Dryad
Published February 23, 2022 | Version v1
Dataset Open

Rare missense functional variants at COL4A1 and COL4A2 in sporadic intracerebral hemorrhage

Creators

  • 1. Massachusetts General Hospital
  • 2. University of Glasgow
  • 3. Korea University
  • 4. University of Michigan–Ann Arbor
  • 5. University of Virginia Health System
  • 6. Mayo Clinic
  • 7. University of Florida
  • 8. Beth Israel Deaconess Medical Center
  • 9. University of Washington
  • 10. University of Arizona
  • 11. University of Cincinnati
  • 12. Wake Forest University
  • 13. University of Edinburgh

Description

Objective
To test the genetic contribution of rare missense variants in COL4A1 and COL4A2 in which common variants are genetically associated with sporadic intracerebral hemorrhage (ICH), we performed rare variant analysis in multiple sequencing data for the risk for sporadic ICH.

Methods
We performed sequencing across 559Kbp at 13q34 including COL4A1 and COL4A2 among 2,133 individuals (1,055 ICH cases; 1,078 controls) in US-based and 1,492 individuals (192 ICH cases; 1,300 controls) from Scotland-based cohorts, followed by sequence annotation, functional impact prediction, genetic association testing, and in silico thermodynamic modeling.

Results
We identified 107 rare nonsynonymous variants in sporadic ICH, of which 2 two missense variants, rs138269346 (COL4A1I110T) and rs201716258 (COL4A2H203L), were predicted to be highly functional and occurred in multiple ICH cases but not in controls from the US-based cohort. The minor allele of rs201716258 was also present in Scottish ICH patients, and rs138269346 was observed in two ICH-free controls with a history of hypertension and myocardial infarction. Rs138269346 was nominally associated with non-lobar ICH risk (P=0.05), but not with lobar ICH (P=0.08), while associations between rs201716258 and ICH subtypes were non-significant (P>0.12). Both variants were considered pathogenic based on minor allele frequency (<0.00035 in EUR), predicted functional impact (deleterious or probably damaging), and in silico modeling studies (substantially altered physical length and thermal stability of collagen).

Conclusions
We identified rare missense variants in COL4A1/A2 in association with sporadic ICH. Our annotation and simulation studies suggest that these variants are highly functional and may represent targets for translational follow-up.

Notes

Funding provided by: National Heart, Lung, and Blood Institute
Crossref Funder Registry ID: http://dx.doi.org/10.13039/100000050
Award Number: HHSN268201100037C

Funding provided by: National Institute of Neurological Disorders and Stroke
Crossref Funder Registry ID: http://dx.doi.org/10.13039/100000065
Award Number: R01NS103924

Funding provided by: Medical Research Council
Crossref Funder Registry ID: http://dx.doi.org/10.13039/501100000265
Award Number: MR/R005567-1

Funding provided by: Stroke Association
Crossref Funder Registry ID: http://dx.doi.org/10.13039/501100000364
Award Number: PPA 2016/02

Funding provided by: Heart Research UK
Crossref Funder Registry ID: http://dx.doi.org/10.13039/501100000327
Award Number: RG 2664/17/20

Funding provided by: Medical Research Council
Crossref Funder Registry ID: http://dx.doi.org/10.13039/501100000265
Award Number: Stroke Association clinical research training fellowship: G0900428

Funding provided by: Wellcome Trust
Crossref Funder Registry ID: http://dx.doi.org/10.13039/100010269
Award Number: 203699/Z/16/Z: clinical research training fellowship

Funding provided by: Medical Research Council
Crossref Funder Registry ID: http://dx.doi.org/10.13039/501100000265
Award Number: G1002605: senior clinical fellowship

Funding provided by: Biotechnology and Biological Sciences Research Council
Crossref Funder Registry ID: http://dx.doi.org/10.13039/501100000268
Award Number:

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