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GWAS Study

Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936.

Hillary RF, McCartney DL, Harris SE et al.

31320639 PubMed ID
GWAS Study Type
750 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HR
Hillary RF
MD
McCartney DL
HS
Harris SE
SA
Stevenson AJ
SA
Seeboth A
ZQ
Zhang Q
LD
Liewald DC
EK
Evans KL
RC
Ritchie CW
TE
Tucker-Drob EM
WN
Wray NR
MA
McRae AF
VP
Visscher PM
DI
Deary IJ
MR
Marioni RE
Chapter II

Abstract

Summary of the research findings

Although plasma proteins may serve as markers of neurological disease risk, the molecular mechanisms responsible for inter-individual variation in plasma protein levels are poorly understood. Therefore, we conduct genome- and epigenome-wide association studies on the levels of 92 neurological proteins to identify genetic and epigenetic loci associated with their plasma concentrations (n = 750 healthy older adults). We identify 41 independent genome-wide significant (P < 5.4 × 10-10) loci for 33 proteins and 26 epigenome-wide significant (P < 3.9 × 10-10) sites associated with the levels of 9 proteins. Using this information, we identify biological pathways in which putative neurological biomarkers are implicated (neurological, immunological and extracellular matrix metabolic pathways). We also observe causal relationships (by Mendelian randomisation analysis) between changes in gene expression (DRAXIN, MDGA1 and KYNU), or DNA methylation profiles (MATN3, MDGA1 and NEP), and altered plasma protein levels. Together, this may help inform causal relationships between biomarkers and neurological diseases.

750 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

750
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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