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Diagnostic value of plasma phosphorylated tau181 in Alzheimer's disease and frontotemporal lobar degeneration

机译:血浆磷酸化TAU181在阿尔茨海默病和额光叶片变性的诊断价值

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摘要

With the potential development of new disease-modifying Alzheimer's disease (AD) therapies, simple, widely available screening tests are needed to identify which individuals, who are experiencing symptoms of cognitive or behavioral decline, should be further evaluated for initiation of treatment. A blood-based test for AD would be a less invasive and less expensive screening tool than the currently approved cerebrospinal fluid or amyloid beta positron emission tomography (PET) diagnostic tests. We examined whether plasma tau phosphorylated at residue 181 (pTau181) could differentiate between clinically diagnosed or autopsy-confirmed AD and frontotemporal lobar degeneration. Plasma pTau181 concentrations were increased by 3.5-fold in AD compared to controls and differentiated AD from both clinically diagnosed (receiver operating characteristic area under the curve of 0.894) and autopsy-confirmed frontotemporal lobar degeneration (area under the curve of 0.878). Plasma pTau181 identified individuals who were amyloid beta-PET-positive regardless of clinical diagnosis and correlated with cortical tau protein deposition measured by F-18-flortaucipir PET. Plasma pTau181 may be useful to screen for tau pathology associated with AD.
机译:随着新疾病修饰的阿尔茨海默病(AD)疗法的潜在发展,需要简单,广泛可用的筛选试验来确定正在进行认知或行为下降的症状的个体,以进一步评估治疗的启动。比目前批准的脑脊液或淀粉样蛋白β正电子发射断层扫描(PET)诊断测试,AD的基于血液的测试是较少的侵入性和更便宜的筛选工具。我们检查了在残留物181(ptau181)的血浆Tau磷酸化是否可以区分临床诊断或尸检确认的广告和额定颞叶退化。与从临床诊断术(曲线下的接收器操作特征区域)的对照和分化的广告相比,血浆PTAU181浓度增加3.5倍,术诊断为0.894的接收器操作特征区域)和尸检确认的额发射叶片变性(曲线下的面积为0.878)。血浆ptau181鉴定为淀粉样蛋白β-peat阳性的个体,无论临床诊断,与由f-18-flortaucipir pet测量的皮质Tau蛋白沉积相关。等离子体ptau181可用于筛选与广告相关的TAU病理学。

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  • 来源
    《Nature medicine》 |2020年第3期|共21页
  • 作者单位

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Eli Lilly &

    Co Indianapolis IN 46285 USA;

    Eli Lilly &

    Co Indianapolis IN 46285 USA;

    Eli Lilly &

    Co Indianapolis IN 46285 USA;

    Eli Lilly &

    Co Indianapolis IN 46285 USA;

    Eli Lilly &

    Co Indianapolis IN 46285 USA;

    Eli Lilly &

    Co Indianapolis IN 46285 USA;

    Univ Gothenburg Inst Neurosci &

    Physiol Dept Psychiat &

    Neurochem Sahlgrenska Acad Molndal;

    Univ Gothenburg Inst Neurosci &

    Physiol Dept Psychiat &

    Neurochem Sahlgrenska Acad Molndal;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Vrije Univ Dept Clin Chem Amsterdam Univ Med Ctr Neurochem Lab Amsterdam Netherlands;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Mayo Clin Dept Neurol Rochester MN USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Eli Lilly &

    Co Indianapolis IN 46285 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Univ Calif San Francisco Dept Neurol Memory &

    Aging Ctr San Francisco CA 94143 USA;

    Mayo Clin Dept Neurol Rochester MN USA;

    Mayo Clin Dept Neurol Rochester MN USA;

    Mayo Clin Dept Neurol Jacksonville FL USA;

    Univ Penn Dept Neurol Philadelphia PA 19104 USA;

    Columbia Univ Dept Psychiat New York NY USA;

    Johns Hopkins Univ Dept Psychiat Baltimore MD USA;

    Univ N Carolina Dept Neurol Chapel Hill NC 27515 USA;

    Univ Alabama Birmingham Dept Neurol Birmingham AL USA;

    Washington Univ Dept Neurol St Louis MO 63110 USA;

    Northwestern Univ Dept Neurol Evanston IL USA;

    Case Western Reserve Univ Dept Neurol Cleveland OH 44106 USA;

    Univ Calif San Diego Dept Neurosci La Jolla CA 92093 USA;

    Univ Texas Southwestern Dept Neurol Dallas TX USA;

    Univ Calif Los Angeles Dept Neurol Los Angeles CA 90024 USA;

    Univ Calif Los Angeles Dept Neurol Los Angeles CA 90024 USA;

    Univ Calif Los Angeles Semel Inst Neurosci &

    Behav Los Angeles CA USA;

    Univ Calif Los Angeles Semel Inst Neurosci &

    Behav Los Angeles CA USA;

    Univ Hlth Network Dept Med Neurology Toronto ON Canada;

    Univ British Columbia Dept Med Div Neurol Vancouver BC Canada;

    Univ British Columbia Dept Pathol &

    Lab Med Vancouver BC Canada;

    Univ Washington Dept Neurol Seattle WA 98195 USA;

    Indiana Univ Natl Cent Repository Alzheimers Dis &

    Related Dem Indianapolis IN 46204 USA;

    Harvard Univ Dept Neurol Boston MA 02115 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医药、卫生;
  • 关键词

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