From the Departments of Neurology (M.E.F., S.J., A.P.S., M.J.P., D.M.R., K.V.P., R.A.B., K.A.J., R.A.S., R.F.B.) and Radiology (J.C.P., J.A.B., H.I.L.J., B.J.H., K.A.J.), Massachusetts General Hospital, Harvard Medical School; Department of Biostatistics (S.J., R.A.B.), Harvard T.H. Chan School of Public Health, Boston, MA; Division of Public Health Sciences (S.J.), Department of Surgery, Washington University School of Medicine in St. Louis, MO; Faculty of Health (H.I.L.J.), Medicine and Life Sciences, School for Mental Health and Neuroscience, Alzheimer Centre Limburg, Maastricht University, the Netherlands; Cliniques Universitaires Saint-Luc (B.J.H.), Université Catholique de Louvain, Brussels, Belgium; Center for Alzheimer Research and Treatment (D.M.R., K.V.P., R.A.S., R.F.B.), Brigham and Women's Hospital, Boston, MA; Department of Molecular Imaging & Therapy (V.L.V.), Austin Health, Melbourne, Australia; Department of Neuroscience (E.C.M.), Stanford University, Palo Alto, CA; Department of Biostatistics (R.A.B.), New York University School of Global Public Health, NY; Center for Alzheimer Research and Treatment, Brigham and Women's Hospital, Boston, MA; and Melbourne School of Psychological Sciences (R.F.B.), University of Melbourne, Australia.
Neurology. 2021 Jan 26;96(4):e619-e631. doi: 10.1212/WNL.0000000000011214. Epub 2020 Nov 16.
As clinical trials move toward earlier intervention, we sought to redefine the β-amyloid (Aβ)-PET threshold based on the lowest point in a baseline distribution that robustly predicts future Aβ accumulation and cognitive decline in 3 independent samples of clinically normal individuals.
Sequential Aβ cutoffs were tested to identify the lowest cutoff associated with future change in cognition (Preclinical Alzheimer Cognitive Composite [PACC]) and Aβ-PET in clinically normal participants from the Harvard Aging Brain Study (n = 342), Australian Imaging, Biomarker and Lifestyle study of aging (n = 157), and Alzheimer's Disease Neuroimaging Initiative (n = 356).
Within samples, cutoffs derived from future Aβ-PET accumulation and PACC decline converged on the same inflection point, beyond which trajectories diverged from normal. Across samples, optimal cutoffs fell within a short range (Centiloid 15-18.5).
These optimized thresholds can help to inform future research and clinical trials targeting early Aβ. Threshold convergence raises the possibility of contemporaneous early changes in Aβ and cognition.
This study provides Class II evidence that among clinically normal individuals a specific Aβ-PET threshold is predictive of cognitive decline.
随着临床试验向早期干预推进,我们试图重新定义β-淀粉样蛋白(Aβ)-PET 阈值,该阈值基于基线分布中的最低点,该点能够可靠地预测 3 个独立的临床正常个体中未来 Aβ 积累和认知下降。
为了确定与临床正常参与者的未来认知变化(前驱性阿尔茨海默病认知复合指标 [PACC])和 Aβ-PET 相关的最低截止值,我们对连续的 Aβ截止值进行了测试,这些参与者来自哈佛衰老大脑研究(n = 342)、澳大利亚影像学、生物标志物和老龄化生活方式研究(n = 157)以及阿尔茨海默病神经影像学倡议(n = 356)。
在样本内,源自未来 Aβ-PET 积累和 PACC 下降的截止值收敛于相同的拐点,超过该拐点,轨迹就会从正常状态中发散。在多个样本中,最佳截止值落在一个狭窄的范围内(百分位值 15-18.5)。
这些优化后的阈值有助于为针对早期 Aβ 的未来研究和临床试验提供信息。截止值的收敛性提高了 Aβ 和认知同时发生早期变化的可能性。
本研究提供了 II 级证据,表明在临床正常个体中,特定的 Aβ-PET 阈值可预测认知下降。