Neurology:特发性REM睡眠行为障碍的新型生物标志物特征

2018-10-01 xing.T MedSci原创

由此可见,该研究结果揭示了RBD发病机制中涉及的蛋白质特征谱、分子途径、机制及其临床表现。这些知识开辟了一条新的途径使其可以更准确、更及时地诊断和确定RBD,这可能最终转化为具有疾病调节作用的新治疗策略。但需要进一步评估已确定的标志物,以确认其诊断价值和指导临床决策的潜力。

近日,神经病学领域权威取杂志Neurology上发表了一篇研究文章,研究人员旨在进行严格、深入的蛋白质组学分析,以确定特发性REM睡眠行为障碍(RBD)的循环生物标志物特征,能够为潜在的致病机制和α-突触核蛋白相关的神经退行性过程提供新的见解。

研究人员对特发性RBD(n=9)患者和健康对照者(n=10)的血清样品进行全面的液相色谱-质谱(MS)/MS蛋白质组学分析,并使用系统生物学方法分析数据以确定RBD患者中改变的代谢途径。

研究人员鉴定了259种蛋白质,其中11种在与对照者相比过程中,RBD患者表现出显著改变的表达水平。血清多巴胺β-羟化酶(DBH)和维生素D结合蛋白(GC)的显著降低分别与去甲肾上腺素能(NErgic)和多巴胺能系统的改变相一致。其他改变的蛋白质谱表明免疫、炎症、补体和凝血也在RBD病理生理学中起作用。

由此可见,该研究结果揭示了RBD发病机制中涉及的蛋白质特征谱、分子途径、机制及其临床表现。这些知识开辟了一条新的途径使其可以更准确、更及时地诊断和确定RBD,这可能最终转化为具有疾病调节作用的新治疗策略。但需要进一步评估已确定的标志物,以确认其诊断价值和指导临床决策的潜力。

原始出处:

Stefania Mondello, et al.Novel biomarker signatures for idiopathic REM sleep behavior disorder A proteomic and system biology approach.neurology.2018. https://doi.org/10.1212/WNL.0000000000006439

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    2019-08-22 yinhl1978
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    2019-08-16 tongyongming
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