system and several cortical and subcortical structures including ACC, OFC, DLPFC, ventral striatum, medial thalamus, ventral tegmental area, among others.
Although recognized as largely treatment resistant, the literature describes several non-pharmacological interventions [43].
From a transdiagnostic lens, pharmacological interventions should be tailored to the apathy subtype identified using the Dimensional Apathy Scale. Pagonabarraga et al. [38] present a reasonable framework to approach psychpharmacology in Apathy. For deficiencies in reward valuation (emotional blunting), dopamine receptor agonists, methylphenidate and bupropion may be used. For deficits in executive dysfunction (decreased interest, cognitive blunting), utilizing acetylcholinesterase inhibitors is recommended. For deficits in autoactivation (lack of self-initiated behaviors which respond to external stimuli), dopamine receptor agonists are indicated [38]. If depression (negative affect, hopelessness, guilt, pessimism) coexists with apathy, non-SSRI antidepressants are recommended as a first line as SSRI may worsen apathy when depressive symptoms are comorbid [38].
No potential conflict of interest relevant to this article was reported.
Conceptualization and Writing: Mario Fahed and David C. Steffens.
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Author ORCID Information Mario Fahed David C. Steffens |
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