Translational Neurodegeneration (Jun 2023)

Head-to-head comparison of plasma and PET imaging ATN markers in subjects with cognitive complaints

  • Jiaying Lu,
  • Xiaoxi Ma,
  • Huiwei Zhang,
  • Zhenxu Xiao,
  • Ming Li,
  • Jie Wu,
  • Zizhao Ju,
  • Li Chen,
  • Li Zheng,
  • Jingjie Ge,
  • Xiaoniu Liang,
  • Weiqi Bao,
  • Ping Wu,
  • Ding Ding,
  • Tzu-Chen Yen,
  • Yihui Guan,
  • Chuantao Zuo,
  • Qianhua Zhao,
  • on behalf of the Shanghai Memory Study (SMS)

DOI
https://doi.org/10.1186/s40035-023-00365-x
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 15

Abstract

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Abstract Background Gaining more information about the reciprocal associations between different biomarkers within the ATN (Amyloid/Tau/Neurodegeneration) framework across the Alzheimer’s disease (AD) spectrum is clinically relevant. We aimed to conduct a comprehensive head-to-head comparison of plasma and positron emission tomography (PET) ATN biomarkers in subjects with cognitive complaints. Methods A hospital-based cohort of subjects with cognitive complaints with a concurrent blood draw and ATN PET imaging (18F-florbetapir for A, 18F-Florzolotau for T, and 18F-fluorodeoxyglucose [18F-FDG] for N) was enrolled (n = 137). The β-amyloid (Aβ) status (positive versus negative) and the severity of cognitive impairment served as the main outcome measures for assessing biomarker performances. Results Plasma phosphorylated tau 181 (p-tau181) level was found to be associated with PET imaging of ATN biomarkers in the entire cohort. Plasma p-tau181 level and PET standardized uptake value ratios of AT biomarkers showed a similarly excellent diagnostic performance for distinguishing between Aβ+ and Aβ− subjects. An increased tau burden and glucose hypometabolism were significantly associated with the severity of cognitive impairment in Aβ+ subjects. Additionally, glucose hypometabolism – along with elevated plasma neurofilament light chain level – was related to more severe cognitive impairment in Aβ− subjects. Conclusion Plasma p-tau181, as well as 18F-florbetapir and 18F-Florzolotau PET imaging can be considered as interchangeable biomarkers in the assessment of Aβ status in symptomatic stages of AD. 18F-Florzolotau and 18F-FDG PET imaging could serve as biomarkers for the severity of cognitive impairment. Our findings have implications for establishing a roadmap to identifying the most suitable ATN biomarkers for clinical use.

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