Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama, 359-8513, Japan.
Laboratory for Mathematics, Premedical Course, National Defense Medical College, Tokorozawa, Saitama, Japan.
Hum Cell. 2021 Mar;34(2):293-299. doi: 10.1007/s13577-021-00485-4. Epub 2021 Jan 31.
Gout is a common type of acute arthritis that results from elevated serum uric acid (SUA) levels. Recent genome-wide association studies (GWASs) have revealed several novel single nucleotide polymorphism (SNPs) associated with SUA levels. Of these, rs10821905 of A1CF and rs1178977 of BAZ1B showed the greatest and the second greatest significant effect size for increasing SUA level in the Japanese population, but their association with gout is not clear. We examined their association with gout using 1411 clinically-defined Japanese gout patients and 1285 controls, and meta-analyzed our previous gout GWAS data to investigate any association with gout. Replication studies revealed both SNPs to be significantly associated with gout (P = 0.0366, odds ratio [OR] with 95% confidence interval [CI]: 1.30 [1.02-1.68] for rs10821905 of A1CF, P = 6.49 × 10, OR with 95% CI: 1.29 [1.07-1.55] for rs1178977 of BAZ1B). Meta-analysis also revealed a significant association with gout in both SNPs (P = 3.16 × 10, OR with 95% CI: 1.39 [1.17-1.66] for rs10821905 of A1CF, P = 7.28 × 10, OR with 95% CI 1.32 [1.15-1.51] for rs1178977 of BAZ1B). This study shows the first known association between SNPs of A1CF, BAZ1B and clinically-defined gout cases in Japanese. Our results also suggest a shared physiological/pathophysiological background between several populations, including Japanese, for both SUA increase and gout susceptibility. Our findings will not only assist the elucidation of the pathophysiology of gout and hyperuricemia, but also suggest new molecular targets.
痛风是一种常见的急性关节炎,其病因是血清尿酸(SUA)水平升高。最近的全基因组关联研究(GWAS)揭示了几个与 SUA 水平相关的新的单核苷酸多态性(SNP)。在这些 SNP 中,A1CF 的 rs10821905 和 BAZ1B 的 rs1178977 在日本人群中对 SUA 水平升高的影响最大和第二大,但它们与痛风的关联尚不清楚。我们使用 1411 例临床确诊的日本痛风患者和 1285 例对照,检测了这两个 SNP 与痛风的关联,并对我们以前的痛风 GWAS 数据进行了荟萃分析,以研究与痛风的任何关联。复制研究显示这两个 SNP 与痛风均显著相关(P=0.0366,A1CF 的 rs10821905 的比值比[OR]及其 95%置信区间[CI]:1.30[1.02-1.68],P=6.49×10,BAZ1B 的 rs1178977 的 OR 及其 95%CI:1.29[1.07-1.55])。荟萃分析还显示这两个 SNP 与痛风均显著相关(P=3.16×10,A1CF 的 rs10821905 的 OR 及其 95%CI:1.39[1.17-1.66],P=7.28×10,BAZ1B 的 rs1178977 的 OR 及其 95%CI:1.32[1.15-1.51])。这项研究首次在日本人群中发现 A1CF、BAZ1B 的 SNP 与临床确诊的痛风病例之间存在关联。我们的研究结果还表明,包括日本人在内的多个人群中,SUA 升高和痛风易感性存在共同的生理/病理生理背景。我们的发现不仅有助于阐明痛风和高尿酸血症的病理生理学,还为新的分子靶点提供了线索。