Introduction
Around 450,000 adults in the UK have a diagnosis of an Autism Spectrum Disorder (ASD) and a growing awareness of the disorder in adulthood has increased the demand for diagnostic services in adulthood (Howlin and Taylor
2015). Diagnosis in adulthood is reflected in recent changes to diagnostic criteria, notably, the removal of the criterion of a specific early age onset (American Psychiatric Association
2013). The increased demand for referrals and this diagnostic change present challenges for clinicians striving to deliver evidence-based assessments in a time-limited environment, and for researchers seeking to better understand the nature of adult ASD and associated difficulties (Russell et al.
2016; Scottish Autism Strategy
2011). In assessment settings, psychometric tools that have been standardised in the general population may provide meaningful information to clinicians who aim to develop a clear profile of the strengths and challenges that are faced by adults who are seeking a first-time ASD diagnosis (Bolte et al.
2011; Dell’Osso et al.
2016).
Changes in diagnostic criteria in ASD sit alongside a growing interest in dimensional approaches to diagnosis within development and psychopathology (Hudziak et al.
2007; Jalbrzikowski et al.
2017; Owen
2014). This shift from a categorical to a dimensional approach may represent a better fit with clinical practice, whereby diagnostic assessments tend to involve developing an individual profile of strengths and difficulties relating to social-communication and cognitive abilities in ASD (National Research Council
2001). Dimensional formulations of ASD have proposed that key traits of behaviour and ability exist in all individuals along a continuum (e.g. Skuse et al.
2004). In this conceptualisation, behaviour associated with ASD is proposed to sit at an ‘extreme’ end of a continuous distribution of multiple dimensions of autistic traits (Kamp-Becker et al.
2010). For example, the empathising–systemising (ES) framework was developed to capture the thinking style associated with ASD, while emphasising that these traits are also present to a greater or lesser extent in the typical population (Baron-Cohen
2009). This framework addresses the social and non-social features of ASD by highlighting variation in empathetic responding (i.e., differences or difficulties with responding emotionally to another person’s thoughts or feelings), alongside intact or superior skills in systemising (i.e. a drive to analyse, understand, predict, control and construct rule-based systems; see Baron-Cohen
2009).
Empathy reflects a degree of perspective taking to recognise another person’s emotion and to make relevant social inferences and appropriate emotional responses (Baez and Ibanez
2014). Empirical studies provide extensive support for a social-cognitive difference in ASD, that is most evident for individuals with increased severity of symptoms and developmental delay (review by Hadwin and Kovshoff
2015). For example, research has demonstrated difficulties in individuals with ASD in identifying others’ thoughts, (e.g. Wellman et al.
2001), recognising social faux pas (e.g. Baron-Cohen et al.
1999), and understanding non-literal expressions such as metaphors, sarcasm and lies (e.g. Kaland et al.
2002). While adults with average or above average intellectual functioning usually succeed in relatively simple social-cognitive tasks, research has demonstrated particular difficulties in advanced social-cognitive abilities. These can include, for example, understanding what one person thinks about another person’s thoughts, understanding non-literal expressions, and understanding the beliefs, intentions and meanings of indirect remarks or sarcasm (e.g. Mathersul et al.
2013).
Social-cognitive differences in individuals diagnosed with ASD are suggested to account for challenges linked to social adaptability observed in daily life, including difficulty initiating and sustaining friendships, making socially inappropriate comments, or misunderstanding social cues (e.g. Peterson et al.
2009). Further research has investigated the proposition that adults with ASD who do not have an intellectual impairment report or experience fewer social challenges and may learn and engage in social skills through logic and reasoning. Livingston and Happé (
2017), for example, describe this process as “socially adapted behaviour” that may be “achieved via overt and conscious strategies, despite core socio-cognitive abilities, such as theory of mind, remaining impaired” (p. 733). In an earlier paper, Hofvander et al. (
2009) proposed that the motivation to develop coping strategies to ‘mask’ autistic traits could stem from childhood negative experiences associated with not ‘fitting in’.
Early social experiences may lead to a type of “camouflaging” (Lai and Baron-Cohen
2015, p. 1013) that reflects observational learning of how to act in a social setting, using social rules and scripts, and that is underpinned by intellectual ability. The notion of camouflaging may be especially pronounced in adults with undetected ASD, who may reveal challenges in social adaptation via self-report, and where any difficulty is not immediately apparent from observation (Lai et al.
2011). This framework suggests that while core symptoms of ASD are present, they may be masked by learned strategies and/or may not become evident until social demands become increasingly complex and effortful. Researchers have further recognised that learned strategies create particular challenges in recognising ASD in adults, where difficulties in social-communication may go unnoticed without further exploration (Lai and Baron-Cohen
2015).
While a large body of research has aimed to understand the strengths and challenges of children and young people referred for an ASD assessment, research that has focused on adults who seek referral is sparse. An increasing number of adults being referred for or requesting an ASD diagnosis has led to calls for more understanding of this population, with the longer term goal of increasing quality of life and well-being (Howlin and Taylor
2015).
The present study aimed to extend current research to explore the social-cognitive profile of a population of individuals who were referred by their general practitioner to a specialist service for an ASD diagnostic assessment in adulthood and whose diagnosis, as part of this referral process, was confirmed or disconfirmed. The study investigated key social skills, including emotion recognition (recognising and labelling emotions from dynamic social scenes) and social inference (the ability to interpret conversational remarks meant literally or non-literally and to make judgments about the thoughts, intentions and feelings of others). Furthermore, it considered autism, empathy and systemising traits in diagnosed and non-diagnosed adults. It aimed to consider whether these dimensional traits differentiated group membership and were important in understanding any differences in the social-cognitive profiles in this population of adults. We utilised a measure of cognitive ability to establish that diagnostic groups were similarly matched. By building a profile of the relative strengths and challenges of adults diagnosed with ASD in adulthood, we aimed to inform the development of support and professional services that work to promote a better quality of life for this population.
Discussion
This study explored social cognition of adults referred to a diagnostic service for an ASD assessment in adulthood. We considered the social-cognitive profile between adults whose ASD diagnosis was confirmed versus those where the diagnosis was not confirmed. In addition, we explored whether individual differences in empathy, as well as autism and systemising traits, were important in explaining emotion understanding and social inference in the two diagnostic groups. The results showed that adults in the ASD diagnosis confirmed group reported more autism traits and fewer empathic skills, compared to adults whose diagnosis was not confirmed. There was a marginal (but not statistically significant) group difference in systemising traits, with the ASD diagnosed group endorsing a greater number. Moreover, fewer self-reported empathic skills were found to be important in mediating social-cognitive differences between diagnostic groups. The results suggest that underpinning empathy differences between diagnostic groups was important in understanding individual differences in emotion understanding.
Consistent with the empathising–systemising theory (Baron-Cohen
2009), the current findings indicated that adults referred for assessment and who received a diagnosis of ASD presented with relative strengths in systemising, alongside poorer empathic skills. Baron-Cohen and Wheelwright (
2004) argued that empathy is a core skill that facilitates effective social interaction, and that underpins the development of social relationships and prosocial behaviour. Consequently, lower empathic ability may reflect less social adaptability (e.g., relationship or friendship difficulties/breakdown), and may be a key factor in understanding reasons for referral in adulthood (Sasson et al.
2013). Geurts and Jansen (
2011) identified that social difficulties were one of the most common reasons for referral to an ASD assessment service, and the current findings suggest that these challenges may arise from difficulties in empathising associated with social interaction. This finding is consistent with recent work in the general population, where social difficulties mediated the relationship between autistic traits and income level (Skylark and Baron-Cohen
2017).
Some researchers have suggested that a diagnosis of ASD in adulthood is associated with fewer autistic traits (e.g. Seltzer et al.
2004), in addition to individuals showing average or above average intellectual functioning (e.g. Aggarwal and Angus
2015). The current study showed that most adults across the sample showed cognitive abilities within a typical range. In addition, cognitive ability was not different between diagnostic groups, but the number of adults endorsing autism traits was greater in the ASD diagnosed group. Clinicians familiar with a particular profile of strengths and deficits in social-cognition, typically seen in ASD, may miss this different presentation in adults seeking first-time diagnosis. NICE guidelines (
2012) endorse the use of self-report measures of autistic traits and empathising ability to aid the complex task of assessment and diagnosis of adults. Consistently, researchers have also supported the use of dimensional measures of cognitive and social functioning in addition to an ASD diagnosis (e.g., Volkmar et al.
2009). The current study supports the exploration of traits using the AQ and EQ screening measures as part of a comprehensive assessment in adults who present for an ASD diagnosis in adulthood.
Although an ASD diagnosis was not directly associated with emotion understanding, lower empathic skills were found to help explain the profile of social-cognitive difficulties for individuals referred for an ASD assessment in adulthood. This finding highlights the important role of understanding dimensional ASD traits, rather than a diagnostic category alone, in interpreting social functioning. An implication is that clinicians should be aware that measures assessing social-cognition may not be sensitive enough to detect difficulties in functioning for adults seeking first-time diagnosis. The findings fit with the proposition of compensation in adult ASD and where adults living with ASD can show intact cognitive ability and good social reasoning skills, but where underpinning psychological constructs are less evident (see Lai and Baron-Cohen
2015; Livingstone and Happé
2017). Consistently, adults diagnosed with ASD in adulthood (versus childhood) have reported that their higher cognitive ability enabled them to use logical reasoning to overcome their difficulties in social functioning (Lovett
2005). This camouflaging of autistic behaviours causes challenges for clinicians attempting to explore the social presentation typically associated with ASD (Bastiaansen et al.
2011), not withstanding the difficulties autistic individuals themselves report experiencing as a function of effortfully masking autistic traits to ‘fit in’ (Hull et al.
2017). Given the potential increased risk for stress, negative impact on self-esteem and exhaustion for adults using these strategies, camouflaging should be neither expected nor encouraged as an intervention (Lai et al.
2011; Hull et al.
2017).
The findings of the current study indicate that adults who receive a diagnosis of ASD in adulthood may welcome an opportunity to develop social skills and where the focus is on empathic processing. A recent review of empathy focused interventions for health professionals indicated that it is possible to enhance empathic skills in adults to increase their social-cognitive understanding via empathic processes utilising role play, video and discussion (Kiosses et al.
2016). Future research should aim to understand if opportunities to explore the role of empathy in the context of social-cognition would be acceptable or beneficial for adults referred for a diagnosis of ASD. In addition, further studies are required to understand the extent to which empathic processes are sensitive to change via intervention programmes.
Alongside possible opportunities to enhance the skills of the person with autism, more emphasis has recently been placed on creating a better ‘person-environment’ fit (Lai and Baron-Cohen
2015). In this case, the focus is on how social contexts react to autistic people. This approach reflects the ‘double empathy problem’, which acknowledges the challenges individuals with autism face in processing and understanding other people, but also highlights that non-autistic individuals need to work harder to understand autistic individuals (Milton
2018). This framework suggests that there is a mutual and reciprocal misunderstanding of both parties, due to experiencing the world in very different ways. Specifically, Milton (
2018) proposes that targets for intervention and further research should focus on empowering individuals with autism, to fostering an understanding and appreciation of their world view, and to bridge the ‘double-empathy gap’ by developing shared interactional expertise.
There are several limitations to this study. Studies to compare diagnosed and nondiagnosed adults who have been referred for assessment in adulthood are sparse; therefore, the findings require independent replication. Given the substantial heterogeneity within ASD, and the focus of the present study on adults with no recorded intellectual disability, one caveat is whether the results from this subgroup of adults will generalise to individuals diagnosed with ASD more broadly. A further limitation of the present study design was that historical information was not obtained for the referred sample about previous diagnoses, referrals or assessments.
Despite these limitations, the study has strength in the large sample size, wide age-range of adults, use of a clinical population, and the clinical relevance of the findings. This novel study addresses the call for real-world research and contributes to furthering our dimensional understanding of the strengths and challenges for adults seeking first-time ASD diagnosis.