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Genome-wide SNP-sex interaction analysis of susceptibility to idiopathic pulmonary fibrosis.

Olivia C LeavyAnne F GoemansAmy D StockwellRichard J AllenBeatriz Guillen-GuioTamara Hernandez-BeeftinkAyodeji AdegunsoyeHelen L Boothnull nullPaul CullinanWilliam A FahyTasha E FingerlinHarvinder S VirkIan P HallSimon P HartMike R HillNik HiraniRichard B HubbardNaftali KaminskiShwu-Fan MaRobin J McAnultyX Rebecca ShengAnn B MillarMaria Molina-MolinaVidyia NavaratnamMargaret NeighborsHelen ParfreyGauri SainiIan SayersMary E StrekMartin D TobinMoira Kb WhyteYingze ZhangToby M MaherPhilip L MolyneauxJustin M OldhamBrian L YaspanCarlos FloresFernando MartinezCarl J ReynoldsDavid A SchwartzImre NothR Gisli JenkinsLouise V Wain
Published in: medRxiv : the preprint server for health sciences (2024)
Although we found some preliminary evidence of genetic variants with sex-specific effects on IPF risk, our analyses suggest that genome-wide genetic risk from common single nucleotide polymorphisms is similar in males and females. This is important when considering integration of polygenic risk scores into clinical prediction models for IPF. There may be other forms of genetic variation, such as complex structural variation or rare variants, not captured in this analysis, that may improve risk prediction for males and females separately.
Keyphrases
  • idiopathic pulmonary fibrosis
  • genome wide
  • dna methylation
  • copy number
  • interstitial lung disease
  • gene expression
  • systemic sclerosis