Sakiyama Masayuki, Matsuo Hirotaka, Nakaoka Hirofumi, Kawamura Yusuke, Kawaguchi Makoto, Higashino Toshihide, Nakayama Akiyoshi, Akashi Airi, Ueyama Jun, Kondo Takaaki, Wakai Kenji, Sakurai Yutaka, Yamamoto Ken, Ooyama Hiroshi, Shinomiya Nariyoshi
Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama, 359-8513, Japan.
Department of Dermatology, National Defense Medical College, Tokorozawa, Japan.
BMC Med Genet. 2018 Jun 7;19(1):96. doi: 10.1186/s12881-018-0583-z.
Gout is a common disease resulting from hyperuricemia which causes acute arthritis. A recent genome-wide association study (GWAS) of gout identified three new loci for gout in Han Chinese: regulatory factor X3 (RFX3), potassium voltage-gated channel subfamily Q member 1 (KCNQ1), and breast carcinoma amplified sequence 3 (BCAS3). The lack of any replication studies of these three loci using other population groups prompted us to perform a replication study with Japanese clinically defined gout cases and controls.
We genotyped the variants of RFX3 (rs12236871), KCNQ1 (rs179785) and BCAS3 (rs11653176) in 723 Japanese clinically defined gout cases and 913 controls by TaqMan method. rs179785 of KCNQ1 is also evaluated by direct sequencing because of difficulties of its genotyping by TaqMan method.
Although the variants of RFX3 and BCAS3 were clearly genotyped by TaqMan method, rs179785 of KCNQ1 was not, because rs179785 (A/G) of KCNQ1 is located at the last nucleotide ("A") of the 12-bp deletion variant (rs200562977) of KCNQ1. Therefore, rs179785 and rs200562977 of KCNQ1 were genotyped by direct sequencing in all samples. Moreover, by direct sequencing with the same primers, we were able to evaluate the genotypes of rs179784 of KCNQ1 which shows strong linkage disequilibrium with rs179785 (D' = 1.0 and r = 0.99). rs11653176, a common variant of BCAS3, showed a significant association with gout (P = 1.66 × 10; odds ratio [OR] = 0.80); the direction of effect was the same as that seen in the previous Han Chinese GWAS. Two variants of KCNQ1 (rs179785 and rs179784) had a nominally significant association (P = 0.043 and 0.044; OR = 0.85 and 0.86, respectively), but did not pass the significance threshold for multiple hypothesis testing using the Bonferroni correction. On the other hand, rs200562977 of KCNQ1 and rs12236871 of RFX3 did not show any significant association with gout.
BCAS3 is a coactivator of estrogen receptor alpha, and the influence of estrogen to serum uric acid level is well known. Our present replication study, as did the previous gout GWAS, demonstrated the common variant of BCAS3 to be associated with gout susceptibility.
痛风是一种由高尿酸血症导致的常见疾病,可引起急性关节炎。最近一项针对痛风的全基因组关联研究(GWAS)在中国汉族人群中确定了三个新的痛风相关基因座:调节因子X3(RFX3)、钾电压门控通道亚家族Q成员1(KCNQ1)和乳腺癌扩增序列3(BCAS3)。由于缺乏使用其他人群对这三个基因座进行的重复研究,我们开展了一项针对日本临床确诊痛风病例和对照的重复研究。
我们采用TaqMan方法对723例日本临床确诊痛风病例和913例对照进行RFX3(rs12236871)、KCNQ1(rs179785)和BCAS3(rs11653176)的基因分型。由于通过TaqMan方法对KCNQ1的rs179785进行基因分型存在困难,因此也通过直接测序对其进行评估。
尽管通过TaqMan方法能够清晰地对RFX3和BCAS3的变异进行基因分型,但无法对KCNQ1的rs179785进行基因分型,因为KCNQ1的rs179785(A/G)位于KCNQ1的12碱基缺失变异(rs200562977)的最后一个核苷酸(“A”)处。因此,对所有样本通过直接测序对KCNQ1的rs179785和rs200562977进行基因分型。此外,使用相同引物进行直接测序时,我们能够评估与rs179785显示出强连锁不平衡(D' = 1.0且r = 0.99)的KCNQ1的rs179784的基因型。BCAS3的常见变异rs11653176与痛风显著相关(P = 1.66×10;优势比[OR] = 0.80);效应方向与之前中国汉族GWAS研究中所见相同。KCNQ1的两个变异(rs179785和rs179784)具有名义上的显著关联(P = 0.043和0.044;OR分别为0.85和0.86),但未通过使用Bonferroni校正进行多重假设检验的显著性阈值。另一方面,KCNQ1的rs200562977和RFX3的rs12236871与痛风未显示出任何显著关联。
BCAS3是雌激素受体α 的共激活因子,雌激素对血清尿酸水平的影响是众所周知的。我们目前的重复研究与之前的痛风GWAS研究一样,证明了BCAS3的常见变异与痛风易感性相关。