Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease.

Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease.
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DOI:
10.1038/ng.3268
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发表时间:
2015-06
期刊:
影响因子:
30.8
通讯作者:
de Balcker, Paul I. W.
de Balcker, Paul I. W.
中科院分区:
生物学1区
文献类型:
--
作者:
Gutierrez-Achury, Javier;Zhernakova, Alexandra;Pulit, Sara L.;Trynka, Gosia;Hunt, Karen A.;Romanos, Jihane;Raychaudhuri, Soumya;van Heel, David A.;Wijmenga, Cisca;de Balcker, Paul I. W.

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尽管膳食麸质是触发因素,但乳糜泻风险受到主要组织相容性复合体(MHC)区域遗传变异的强烈影响。我们对MHC关联信号进行了精细映射,以确定独立于HLA-DQ等位基因的其他风险因素,并观察到五种新的关联,占遗传风险的18%。加上57个已知的非MHC基因座,遗传变异现在可以解释高达48%的乳糜泻遗传性。
Although dietary gluten is the trigger, celiac disease risk is strongly influenced by genetic variation in the major histocompatibility complex (MHC) region. We fine-mapped the MHC association signal to identify additional risk factors independent of the HLA-DQ alleles and observed five novel associations that account for 18% of the genetic risk. Together with the 57 known non-MHC loci, genetic variation can now explain up to 48% of celiac disease heritability.
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