GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibility

Autoimmune Addison’s disease is a rare complex disease, which has not yet been characterized by non-biased genetic studies. Here, the authors perform the first GWAS for the disease, identifying nine loci including two coding variants in the gene Autoimmune Regulator (AIRE).

Bibliographic Details
Main Authors: Daniel Eriksson, Ellen Christine Røyrvik, Maribel Aranda-Guillén, Amund Holte Berger, Nils Landegren, Haydee Artaza, Åsa Hallgren, Marianne Aardal Grytaas, Sara Ström, Eirik Bratland, Ileana Ruxandra Botusan, Bergithe Eikeland Oftedal, Lars Breivik, Marc Vaudel, Øyvind Helgeland, Alberto Falorni, Anders Palmstrøm Jørgensen, Anna-Lena Hulting, Johan Svartberg, Olov Ekwall, Kristian Johan Fougner, Jeanette Wahlberg, Bjørn Gunnar Nedrebø, Per Dahlqvist, The Norwegian Addison Registry Study Group, The Swedish Addison Registry Study Group, Per Morten Knappskog, Anette Susanne Bøe Wolff, Sophie Bensing, Stefan Johansson, Olle Kämpe, Eystein Sverre Husebye
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-021-21015-8
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spelling doaj-0be85e9204274eff9b1cb72be80b22052021-02-14T12:11:49ZengNature Publishing GroupNature Communications2041-17232021-02-0112111410.1038/s41467-021-21015-8GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibilityDaniel Eriksson0Ellen Christine Røyrvik1Maribel Aranda-Guillén2Amund Holte Berger3Nils Landegren4Haydee Artaza5Åsa Hallgren6Marianne Aardal Grytaas7Sara Ström8Eirik Bratland9Ileana Ruxandra Botusan10Bergithe Eikeland Oftedal11Lars Breivik12Marc Vaudel13Øyvind Helgeland14Alberto Falorni15Anders Palmstrøm Jørgensen16Anna-Lena Hulting17Johan Svartberg18Olov Ekwall19Kristian Johan Fougner20Jeanette Wahlberg21Bjørn Gunnar Nedrebø22Per Dahlqvist23The Norwegian Addison Registry Study GroupThe Swedish Addison Registry Study GroupPer Morten Knappskog24Anette Susanne Bøe Wolff25Sophie Bensing26Stefan Johansson27Olle Kämpe28Eystein Sverre Husebye29Centre for Molecular Medicine, Department of Medicine (Solna), Karolinska InstitutetDepartment of Clinical Science, University of BergenCentre for Molecular Medicine, Department of Medicine (Solna), Karolinska InstitutetDepartment of Clinical Science, University of BergenCentre for Molecular Medicine, Department of Medicine (Solna), Karolinska InstitutetDepartment of Clinical Science, University of BergenCentre for Molecular Medicine, Department of Medicine (Solna), Karolinska InstitutetDepartment of Clinical Science, University of BergenDepartment of Endocrinology, Metabolism and Diabetes, Karolinska University HospitalDepartment of Clinical Science, University of BergenDepartment of Endocrinology, Metabolism and Diabetes, Karolinska University HospitalDepartment of Clinical Science, University of BergenDepartment of Clinical Science, University of BergenCenter for Diabetes Research, Department of Clinical Science, University of BergenCenter for Diabetes Research, Department of Clinical Science, University of BergenDepartment of Medicine, University of PerugiaSection of Specialized Endocrinology, Department of Endocrinology, Oslo University HospitalDepartment of Molecular Medicine and Surgery, Karolinska InstitutetTromsø Endocrine Research Group, Department of Clinical Medicine, UiT The Arctic University of NorwayDepartment of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of GothenburgDepartment of Endocrinology, St. Olavs HospitalDepartment of Endocrinology, Linköping UniversityDepartment of Clinical Science, University of BergenDepartment of Public Health and Clinical Medicine, Umeå UniversityDepartment of Clinical Science, University of BergenDepartment of Clinical Science, University of BergenDepartment of Endocrinology, Metabolism and Diabetes, Karolinska University HospitalDepartment of Clinical Science, University of BergenCentre for Molecular Medicine, Department of Medicine (Solna), Karolinska InstitutetCentre for Molecular Medicine, Department of Medicine (Solna), Karolinska InstitutetAutoimmune Addison’s disease is a rare complex disease, which has not yet been characterized by non-biased genetic studies. Here, the authors perform the first GWAS for the disease, identifying nine loci including two coding variants in the gene Autoimmune Regulator (AIRE).https://doi.org/10.1038/s41467-021-21015-8
collection DOAJ
language English
format Article
sources DOAJ
author Daniel Eriksson
Ellen Christine Røyrvik
Maribel Aranda-Guillén
Amund Holte Berger
Nils Landegren
Haydee Artaza
Åsa Hallgren
Marianne Aardal Grytaas
Sara Ström
Eirik Bratland
Ileana Ruxandra Botusan
Bergithe Eikeland Oftedal
Lars Breivik
Marc Vaudel
Øyvind Helgeland
Alberto Falorni
Anders Palmstrøm Jørgensen
Anna-Lena Hulting
Johan Svartberg
Olov Ekwall
Kristian Johan Fougner
Jeanette Wahlberg
Bjørn Gunnar Nedrebø
Per Dahlqvist
The Norwegian Addison Registry Study Group
The Swedish Addison Registry Study Group
Per Morten Knappskog
Anette Susanne Bøe Wolff
Sophie Bensing
Stefan Johansson
Olle Kämpe
Eystein Sverre Husebye
spellingShingle Daniel Eriksson
Ellen Christine Røyrvik
Maribel Aranda-Guillén
Amund Holte Berger
Nils Landegren
Haydee Artaza
Åsa Hallgren
Marianne Aardal Grytaas
Sara Ström
Eirik Bratland
Ileana Ruxandra Botusan
Bergithe Eikeland Oftedal
Lars Breivik
Marc Vaudel
Øyvind Helgeland
Alberto Falorni
Anders Palmstrøm Jørgensen
Anna-Lena Hulting
Johan Svartberg
Olov Ekwall
Kristian Johan Fougner
Jeanette Wahlberg
Bjørn Gunnar Nedrebø
Per Dahlqvist
The Norwegian Addison Registry Study Group
The Swedish Addison Registry Study Group
Per Morten Knappskog
Anette Susanne Bøe Wolff
Sophie Bensing
Stefan Johansson
Olle Kämpe
Eystein Sverre Husebye
GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibility
Nature Communications
author_facet Daniel Eriksson
Ellen Christine Røyrvik
Maribel Aranda-Guillén
Amund Holte Berger
Nils Landegren
Haydee Artaza
Åsa Hallgren
Marianne Aardal Grytaas
Sara Ström
Eirik Bratland
Ileana Ruxandra Botusan
Bergithe Eikeland Oftedal
Lars Breivik
Marc Vaudel
Øyvind Helgeland
Alberto Falorni
Anders Palmstrøm Jørgensen
Anna-Lena Hulting
Johan Svartberg
Olov Ekwall
Kristian Johan Fougner
Jeanette Wahlberg
Bjørn Gunnar Nedrebø
Per Dahlqvist
The Norwegian Addison Registry Study Group
The Swedish Addison Registry Study Group
Per Morten Knappskog
Anette Susanne Bøe Wolff
Sophie Bensing
Stefan Johansson
Olle Kämpe
Eystein Sverre Husebye
author_sort Daniel Eriksson
title GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibility
title_short GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibility
title_full GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibility
title_fullStr GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibility
title_full_unstemmed GWAS for autoimmune Addison’s disease identifies multiple risk loci and highlights AIRE in disease susceptibility
title_sort gwas for autoimmune addison’s disease identifies multiple risk loci and highlights aire in disease susceptibility
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2021-02-01
description Autoimmune Addison’s disease is a rare complex disease, which has not yet been characterized by non-biased genetic studies. Here, the authors perform the first GWAS for the disease, identifying nine loci including two coding variants in the gene Autoimmune Regulator (AIRE).
url https://doi.org/10.1038/s41467-021-21015-8
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