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Blood platelet research in autism spectrum disorders: In search of biomarkers

机译:自闭症谱系障碍中的血小板研究:寻找生物标志物

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Autism spectrum disorder (ASD) is a clinically heterogeneous neurodevelopmental disorder that is caused by gene‐environment interactions. To improve its diagnosis and treatment, numerous efforts have been undertaken to identify reliable biomarkers for autism. None of them have delivered the holy grail that represents a reproducible, quantifiable, and sensitive biomarker. Though blood platelets are mainly known to prevent bleeding, they also play pivotal roles in cancer, inflammation, and neurological disorders. Platelets could serve as a peripheral biomarker or cellular model for autism as they share common biological and molecular characteristics with neurons. In particular, platelet‐dense granules contain neurotransmitters such as serotonin and gamma‐aminobutyric acid. Molecular players controlling granule formation and secretion are similarly regulated in platelets and neurons. The major platelet integrin receptor αIIbβ3 has recently been linked to ASD as a regulator of serotonin transport. Though many studies revealed associations between platelet markers and ASD, there is an important knowledge gap in linking these markers with autism and explaining the altered platelet phenotypes detected in autism patients. The present review enumerates studies of different biomarkers detected in ASD using platelets and highlights the future needs to bring this research to the next level and advance our understanding of this complex disorder.
机译:自闭症谱系障碍(ASD)是一种临床异质性神经发育障碍,由基因-环境相互作用引起。为了改善其诊断和治疗,已经进行了许多努力以鉴定可靠的自闭症生物标志物。他们都没有交付代表可再现,可量化和敏感的生物标志物的圣杯。尽管众所周知,血小板主要是预防出血,但它们在癌症,炎症和神经系统疾病中也起着关键作用。血小板可以作为自闭症的外周生物标志物或细胞模型,因为它们与神经元具有共同的生物学和分子特征。尤其是血小板密集的颗粒含有神经递质,例如血清素和γ-氨基丁酸。在血小板和神经元中类似地调节控制颗粒形成和分泌的分子参与者。最近,主要的血小板整联蛋白受体αIIbβ3已与ASD相连,作为5-羟色胺转运的调节剂。尽管许多研究揭示了血小板标志物与ASD之间的关联,但是在将这些标志物与自闭症联系起来并解释自闭症患者中检测到的血小板表型改变方面存在重要的知识鸿沟。本综述列举了使用血小板在ASD中检测到的不同生物标志物的研究,并强调了将这项研究提高到一个新水平并加深我们对这种复杂疾病的理解的未来需求。

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