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日本人群中 等位基因相互作用对 ACPA(+)类风湿关节炎易感性和 ACPA 水平影响的遗传图谱。

Genetic landscape of interactive effects of alleles on susceptibility to ACPA(+) rheumatoid arthritis and ACPA levels in Japanese population.

机构信息

Center for Genomic Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Center for the Promotion of Interdisciplinary Education and Research, Kyoto University, Kyoto, Japan.

出版信息

J Med Genet. 2017 Dec;54(12):853-858. doi: 10.1136/jmedgenet-2017-104779. Epub 2017 Oct 12.

Abstract

BACKGROUND

is the strongest susceptibility gene to rheumatoid arthritis (RA). alleles showed significant non-additive and interactive effects on susceptibility to RA in the European population, but these effects on RA susceptibility should vary between populations due to the difference in allelic distribution. Furthermore, non-additive or interactive effects on the phenotypes of RA are not fully known. We evaluated the non-additive and interactive effects of alleles on RA susceptibility and anticitrullinated protein/peptide antibody (ACPA) levels in Japanese patients.

METHODS

A total of 5581 ACPA(+) RA and 19 170 controls were genotyped or imputed for alleles. Logistic regression analysis was performed for both allelic non-additive effects and interactive effects of allelic combinations. The significant levels were set by Bonferroni's correction. A total of 4371 ACPA(+) RA were analysed for ACPA levels.

RESULTS

We obtained evidence of non-additive and interactive effects of on ACPA(+) RA susceptibility (p=2.5×10 and 1.5×10, respectively). Multiple alleles including *04:05, the most common susceptibility allele in the Japanese, showed significant non-additive effects (p≤0.0043). We identified multiple allelic combinations with significant interactive effects including a common combination with the European population as well as novel combinations. Additional variance of ACPA(+) RA susceptibility could be explained substantially by heterozygote dominance or interactive effects. We did not find evidence of non-additive and interactive effects on levels of ACPA.

CONCLUSION

HLA allelic non-additive and interactive effects on ACPA(+) RA susceptibility were observed in the Japanese population. The allelic non-additive and interactive effects depend on allelic distribution in populations.

摘要

背景

是类风湿关节炎(RA)最强的易感基因。在欧洲人群中, 等位基因对 RA 的易感性表现出显著的非加性和交互作用,但由于等位基因分布的差异,这些对 RA 易感性的影响在不同人群中应该有所不同。此外,RA 表型的非加性或交互作用尚不完全清楚。我们评估了 等位基因对日本患者 RA 易感性和抗瓜氨酸化蛋白/肽抗体(ACPA)水平的非加性和交互作用。

方法

共对 5581 例 ACPA(+) RA 和 19170 例对照进行了 等位基因的基因分型或推断。对等位基因的非加性效应和等位基因组合的交互作用进行了逻辑回归分析。显著水平通过 Bonferroni 校正确定。对 4371 例 ACPA(+) RA 进行了 ACPA 水平分析。

结果

我们获得了 等位基因对 ACPA(+) RA 易感性的非加性和交互作用的证据(p=2.5×10和 1.5×10,分别)。包括在日本人中最常见的易感等位基因 *04:05 在内的多个 等位基因表现出显著的非加性效应(p≤0.0043)。我们确定了多个具有显著交互作用的等位基因组合,包括与欧洲人群相同的常见组合以及新的组合。杂合优势或交互作用可以显著解释 ACPA(+) RA 易感性的额外方差。我们没有发现 ACPA 水平的非加性和交互作用的证据。

结论

在日本人群中观察到 HLA 等位基因对 ACPA(+) RA 易感性的非加性和交互作用。等位基因的非加性和交互作用取决于人群中的等位基因分布。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5acf/6724214/b4c4e0a1b553/nihms-1047778-f0001.jpg

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