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Distinct Subtypes of Apathy Revealed by the Apathy Motivation Index

Yuen-Siang Ang, Patricia Lockwood, Matthew A. J. Apps and 2 more

PLOS ONE · 2017 · CC BY

doi:10.1371/journal.pone.0169938

Abstract

Apathy is a debilitating but poorly understood disorder characterized by a reduction in motivation. As well as being associated with several brain disorders, apathy is also prevalent in varying degrees in healthy people. Whilst many tools have been developed to assess levels of apathy in clinical disorders, surprisingly there are no measures of apathy suitable for healthy people. Moreover, although apathy is commonly comorbid with symptoms of depression, anhedonia and fatigue, how and why these symptoms are associated is unclear. Here we developed the Apathy-Motivation Index (AMI), a brief self-report index of apathy and motivation. Using exploratory factor analysis (in a sample of 505 people), and then confirmatory analysis (in a different set of 479 individuals), we identified subtypes of apathy in behavioural, social and emotional domains. Latent profile analyses showed four different profiles of apathy that were associated with varying levels of depression, anhedonia and fatigue. The AMI is a novel and reliable measure of individual differences in apathy and might provide a useful means of probing different mechanisms underlying sub-clinical lack of motivation in otherwise healthy individuals. Moreover, associations between apathy and comorbid states may be reflective of problems in different emotional, social and behavioural domains.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 20, 2026. Paragraph numbers are ours, so an answer can point at one.

Introduction

Apathy is a disorder of motivation characterised by reduced action initiation and goal-directed behaviour. Although it often occurs in several neurological and psychiatric disorders, it is also apparent to varying degrees in healthy people. A lack of motivation can significantly affect everyday life, particularly in education and employment opportunities. Theoretical accounts have proposed that apathy is a multidimensional construct which actually covers motivation within dissociable domains: cognitive, emotional/affective and behavioural. Self-report and clinician administered measures have now been developed to characterise apathy in clinical samples based on this multidimensional construct (Lille Apathy Rating Scale, Dimensional Apathy Scale). However, currently there are no validated assessments of apathy in healthy people. As a result, the mechanisms underlying variability in apathy are still poorly understood. It is also unknown whether different domains of apathy can be identified in healthy people, and whether they might be dissociable across individuals.

Whilst apathy is a common syndrome associated with altered motivation, it is also frequently comorbid with other states which may have symptoms of reduced motivation, particularly depression, anhedonia and fatigue. This raises the question of the extent to which apathy can be meaningfully distinguished from these other conditions and whether they might perhaps be associated with discrete dimensions of apathy in healthy individuals.

In clinical disorders such as Parkinson’s disease (PD), it is now established that apathy is frequently linked to depression, with many overlapping symptoms including loss of interest and lack of initiative. However, there is also evidence that apathy and depression may be separable, particularly in the domain of affect. Thus anhedonia, or loss in pleasure derived from activities one used to enjoy, is correlated with apathy in PD and items used in the assessment of both symptoms are often overlapping. Recently fatigue—the feeling of exhaustion caused by the exertion of effort, which is unrelated to actual exertion of energy by muscles—has also been shown to associate with apathy in clinical disorders such as PD and multiple sclerosis. However, despite the evidence of links between apathy and depression, anhedonia and fatigue in neurological conditions, it remains to be established whether there are similar specific links in the healthy population. Furthermore, are these different symptoms associated with distinct profiles of apathy in healthy people?

Here, we adapted the Lille Apathy Rating Scale (LARS), a tool first developed to measure apathy in PD, to produce and validate a novel measure to assess and dissect the profile of apathy in healthy people: the Apathy Motivation Index (AMI). Using the most rigorous psychometric procedures, we then dissected out the different factors that comprise the AMI and determined whether depression, anhedonia and fatigue are related to distinct profiles of apathy. We hypothesized that, after developing our new index, we would identify distinct subtypes of apathy in the general population and that these subtypes would be differentially associated with depression, anhedonia and fatigue.

Participants

505 people (211 males, 271 females, 23 gender undisclosed, mean age = 28.7 years, SD = 14.9, range = 16–85, N = 27 age undisclosed), recruited from the local communities via online adverts and posters, completed a preliminary 51-item scale. All participants gave written informed consent and the study was approved by the University of Oxford ethics committee. Methods were carried out in accordance with the relevant guidelines and regulations.

Procedure

Our initial item validation was adapted from the LARS. To create a comparable measure suitable for the general population, a team of clinical neurologists and university researchers developed, based on their experience with clinically apathetic patients, novel items to specifically reflect each domain of the LARS. Items from the clinical LARS that were deemed to be applicable to healthy people were also adapted. This gave rise to a preliminary 51-item scale. Participants were asked to self-rate each item on a five-point Likert scale by deciding how true that statement was based on the past two weeks of their life. The scale ranged from 0–4 (with 0 = ‘completely untrue’, 4 = ‘completely true’). An “N/A” option was also available for items that were not applicable. Each item was reverse-scored so that a higher rating indicated more apathy.

Data analysis

An exploratory factor analysis (EFA) with promax rotation was conducted in MPlus to examine the latent structure of this 51-item apathy questionnaire. The exploratory-derived solutions were assessed by scree plot and two absolute fit indices: Root Mean Square Error of Approximation (RMSEA) and Standardised Root Mean Square Residual (SRMR). A value of RMSEA and SRMR less than 0.08 is generally considered to be reasonable.

Results

A simple three-factor structure was the most parsimonious account of the data. This structure had good model fit (RMSEA = 0.051 with 90% CI of 0.048–0.053, SRMR = 0.05) and was supported by scree plot, which showed the characteristic “elbow” or plateau in eigenvalues after 3 factors. After the EFA, twenty-one items were excluded, as their loadings were less than 0.40.

Item reduction

Next, the six highest loading items for each factor were retained to form a revised 18-item Apathy-Motivation Index (AMI). These three factors were labelled according to their common themes as (1) behavioural activation (BA): tendency to self-initiate goal-directed behaviour (e.g. I get things done when they need to be done, without requiring reminders from others), (2) social motivation (SM): level of engagement in social interactions (e.g. I start conversations without being prompted), and (3) emotional sensitivity (ES): feelings of positive and negative affection (e.g. I feel awful if I say something insensitive). Each of the six questions for the three subscales is shown in Table 1. The factor loadings for each subscale were good (BA: 0.56–0.75; SM: 0.54–0.66; ES: 0.46–0.78).

Participants

Data from a new group of 479 people recruited via online adverts and Prolific Academic (www.prolific.ac) was used for the analysis (for demographic information see Table 2). Exclusion criteria were self-reported neurological or psychiatric disorder. All participants gave electronic informed consent and the study was approved by the University of Oxford ethics committee. 63 of these participants also completed the AMI a second time between 6–8 days after initial completion to assess test-retest reliability.

Procedure

Participants completed the AMI to confirm the proposed three-factor structure. In addition, they were also asked to complete a set of established related measures to assess construct validity, noted below. Descriptive statistics of these additional measures are provided in Table 3.

Apathy Evaluation Scale (AES)

The AES is an 18-item scale that measures apathy as a single construct. Each item was scored on a 4-point Likert scale, with a higher total score indicating greater apathy (1–4: 1 = ‘very true’, 4 = ‘not true at all’ for positively scored items).

Dimensional Apathy Scale (DAS)

The DAS is a 24-item scale that assesses apathy on three different subscales, namely executive, emotional and behavioural/cognitive initiation. Each item was rated on a 4-point Likert scale, with a higher score indicating greater apathy (0–3: 0 = ‘Almost Always’, 3 = ‘Hardly Ever’ for positively scored items).

Beck’s Depression Inventory (BDI)

The BDI is 21-item scale that measures the severity of depression. Each item relates to a symptom of depression, e.g., hopelessness, and was scored on a 4-point Likert scale (0–3: 0 = least severe, 3 = most severe). A higher total score indicates greater depression.

Snaith Hamilton Pleasure Scale (SHAPS)

The SHAPS is a 14-item scale that assesses hedonic tone, or ability to experience pleasure. While responses were made on a 4-point scale, for simplicity, Snaith et al. scored each item in a binary manner (0–1: 0 = either ‘Strongly Agree’ or ‘Agree’, 1 = either ‘Strongly Disagree’ or ‘Disagree’). We followed Pluck and Brown and Franken et al. and scored responses using a 4-point Likert-style instead (1–4: 1 = ‘Strongly Disagree’, 4 = ‘Strongly Agree’) with higher scores reflecting greater hedonic tone. Conversely, lower scores indicated higher levels of anhedonia.

Modified Fatigue Impact Scale (MFIS)

The MFIS is a 21-item scale that measures how fatigue affects daily life, with each item being rated on a 5-point Likert scale (0–4: 0 = ‘Never’, 4 = ‘Almost Always’). A higher score indicates a greater impact of fatigue on the individual.

Data analysis

A confirmatory factor analysis (CFA) was conducted in MPlus. Model fit was assessed using RMSEA, SRMR, and Comparative Fit Index (CFI). While a CFI of at least 0.90 is normally taken to indicate an acceptable model, it should be noted that this index calculates the fit difference between a null independence model (i.e. zero correlation between all observed variables) and the hypothesized model. This means that for a model with low item inter-correlations, the CFI may be lowered even if it describes the data adequately. Thus, it has been suggested that in the event of substantial low item inter-correlations, the CFI criterion could be relaxed to > 0.80. Approximately 65% of the inter-correlations in our data were low (< 0.20), hence, we adopted the relaxed CFI cut-off of 0.80 while ensuring that the cut-offs for RMSEA and SRMR were < 0.08.

Results

The three-factor structure of the 18-item AMI (Table 1) was confirmed, and had good model fit indices (RMSEA = 0.076 with 90% CI of 0.068–0.083, SRMR = 0.071, CFI = 0.83). This model is schematically illustrated in Fig 1. Each item on the AMI was scored from 0–4, with a higher score indicating greater apathy. We propose cut-offs for moderate and severe apathy on the AMI to be respectively > 1 S.D. and > 2 S.D. above the mean (Table 4). While SM correlated significantly with BA and ES components of motivation, BA did not correlate significantly with ES. (**: p < 0.01).

To assess internal reliability, Cronbach’s coefficient alpha values were calculated for both the total score and subscales. They showed adequate values, indicating acceptable internal consistency (αoverall = 0.77, αBA = 0.79, αSM = 0.75, αES = 0.75). Test-retest reliability coefficients for the scale and subscales were also satisfactory, indicating stable responses across time (roverall: 0.83, rBA: 0.88, rSM: 0.84, rES: 0.72).

To examine construct validity, correlational analyses between the overall and subscale scores of the AMI and other related measures were conducted. The Benjamini and Hochberg method was used to control for false discovery on multiple comparisons. We briefly summarize key correlational results here in text (details in Table 5 and Fig 2). AMI total score showed positive correlations with existing assessments of apathy: DAS total (r = 0.62, p < 0.01) and AES (r = 0.61, p < 0.01). It was also positively associated with the BDI (ρ = 0.26, p < 0.01) and MFIS total (r = 0.19, p < 0.01). Finally, the AMI total score was negatively correlated with the SHAPS (r = - 0.46, p < 0.01), indicating that apathetic people experience greater anhedonia. Overall, these findings indicated that the AMI had good construct validity.

Participants

Participants were the same as in Study 2.

Data analysis procedure

To examine whether we could identify distinct profiles of apathy and how these are differentially predictive of comorbid states (depression, anhedonia and fatigue), we conducted a latent profile analysis (LPA) using the data acquired in study 2. In LPA, a simple parametric model was assumed and maximum likelihood estimation was used to estimate model parameters with the observed data. This allowed us to define the classes. Each individual’s probability of class membership was also estimated together with the overall model so that they can be placed into the appropriate class.

We investigated models with one to five classes and determined the optimal number of classes for our sample with several statistical indicators. The Lo-Mendell-Rubin Adjusted Likelihood Ratio Test (LMRT) and Bootstrapped Likelihood Ratio Test (BLRT) compares the fit of the current model with K classes to one with K-1 classes. A small p-value (< 0.05) indicates that the solution with K classes fit better. The Akaike Information Criterion (AIC) and sample-size adjusted Bayesian Information Criterion (sBIC) are descriptive fit indices with lower values indicating more optimal model fit.

Results

The 4-class model was the most appropriate (Table 6). By iteratively comparing models one class apart (i.e. 1- versus 2-class, then 2- versus 3-class etc.) with the LMRT and BLRT p-values, we found the 4-class model had the best fit. Furthermore, the 4- and 5-class models had the lowest AIC and BIC values.

To interpret each class, we compared the conditional response means with the overall sample means on each AMI subscale (Table 7, Fig 3). We then labelled these classes according to their profile on apathy subtypes:

Class 1 consisted of 57 individuals (11.9%) and was labelled “emotionally apathetic” as their mean ES subscale score was higher than that of the overall sample mean.

Class 2 contained 121 individuals (25.3%) and was labelled “behaviourally/socially apathetic” due to a higher mean BA and SM subscale score than the overall sample mean.

All conditional response means for Class 3 were lower than the overall sample means, thus, we referred to this class of 291 individuals (60.8%) as “generally motivated”.

Class 4 consisted 10 individuals (2.1%) who had substantially higher conditional response means than the overall sample means on every subscale. Accordingly, they were referred to as “generally apathetic”.

ANOVA was used to examine differences among the four apathy-motivation subtypes on independent measures of depression, anhedonia and fatigue (Fig 4). Significant differences were found between classes for all three measures (BDI: F(3,475) = 14.7, p < 0.001; SHAPS: F(3,475) = 29.9, p < 0.001; MFIS: F(3,475) = 8.63, p < 0.001).

Post-hoc comparisons showed that the behaviourally/socially apathetic class were significantly more depressed and fatigued than the emotionally apathetic and generally motivated classes. The generally motivated class also experienced greater fatigue than the emotionally apathetic class (Fig 4A and 4C). For anhedonia, the generally motivated class experienced more pleasure than each of the other classes. The emotionally apathetic people were also more hedonic than the generally apathetic class (Fig 4B).

All post-hoc comparison differences were significant at p < 0.05 (Emotionally apathetic: BDI mean = 8.0, SD = 8.8, SHAPS mean = 47.6, SD = 5.6, MFIS mean = 20.9, SD = 14.0; Behaviourally/socially apathetic: BDI mean = 16.2, SD = 11.8, SHAPS mean = 45.7, SD = 5.8, MFIS mean = 34.9, SD = 17.6; Generally motivated: BDI mean = 9.7, SD = 9.0, SHAPS mean = 50.4, SD = 4.9, MFIS mean = 29.3, SD = 17.3; Generally apathetic: BDI mean = 12.8, SD = 13.0, SHAPS mean = 42.3, SD = 6.6, MFIS mean = 29.3, SD = 26.7). Together, these results suggest that different subtypes of apathy are differentially predictive of depression, anhedonia and fatigue.

Discussion

Here we developed the Apathy Motivation Index (AMI; Table 1), a new instrument suitable for assessing levels of apathy and motivation in the healthy population. Results of factor analyses—both exploratory (EFA) and confirmatory (CFA)–in large samples indicated that the AMI has a clear three-factor structure with good psychometric properties. We also showed for the first time that different subtypes of apathy are predictive of different associations with depression, anhedonia and fatigue in healthy people (Fig 4).

We identified three domains of apathy, namely behavioural activation (BA), emotional sensitivity (ES) and social motivation (SM). The BA subscale focused on the individual’s tendency to self-initiate goal-directed behaviour. This appears to relate closely to Stuss's executive process of ‘energization’ or the initiating and maintaining of task-relevant responses. By contrast, the ES subscale contained items that probe an individual’s feelings of positive and negative affection, which seems similar to the emotional blunting often observed in some patients with apathy. We also found that these two subscales were not significantly correlated, suggesting some dissociation between behavioural and emotional aspects of apathy.

Comparing these two subscales to the conceptualisation of apathy by Levy and Dubois suggests that the BA subscale likely encompasses the ‘cognitive’ and ‘auto-activation’ aspects, while the ES domain appears to correspond more to the ‘emotional-affective’ subtype. This is supported by positive associations found between the AMI BA subscale with DAS (Dimensional Apathy Scale) executive and behavioural/cognitive initiation but not the emotional subscale. Conversely, the AMI ES subscale was correlated with the DAS emotional subscale but not behavioural/cognitive initiation subscale.

The SM subscale contained items that examine a person’s engagement in social interactions. Impaired social life was highlighted by Sockeel et al. as a domain of apathy during the development of the LARS, although it is not specified within other cognitive-behaviour-emotion frameworks of apathy. We observed that the AMI SM was correlated with both the BA and ES subscales. It also correlated positively with all three subscales of the DAS. This suggests that although separate factors of SM, BA and ES comprise apathy there is also some degree of shared variance between items assessing SM with BA and ES (Fig 1).

As expected, the AMI correlated with established assessments of apathy, depression, anhedonia and fatigue, providing evidence of good construct validity (Table 5). Rather than discuss every individual association between the scale/subscales, we highlight key findings here. Distinguishing apathy from depression is challenging due to the overlaps in symptoms, e.g., lack of initiation. Nonetheless, it is recognised that apathy may be characterised by emotional blunting whereas depression is an affective disorder featured by extreme emotional fluctuations. In support of this, we observed that while the AMI BA and SM subscales correlated positively with the BDI, the ES subscale was negatively associated.

Anhedonia is a mood disorder characterised by an inability to derive pleasure. It has long been established that positive reinforcement is essential to maintain goal-directed behaviour. Given this relationship between motivation and reward, we predicted that anhedonia and apathy would be linked. In support, we found that all subscales of the AMI were related to the SHAPS. Our finding suggests that apathy and anhedonia have a close relationship in the general population, with those individuals characterised by higher levels of apathy also more likely to report experiencing anhedonia. However, these measures were not perfectly correlated suggesting that there are also unique aspects of anhedonia not related to apathy.

Fatigue can be a symptom of reduced motivation characterised by the lack of energy to perform actions. Although similar in symptomology to apathy, few studies have investigated their relationship. We observed that the AMI BA and SM subscales associated positively with all subscales of the MFIS (namely physical, cognitive and psychosocial). Conversely, the ES subscale correlated negatively with these MFIS domains. These observations suggest that there is a partial overlap between apathy and fatigue. Specifically, while individuals who were behaviourally and/or socially more apathetic were likely to be more fatigued, people who were emotionally apathetic experienced less fatigue in general. Thus, there is also dissociation between fatigue and subtypes of apathy.

By using latent profile analysis (LPA) to group individuals with similar AMI profiles, we identified four subtypes of apathy-motivation in our healthy people (Table 7; Fig 3). Most people (60.8%) were identified as ‘generally motivated’ with their group average on each AMI subscale being lower than the overall mean. A small number (2.1%), on the other hand, scored higher than the global mean on all AMI subscales. Thus, these individuals were classified as ‘generally apathetic’. The other subtypes were labelled ‘emotionally apathetic’ (11.9%) and ‘behaviourally/socially apathetic’ (25.3%) as they had a lower average score than overall only on that/those particular AMI subscale(s).

Intriguingly, these different apathy subtypes were predictive of different associations with depression, anhedonia and fatigue. People identified as ‘behaviourally/socially apathetic’ were significantly more depressed and fatigued than people who were ‘emotionally apathetic’ or ‘generally motivated’. In addition, individuals who were ‘emotionally apathetic’, ‘behaviourally/socially apathetic’ or ‘generally apathetic’ were significantly more anhedonic than those who were ‘generally motivated’. These results indicated that the four apathy subtypes were distinct and overlapped differently with the closely related outcomes of depression, anhedonia and fatigue. Moreover, having high levels of behavioural and social apathy are more associated with other negative states, whereas experiencing emotional apathy on its own may not be associated with higher levels of depression and fatigue.

Conclusion

The AMI is a reliable instrument suitable for assessing apathy and motivation in the healthy population and in clinical disorders. The findings presented here show for the first time that apathy in the healthy population can be dissected into four subtypes: ‘emotionally apathetic’, ‘behaviourally/socially apathetic’, ‘generally motivated’ and ‘generally apathetic’. These classes showed different propensities for depression, anhedonia and fatigue. Our data suggest that there may be particular subtypes of apathy that are more likely to co-occur with these symptoms. Future longitudinal studies would benefit from investigating how particular profiles of apathy are risk factors for the development of depression, anhedonia and fatigue.

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    Not in our library10.1038/nn1579

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