Mass spectrometry as a tool for studying autism spectrum disorder View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2013-12

AUTHORS

Alisa G Woods, Armand G Ngounou Wetie, Izabela Sokolowska, Stefanie Russell, Jeanne P Ryan, Tanja Maria Michel, Johannes Thome, Costel C Darie

ABSTRACT

Autism spectrum disorders (ASDs) are increasing in incidence but have an incompletely understood etiology. Tools for uncovering clues to the cause of ASDs and means for diagnoses are valuable to the field. Mass Spectrometry (MS) has been a useful method for evaluating differences between individuals with ASDs versus matched controls. Different biological substances can be evaluated using MS, including urine, blood, saliva, and hair. This technique has been used to evaluate relatively unsupported hypotheses based on introduction of exogenous factors, such as opiate and heavy metal excretion theories of ASDs. MS has also been used to support disturbances in serotonin-related molecules, which have been more consistently observed in ASDs. Serotonergic system markers, markers for oxidative stress, cholesterol system disturbances, peptide hypo-phosphorylation and methylation have been measured using MS in ASDs, although further analyses with larger numbers of subjects are needed (as well as consideration of behavioral data). Refinements in MS and data analysis are ongoing, allowing for the possibility that future studies examining body fluids and specimens from ASD subjects could continue to yield novel insights. This review summarizes MS investigations that have been conducted to study ASD to date and provides insight into future promising applications for this technique, with focus on proteomic studies. More... »

PAGES

6

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1186/2049-9256-1-6

    DOI

    http://dx.doi.org/10.1186/2049-9256-1-6

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1007448863

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/25408899


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