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News about the Role of Fluid and Imaging Biomarkers in Neurodegenerative Diseases

机译:关于液体和成像生物标志物在神经变性疾病中的作用的新闻

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摘要

Biomarkers are molecules that are variable in their origin, nature, and mechanism of action; they are of great relevance in biology and also in medicine because of their specific connection with a single or several diseases. Biomarkers are of two types, which in some cases are operative with each other. Fluid biomarkers, started around 2000, are generated in fluid from specific proteins/peptides and miRNAs accumulated within two extracellular fluids, either the central spinal fluid or blood plasma. The switch of these proteins/peptides and miRNAs, from free to segregated within extracellular vesicles, has induced certain advantages including higher levels within fluids and lower operative expenses. Imaging biomarkers, started around 2004, are identified in vivo upon their binding by radiolabeled molecules subsequently revealed in the brain by positron emission tomography and/or other imaging techniques. A positive point for the latter approach is the quantitation of results, but expenses are much higher. At present, both types of biomarker are being extensively employed to study Alzheimer’s and other neurodegenerative diseases, investigated from the presymptomatic to mature stages. In conclusion, biomarkers have revolutionized scientific and medical research and practice. Diagnosis, which is often inadequate when based on medical criteria only, has been recently improved by the multiplicity and specificity of biomarkers. Analogous results have been obtained for prognosis. In contrast, improvement of therapy has been limited or fully absent, especially for Alzheimer’s in which progress has been inadequate. An urgent need at hand is therefore the progress of a new drug trial design together with patient management in clinical practice.
机译:生物标志物是它们的起源,性质和作用机制变异的分子;由于与单一或几种疾病的特定联系,它们在生物学和医学中具有很大的相关性。生物标志物是两种类型,在某些情况下,彼此可操作。从2000年开始的流体生物标志物在来自累积在两个细胞外液中的特定蛋白质/肽和miRNA的流体中产生,无论是中央脊髓液还是血浆。这些蛋白质/肽和miRNA的开关从室内囊泡中自由偏离,诱导某些优点,包括液体内的更高水平和更低的操作费用。成像生物标志物于2004年开始,在通过正电子发射断层扫描和/或其他成像技术随后在脑中揭示的放射性标记分子的结合时在体内鉴定。后一种方法的积极点是结果的定量,但费用要高得多。目前,两种类型的生物标志物都广泛用于研究阿尔茨海默和其他神经变性疾病,从假设到成熟阶段研究。总之,生物标志物彻底改变了科学和医学研究和实践。最近通过生物标志物的多重性和特异性来改善了诊断,这通常是在基于医学标准时的增加。已经获得了类似结果的预后。相比之下,治疗的改善受到限制或充分缺席,特别是对于阿尔茨海默氏症的进展不足。因此,迫切需要在临床实践中与患者管理一起进行新的药物试验设计。

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