Autism spectrum disorder: difficulties in diagnosis and microRNA biomarkers

被引:0
|
作者
Martinez, Bridget [1 ,2 ]
Peplow, Philip V. [3 ]
机构
[1] Univ Nevada Reno, Dept Pharmacol, Reno, NV USA
[2] Univ Nevada Reno, Dept Med, Reno, NV USA
[3] Univ Otago, Dept Anat, Dunedin, New Zealand
关键词
autism spectrum disorder; biomarker; blood cells; blood plasma; blood serum; diagnosis; microRNA; peripheral blood mononuclear cells; serum neural cell adhesion molecule L1-captured extracellular vesicles; whole blood; DISABILITIES MONITORING NETWORK; AGED; 8; YEARS; SYNAPTIC PLASTICITY; UNITED-STATES; RATING-SCALE; GENOME-WIDE; 11; SITES; CHILDREN; PREVALENCE; EXPRESSION;
D O I
10.4103/NRR.NRR-D-24-00712
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We performed a PubMed search for microRNAs in autism spectrum disorder that could serve as diagnostic biomarkers in patients and selected 17 articles published from January 2008 to December 2023, of which 4 studies were performed with whole blood, 4 with blood plasma, 5 with blood serum, 1 with serum neural cell adhesion molecule L1-captured extracellular vesicles, 1 with blood cells, and 2 with peripheral blood mononuclear cells. Most of the studies involved children and the study cohorts were largely males. Many of the studies had performed microRNA sequencing or quantitative polymerase chain reaction assays to measure microRNA expression. Only five studies had used real-time polymerase chain reaction assay to validate microRNA expression in autism spectrum disorder subjects compared to controls. The microRNAs that were validated in these studies may be considered as potential candidate biomarkers for autism spectrum disorder and include miR-500a-5p, -197-5p, -424-5p, -664a-3p, -365a-3p, -619-5p, -664a-3p, -3135a, -328-3p, and -500a-5p in blood plasma and miR-151a-3p, -181b-5p, -320a, -328, -433, -489, -572, -663a, -101-3p, -106b-5p, -19b-3p, -195-5p, and -130a-3p in blood serum of children, and miR-15b-5p and -6126 in whole blood of adults. Several important limitations were identified in the studies reviewed, and need to be taken into account in future studies. Further studies are warranted with children and adults having different levels of autism spectrum disorder severity and consideration should be given to using animal models of autism spectrum disorder to investigate the effects of suppressing or overexpressing specific microRNAs as a novel therapy.
引用
收藏
页码:2776 / 2786
页数:11
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