Neurodegenerative Disorder Research Center and Brain Bank, Material Science at Microscale National Laboratory, School of Life Sciences, Key Laboratory of Brain Function and Disease, Chinese Academy of Sciences, University of Science and Technology of China, Hefei; Center for Advanced, Therapeutic Strategies for Brain Disorders, Sarasota; Department of Neurology, University of Florida College of Medicine, Gainesville, Florida.
Roskamp Institute, Sarasota.
Biol Psychiatry. 2018 Mar 1;83(5):447-455. doi: 10.1016/j.biopsych.2017.02.007. Epub 2017 Mar 27.
Increased beta-secretase 1 (BACE1) activity has consistently been detected in brain tissue and cerebrospinal fluid of subjects with mild cognitive impairment (MCI) and probable Alzheimer's disease (AD) compared with control subjects. The collection of cerebrospinal fluid by lumbar puncture is invasive. We sought to identify the presence of plasma BACE1 activity and determine potential alterations in subjects with MCI with clinical follow-up examinations for 3 years using patients with diagnosed probable AD dementia compared with healthy control subjects.
Seventy-five patients with probable AD, 96 individuals with MCI, and 53 age-matched and sex-matched healthy control subjects were recruited from three independent international academic memory clinics and AD research expert centers. Plasma BACE1 activity was measured by a synthetic fluorescence substrate enzyme-linked immunosorbent assay. BACE1 protein expression was assessed by Western blotting using three different antibodies that recognize the epitopes of the N-terminus, C-terminus, and full-length BACE1.
Compared with healthy control subjects, plasma BACE1 activity (V) significantly increased by 53.2% in subjects with MCI and by 68.9% in patients with probable AD. Subjects with MCI who converted to probable AD dementia at follow-up examinations exhibited significantly higher BACE1 activity compared with cognitively stable MCI nonconverters and showed higher levels of BACE1 activity than patients with AD.
Plasma BACE1 activity is significantly increased in MCI converters and patients with probable AD. The sensitivities and specificities of BACE1 activity for the patients were 84% and 88%, respectively. Our results indicate that plasma BACE1 activity may be a biomarker for AD risk and could predict progression from prodromal to probable AD dementia.
与对照组相比,轻度认知障碍(MCI)和可能的阿尔茨海默病(AD)患者的脑组织和脑脊液中β-分泌酶 1(BACE1)活性持续增加。腰椎穿刺采集脑脊液具有侵袭性。我们试图通过与诊断为可能的 AD 痴呆的患者进行临床随访检查 3 年,来确定 MCI 患者是否存在血浆 BACE1 活性,并确定其潜在变化,这些患者与健康对照组相匹配。
从三个独立的国际学术记忆诊所和 AD 研究专家中心招募了 75 名可能的 AD 患者、96 名 MCI 患者和 53 名年龄和性别相匹配的健康对照组。使用合成荧光底物酶联免疫吸附测定法测量血浆 BACE1 活性。通过 Western 印迹使用三种不同的抗体评估 BACE1 蛋白表达,这些抗体识别 N 端、C 端和全长 BACE1 的表位。
与健康对照组相比,MCI 患者的血浆 BACE1 活性(V)显著增加了 53.2%,而可能的 AD 患者的血浆 BACE1 活性增加了 68.9%。在随访检查中转换为可能的 AD 痴呆的 MCI 患者的 BACE1 活性明显高于认知稳定的 MCI 非转换者,并且其 BACE1 活性水平高于 AD 患者。
MCI 转化者和可能的 AD 患者的血浆 BACE1 活性显著增加。BACE1 活性对患者的灵敏度和特异性分别为 84%和 88%。我们的结果表明,血浆 BACE1 活性可能是 AD 风险的生物标志物,并可预测从前驱期到可能的 AD 痴呆的进展。