Identification of a novel missense variant in SPDL1 associated with idiopathic pulmonary fibrosis
Identification of a novel missense variant in SPDL1 associated with idiopathic pulmonary fibrosis
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Author / Creator
Dhindsa, Ryan S , Mattsson, Johan , Nag, Abhishek , Wang, Quanli , Wain, Louise V , Allen, Richard , Wigmore, Eleanor M , Ibanez, Kristina , Vitsios, Dimitrios , Sri Vv Deevi , Wasilewski, Sebastian , Karlsson, Maria , Lassi, Glenda , Olsson, Henric , Muthas, Daniel , Mackay, Alex , Murray, Lynne , Young, Simon , Haefliger, Carolina , Consortium, Finngen , Maher, Toby M , Belvisi, Maria G , Jenkins, Gisli , Molyneaux, Philip , Platt, Adam and Petrovski, Slavé
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Cold Spring Harbor: Cold Spring Harbor Laboratory Press
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English
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Cold Spring Harbor: Cold Spring Harbor Laboratory Press
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Contents
Idiopathic pulmonary fibrosis (IPF) is a fatal disorder characterised by progressive, destructive lung scarring. Despite significant progress, the genetic determinants of this disease remain incompletely defined. Using next generation sequencing data from 752 individuals with sporadic IPF and 119,055 controls, we performed both variant- and gene-level analyses to identify novel IPF genetic risk factors. Our variant-level analysis revealed a novel rare missense variant in SPDL1 (NM_017785.5 p.Arg20Gln; p = 2.4 x 10-7, odds ratio = 2.87). This signal was independently replicated in the FinnGen cohort (combined p = 2.2 x 10-20), firmly associating this variant as a novel IPF risk allele. SPDL1 encodes Spindly, a protein involved in mitotic checkpoint signalling during cell division that has not been previously described in fibrosis. Our results highlight a novel mechanism underlying IPF, providing the potential for new therapeutic discoveries in a disease of great unmet need. Competing Interest Statement L.W. holds a GSK/British Lung Foundation Chair in Respiratory Research. The research was partially supported by the National Institute for Health Research (NIHR) Leicester Biomedical Research Centre; the views expressed are those of the author(s) and not necessarily those of the National Health Service (NHS), the NIHR or the Department of Health. P.L.M. is supported by an Action for Pulmonary Fibrosis Mike Bray fellowship. T.M.M. is supported by a National Institute for Health Research Clinician Scientist Fellowship (NIHR ref: CS-2013-13-017) and is a British Lung Foundation Chair in Respiratory Research (C17-3). The FinnGen project is funded by two grants from Business Finland (HUS 4685/31/2016 and UH 4386/31/2016) and eleven industry partners (AbbVie Inc, AstraZeneca UK Ltd, Biogen MA Inc, Celgene Corporation, Celgene International II Sarl, Genentech Inc, Merck Sharp & Dohme Corp, Pfizer Inc., GlaxoSmithKline, Sanofi, Maze Therapeutics Inc., Janssen Biotech Inc). Following biobanks are acknowledged for collecting the FinnGen project samples: Auria Biobank (www.auria.fi/biopankki), THL Biobank (www.thl.fi/biobank), Helsinki Biobank (www.helsinginbiopankki.fi), Biobank Borealis of Northern Finland (
Alternative Titles
Full title
Identification of a novel missense variant in SPDL1 associated with idiopathic pulmonary fibrosis
Authors, Artists and Contributors
Author / Creator
Mattsson, Johan
Nag, Abhishek
Wang, Quanli
Wain, Louise V
Allen, Richard
Wigmore, Eleanor M
Ibanez, Kristina
Vitsios, Dimitrios
Sri Vv Deevi
Wasilewski, Sebastian
Karlsson, Maria
Lassi, Glenda
Olsson, Henric
Muthas, Daniel
Mackay, Alex
Murray, Lynne
Young, Simon
Haefliger, Carolina
Consortium, Finngen
Maher, Toby M
Belvisi, Maria G
Jenkins, Gisli
Molyneaux, Philip
Platt, Adam
Petrovski, Slavé
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TN_cdi_proquest_journals_2418457295
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2418457295
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E-ISSN
2692-8205
DOI
10.1101/2020.06.29.178079
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https://www.proquest.com/docview/2418457295?pq-origsite=primo&accountid=13902