Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis

• Published in: Communications biology Vol. 4; no. 1; p. 392
• Main Authors: Dhindsa, Ryan S., Mattsson, Johan, Nag, Abhishek, Wang, Quanli, Wain, Louise V., Allen, Richard, Wigmore, Eleanor M., Ibanez, Kristina, Vitsios, Dimitrios, Deevi, Sri V. V., Wasilewski, Sebastian, Karlsson, Maria, Lassi, Glenda, Olsson, Henric, Muthas, Daniel, Monkley, Susan, Mackay, Alex, Murray, Lynne, Young, Simon, Haefliger, Carolina, Maher, Toby M., Belvisi, Maria G., Jenkins, Gisli, Molyneaux, Philip L., Platt, Adam, Petrovski, Slavé
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 23.03.2021; Nature Publishing Group; Nature Portfolio
• Subjects: 38/61; 45/23; 45/43; 631/208/205; 692/699/1785; Aged; Biology; Biomedical and Life Sciences; Case-Control Studies; Cell Cycle Proteins - genetics; Cell division; Exome Sequencing; Female; Fibrosis; Genetic Predisposition to Disease; Genome-Wide Association Study; Genomes; Humans; Idiopathic Pulmonary Fibrosis - diagnosis; Idiopathic Pulmonary Fibrosis - genetics; Life Sciences; Lung diseases; Male; Mutation, Missense; Phenotype; Pulmonary fibrosis; Risk factors
• ISSN: 2399-3642; 2399-3642
• DOI: 10.1038/s42003-021-01910-y

Idiopathic pulmonary fibrosis (IPF) is a fatal disorder characterised by progressive, destructive lung scarring. Despite substantial progress, the genetic determinants of this disease remain incompletely defined. Using whole genome and whole exome sequencing data from 752 individuals with sporadic IPF and 119,055 UK Biobank controls, we performed a variant-level exome-wide association study (ExWAS) and gene-level collapsing analyses. Our variant-level analysis revealed a novel association between a rare missense variant in SPDL1 and IPF (NM_017785.5:g.169588475 G > A p.Arg20Gln; p  = 2.4 × 10 −7 , odds ratio = 2.87, 95% confidence interval: 2.03–4.07). This signal was independently replicated in the FinnGen cohort, which contains 1028 cases and 196,986 controls (combined p  = 2.2 × 10 −20 ), firmly associating this variant as an IPF risk allele. SPDL1 encodes Spindly, a protein involved in mitotic checkpoint signalling during cell division that has not been previously described in fibrosis. To the best of our knowledge, these results highlight a novel mechanism underlying IPF, providing the potential for new therapeutic discoveries in a disease of great unmet need. Ryan Dhindsa et al. conducted an exome-wide association study to identify a rare variant in SPDL1 as a risk factor for idiopathic pulmonary fibrosis (IPF). Their findings implicate mitotic checkpoint signalling as a new mechanism underlying IPF.