Pleiotropy analysis between lobar intracerebral hemorrhage and CSF β-amyloid highlights new and established associations.

TitlePleiotropy analysis between lobar intracerebral hemorrhage and CSF β-amyloid highlights new and established associations.
Publication TypeJournal Article
Year of Publication2023
AuthorsMarini S, Chung J, Han X, Sun X, Parodi L, Farrer LA, Rosand J, Romero JRafael, Anderson CD
JournalInt J Stroke
Volume18
Issue7
Pagination804-811
Date Published08/2023
ISSN1747-4949
KeywordsAmyloid beta-Peptides, Brain, Cerebral Amyloid Angiopathy, Cerebral Hemorrhage, Genome-Wide Association Study, Humans, Magnetic Resonance Imaging, Stroke
Abstract

BACKGROUND AND AIMS: Combining biologically related traits in genome-wide association studies (GWAS) increases the power for genetic discovery. Given the established relationship between lobar intracerebral hemorrhage (ICH) and cerebral amyloid angiopathy (CAA), and between the latter and levels of cerebrospinal fluid amyloid-β 42 (CSF-Aβ42), we leveraged genetic predisposition for lower CSF-Aβ42 levels as a proxy phenotype for CAA to identify new genes associated with lobar ICH.

METHODS: We used publicly available GWAS data for CSF-Aβ42 levels (n = 3146) and for lobar ICH (n = 2094). First, we evaluated the association between lobar ICH risk and CSF-Aβ42 in lobar ICH patients using a polygenic risk score (PRS) for CSF-Aβ42. Next, we conducted multi-trait analysis of GWAS (MTAG) for pleiotropy analysis of lobar ICH and CSF-Aβ42. MTAG results were further tested using Expression Quantitative Trait Locus and Differential Gene Expression Analyses.

RESULTS: CSF-Aβ42 PRS was associated with lobar ICH risk (p = 0.04). MTAG analysis identified a novel association within (rs1007589; minor allele frequency = 0.09; MTAG p = 5.4 × 10; lobar ICH odds ratio = 1.4 and p = 2.4 × 10; CSF-Aβ42 β = -0.03 and p = 4.5 × 10). rs1007589 was significantly associated with the expression levels of in temporal and occipital cortices, regions known to preferentially accumulate microhemorrhages in CAA.

CONCLUSION: Our pleiotropy analysis suggested a variant possibly implicated with lobar ICH driven by amyloid-related mechanisms in and associated with differential expression in brain regions characteristically affected by CAA. CDH9 is one subtype of the cadherin superfamily, which regulates intercellular adhesion, is involved in blood-brain barrier integrity, and is elevated in Alzheimer's disease patients. Further analyses are warranted to understand the effects of the variant on the pathogenesis of ICH and its clinical significance.

DOI10.1177/17474930231155816
Alternate JournalInt J Stroke
PubMed ID36705426
Grant ListU19 AG068753 / AG / NIA NIH HHS / United States
RF1 AG057519 / AG / NIA NIH HHS / United States
R01 AG048927 / AG / NIA NIH HHS / United States
U01 AG062602 / AG / NIA NIH HHS / United States
U01 AG032984 / AG / NIA NIH HHS / United States
K23 NS086873 / NS / NINDS NIH HHS / United States