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Blood Phosphorylated Tau 181 as a Biomarker for Amyloid Burden on Brain PET in Cognitively Healthy Adults.
McGrath, Emer R; Beiser, Alexa S; O'Donnell, Adrienne; Yang, Qiong; Ghosh, Saptaparni; Gonzales, Mitzi M; Himali, Jayandra J; Satizabal, Claudia L; Johnson, Keith A; Tracy, Russell P; Seshadri, Sudha.
Afiliação
  • McGrath ER; HRB Clinical Research Facility, National University of Ireland Galway, Galway, Ireland.
  • Beiser AS; The Framingham Heart Study, Framingham, MA, USA.
  • O'Donnell A; The Framingham Heart Study, Framingham, MA, USA.
  • Yang Q; Boston University School of Public Health, Boston, MA, USA.
  • Ghosh S; Boston University School of Medicine, Boston, MA, USA.
  • Gonzales MM; The Framingham Heart Study, Framingham, MA, USA.
  • Himali JJ; Boston University School of Public Health, Boston, MA, USA.
  • Satizabal CL; The Framingham Heart Study, Framingham, MA, USA.
  • Johnson KA; Boston University School of Public Health, Boston, MA, USA.
  • Tracy RP; The Framingham Heart Study, Framingham, MA, USA.
  • Seshadri S; Boston University School of Medicine, Boston, MA, USA.
J Alzheimers Dis ; 87(4): 1517-1526, 2022.
Article em En | MEDLINE | ID: mdl-35491781
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-ß (Aß) 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 Aß-precuneus, Aß-FLR (frontal, lateral, and retrosplenial cortices) and tau-global composite region PET deposition. Secondary outcomes included individual regional Aß 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 Aß deposition in the FLR (ß±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 Aß 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-Aß 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 Aß 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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Amiloidose Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Alzheimers Dis Assunto da revista: GERIATRIA / NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Irlanda País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Amiloidose Tipo de estudo: Prognostic_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Alzheimers Dis Assunto da revista: GERIATRIA / NEUROLOGIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Irlanda País de publicação: Holanda