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没有证据表明6号染色体p21区域存在多个影响类风湿关节炎风险的基因座。

No evidence for multiple loci affecting rheumatoid arthritis risk on chromosome 6p21.

作者信息

Sherva Richard, Sun Lingwei, Biernacka Joanna, Neuman Rosalind

机构信息

Department of Psychiatry, Washington University School of Medicine, 660 South Euclid Avenue, St. Louis, Missouri 63104, USA.

Institute of Human Genetics, Newcastle University, International Centre for Life, Central Parkway, Newcastle upon Tyne, NE1 3BZ, UK.

出版信息

BMC Proc. 2007;1 Suppl 1(Suppl 1):S42. doi: 10.1186/1753-6561-1-s1-s42. Epub 2007 Dec 18.

Abstract

The influence of certain alleles of the HLA-DRB1 locus on risk for rheumatoid arthritis has been well established through linkage and association studies. In addition, other loci in the HLA region on 6p21 may also affect an individual's risk profile. Here, we used a method to detect excess identity-by-descent sharing between affected sib pairs conditional on the observed genotypes at the hypothesized causal locus to test for the presence of additional arthritis risk loci in the linked region. We used affected sib pairs from two different studies. Because the test depends heavily on specifying accurate allele frequency estimates at the proposed causal locus, we used HLA-DRB1 allele frequency estimates from a large, population-based sample. We also discuss an alternate form of the test in which we could condition on parental genotypes, thereby eliminating the need for actual allele frequencies. The test showed no evidence for the presence of additional arthritis risk loci in the region in the British or North American samples made available for Genetic Analysis Workshop 15. Given the prior knowledge that there likely are arthritis risk loci other than HLA-DRB1 in the region, it appears the tests may have inadequate power to detect the presence of these loci in certain cases.

摘要

通过连锁和关联研究,HLA - DRB1基因座的某些等位基因对类风湿性关节炎风险的影响已得到充分证实。此外,位于6p21的HLA区域中的其他基因座也可能影响个体的风险状况。在此,我们使用了一种方法,以假设的因果基因座处观察到的基因型为条件,检测患病同胞对之间过度的同源性,以检验连锁区域中是否存在其他关节炎风险基因座。我们使用了来自两项不同研究的患病同胞对。由于该检验在很大程度上依赖于在所提议的因果基因座处指定准确的等位基因频率估计值,因此我们使用了来自一个大型基于人群样本的HLA - DRB1等位基因频率估计值。我们还讨论了该检验的另一种形式,即可以以亲本基因型为条件,从而无需实际的等位基因频率。对于提供给遗传分析研讨会15的英国或北美样本,该检验未显示该区域存在其他关节炎风险基因座的证据。鉴于之前已知该区域可能存在除HLA - DRB1之外的关节炎风险基因座,在某些情况下,这些检验似乎可能没有足够的能力来检测这些基因座的存在。

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