Autoimmune hypothyroidism GWAS reveals independent autoimmune and thyroid-specific contributions and an inverse relation with cancer risk

Author:

Reeve Mary1,Kanai Masahiro2ORCID,Graham Daniel3ORCID,Karjalainen Juha4,Luo Shuang1,Kolosov Nikita5,Adams Cameron6,Ritari Jarmo7,Karczewski Konrad3ORCID,Kiiskinen Tuomo8ORCID,Fuller Zachary3ORCID,Mehtonen Juha9ORCID,Kurki Mitja2,Khan Zia6,Partanen Jukka10ORCID,McCarthy Mark6,Artomov Mykyta11ORCID,Tuomi Tiinamaija12ORCID,Pirinen Matti9ORCID,Kero Jukka13,Xavier Ramnik2,Daly Mark3ORCID,Ripatti Samuli14ORCID,FinnGen 15

Affiliation:

1. Institute for Molecular Medicine Finland (FiMM)

2. Broad Institute of MIT and Harvard

3. Broad Institute

4. Institute for Molecular Medicine Finland (FIMM), University of Helsinki

5. Northwest Cancer Research Hospital

6. Genentech

7. Veripalvelu

8. Institute for Molecular Medicine Finland

9. University of Helsinki

10. Finnish Red Cross Blood Service

11. Nationwide Children's Hospital

12. Helsinki University Hospital

13. Research Centre for Integrative Physiology and Pharmacology,Institute of Biomedicine, University of Turku, Turku

14. Institute for Molecular Medicine Finland, FIMM, HiLIFE, University of Helsinki, Helsinki

15. FinnGen

Abstract

Abstract

The high prevalence of autoimmune hypothyroidism (AIHT) - more than 5% in human populations - provides a unique opportunity to unlock the most complete picture to date of genetic loci that underlie systemic and organ-specific autoimmunity. Using a meta-analysis of 81,718 AIHT cases in FinnGen and the UK Biobank, we dissect associations along axes of thyroid dysfunction and autoimmunity. This largest-to-date scan of hypothyroidism identifies 418 independent associations (p < 5x10− 8), more than half of which have not previously been documented in thyroid disease. In 48 of these, a protein-coding variant is the lead SNP or is highly correlated (r2 > 0.95) with the lead SNP at the locus, including low-frequency coding variants at LAG3, ZAP70, TG, TNFSF11, IRF3, S1PR4, HABP2, ZNF429 as well as established variants at ADCY7, IFIH1 and TYK2. The variants at LAG3 (P67T), ZAP70 (T155M), and TG (Q655X) are highly enriched in Finland and functional experiments in T-cells demonstrate that the ZAP70:T155M allele reduces T-cell activation. By employing a large-scale scan of non-thyroid autoimmunity and a published meta-analysis of TSH levels, we use a Bayesian classifier to dissect the associated loci into distinct groupings and from this estimate, a significant proportion are involved in systemic (i.e., general to multiple autoimmune conditions) autoimmunity (34%) and another subset in thyroid-specific dysfunction (17%). By comparing these association results further to other common disease endpoints, we identify a noteworthy overlap with skin cancer, with 10% of AIHT loci showing a consistent but opposite pattern of association where alleles that increase the risk of hypothyroidism have protective effects for skin cancer. The association results, including genes encoding checkpoint inhibitors and other genes affecting protein levels of PD1, bolster the causal role of natural variation in autoimmunity influencing cancer outcomes.

Publisher

Springer Science and Business Media LLC

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