Neurodivergent Children Are Twice as Likely To Experience Chronic Disabling Fatigue
New research shows that children with neurodivergent traits are twice as likely to experience chronic fatigue by age 18.
Complete the form below to unlock access to ALL audio articles.
A groundbreaking study led by researchers in the Department of Neuroscience at Brighton and Sussex Medical School (BSMS) and funded by the Medical Research Council (MRC) has found that children who exhibit neurodivergent traits, such as those associated with autism and ADHD, are twice as likely to experience chronic disabling fatigue by age 18.
The research, led by Dr Lisa Quadt, Research Fellow in Psychiatry at BSMS and Dr Jessica Eccles, Reader in Brain-Body Medicine at BSMS, highlights a significant link between neurodivergence and chronic fatigue.
The study found that increased inflammation in childhood, often resulting from heightened stress levels, may be a contributing factor. This supports previous findings that suggest chronic fatigue can be rooted in inflammatory processes.
“These results show the importance of trans-diagnostic screening for children and the need for better support for neurodivergent children” says Dr Quadt. “Children with neurodivergent traits, diagnosed or not, often experience heightened stress, which is likely one reason for their increased inflammatory levels. Our study indicates that this may be a risk factor for developing chronic disabling fatigue, which dramatically decreases quality of life.”
Want more breaking news?
Subscribe to Technology Networks’ daily newsletter, delivering breaking science news straight to your inbox every day.
Subscribe for FREEThe study's findings advocate for better screening practices and enhanced support systems for neurodivergent children to mitigate the risk of chronic fatigue and improve overall quality of life.
Reference: Quadt L, Csecs J, Bond R, et al. Childhood neurodivergent traits, inflammation and chronic disabling fatigue in adolescence: a longitudinal case–control study. BMJ Open. 2024;14(7):e084203. doi: 10.1136/bmjopen-2024-084203
This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source. Our press release publishing policy can be accessed here.