Department of Epidemiology, school of public health, Tianjin Medical University, China.
J Neurol Sci. 2011 Jun 15;305(1-2):92-6. doi: 10.1016/j.jns.2011.03.005. Epub 2011 Mar 26.
Amyloid β(Aβ) peptides are important components of plaques in Alzheimer's disease(AD). A decrease in the CSF concentration of Aβ40 and Aβ42 is a potential biomarker for incident AD. In contrast, studies on plasma Aβ40 and Aβ42 concentrations have yielded contradictory results. To explore the relationship between plasma Aβ40 and Aβ42 concentrations and AD in aging individuals with mild cognitive impairment (MCI), evaluate the sensitivity and the specificity of plasma Aβ and their ratio as a marker for progression to AD. We measured baseline concentrations of Aβ40 and Aβ42, and their ratio in plasma of patients carefully categorized clinically and neurochemically as having AD or other dementias from a cohort of patients with MCI (n=588) after 4-6 years of follow-up time. Plasma concentrations of Aβ40, Aβ42 were measured using a sandwich enzyme-linked immunosorbent assay technology. The association between plasma Aβ concentrations and the risk of dementia was assessed using Cox proportional hazard models. Optimal sensitivity and specificity of Aβ measurements were determined by ROC curve analysis. Plasma Aβ42 concentration and the Aβ42/Aβ40 ratio at baseline were significantly decreased in the MCI patients who developed AD as compared to cognitively stable MCI patients. The baseline concentrations of Aβ40 were similar in all MCI groups. The Aβ42/Aβ40 ratio was superior to Aβ42 concentration with regard to identify incipient AD in MCI. The ratio of Aβ42 to Aβ40 rather than absolute levels of the peptides can aid in the identification of incipient AD among MCI patients. A potential role of plasma Aβ concentrations as a marker of incipient dementia warrants further investigation.
淀粉样蛋白 β(Aβ)肽是阿尔茨海默病(AD)斑块的重要组成部分。脑脊液中 Aβ40 和 Aβ42 浓度的降低是 AD 发病的潜在生物标志物。相比之下,血浆 Aβ40 和 Aβ42 浓度的研究结果却相互矛盾。为了探讨在有轻度认知障碍(MCI)的老化个体中,血浆 Aβ40 和 Aβ42 浓度与 AD 之间的关系,评估血浆 Aβ及其比值作为 AD 进展标志物的敏感性和特异性。我们在经过 4-6 年的随访时间后,对来自 MCI 患者队列的患者进行了仔细的临床和神经化学分类,测量了基线时 Aβ40 和 Aβ42 的浓度及其比值。使用夹心酶联免疫吸附测定技术测量血浆 Aβ40 和 Aβ42 的浓度。使用 Cox 比例风险模型评估血浆 Aβ浓度与痴呆风险之间的关系。通过 ROC 曲线分析确定 Aβ 测量的最佳敏感性和特异性。与认知稳定的 MCI 患者相比,发生 AD 的 MCI 患者的血浆 Aβ42 浓度和 Aβ42/Aβ40 比值在基线时显著降低。所有 MCI 组的 Aβ40 基线浓度相似。在 MCI 中,Aβ42/Aβ40 比值在识别早期 AD 方面优于 Aβ42 浓度。Aβ42 与 Aβ40 的比值而不是肽的绝对水平可以帮助识别 MCI 患者中的早期 AD。血浆 Aβ 浓度作为早期痴呆标志物的潜在作用值得进一步研究。