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Finding potential autism biomarkers
MADISON, Wis.—Metabolic signatures in the blood of children with autism spectrum disorder (ASD) may lead to earlier diagnosis of the condition for some, according to newly published research. The findings appeared online yesterday in Biological Psychiatry in a publication entitled “Amino acid dysregulation metabotypes: potential biomarkers for diagnosis and individualized treatment for subtypes of autism spectrum disorder.” David G. Amaral, Ph.D. of the University of California, Davis MIND Institute and scientists from NeuroPointDX, a division of Stemina Biomarker Discovery, authored the publication, which is the first resulting from the Children’s Autism Metabolome Project (CAMP), the largest study of the metabolism of children with ASD.
These biochemical signatures provide insight into how the body metabolizes certain amino acids important to typical neurodevelopment. Children with these metabolic signatures are placed into metabolic subtypes, or metabotypes, that are highly associated with an ASD diagnosis. No reliable, objective biomarkers exist to aid in the diagnosis of the disorder, which is currently diagnosed based on the behavioral characteristics exhibited by an affected child. While a diagnosis is possible in children as young as 24 months, the average age of ASD diagnosis in the United States is over four years old.
“Using a metabolomics approach to detect ASD risk holds substantial promise for the identification of objective ASD biomarkers because metabolism is sensitive to interactions among the genome, gastrointestinal microbiome, diet, and environmental factors that all contribute to an individual’s unique metabolic signature,” noted Elizabeth Donley, NeuroPointDX Chief Executive Officer, a co-author of the publication. “Metabolic testing can provide important biochemical signatures that help identify disruptions in biological processes that underlie an individual’s ASD.”
Past studies have been too small to reliably detect these metabolic dysregulations and characterize them into metabotypes. To test for metabolic imbalances that could reveal metabotypes and potential diagnostic biomarkers of ASD, the researchers conducted CAMP, a large-scale, eight-site study that recruited 1,100 children (ages 18 months to 48 months) with clinically confirmed ASD, developmental delay, or typical development. Prior research by this team and others, as well as preliminary analysis of the CAMP samples, suggested that analysis of amino acid dysregulation might be a useful approach to identifying unique metabotypes with the potential to serve as objective biomarkers of ASD.
When scientists at NeuroPointDX compared plasma metabolites from 516 children with ASD with those from 164 age-matched typically developing children from the CAMP study, they were able to stratify the ASD children into subpopulations, based on shared metabolic signatures. Imbalances in glutamine, glycine, and ornithine with lowered branched chain amino acids (BCAA: leucine, isoleucine, and valine) identified three ASD-associated amino acid dysregulation metabotypes (AADM). These three AADMs together were present in 16.7% of the CAMP ASD subjects, and were detectable with a specificity of 96.3% and an accuracy (PPV) of 93.5%.
“It is unlikely that a single marker will detect all autism,” said lead author Amaral. “This paper demonstrates that alterations in metabolic profiles can detect sizable subsets of individuals with autism. The hope is that we will be able to generate a panel of biomarkers that will detect a large proportion of people at risk. Moreover, this approach highlights metabolic pathways that may be targets for therapeutic intervention.
“One of the major goals of the MIND Institute is the development of early biological markers for detecting the risk of autism spectrum disorder. It would have been difficult for the MIND Institute to carry out the CAMP study on its own,” Amaral continued. “CAMP is an excellent example of an academic/corporate partnership that has the promise of benefitting the autism community.”
NeuroPointDX continues to analyze the CAMP study samples to identify additional metabotypes that will be diagnostic for other subsets of children with ASD. By combining such ASD-associated metabotypes into a diagnostic panel, NeuroPointDX believes it should be possible to develop an objective blood test that enables a substantial percentage of children at risk for ASD to be identified at a very early age, when therapeutic intervention can provide the greatest benefit.
“One of the critical and currently unmet clinical and research needs in the field of autism is a reliable early biological marker,” said Geraldine Dawson, PhD, FAPA, FAPS, Professor of Psychiatry and Behavioral Sciences and Director, Duke Center for Autism and Brain Development, Duke Institute for Brain Sciences, who was not involved in the study. “The sooner families can receive information that their child is at high risk for autism, the sooner they can begin effective behavioral or other therapies. The research in this paper is an important milestone towards establishing metabolomics biomarkers of autism.”