Potential Biomarkers for Diagnosis and Screening of Autism Spectrum Disorders

被引:0
|
作者
Meiliana, Anna [1 ,2 ]
Wijaya, Andi [2 ,3 ]
机构
[1] Padjadjaran State Univ, Postgrad Program Clin Pharm, Jl Eijkman 8, Bandung, Indonesia
[2] Prodia Clin Lab, Bandung, Indonesia
[3] Hasanuddin Univ, Postgrad Program Clin Biochem, Makassar, Indonesia
来源
INDONESIAN BIOMEDICAL JOURNAL | 2014年 / 6卷 / 03期
关键词
ASD; autism; biomarkers; newborn screening; diagnosis;
D O I
10.18585/inabj.v6i3.27
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BACKGROUND: Autism spectrum disorder (ASD) is a highly heritable neurodevelopmental condition, which is typically characterized by a triad of symptoms: impaired social communication, social reciprocity and repetitive stereotypic behavior. While the behavioral phenotype of ASD is well described, the search for reliable 'autism biomarkers' continues. CONTENT: Insulin growth factor (IGF) is essential for the myelination of developing fetal neurons; this is in addition to the well-known links between IGF, maternal inlammation, infection and autism supporting IGF as a potential marker. Combining IGF data with data regarding levels of the known markers, serotonin and anti-myelin basic protein, in order to calculate an autism index, could provide a new diagnostic method for at-risk neonates. Disruptions to multiple pathophysiological systems, including redox, folate, methylation, tryptophan metabolism, and mitochondrial metabolism, have been well documented in autistic patients. Maternal infection and inlammation have known links with autism. Autoimmunity has therefore been a well-studied area of autism research. The potential of using autoantibodies as novel biomarkers for autism, in addition to providing insights into the neurodevelopmental processes that lead to autism. SUMMARY: The six proposed causes of autism involve both metabolic and immunologic dysfunctions and include: increased oxidative stress; decreased methionine metabolism and trans-sulfuration: aberrant free and bound metal burden; gastrointestinal (GI) disturbances; immune/inlammation dysregulation; and autoimmune targeting. A newborn screening program for early-onset ASD should be capable of utilizing a combination of ASD-associated biomarkers representative of the six proposed causes of autism in order to identify newborns at risk. The biomarkers discussed in this article are useful to guide the selection, eficacy, and suficiency of biomedical interventions, which would likely include nutritional supplementation, dietary changes, and speciic medications for treating GI pathogens and reducing inlammation.
引用
收藏
页码:137 / 156
页数:20
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