Autism spectrum disorder
Why is cognitive assessment important in autism?
Why is it important to do research in autism?
Individuals with autism spectrum disorder often exhibit cognitive deficits that reflect underlying abnormalities in brain structure and function5,6. Our recommended test battery for research of autism spectrum disorder’s assesses the core domains impaired in ASD, as well as those likely to be affected by novel interventions. Â
The search is on for treatments that can ameliorate the core symptoms of ASD, and cognitive impairment, in order to maximise long-term outcomes and quality of life for affected individuals.Â
What is autism?
Autism is a neurodevelopmental disorder associated with problems with social communication and/or interaction, and occurrences of restricted or repetitive patterns of behaviour, interests, or activities.Â
Autism was previously distinguished from Asperger’s syndrome, but the latest version of the Diagnostic and Statistical Manual (DSM-5) instead uses a broader ‘umbrella’ category of Autism Spectrum Disorder (ASD).Â
The condition affects approximately 1 in every 100 children. It is not fully known what causes autism but it is thought to include a mixture of environmental and genetic factors1.Â
The UK National Institute for Health and Care Excellence (NICE) has a number of guidelines regarding the recognition, diagnosis, and treatment of autism2-4. Generally speaking, people with autism should be supported via a multidisciplinary approach, by people with expertise in the disorder. This can involve support from clinical psychologists, nurses, occupational therapists, psychiatrists, social workers, speech and language therapists, and other support staff.Â
What is ADHD?
Attention-Deficit Hyperactivity Disorder (ADHD), otherwise known as hyperkinetic disorder, is a condition that affects people’s behaviour. ADHD can cause restlessness, trouble concentrating and impulsive behaviour1. For example, children with ADHD may blurt out answers in the classroom, fidget and find it impossible to keep still and struggle to focus on what a person is saying.Â
ADHD is the most common psychiatric disorder of childhood, affecting at least 5% of children globally. Symptoms persist into adulthood in up to 60% of childhood cases2.Â
For a diagnosis of ADHD to be given, the symptoms must be functionally impairing and occur in at least two distinct settings, for example at home and at school.Â
Considerable research has examined the long-term consequences of ADHD, highlighting its global importance for society. In a systematic review of the data, untreated ADHD was associated with poorer long-term outcomes across all categories considered: these included academic performance, job performance and employment status, self-esteem, quality of life, and risk of driving accidents3.Â
ADHD is a treatable psychiatric disorder, with medium to large effect sizes in terms of symptomatic improvement, versus control conditions, over the short-medium term4.Â
ADHD is often misdiagnosed, and is frequently comorbid with other mental (and physical health) disorders. First-line treatment options for ADHD can include consideration of psychotherapy and/or medication, but these should always be offered as part of a comprehensive package of care. The most appropriate treatment options and sequencing of treatment options can vary considerably depending on factors such as the age of the individual, severity of disease, and patient/family preference.Â
Why it is important to do research in ADHD?
The core symptoms of attention deficit disorders are cognitive in nature (inattention, hyperactivity, and/or impulsivity). These cognitive deficits often reflect underlying brain circuitry dysfunction (including prefrontal regions) and of neurochemical transmission, including the dopamine and noradrenaline/norepinephrine pathways5-9. Our recommended test battery for attention deficit disorders assesses the cognitive domains most likely to be impaired, as well as those likely to be affected by interventions.Â
Sample CANTAB test battery for autism
We have developed the cognitive battery listed below as a starting point to aid the discussion between our clinical scientists and the sponsor’s clinical team regarding your specific study protocol, clinical population and the study goals.
The tests in this battery are sensitive to cognitive dysfunction across the spread of disorder severities and across age ranges (childhood, adolescent, and adult ASD)7-10.Â
Endpoints measured
Executive function
Episodic memory
Planning
Processing speed
Key research for CANTAB® in autism spectrum disorders
These tests have been shown to discriminate neuropsychological differences between ASD and other common comorbid conditions, such as Attention-Deficit Hyperactivity Disorder (ADHD) and depression11.Â
Research has demonstrated that the Spatial Working Memory (SWM) test is highly sensitive to cognitive dysfunction in autism, highlighting that deficits in this cognitive process are prevalent within individuals with autism5.Â
Pathology and functional impact of autism spectrum disorders
As with most psychiatric disorders, the causes and brain basis of ASD is not fully understood. Genetic factors are important, with heritability estimates for ASD being 77-99%, higher than for many other prevalent neurodevelopmental disorders13.Â
Environmental factors also play a role in the aetiology of ASD. For example, premature birth and maternal diabetes have been associated with elevated risk of offspring developing ASD14,15 though the causal pathways are unclear. Abnormalities of the cortex and cerebellum, which play key roles in cognition, are commonly reported in ASD compared to healthy controls16.Â
Common findings include excessive brain volumes and other morphological abnormalities in frontal regions and in the amygdala; coupled with lack of sufficient connectivity between brain regions16.Â
Other research into ASD suggests that there are underlying abnormalities in antioxidant capacity and immune function, including changes to immune cells in the central nervous system17. Consistent with underlying brain changes in ASD, studies report a range of cognitive deficits in such individuals18.Â
Further readingÂ
You can find more papers about autism spectrum disorders in our bibliography.Â
Here are some other papers that might be of interest:Â
Kenworthy L., et al (2008). Understanding executive control in autism spectrum disorders in the lab and in the real world. Neuropsychol Rev.Â
Buescher A.V., (2014). Costs of autism spectrum disorders in the United Kingdom and the United States. JAMA Pediatr.Â
Parellada M., (2014). The neurobiology of autism spectrum disorders. Eur Psychiatry.Â
Matsuura N.,et al (2014). Distinguishing between autism spectrum disorder and attention deficit hyperactivity disorder by using behavioral checklists, cognitive assessments, and neuropsychological test battery. Asian J Psychiatr.Â
Ozonoff S., et al (2004). Performance on Cambridge Neuropsychological Test Automated Battery subtests sensitive to frontal lobe function in people with autistic disorder: evidence from the Collaborative Programs of Excellence in Autism network. J Autism Dev Disord.Â
References
- https://www.who.int/news-room/fact-sheets/detail/autism-spectrum-disorders Â
- NICE guidelines [CG128]. Autism diagnosis in children and young people: Recognition, referral and diagnosis of children and young people on the autism spectrum. Published date: September 2011.Â
- NICE quality standard [QS51]. Autism. Published date: January 2014.Â
- NICE guidelines [CG142] Autism: recognition, referral, diagnosis and management of adults on the autism spectrum. Published date: June 2012.Â
- Parellada M, Penzol MJ, Pina L, Moreno C, González-Vioque E, Zalsman G, Arango C. The neurobiology of autism spectrum disorders. Eur Psychiatry. 2014 Jan;29(1):11-9.Â
- Kenworthy L, Yerys BE, Anthony LG, Wallace GL. Understanding executive control in autism spectrum disorders in the lab and in the real world. Neuropsychol Rev. 2008 Dec;18(4):320-38.Â
- Chien YL, Gau SS, Shang CY, Chiu YN, Tsai WC, Wu YY. Visual memory and sustained attention impairment in youths with autism spectrum disorders. Psychol Med. 2015 Aug;45(11):2263-73.Â
- Van Eylen L, Boets B, Steyaert J, Wagemans J, Noens I. Executive functioning in autism spectrum disorders: influence of task and sample characteristics and relation to symptom severity. Eur Child Adolesc Psychiatry. 2015 Feb 20. [Epub ahead of print]Â
- Jiang YV, Capistrano CG, Palm BE. Spatial working memory in children with high-functioning autism: intact configural processing but impaired capacity. J Abnorm Psychol. 2014 Feb;123(1):248-57.Â
- Ozonoff S, Cook I, Coon H, Dawson G, Joseph RM, Klin A, McMahon WM, Minshew N, Munson JA, Pennington BF, Rogers SJ, Spence MA, Tager-Flusberg H, Volkmar FR, Wrathall D. Performance on Cambridge Neuropsychological Test Automated Battery subtests sensitive to frontal lobe function in people with autistic disorder: evidence from the Collaborative Programs of Excellence in Autism network. J Autism Dev Disord. 2004 Apr;34(2):139-50.Â
- Matsuura N, Ishitobi M, Arai S, Kawamura K, Asano M, Inohara K, Narimoto T, Wada Y, Hiratani M, Kosaka H. Distinguishing between autism spectrum disorder and attention deficit hyperactivity disorder by using behavioral checklists, cognitive assessments, and neuropsychological test battery. Asian J Psychiatr. 2014 Dec;12:50-7.Â
- Steele SD, Minshew, NJ, Luna B, Sweeney JA. Spatial working memory deficits in autism. J Autism Dev Disord (2007) 37:605–612 DOI 10.1007/s10803-006-0202-2Â
- Colvert E, Tick B, McEwen F, Stewart C, Curran SR, Woodhouse E, Gillan N, Hallett V, Lietz S, Garnett T, Ronald A, Plomin R, Rijsdijk F, Happé F, Bolton P. Heritability of Autism Spectrum Disorder in a UK Population-Based Twin Sample. JAMA Psychiatry. 2015 May;72(5):415-23.Â
- Pyhälä R, Hovi P, Lahti M, Sammallahti S, Lahti J, Heinonen K, Pesonen AK, Strang-Karlsson S, Eriksson JG, Andersson S, Järvenpää AL, Kajantie E, Räikkönen K. Very low birth weight, infant growth, and autism-spectrum traits in adulthood. Pediatrics. 2014 Dec;134(6):1075-83.Â
- Xu G, Jing J, Bowers K, Liu B, Bao W. Maternal diabetes and the risk of autism spectrum disorders in the offspring: a systematic review and meta-analysis. J Autism Dev Disord. 2014 Apr;44(4):766-75.Â
- Parellada M, Penzol MJ, Pina L, Moreno C, González-Vioque E, Zalsman G, Arango C. The neurobiology of autism spectrum disorders. Eur Psychiatry. 2014 Jan;29(1):11-9.Â
- Mead J, Ashwood P. Evidence supporting an altered immune response in ASD. Immunol Lett. 2015 Jan;163(1):49-55.Â
- Kenworthy L, Yerys BE, Anthony LG, Wallace GL. Understanding executive control in autism spectrum disorders in the lab and in the real world. Neuropsychol Rev. 2008 Dec;18(4):320-38.Â
- Â