Variants at the Interleukin 1 Gene Locus and Pericarditis

Author:

Thorolfsdottir Rosa B.1,Jonsdottir Andrea B.1,Sveinbjornsson Gardar1,Aegisdottir Hildur M.1,Oddsson Asmundur1,Stefansson Olafur A.1,Halldorsson Gisli H.12,Saevarsdottir Saedis134,Thorleifsson Gudmar1,Stefansdottir Lilja1,Pedersen Ole B.56,Sørensen Erik7,Ghouse Jonas89,Raja Anna Axelsson8,Zheng Chaoqun8,Silajdzija Elvira8,Rand Søren Albertsen89,Erikstrup Christian1011,Ullum Henrik12,Mikkelsen Christina713,Banasik Karina1415,Brunak Søren15,Ivarsdottir Erna V.1,Sigurdsson Asgeir1,Beyter Doruk1,Sturluson Arni1,Einarsson Hafsteinn12,Tragante Vinicius1,Helgason Hannes12,Lund Sigrun H.1,Halldorsson Bjarni V.116,Sigurpalsdottir Brynja D.116,Olafsson Isleifur17,Arnar David O.134,Thorgeirsson Gudmundur1,Knowlton Kirk U.1819,Nadauld Lincoln D.2021,Gretarsdottir Solveig1,Helgadottir Anna1,Ostrowski Sisse R.67,Gudbjartssson Daniel F.12,Jonsdottir Ingileif1322,Bundgaard Henning68,Holm Hilma1,Sulem Patrick1,Stefansson Kari13,Banasik Karina23,Bay Jakob23,Boldsen Jens K.23,Brodersen Thorsten23,Brunak Søren23,Burgdorf Kristoffer23,Chalmer Mona A.23,Didriksen Maria23,Dinh Khoa M.23,Dowsett Joseph23,Erikstrup Christian23,Feenstra Bjarke23,Geller Frank23,Gudbjartsson Daniel23,Hansen Thomas F.23,Hindhede Lotte23,Hjalgrim Henrik23,Jacobsen Rikke L.23,Jemec Gregor23,Jensen Bitten A.23,Kaspersen Katrine23,Kjerulff Bertram D.23,Kogelman Lisette23,Larsen Margit A. H.23,Louloudis Ioannis23,Lundgaard Agnete23,Mikkelsen Susan23,Mikkelsen Christina23,Nissen Ioanna23,Nyegaard Mette23,Ostrowski Sisse R.23,Pedersen Ole B.23,Henriksen Alexander P.23,Rohde Palle D.23,Rostgaard Klaus23,Schwinn Michael23,Stefansson Kari23,Stefánsson Hreinn23,Sørensen Erik23,Thorsteinsdóttir Unnur23,Thørner Lise W.23,Topholm Bruun Mie23,Ullum Henrik23,Werge Thomas23,Westergaard David23,

Affiliation:

1. deCODE genetics, Amgen, Reykjavik, Iceland

2. School of Engineering and Natural Sciences, University of Iceland, Reykjavik, Iceland

3. Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland

4. Department of Medicine, Landspitali, The National University Hospital of Iceland, Reykjavik, Iceland

5. Department of Clinical Immunology, Zealand University Hospital, Køge, Denmark

6. Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark

7. Department of Clinical Immunology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark

8. Department of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark

9. Laboratory for Molecular Cardiology, Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark

10. Department of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark

11. Department of Clinical Medicine, Aarhus University, Aarhus, Denmark

12. Statens Serum Institut, Copenhagen, Denmark

13. Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark

14. Department of Obstetrics and Gynaecology, Copenhagen University Hospital Hvidovre, Hvidovre, Denmark

15. Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark

16. School of Technology, Reykjavik University, Reykjavik, Iceland

17. Department of Clinical Biochemistry, Landspitali, National University Hospital of Iceland, Reykjavik, Iceland

18. Intermountain Medical Center, Intermountain Heart Institute, Salt Lake City, Utah

19. School of Medicine, University of Utah, Salt Lake City

20. Precision Genomics, Intermountain Healthcare, Saint George, Utah

21. School of Medicine, Stanford University, Stanford, California

22. Department of Immunology, Landspitali, The National University Hospital of Iceland, Reykjavik, Iceland

23. for the Danish Blood Donor Study Genomic Consortium

Abstract

ImportanceRecurrent pericarditis is a treatment challenge and often a debilitating condition. Drugs inhibiting interleukin 1 cytokines are a promising new treatment option, but their use is based on scarce biological evidence and clinical trials of modest sizes, and the contributions of innate and adaptive immune processes to the pathophysiology are incompletely understood.ObjectiveTo use human genomics, transcriptomics, and proteomics to shed light on the pathogenesis of pericarditis.Design, Setting, and ParticipantsThis was a meta-analysis of genome-wide association studies of pericarditis from 5 countries. Associations were examined between the pericarditis-associated variants and pericarditis subtypes (including recurrent pericarditis) and secondary phenotypes. To explore mechanisms, associations with messenger RNA expression (cis-eQTL), plasma protein levels (pQTL), and CpG methylation of DNA (ASM-QTL) were assessed. Data from Iceland (deCODE genetics, 1983-2020), Denmark (Copenhagen Hospital Biobank/Danish Blood Donor Study, 1977-2022), the UK (UK Biobank, 1953-2021), the US (Intermountain, 1996-2022), and Finland (FinnGen, 1970-2022) were included. Data were analyzed from September 2022 to August 2023.ExposureGenotype.Main Outcomes and MeasuresPericarditis.ResultsIn this genome-wide association study of 4894 individuals with pericarditis (mean [SD] age at diagnosis, 51.4 [17.9] years, 2734 [67.6%] male, excluding the FinnGen cohort), associations were identified with 2 independent common intergenic variants at the interleukin 1 locus on chromosome 2q14. The lead variant was rs12992780 (T) (effect allele frequency [EAF], 31%-40%; odds ratio [OR], 0.83; 95% CI, 0.79-0.87; P = 6.67 × 10−16), downstream of IL1B and the secondary variant rs7575402 (A or T) (EAF, 45%-55%; adjusted OR, 0.89; 95% CI, 0.85-0.93; adjusted P = 9.6 × 10−8). The lead variant rs12992780 had a smaller odds ratio for recurrent pericarditis (0.76) than the acute form (0.86) (P for heterogeneity = .03) and rs7575402 was associated with CpG methylation overlapping binding sites of 4 transcription factors known to regulate interleukin 1 production: PU.1 (encoded by SPI1), STAT1, STAT3, and CCAAT/enhancer-binding protein β (encoded by CEBPB).Conclusions and RelevanceThis study found an association between pericarditis and 2 independent sequence variants at the interleukin 1 gene locus. This finding has the potential to contribute to development of more targeted and personalized therapy of pericarditis with interleukin 1–blocking drugs.

Publisher

American Medical Association (AMA)

Subject

Cardiology and Cardiovascular Medicine

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