Autism spectrum disorder: difficulties in diagnosis and microRNA biomarkers.

IF 5.9 2区 医学 Q2 CELL BIOLOGY
Neural Regeneration Research Pub Date : 2025-10-01 Epub Date: 2024-09-24 DOI:10.4103/NRR.NRR-D-24-00712
Bridget Martinez, Philip V Peplow
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引用次数: 0

Abstract

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.

自闭症谱系障碍:诊断困难与 microRNA 生物标记物。
我们在PubMed上搜索了自闭症谱系障碍中可作为患者诊断生物标志物的microRNAs,选取了17篇发表于2008年1月至2023年12月的文章,其中4篇研究使用了全血,4篇使用了血浆,5篇使用了血清,1篇使用了血清神经细胞粘附分子L1捕获的细胞外囊泡,1篇使用了血细胞,2篇使用了外周血单核细胞。大多数研究涉及儿童,研究群体大多为男性。许多研究都采用了 microRNA 测序或定量聚合酶链反应测定法来测量 microRNA 的表达。只有五项研究使用实时聚合酶链反应测定法来验证自闭症谱系障碍受试者与对照组相比的 microRNA 表达情况。这些研究验证的 microRNA 可被视为自闭症谱系障碍的潜在候选生物标志物,包括 miR-500a-5p、-197-5p、-424-5p、-664a-3p、-365a-3p、-619-5p、-664a- 3p、-3135a、-328-3p、血浆中的 miR-151a-3p、-181b-5p、-320a、-328、-433、-489、-572、-663a、-101-3p、-106b-5p、-19b-3p、-195-5p 和-130a-3p,以及成人全血中的 miR-15b-5p 和 -6126。在回顾的研究中发现了一些重要的局限性,需要在今后的研究中加以考虑。有必要对自闭症谱系障碍严重程度不同的儿童和成人进行进一步研究,并应考虑使用自闭症谱系障碍动物模型来研究抑制或过表达特定 microRNA 作为新疗法的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neural Regeneration Research
Neural Regeneration Research CELL BIOLOGY-NEUROSCIENCES
CiteScore
8.00
自引率
9.80%
发文量
515
审稿时长
1.0 months
期刊介绍: Neural Regeneration Research (NRR) is the Open Access journal specializing in neural regeneration and indexed by SCI-E and PubMed. The journal is committed to publishing articles on basic pathobiology of injury, repair and protection to the nervous system, while considering preclinical and clinical trials targeted at improving traumatically injuried patients and patients with neurodegenerative diseases.
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