Prospective Study to Determine the Prevalence of Signs of Central Sensitization in Adults With ASD Without Intellectual Developmental Disorders

Autism is a neurodevelopmental disorder (NDD) characterized by two key features: persistent deficits in communication and social interaction, and restricted, repetitive behaviors, interests, and activities. 95% of children aged 3 to 6 with autism spectrum disorder (ASD) have sensory peculiarities. In adulthood, this figure is estimated to be 90%.. This atypical sensory perception has been included in the diagnostic criteria of the Diagnostic and Statistical Manual of Mental Disorders (DSM) since 2013, and recommendations advocate for sensory assessment (HAS, 2010) as part of treatment. Each sense can be affected by hypo- or hypersensitivity. Pain is now defined by international consensus as an unpleasant sensory and emotional experience, which may or may not be associated with injury. In the continuum of this particular sensory experience, pain can be very present but also difficult to detect and manage. It is now established that there are other characteristics that impact pain in ASD: information processing time may be longer, referred to as "latency time," but there are also difficulties in representing body image and difficulties in identifying and/or interpreting perceptions. The expression of pain may be atypical, with an apparent lack of reaction to pain due to a lack of flexibility. All of these characteristics themselves vary over time, with age, the menstrual cycle, lack of sleep, fatigue, etc., to the point that even pain specialists in pain clinics may not recognize it. It is therefore essential to carry out appropriate and individualized assessments. The scientific literature refers to the high frequency of painful events in ASD. For example, the prevalence of gastrointestinal disorders with associated abdominal pain is significantly higher. Recent research has revealed that 82.4% of children and adolescents with ASD have at least one gastrointestinal symptom. Researchers have found that children with ASD are almost eight times more likely to have one or more chronic gastrointestinal symptoms than typically developing children. In addition, there are more common comorbidities that facilitate or maintain chronic pain : Ehler Danlos syndrome and hypermobility spectrum disorders, IBD, ADHD, post-traumatic stress disorder, depression, migraines and tension headaches, anxiety disorders, epilepsy, small fiber pathologies, nutritional deficiencies, and musculoskeletal disorders. Mutations in certain genes involved in ASD (such as SCN9A, SHANK3, and CNTNAP2) lead to impaired neuronal function, producing different responses to pain, as demonstrated in both mouse and human models. The links between ASD and chronic pain are therefore complex. In some cases, it is the unusual characteristics of the pain that can lead to a diagnosis of ASD. Pain can be nociceptive (due to lesions that stimulate peripheral receptors) or neuropathic (related to a lesion or pathology of the nervous system). A third mechanism of pain is now being discussed, linked to the plasticity of the nervous system, known as nociplastic pain. The concept of central sensitization (CS) underlying this type of pain helps explain the state of painful hypersensitivity and conditions such as fibromyalgia and irritable bowel syndrome. There are close links between these conditions and ASD. Grant et al. in 2022 found that 21% of adults with ASD surveyed in the cohort reported having a diagnosis related to central sensitization syndrome (CSS), but 60% scored 40 or higher, the cut-off point for the Central Sensitization Index, which rates symptoms of CS. These signs of CS are therefore thought to be common and may explain why the prevalence of chronic pain (lasting more than three months) is high in ASD. This suggests that CS symptoms such as pain and fatigue are very common in people with autism and may be more prevalent than in the general population. In comparison, the prevalence of chronic pain in France is estimated at 31.7%. According to Grant et al., autistic women are more likely to report a diagnosis of CFS and exhibit more symptoms of CF than men. Sensory sensitivity, anxiety, age, and gender were significant predictors of CF symptoms, with sensory sensitivity and anxiety modulating the relationship between autistic traits and CF symptoms. Three-quarters of women diagnosed with ASD and/or ADHD in childhood report chronic pain in adulthood. The issue is the disability associated with this chronic pain and the impairment of quality of life. There is no specific tool for assessing nociplastic pain. The Central Sensitization Inventory (CSI) is a self-report questionnaire validated in 2014 by Neblett et al. that attempts to measure central sensitization. The cut-off point was set at 40. In the study by Grant et al., which surveyed adults with ASD without TDI using this tool, the group with SSC had an average score of 55.3 (versus 52.4 in Neblett's cohort), but the group without diagnosed SSC had a score of 40.6 (versus 30.9 in Neblett's cohort). This suggests that pain and fatigue are very common in people on the autism spectrum. They could explain why the prevalence of chronic pain (i.e., lasting more than 3 months) is high in ASD and why the nociplastic nature of this pain must be taken into account. On the other hand, there is a FIRST self-administered questionnaire for fibromyalgia that allows for simple screening for this condition, which is at the top of the list of CSDs. Finally, as Grant et al. Investigator investigate the relationship between autistic traits and central sensitization syndromes by studying the correlation with the 10-item Autism Spectrum Quotient (AQ) and the relationship between sensory perception and central sensitization syndromes by studying the correlation with the Sensory Perception Quotient (SPQ) and SSC. Chronic pain is common in ASD, and its nociplastic nature is poorly understood. In this context, the objective of this study is to determine the prevalence of signs of central sensitization in adults with ASD (without intellectual developmental disorder).