Literature DB >> 32586852

Regional hyperperfusion in cognitively normal APOE ε4 allele carriers in mid-life: analysis of ASL pilot data from the PREVENT-Dementia cohort.

Elizabeth Frances McKiernan1, Elijah Mak2, Maria-Eleni Dounavi2, Katie Wells3, Craig Ritchie4, Guy Williams5, Li Su2, John O'Brien2.   

Abstract

BACKGROUND: Regional cerebral hypoperfusion is characteristic of Alzheimer's disease (AD). Previous studies report conflicting findings in cognitively normal individuals at high risk of AD. Understanding early preclinical perfusion alterations may improve understanding of AD pathogenesis and lead to new biomarkers and treatment targets.
METHODS: 3T arterial spin labelling MRI scans from 162 participants in the PREVENT-Dementia cohort were analysed (cognitively normal participants aged 40-59, stratified by future dementia risk). Cerebral perfusion was compared vertex-wise according to APOE ε4 status and family history (FH). Correlations between individual perfusion, age and cognitive scores (COGNITO battery) were explored.
RESULTS: Regional hyperperfusion was found in APOE ε4+group (left cingulate and lateral frontal and parietal regions p<0.01, threshold-free cluster enhancement, TFCE) and in FH +group (left temporal and parietal regions p<0.01, TFCE). Perfusion did not correlate with cognitive test scores.
CONCLUSIONS: Regional cerebral hyperperfusion in individuals at increased risk of AD in mid-life may be a very early marker of functional brain change related to AD. Increased perfusion may reflect a functional 'compensation' mechanism, offsetting the effects of early neural damage or may itself be risk factor for accelerating spread of degenerative pathology. © Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Year:  2020        PMID: 32586852     DOI: 10.1136/jnnp-2020-322924

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  4 in total

Review 1.  Causes and consequences of baseline cerebral blood flow reductions in Alzheimer's disease.

Authors:  Oliver Bracko; Jean C Cruz Hernández; Laibaik Park; Nozomi Nishimura; Chris B Schaffer
Journal:  J Cereb Blood Flow Metab       Date:  2021-01-14       Impact factor: 6.200

2.  Mediation of the APOE Associations With Cognition Through Cerebral Blood Flow: The CIBL Study.

Authors:  Yan-Li Wang; Mengfan Sun; Fang-Ze Wang; Xiaohong Wang; Ziyan Jia; Yuan Zhang; Runzhi Li; Jiwei Jiang; Linlin Wang; Wenyi Li; Yongan Sun; Jinglong Chen; Cuicui Zhang; Baolin Shi; Jianjian Liu; Xiangrong Liu; Jun Xu
Journal:  Front Aging Neurosci       Date:  2022-06-30       Impact factor: 5.702

3.  The Open-Access European Prevention of Alzheimer's Dementia (EPAD) MRI dataset and processing workflow.

Authors:  Luigi Lorenzini; Silvia Ingala; Alle Meije Wink; Joost P A Kuijer; Viktor Wottschel; Mathijs Dijsselhof; Carole H Sudre; Sven Haller; José Luis Molinuevo; Juan Domingo Gispert; David M Cash; David L Thomas; Sjoerd B Vos; Ferran Prados; Jan Petr; Robin Wolz; Alessandro Palombit; Adam J Schwarz; Gaël Chételat; Pierre Payoux; Carol Di Perri; Joanna M Wardlaw; Giovanni B Frisoni; Christopher Foley; Nick C Fox; Craig Ritchie; Cyril Pernet; Adam Waldman; Frederik Barkhof; Henk J M M Mutsaerts
Journal:  Neuroimage Clin       Date:  2022-07-07       Impact factor: 4.891

4.  Evidence of cerebral hemodynamic dysregulation in middle-aged APOE ε4 carriers: The PREVENT-Dementia study.

Authors:  Maria-Eleni Dounavi; Audrey Low; Elizabeth F McKiernan; Elijah Mak; Graciela Muniz-Terrera; Karen Ritchie; Craig W Ritchie; Li Su; John T O'Brien
Journal:  J Cereb Blood Flow Metab       Date:  2021-06-02       Impact factor: 6.200

  4 in total

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