Scientists based at the University of Warwick, UK have developed tests that can indicate autism in children.
The researchers believe that the new blood and urine tests, which search for damage to proteins, are the first of their kind. The tests could lead to earlier detection of autism spectrum disorders (ASD) and consequently much earlier treatment.
Currently there is no biological test for autism. Diagnosis relies on assessing a wide range of ASD symptoms and can be difficult and uncertain, particularly at the early stages of development.
Thehas been published in the journal Molecular Autism. The team was led by Dr Naila Rabbani, Reader of Experimental Systems Biology at the University of Warwick. Dr Rabbani said:
Our discovery could lead to earlier diagnosis and intervention. We hope the tests will also reveal new causative factors. With further testing we may reveal specific plasma and urinary profiles or “fingerprints” of compounds with damaging modifications. This may help us improve the diagnosis of ASD and point the way to new causes of ASD.
The team, which is based at the University’s Warwick Medical School, involves academics at the University of Warwick’s Warwick Systems Biology group, the University of Birmingham, the University of Bologna, the Institute of Neurological Sciences, Bologna, and the Don Carlo Gnocchi Foundation ONLUS.
They found a link between ASD and damage to proteins in blood plasma by oxidation and glycation — processes where reactive oxygen species (ROS) and sugar molecules spontaneously modify proteins. They found the most reliable of the tests they developed was examining protein in blood plasma where, when tested, children with ASD were found to have higher levels of the oxidation-marker dityrosine (DT) and certain sugar-modified compounds called ‘advanced glycation endproducts’ (AGEs).
Genetic causes have been found in 30–35 per cent of cases of ASD and the remaining 65–70 per cent of cases are thought to be caused by a combination of environmental factors, multiple mutations, and rare genetic variants.
The team’s research also confirmed the previously held belief that mutations of amino acid transporters are a genetic variant associated with ASD. The Warwick team worked with collaborators at the University of Bologna, Italy, who recruited locally 38 children who were diagnosed as having ASD (29 boys and nine girls) and a control group of 31 children (23 boys and eight girls) between the ages of five and 12. Blood and urine samples were taken from the children for analysis.
The University of Warwick team discovered that there were chemical differences between the two groups. Working with a further collaborator at the University of Birmingham, the changes in multiple compounds were combined together using artificial intelligence algorithms techniques to develop a mathematical equation or ‘algorithm’ to distinguish between ASD and controls. The outcome was a diagnostic test better than any method currently available.
The next steps are to repeat the study with further groups of children to confirm the good diagnostic performance and to assess if the test can identify ASD at very early stages and if treatments are working.