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Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study.


ABSTRACT: Systemic lupus erythematosus (SLE) is a chronic heterogeneous autoimmune disorder characterized by the loss of tolerance to self-antigens and dysregulated interferon responses. The etiology of SLE is complex, involving both heritable and environmental factors. Candidate-gene studies and genome-wide association (GWA) scans have been successful in identifying new loci that contribute to disease susceptibility; however, much of the heritable risk has yet to be identified. In this study, we sought to replicate 1,580 variants showing suggestive association with SLE in a previously published GWA scan of European Americans; we tested a multiethnic population consisting of 7,998 SLE cases and 7,492 controls of European, African American, Asian, Hispanic, Gullah, and Amerindian ancestry to find association with the disease. Several genes relevant to immunological pathways showed association with SLE. Three loci exceeded the genome-wide significance threshold: interferon regulatory factor 8 (IRF8; rs11644034; p(meta-Euro) = 2.08 × 10(-10)), transmembrane protein 39A (TMEM39A; rs1132200; p(meta-all) = 8.62 × 10(-9)), and 17q21 (rs1453560; p(meta-all) = 3.48 × 10(-10)) between IKAROS family of zinc finger 3 (AIOLOS; IKZF3) and zona pellucida binding protein 2 (ZPBP2). Fine mapping, resequencing, imputation, and haplotype analysis of IRF8 indicated that three independent effects tagged by rs8046526, rs450443, and rs4843869, respectively, were required for risk in individuals of European ancestry. Eleven additional replicated effects (5 × 10(-8) < p(meta-Euro) < 9.99 × 10(-5)) were observed with CFHR1, CADM2, LOC730109/IL12A, LPP, LOC63920, SLU7, ADAMTSL1, C10orf64, OR8D4, FAM19A2, and STXBP6. The results of this study increase the number of confirmed SLE risk loci and identify others warranting further investigation.

SUBMITTER: Lessard CJ 

PROVIDER: S-EPMC3322228 | biostudies-literature | 2012 Apr

REPOSITORIES: biostudies-literature

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Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study.

Lessard Christopher J CJ   Adrianto Indra I   Ice John A JA   Wiley Graham B GB   Kelly Jennifer A JA   Glenn Stuart B SB   Adler Adam J AJ   Li He H   Rasmussen Astrid A   Williams Adrienne H AH   Ziegler Julie J   Comeau Mary E ME   Marion Miranda M   Wakeland Benjamin E BE   Liang Chaoying C   Ramos Paula S PS   Grundahl Kiely M KM   Gallant Caroline J CJ   Alarcón-Riquelme Marta E ME   Alarcón Graciela S GS   Anaya Juan-Manuel JM   Bae Sang-Cheol SC   Boackle Susan A SA   Brown Elizabeth E EE   Chang Deh-Ming DM   Cho Soo-Kyung SK   Criswell Lindsey A LA   Edberg Jeffrey C JC   Freedman Barry I BI   Gilkeson Gary S GS   Jacob Chaim O CO   James Judith A JA   Kamen Diane L DL   Kimberly Robert P RP   Kim Jae-Hoon JH   Martin Javier J   Merrill Joan T JT   Niewold Timothy B TB   Park So-Yeon SY   Petri Michelle A MA   Pons-Estel Bernardo A BA   Ramsey-Goldman Rosalind R   Reveille John D JD   Scofield R Hal RH   Song Yeong Wook YW   Stevens Anne M AM   Tsao Betty P BP   Vila Luis M LM   Vyse Timothy J TJ   Yu Chack-Yung CY   Guthridge Joel M JM   Kaufman Kenneth M KM   Harley John B JB   Wakeland Edward K EK   Langefeld Carl D CD   Gaffney Patrick M PM   Montgomery Courtney G CG   Moser Kathy L KL  

American journal of human genetics 20120329 4


Systemic lupus erythematosus (SLE) is a chronic heterogeneous autoimmune disorder characterized by the loss of tolerance to self-antigens and dysregulated interferon responses. The etiology of SLE is complex, involving both heritable and environmental factors. Candidate-gene studies and genome-wide association (GWA) scans have been successful in identifying new loci that contribute to disease susceptibility; however, much of the heritable risk has yet to be identified. In this study, we sought t  ...[more]

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