Blood DNA methylation signatures to detect dementia prior to overt clinical symptoms

  • Peter Daniel Fransquet
  • , Paul Lacaze
  • , Richard Saffery
  • , James Phung
  • , Emily Parker
  • , Raj Shah
  • , Anne Murray
  • , Robyn L. Woods
  • , Joanne Ryan

Research output: Contribution to journalArticlepeer-review

29 Citations (Scopus)

Abstract

Introduction: This study determined whether blood DNA methylation (DNAm) patterns differentiate individuals with presymptomatic dementia compared to controls. Methods: DNAm was measured in 73 individuals prior to dementia diagnosis and 87 cognitively healthy controls matched for age, sex, smoking, education, and baseline cognition. DNAm was also measured at 3 years follow-up in 25 dementia cases, and 24 controls. Results: Cases and controls differed in DNAm (unadjusted P <.01) at the time of diagnosis (n = 28,787 probes), and pre-diagnosis (n = 15,111 probes), with cg01404610 (General transcription factor IIA subunit 1 gene) significant after correction for multiple testing. Overall, 1150 probes overlapped between analyses (methylation differences from –10.6% to +11.0%), and effect sizes increased from pre-diagnosis to diagnosis. Discussion: Discernible blood DNAm signatures are in dementia cases before the appearance of overt clinical symptoms. Blood-based methylation may serve as a potential biomarker of dementia, but further investigation is needed to determine their true clinical utility.

Original languageEnglish (US)
Article numbere12056
JournalAlzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring
Volume12
Issue number1
DOIs
Publication statusPublished - 2020
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • biomarker
  • dementia
  • epigenome-wide association study
  • methylation
  • pre-diagnosis

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