Department of Biochemistry, University of Otago, Dunedin, New Zealand.
Genes Immun. 2010 Jun;11(4):351-6. doi: 10.1038/gene.2010.11. Epub 2010 Feb 25.
The location of CARD8 within an inflammatory bowel disease (IBD) locus and its role in the NALP3 inflammasome and as a nuclear factor (NF)kappaB inhibitor make it an attractive candidate risk gene for IBD. However, studies testing for the association of the CARD8 loss-of-function single-nucleotide polymorphism (SNP) rs2043211 with IBD have yielded mixed results. A recent study provided evidence that this discordance may result from an interaction of rs2043211 with loss-of-function variants in nucleotide-binding oligomerization domain protein 2 (NOD2) and a gain-of-function SNP (rs35829419) in NALP3. To confirm this interaction, we conducted a replication in an independent IBD sample set (n=1009 patients, n=517 controls). We found that the presence of the minor allele of rs2043211 with the major allele of rs35829419 conferred a protective effect against Crohn's disease (and vice versa), which intensified in the absence of NOD2 mutations (P(1,2/1,1)=0.009, odds ratio (OR)=0.66, 95% confidence interval (CI) (0.48-0.90); P(1,1/1,2)=0.015, OR=0.35, 95% CI (0.15-0.82)). We propose that these genotype combinations protect against gut inflammation by preventing the NALP3 inflammasome from producing excessive interleukin-1beta.
CARD8 位于炎症性肠病(IBD)基因座内,其在 NALP3 炎性小体和核因子(NF)kappaB 抑制剂中的作用使其成为 IBD 的一个有吸引力的候选风险基因。然而,检测 CARD8 功能丧失单核苷酸多态性(SNP)rs2043211 与 IBD 关联的研究结果喜忧参半。最近的一项研究提供了证据,表明这种不一致可能是由于 rs2043211 与核苷酸结合寡聚化结构域蛋白 2(NOD2)的功能丧失变异体和 NALP3 中的功能获得性 SNP(rs35829419)相互作用所致。为了证实这种相互作用,我们在一个独立的 IBD 样本集中进行了复制(n=1009 例患者,n=517 例对照)。我们发现,rs2043211 的次要等位基因与 rs35829419 的主要等位基因共存会对克罗恩病产生保护作用(反之亦然),而在没有 NOD2 突变的情况下,这种作用会加强(P(1,2/1,1)=0.009,比值比(OR)=0.66,95%置信区间(CI)(0.48-0.90);P(1,1/1,2)=0.015,OR=0.35,95%CI(0.15-0.82))。我们提出,这些基因型组合通过防止 NALP3 炎性小体产生过多的白细胞介素-1β,从而保护肠道免受炎症。