Identification of Novel Genetic Loci Associated with Thyroid Peroxidase Antibodies and Clinical Thyroid Disease

Marco Medici, Eleonora Porcu, Giorgio Pistis, Alexander Teumer, Suzanne J. Brown, Richard A. Jensen, Rajesh Rawal, Greet L. Roef, Theo S. Plantinga, Sita H. Vermeulen, Jari Lahti, Matthew J. Simmonds, Lise Lotte N. Husemoen, Rachel M. Freathy, Beverley M. Shields, Diana Pietzner, Rebecca Nagy, Linda Broer, Layal Chaker, Tim I.M. KorevaarMaria Grazia Plia, Cinzia Sala, Uwe Völker, J. Brent Richards, Fred C. Sweep, Christian Gieger, Tanguy Corre, Eero Kajantie, Betina Thuesen, Youri E. Taes, W. Edward Visser, Andrew T. Hattersley, Jürgen Kratzsch, Alexander Hamilton, Wei Li, Georg Homuth, Monia Lobina, Stefano Mariotti, Nicole Soranzo, Massimiliano Cocca, Matthias Nauck, Christin Spielhagen, Alec Ross, Alice Arnold, Martijn van de Bunt, Sandya Liyanarachchi, Margit Heier, Hans Jörgen Grabe, Corrado Masciullo, Tessel E. Galesloot, Ee M. Lim, Eva Reischl, Peter J. Leedman, Sandra Lai, Alessandro Delitala, Alexandra P. Bremner, David I.W. Philips, John P. Beilby, Antonella Mulas, Matteo Vocale, Goncalo Abecasis, Tom Forsen, Alan James, Elisabeth Widen, Jennie Hui, Holger Prokisch, Ernst E. Rietzschel, Aarno Palotie, Peter Feddema, Stephen J. Fletcher, Katharina Schramm, Jerome I. Rotter, Alexander Kluttig, Dörte Radke, Michela Traglia, Gabriela L. Surdulescu, Huiling He, Jayne A. Franklyn, Daniel Tiller, Bijay Vaidya, Tim de Meyer, Torben Jørgensen, Johan G. Eriksson, Peter C. O'Leary, Eric Wichmann, Ad R. Hermus, Bruce M. Psaty, Till Ittermann, Albert Hofman, Emanuele Bosi, David Schlessinger, Henri Wallaschofski, Nicola Pirastu, Yurii S. Aulchenko, Albert de la Chapelle, Romana T. Netea-Maier, Stephen C.L. Gough, Henriette Meyer zu Schwabedissen, Timothy M. Frayling, Jean Marc Kaufman, Allan Linneberg, Katri Räikkönen, Johannes W.A. Smit, Lambertus A. Kiemeney, Fernando Rivadeneira, André G. Uitterlinden, John P. Walsh, Christa Meisinger, Martin den Heijer, Theo J. Visser, Timothy D. Spector, Scott G. Wilson, Henry Völzke, Anne Cappola, Daniela Toniolo, Serena Sanna, Silvia Naitza, Robin P. Peeters

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

149 Citaten (Scopus)

Samenvatting

Autoimmune thyroid diseases (AITD) are common, affecting 2-5% of the general population. Individuals with positive thyroid peroxidase antibodies (TPOAbs) have an increased risk of autoimmune hypothyroidism (Hashimoto's thyroiditis), as well as autoimmune hyperthyroidism (Graves' disease). As the possible causative genes of TPOAbs and AITD remain largely unknown, we performed GWAS meta-analyses in 18,297 individuals for TPOAb-positivity (1769 TPOAb-positives and 16,528 TPOAb-negatives) and in 12,353 individuals for TPOAb serum levels, with replication in 8,990 individuals. Significant associations (P<5×10-8) were detected at TPO-rs11675434, ATXN2-rs653178, and BACH2-rs10944479 for TPOAb-positivity, and at TPO-rs11675434, MAGI3-rs1230666, and KALRN-rs2010099 for TPOAb levels. Individual and combined effects (genetic risk scores) of these variants on (subclinical) hypo- and hyperthyroidism, goiter and thyroid cancer were studied. Individuals with a high genetic risk score had, besides an increased risk of TPOAb-positivity (OR: 2.18, 95% CI 1.68-2.81, P = 8.1×10-8), a higher risk of increased thyroid-stimulating hormone levels (OR: 1.51, 95% CI 1.26-1.82, P = 2.9×10-6), as well as a decreased risk of goiter (OR: 0.77, 95% CI 0.66-0.89, P = 6.5×10-4). The MAGI3 and BACH2 variants were associated with an increased risk of hyperthyroidism, which was replicated in an independent cohort of patients with Graves' disease (OR: 1.37, 95% CI 1.22-1.54, P = 1.2×10-7 and OR: 1.25, 95% CI 1.12-1.39, P = 6.2×10-5). The MAGI3 variant was also associated with an increased risk of hypothyroidism (OR: 1.57, 95% CI 1.18-2.10, P = 1.9×10-3). This first GWAS meta-analysis for TPOAbs identified five newly associated loci, three of which were also associated with clinical thyroid disease. With these markers we identified a large subgroup in the general population with a substantially increased risk of TPOAbs. The results provide insight into why individuals with thyroid autoimmunity do or do not eventually develop thyroid disease, and these markers may therefore predict which TPOAb-positives are particularly at risk of developing clinical thyroid dysfunction.

Originele taal-2Engels
Artikelnummere1004123
TijdschriftPLoS Genetics
Volume10
Nummer van het tijdschrift2
DOI's
StatusGepubliceerd - feb. 2014
Extern gepubliceerdJa

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