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Deep Resequencing of the 1q22 Locus in Non-Lobar Intracerebral Hemorrhage

  • Livia Parodi
  • , Mary E. Comeau
  • , Marios K. Georgakis
  • , Ernst Mayerhofer
  • , Jaeyoon Chung
  • , Guido J. Falcone
  • , Rainer Malik
  • , Stacie L. Demel
  • , Bradford B. Worrall
  • , Sebastian Koch
  • , Fernando D. Testai
  • , Steven J. Kittner
  • , Jacob L. McCauley
  • , Christiana E. Hall
  • , Douglas J. Mayson
  • , Mitchell S.V. Elkind
  • , Michael L. James
  • , Daniel Woo
  • , Jonathan Rosand
  • , Carl D. Langefeld
  • Christopher D. Anderson
  • Massachusetts General Hospital
  • The Broad Institute of MIT and Harvard
  • Brigham and Women’s Hospital
  • Wake Forest University
  • Ludwig Maximilian University of Munich
  • Boston University
  • Yale University
  • University of Cincinnati
  • University of Virginia
  • University of Miami
  • University of Illinois at Chicago
  • University of Maryland, Baltimore
  • University of Texas Southwestern Medical Center
  • MedStar Georgetown University Hospital
  • Columbia University
  • Duke University

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Abstract

Objective: Genome-wide association studies have identified 1q22 as a susceptibility locus for cerebral small vessel diseases, including non-lobar intracerebral hemorrhage (ICH) and lacunar stroke. In the present study, we performed targeted high-depth sequencing of 1q22 in ICH cases and controls to further characterize this locus and prioritize potential causal mechanisms, which remain unknown. Methods: A total of 95,000 base pairs spanning 1q22, including SEMA4A, SLC25A44, and PMF1/PMF1-BGLAP were sequenced in 1,055 spontaneous ICH cases (534 lobar and 521 non-lobar) and 1,078 controls. Firth regression and Rare Variant Influential Filtering Tool analysis were used to analyze common and rare variants, respectively. Chromatin interaction analyses were performed using Hi-C, chromatin immunoprecipitation followed by sequencing, and chromatin interaction analysis with paired-end tag databases. Multivariable Mendelian randomization assessed whether alterations in gene-specific expression relative to regionally co-expressed genes at 1q22 could be causally related to ICH risk. Results: Common and rare variant analyses prioritized variants in SEMA4A 5′-UTR and PMF1 intronic regions, overlapping with active promoter and enhancer regions based on ENCODE annotation. Hi-C data analysis determined that 1q22 is spatially organized in a single chromatin loop, and that the genes therein belong to the same topologically associating domain. Chromatin immunoprecipitation followed by sequencing and chromatin interaction analysis with paired-end tag data analysis highlighted the presence of long-range interactions between the SEMA4A-promoter and PMF1-enhancer regions prioritized by association testing. Multivariable Mendelian randomization analyses demonstrated that PMF1 overexpression could be causally related to non-lobar ICH risk. Interpretation: Altered promoter–enhancer interactions leading to PMF1 overexpression, potentially dysregulating polyamine catabolism, could explain demonstrated associations with non-lobar ICH risk at 1q22, offering a potential new target for prevention of ICH and cerebral small vessel disease. ANN NEUROL 2024;95:325–337.

Original languageEnglish
Pages (from-to)325-337
Number of pages13
JournalAnnals of Neurology
Volume95
Issue number2
DOIs
StatePublished - Feb 2024

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