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CSF Aß42 and tau biomarkers in cognitively unimpaired Aß- middle-aged and older APOE ε4 carriers.
Lim, Yen Ying; Yassi, Nawaf; Bransby, Lisa; Ayton, Scott; Buckley, Rachel F; Eratne, Dhamidhu; Velakoulis, Dennis; Li, Qiao-Xin; Fowler, Christopher; Masters, Colin L; Maruff, Paul.
Afiliação
  • Lim YY; Turner Institute of Brain and Mental Health, School of Psychological Sciences, Monash University, Clayton, Australia. Electronic address: yenying.lim@monash.edu.
  • Yassi N; Population Health and Immunity Division, Walter and Eliza Hall Institute of Medical Research, Parkville, Australia; Department of Neurology, Melbourne Brain Centre at the Royal Melbourne Hospital, University of Melbourne, Parkville, Australia.
  • Bransby L; Turner Institute of Brain and Mental Health, School of Psychological Sciences, Monash University, Clayton, Australia.
  • Ayton S; Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Australia.
  • Buckley RF; Department of Neurology, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.
  • Eratne D; Melbourne Neuropsychiatry Centre, University of Melbourne, Parkville, Australia.
  • Velakoulis D; Melbourne Neuropsychiatry Centre, University of Melbourne, Parkville, Australia.
  • Li QX; Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Australia.
  • Fowler C; Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Australia.
  • Masters CL; Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Australia.
  • Maruff P; Turner Institute of Brain and Mental Health, School of Psychological Sciences, Monash University, Clayton, Australia; Florey Institute of Neuroscience and Mental Health, University of Melbourne, Parkville, Australia; Cogstate Ltd., Melbourne, Australia.
Neurobiol Aging ; 129: 209-218, 2023 09.
Article em En | MEDLINE | ID: mdl-37399739
ABSTRACT
This study aimed to determine the relationship between the apolipoprotein E (APOE) ε4 allele and cerebrospinal fluid (CSF) and neuroimaging biomarkers of Alzheimer's disease, and cognition in cognitively unimpaired (CU) middle-aged adults (n = 82; Mage = 58.2), and in Aß- CU older adults (n = 71; Mage = 71.8). Aß- CU middle-aged ε4 carriers showed lower CSF Aß42 levels, higher levels of CSF total tau (t-tau) and neurofilament light (NfL), and poorer cognitive performance compared to noncarriers (Cohen's d 0.30-0.56). In Aß- CU older adults, ε4 carriers also had lower CSF Aß42 levels and higher levels of CSF t-tau and p-tau181, compared to noncarriers (Cohen's d 0.65-0.74). In both Aß- middle-aged and older adults, hippocampal and total brain volume were equivalent between ε4 carriers and noncarriers. In Aß- CU middle-aged adults, APOE ε4 is associated with decreased levels of Aß, increased tau and NfL, and poorer cognition. Similar relationships were observed in Aß- CU older adults. These results have implications for understanding clinicopathological relationships between APOE ε4 and the emergence of cognitive and biomarker abnormalities in Aß- adults.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Apolipoproteína E4 / Doença de Alzheimer Limite: Aged / Humans / Middle aged Idioma: En Revista: Neurobiol Aging Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Apolipoproteína E4 / Doença de Alzheimer Limite: Aged / Humans / Middle aged Idioma: En Revista: Neurobiol Aging Ano de publicação: 2023 Tipo de documento: Article