Roeben Benjamin, Maetzler Walter, Vanmechelen Eugeen, Schulte Claudia, Heinzel Sebastian, Stellos Konstantinos, Godau Jana, Huber Heiko, Brockmann Kathrin, Wurster Isabel, Gaenslen Alexandra, Grüner Eva, Niebler Raphael, Eschweiler Gerhard W, Berg Daniela
Department of Neurodegeneration, Hertie Institute for Clinical Brain Research (HIH), University of Tübingen, Tübingen, Germany.
German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
J Alzheimers Dis. 2016 Mar 16;52(1):161-9. doi: 10.3233/JAD-150575.
BACKGROUND/OBJECTIVE: Plasma levels of amyloid-beta (Aβ) 1-40 peptide have been proposed to be associated with cardiovascular mortality in patients with coronary artery disease (CAD). Therefore, we aimed to investigate the association of plasma Aβ levels with CAD, cardiovascular risk factors (CVRF), and APOE genotype in non-demented elderly individuals.
Plasma Aβ1 - 40 and Aβ1 - 42 levels of 526 individuals (mean age of 63.0±7.3 years) were quantified with the INNO-BIA plasma Aβ forms assay based on multiplextrademark technique. APOE genotype was determined with an established protocol. Presence of CAD and CVRFs were ascertained using a questionnaire and/or medical records.
Plasma Aβ1 - 40 levels were significantly higher in individuals with CAD (p = 0.043) and, independently, in individuals with diabetes mellitus (DM) type 2 (p = 0.001) while accounting for age- and gender-effects. Plasma Aβ1 - 42 levels were higher in APOEɛ4 carriers (p = 0.004), but were neither relevantly associated with CAD nor with any CVRF. Plasma Aβ1 - 40 showed no association with APOE genotype.
Our findings argue for an association of circulating plasma Aβ1 - 40 peptides with incident CAD and DM. Further investigations are needed to entangle the role of Aβ1 - 40 role in the pathophysiology of cardiovascular disease independent of its known role in Alzheimer's disease.
背景/目的:已有研究表明,冠状动脉疾病(CAD)患者血浆中β-淀粉样蛋白(Aβ)1-40肽水平与心血管疾病死亡率相关。因此,我们旨在研究非痴呆老年个体血浆Aβ水平与CAD、心血管危险因素(CVRF)及载脂蛋白E(APOE)基因型之间的关系。
采用基于多重技术的INNO-BIA血浆Aβ形式检测法,对526名个体(平均年龄63.0±7.3岁)的血浆Aβ1-40和Aβ1-42水平进行定量检测。采用既定方案确定APOE基因型。通过问卷调查和/或病历确定CAD和CVRF的存在情况。
在校正年龄和性别影响后,CAD患者的血浆Aβ1-40水平显著升高(p = 0.043),独立来看,2型糖尿病(DM)患者的血浆Aβ1-40水平也显著升高(p = 0.001)。APOEɛ4携带者的血浆Aβ1-42水平较高(p = 0.004),但与CAD及任何CVRF均无显著相关性。血浆Aβ1-40与APOE基因型无关联。
我们的研究结果表明循环血浆Aβ1-40肽与新发CAD和DM有关。需要进一步研究以阐明Aβ1-40在心血管疾病病理生理学中的作用,而不依赖于其在阿尔茨海默病中的已知作用。