血液磷酸化Tau 181作为认知健康成人脑PET淀粉样蛋白负荷的生物标志物

Emer R. McGrath, A. Beiser, A. O’Donnell, Qiong Yang, Saptaparni Ghosh, M. Gonzales, J. Himali, C. Satizabal, Keith A. Johnson, R. Tracy, S. Seshadri
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Our primary outcomes included Aβ-precuneus, Aβ-FLR (frontal, lateral, and retrosplenial cortices) and tau-global composite region PET deposition. Secondary outcomes included individual regional Aβ and tau PET-deposition. P-tau181 was compared with plasma neurofilament light chain (NFL) and glial fibrillary acidic protein (GFAP) in predicting PET outcomes.\n\n\nRESULTS\nP-tau181 was associated with increased Aβ deposition in the FLR (β±SE, 1.25±0.30, p < 0.0001), precuneus (1.35±0.29, p < 0.001), and other cortical regions. Plasma NFL (1.30±0.49, p = 0.01) and GFAP (1.46±0.39, p < 0.001) were also associated with FLR Aβ deposition. In models including all three biomarkers adjusted for age, sex, APOE E4 allele, AD polygenic risk score and cortical atrophy score, p-tau181 (0.93±0.31, p < 0.01, R2 = 0.18) and GFAP (0.93±0.41, p = 0.03, R2 = 0.11), but not NFL (0.25±0.51, p = 0.62, R2 = 0.01), were associated with FLR-Aβ deposition. 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引用次数: 6

摘要

血浆磷酸化tau181 (p-tau181)是一种很有前景的阿尔茨海默病(AD)生物标志物,可能为预测临床前疾病提供实用价值。目的评估认知功能正常个体血浆p-tau181与淀粉样蛋白-β (Aβ)和tau-PET沉积的前瞻性关联。方法在基线时测量52名[48%的女性,平均64.4 (SD 5.5)年]认知未受损的Framingham Offspring队列参与者的血浆p-tau181水平,使用2011-2014年间存储的样本,随后进行11C-Pittsburgh复合物- b (PiB)-PET和/或18F-Flortaucipir (FTP)-PET扫描(n = 18, tau-PET),平均6.8年(SD 0.6)年后。我们的主要结局包括a β-楔前叶、Aβ-FLR(额皮质、外侧皮质和脾后皮质)和tau-全球复合区PET沉积。次要结局包括个别区域的Aβ和tau pet沉积。比较P-tau181与血浆神经丝轻链(NFL)和胶质纤维酸性蛋白(GFAP)预测PET预后的相关性。结果tsp -tau181与FLR (β±SE, 1.25±0.30,p < 0.0001)、楔前叶(1.35±0.29,p < 0.001)及其他皮质区Aβ沉积增加相关。血浆NFL(1.30±0.49,p = 0.01)和GFAP(1.46±0.39,p < 0.001)也与FLR Aβ沉积相关。在包括年龄、性别、APOE E4等位基因、AD多基因风险评分和皮质萎缩评分的三种生物标志物的模型中,p-tau181(0.93±0.31,p < 0.01, R2 = 0.18)和GFAP(0.93±0.41,p = 0.03, R2 = 0.11)与flr - a - β沉积相关,但NFL(0.25±0.51,p = 0.62, R2 = 0.01)与flr - a - β沉积无关。血浆p-tau181与tau-PET负荷无关。结论:在认知功能未受损的成年人中,血浆p-tau181升高与未来多脑区Aβ沉积增加有关。我们的研究结果强调了p-tau181作为血液生物标志物在社区环境中筛查认知健康个体脑淀粉样蛋白沉积的潜在效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Blood Phosphorylated Tau 181 as a Biomarker for Amyloid Burden on Brain PET in Cognitively Healthy Adults.
BACKGROUND Plasma phosphorylated-tau181 (p-tau181) is a promising biomarker for Alzheimer's disease (AD) and may offer utility for predicting preclinical disease. OBJECTIVE To evaluate the prospective association between plasma p-tau181 and amyloid-β (Aβ) and tau-PET deposition in cognitively unimpaired individuals. METHODS Plasma p-tau181 levels were measured at baseline in 52 [48% women, mean 64.4 (SD 5.5) years] cognitively unimpaired Framingham Offspring cohort participants using samples stored between 2011-2014 who subsequently underwent 11C-Pittsburgh Compound-B (PiB)-PET and/or 18F-Flortaucipir (FTP)-PET scans (n = 18 with tau-PET) a mean of 6.8 (SD 0.6) years later. Our primary outcomes included Aβ-precuneus, Aβ-FLR (frontal, lateral, and retrosplenial cortices) and tau-global composite region PET deposition. Secondary outcomes included individual regional Aβ and tau PET-deposition. P-tau181 was compared with plasma neurofilament light chain (NFL) and glial fibrillary acidic protein (GFAP) in predicting PET outcomes. RESULTS P-tau181 was associated with increased Aβ deposition in the FLR (β±SE, 1.25±0.30, p < 0.0001), precuneus (1.35±0.29, p < 0.001), and other cortical regions. Plasma NFL (1.30±0.49, p = 0.01) and GFAP (1.46±0.39, p < 0.001) were also associated with FLR Aβ deposition. In models including all three biomarkers adjusted for age, sex, APOE E4 allele, AD polygenic risk score and cortical atrophy score, p-tau181 (0.93±0.31, p < 0.01, R2 = 0.18) and GFAP (0.93±0.41, p = 0.03, R2 = 0.11), but not NFL (0.25±0.51, p = 0.62, R2 = 0.01), were associated with FLR-Aβ deposition. Plasma p-tau181 was not associated with tau-PET burden. CONCLUSION In cognitively unimpaired adults, elevated plasma p-tau181 is associated with future increased Aβ deposition across multiple brain regions. Our results highlight the potential utility of p-tau181 as a blood-biomarker to screen for brain-amyloid deposition in cognitively healthy individuals in a community-setting.
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