Ruiz Agustín, Pesini Pedro, Espinosa Ana, Pérez-Grijalba Virginia, Valero Sergi, Sotolongo-Grau Oscar, Alegret Montserrat, Monleón Inmaculada, Lafuente Asunción, Buendía Mar, Ibarria Marta, Ruiz Susana, Hernández Isabel, San José Itziar, Tárraga Lluís, Boada Mercè, Sarasa Manuel
Alzheimer Research Center and Memory Clinic, Fundació ACE, Institut Català de Neurociències Aplicades, Barcelona, Spain.
PLoS One. 2013 Nov 27;8(11):e81334. doi: 10.1371/journal.pone.0081334. eCollection 2013.
Plasma amyloid beta (Aβ) levels are being investigated as potential biomarkers for Alzheimer's disease. In AB128 cross-sectional study, a number of medical relevant correlates of blood Aβ40 or Aβ42 were analyzed in 140 subjects (51 Alzheimer's disease patients, 53 healthy controls and 36 individuals diagnosed with mild cognitive impairment). We determined the association between multiple variables with Aβ40 and Aβ42 levels measured in three different blood compartments called i) Aβ directly accessible (DA) in the plasma, ii) Aβ recovered from the plasma matrix (RP) after diluting the plasma sample in a formulated buffer, and iii) associated with the remaining cellular pellet (CP). We confirmed that diastolic blood pressure (DBP) is consistently correlated with blood DA Aβ40 levels (r=-0.19, P=0.032). These results were consistent in the three phenotypic groups studied. Importantly, the observation resisted covariation with age, gender or creatinine levels. Observed effect size and direction of Aβ40 levels/DBP correlation are in accordance with previous reports. Of note, DA Aβ40 and the RP Aβ40 were also strongly associated with creatinine levels (r=0.599, P<<0.001) and to a lesser extent to urea, age, hematocrit, uric acid and homocysteine (p<0.001). DBP and the rest of statistical significant correlates identified should be considered as potential confounder factors in studies investigating blood Aβ levels as potential AD biomarker. Remarkably, the factors affecting Aβ levels in plasma (DA, RP) and blood cell compartments (CP) seem completely different.
血浆β淀粉样蛋白(Aβ)水平正作为阿尔茨海默病的潜在生物标志物进行研究。在AB128横断面研究中,对140名受试者(51名阿尔茨海默病患者、53名健康对照者和36名被诊断为轻度认知障碍的个体)血液中Aβ40或Aβ42的一些医学相关关联因素进行了分析。我们确定了多个变量与在三个不同血液成分中测量的Aβ40和Aβ42水平之间的关联,这三个成分分别为:i)血浆中直接可及的Aβ(DA);ii)在配制缓冲液中稀释血浆样品后从血浆基质中回收的Aβ(RP);iii)与剩余细胞沉淀(CP)相关的Aβ。我们证实舒张压(DBP)与血液DA Aβ40水平始终相关(r = -0.19,P = 0.032)。这些结果在所研究的三个表型组中是一致的。重要的是,该观察结果不受年龄、性别或肌酐水平的协变量影响。观察到的Aβ40水平/DBP相关性的效应大小和方向与先前的报告一致。值得注意的是,DA Aβ40和RP Aβ40也与肌酐水平密切相关(r = 0.599,P << 0.001),在较小程度上与尿素、年龄、血细胞比容、尿酸和同型半胱氨酸相关(p < 0.001)。在将血液Aβ水平作为潜在AD生物标志物的研究中,DBP和其他确定的统计学显著相关因素应被视为潜在的混杂因素。值得注意的是,影响血浆(DA、RP)和血细胞成分(CP)中Aβ水平的因素似乎完全不同。