4.7 Article

Extended exome sequencing identifies BACH2 as a novel major risk locus for Addison's disease

期刊

JOURNAL OF INTERNAL MEDICINE
卷 280, 期 6, 页码 595-608

出版社

WILEY
DOI: 10.1111/joim.12569

关键词

Addison Disease; BACH2 protein; genetic; genetic association studies; genetic predisposition to disease; human; polymorphism

资金

  1. Swedish Research Council
  2. Torsten Foundation
  3. Ragnar Soderberg Foundation
  4. European Union [201167]
  5. Stockholm County Council
  6. Karolinska Institutet
  7. Swedish Society for Medical Research
  8. Swedish Society of Medicine
  9. NovoNordisk Foundation
  10. Tore Nilson's Foundation for Medical Research
  11. Swedish Research Council Formas
  12. Knut and Alice Wallenberg Foundation
  13. Marianne and Marcus Wallenberg Foundation
  14. Swedish Reumatism Foundation
  15. King Gustaf V's 80-year Foundation
  16. Ake Wiberg Foundation
  17. AstraZeneca Science for Life Laboratory Research Collaboration grant (DIS-SECT)
  18. Novo Nordisk Fonden [NNF13OC0005975, NNF14OC0011003] Funding Source: researchfish

向作者/读者索取更多资源

BackgroundAutoimmune disease is one of the leading causes of morbidity and mortality worldwide. In Addison's disease, the adrenal glands are targeted by destructive autoimmunity. Despite being the most common cause of primary adrenal failure, little is known about its aetiology. MethodsTo understand the genetic background of Addison's disease, we utilized the extensively characterized patients of the Swedish Addison Registry. We developed an extended exome capture array comprising a selected set of 1853 genes and their potential regulatory elements, for the purpose of sequencing 479 patients with Addison's disease and 1394 controls. ResultsWe identified BACH2 (rs62408233-A, OR = 2.01 (1.71-2.37), P = 1.66 x 10(-15), MAF 0.46/0.29 in cases/controls) as a novel gene associated with Addison's disease development. We also confirmed the previously known associations with the HLA complex. ConclusionWhilst BACH2 has been previously reported to associate with organ-specific autoimmune diseases co-inherited with Addison's disease, we have identified BACH2 as a major risk locus in Addison's disease, independent of concomitant autoimmune diseases. Our results may enable future research towards preventive disease treatment.

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