4.6 Article

Plasma biomarker profiles and the correlation with cognitive function across the clinical spectrum of Alzheimer's disease

Journal

ALZHEIMERS RESEARCH & THERAPY
Volume 13, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13195-021-00864-x

Keywords

Plasma p-tau181; Simoa; Cognitive domain; CDR; Alzheimer's disease

Funding

  1. Clinical Research Plan of SHDC [SHDC2020CR4007]
  2. Key Projects of Special Development Funds for the Shanghai Zhangjiang National Innovation Demonstration Zone [201905-XHCHJ-H25-201]
  3. MOE Frontiers Center for Brain Science [JIH2642001/028]
  4. Scientific Research Plan Project of Shanghai Science and Technology Committee [17411950106, 17411950701]
  5. National Project of Chronic Disease [2016YFC1306402]
  6. National Natural Science Foundation of China [82071200, 81773513, 21874091, 31927803]
  7. Shanghai Municipal Science and Technology Major Project [2018SHZDZX01]
  8. ZJLab

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Plasma biomarkers in Alzheimer's disease (AD) diagnosis and management are promising, but their profiles and associations with cognition across cognitive stages have been rarely reported. Plasma p-tau181 showed correlations with broader cognitive domains, suggesting its potential as a promising clinical-relevant blood-based biomarker.
Background Plasma biomarkers showed a promising value in the disease diagnosis and management of Alzheimer's disease (AD). However, profiles of the biomarkers and the associations with cognition across a spectrum of cognitive stages have seldom been reported. Methods We recruited 320 individuals with cognitive impairment and 131 cognitively normal participants from a memory clinic and a community cohort. Participants were classified into 6 groups based on their Clinical Dementia Rating (CDR) scores and clinical diagnosis, including AD, amnestic mild cognitive impairment (aMCI), and normal cognition (NC). A battery of neuropsychological tests was used to assess the global and domain-specific cognition. Plasma A beta(1-40), A beta(1-42), A beta(1-42)/A beta(1-40), total tau (t-tau), neurofilament protein light chain (NfL), and phosphorylated tau at threonine 181 (p-tau181) were quantified using the single-molecule array (Simoa) platform. Results All the plasma markers (A beta(1-40), A beta(1-42), A beta(1-42)/A beta(1-40), t-tau, NfL, p-tau181) showed certain discrepancies among NC, aMCI, and AD groups. The p-tau181 level showed a continuous escalating trend as the CDR scores increased from 0 (NC group) to 3 (severe AD). Compared with other biomarkers, p-tau181 had correlations with broader cognitive domains, covering global cognition (r = -0.536, P < 0.0001), memory (r = -0.481, P < 0.0001), attention (r = -0.437, P < 0.0001), visuospatial function (r = -0.385, P < 0.0001), and language (r = -0.177, P = 0.0003). Among participants with CDR >= 1, higher p-tau181 was correlated with worse global cognition (r = -0.301, P < 0.001). Conclusions Plasma p-tau181 had correlations with broader cognitive domains, suggesting its potential as a promising clinical-relevant blood-based biomarker.

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