Niemantsverdriet Ellis, Ottoy Julie, Somers Charisse, De Roeck Ellen, Struyfs Hanne, Soetewey Femke, Verhaeghe Jeroen, Van den Bossche Tobi, Van Mossevelde Sara, Goeman Johan, De Deyn Peter Paul, Mariën Peter, Versijpt Jan, Sleegers Kristel, Van Broeckhoven Christine, Wyffels Leonie, Albert Adrien, Ceyssens Sarah, Stroobants Sigrid, Staelens Steven, Bjerke Maria, Engelborghs Sebastiaan
Reference Center for Biological Markers of Dementia (BIODEM), Laboratory of Neurochemistry and Behavior, Institute Born-Bunge, UAntwerp, Antwerp, Belgium.
Molecular Imaging Center Antwerp (MICA), UAntwerp, Antwerp, Belgium.
J Alzheimers Dis. 2017;60(2):561-576. doi: 10.3233/JAD-170327.
Evidence suggests that the concordance between amyloid-PET and cerebrospinal fluid (CSF) amyloid-β (Aβ) increases when the CSF Aβ1-42/Aβ1-40 ratio is used as compared to CSF Aβ1-42 levels alone.
In order to test this hypothesis, we set up a prospective longitudinal study comparing the concordance between different amyloid biomarkers for Alzheimer's disease (AD) in a clinical setting.
Seventy-eight subjects (AD dementia (n = 17), mild cognitive impairment (MCI, n = 48), and cognitively healthy controls (n = 13)) underwent a [18F]Florbetapir ([18F]AV45) PET scan, [18F]FDG PET scan, MRI scan, and an extensive neuropsychological examination. In a large subset (n = 67), a lumbar puncture was performed and AD biomarkers were analyzed (Aβ1-42, Aβ1-40, T-tau, P-tau181).
We detected an increased concordance in the visual and quantitative (standardized uptake value ratio (SUVR) and total volume of distribution (VT)) [18F]AV45 PET measures when the CSF Aβ1-42/Aβ1-40 was applied compared to Aβ1-42 alone. CSF biomarkers were stronger associated to [18F]AV45 PET for SUVR values when considering the total brain white matter as reference region instead of cerebellar grey matterConclusions:The concordance between CSF Aβ and [18F]AV45 PET increases when the CSF Aβ1-42/Aβ1-40 ratio is applied. This finding is of most importance for the biomarker-based diagnosis of AD as well as for selection of subjects for clinical trials with potential disease-modifying therapies for AD.
有证据表明,与仅使用脑脊液Aβ1-42水平相比,当使用脑脊液Aβ1-42/Aβ1-40比值时,淀粉样蛋白PET与脑脊液(CSF)淀粉样蛋白-β(Aβ)之间的一致性会增加。
为了验证这一假设,我们开展了一项前瞻性纵向研究,在临床环境中比较不同阿尔茨海默病(AD)淀粉样生物标志物之间的一致性。
78名受试者(AD痴呆患者(n = 17)、轻度认知障碍(MCI,n = 48)和认知健康对照者(n = 13))接受了[18F]氟代贝他吡([18F]AV45)PET扫描、[18F]FDG PET扫描、MRI扫描以及全面的神经心理学检查。在一个大的亚组(n = 67)中,进行了腰椎穿刺并分析了AD生物标志物(Aβ1-42、Aβ1-40、总tau蛋白(T-tau)、磷酸化tau蛋白181(P-tau181))。
与仅使用Aβ1-42相比,当应用脑脊液Aβ1-42/Aβ1-40时,我们在视觉和定量(标准化摄取值比值(SUVR)和分布总体积(VT))[18F]AV45 PET测量中检测到一致性增加。当将全脑白质作为参考区域而非小脑灰质时,脑脊液生物标志物与[18F]AV45 PET的SUVR值相关性更强。
当应用脑脊液Aβ1-42/Aβ1-40比值时,脑脊液Aβ与[18F]AV45 PET之间的一致性增加。这一发现对于基于生物标志物的AD诊断以及选择可能采用疾病修饰疗法进行AD临床试验的受试者最为重要。