Center for Brain Health, New York, NY 10016, USA.
Front Biosci (Landmark Ed). 2013 Jun 1;18(3):1150-73. doi: 10.2741/4170.
Numerous studies have shown that Alzheimer's Disease (AD) pathology begins before the onset of clinical symptoms. Because therapies are likely to be more effective if they are implemented early in the disease progression, it is necessary to identify reliable biomarkers to detect AD pathology in the early stages of the disease, ideally in presymptomatic individuals. Recent research has identified three candidate cerebrospinal fluid (CSF) biomarkers that reflect AD pathology: amyloid beta, total tau protein (t-tau), and tau protein phosphorylated at AD-specific epitopes (p-tau). They are useful in supporting the AD diagnosis and have predictive value for AD when patients are in the stage of mild cognitive impairment (MCI). However, their predictive utility in cognitively healthy subjects is still being evaluated. We conducted a review of studies published between 1993 and 2011 and summarized their findings on the role of CSF biomarkers for AD in healthy elderly.
大量研究表明,阿尔茨海默病(AD)的病理学改变早在临床症状出现之前就已经开始了。由于如果在疾病进展的早期实施治疗,治疗方法可能会更有效,因此有必要确定可靠的生物标志物,以便在疾病的早期阶段(理想情况下是在出现症状前)检测 AD 病理学。最近的研究已经确定了三种候选的脑脊液(CSF)生物标志物,它们反映了 AD 的病理学改变:β淀粉样蛋白、总 tau 蛋白(t-tau)和 AD 特异性表位磷酸化的 tau 蛋白(p-tau)。它们在支持 AD 诊断方面非常有用,并且在患者处于轻度认知障碍(MCI)阶段时对 AD 具有预测价值。然而,它们在认知健康受试者中的预测效用仍在评估中。我们对 1993 年至 2011 年间发表的研究进行了综述,并总结了它们关于 CSF 生物标志物在健康老年人 AD 中的作用的发现。