National Clinical Research Base of Traditional Chinese Medicine, Traditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University, Urumqi, Xinjiang, China (mainland).
Xinjiang Respiratory Disease Laboratory, Traditional Chinese Medicine Hospital Affiliated to Xinjiang Medical University, Urumqi, Xinjiang, China (mainland).
Med Sci Monit. 2018 Sep 10;24:6305-6312. doi: 10.12659/MSM.908552.
BACKGROUND This study investigated the relationship between hyperuricemia (with phlegm/non-phlegm block) and ABCG2 gene polymorphism in Han and Uygur people from Xinjiang, China. MATERIAL AND METHODS We recruited 600 hyperuricemia patients with phlegm/non-phlegm block. Genomic DNA was extracted from the whole blood. Gene polymorphism was classified by SnaPshot method. RESULTS The SNP loci rs2725220 and rs2231137 of the ABCG2 gene, but not rs2231142, were significantly different between patients with non-phlegm block and phlegm block (P<0.05). The rs2231142 allele G was the protective factor in Uygur hyperuricemia patients. In both Han and hyperuricemia patients, the rs2725220 allele G was a protective factor and the rs2231137 allele C was a risk factor. For non-phlegm-block hyperuricemia, the rs2231142 and rs2231137 genotypes were significantly different between Uygur and Han patients (P<0.05). The rs2231142 allele G was 1.563 times higher in the Uygur patients compared with Han, and rs2231137 allele C was 1.673 times higher in the Uygur patients compared with the Han. For phlegm-block hyperuricemia, rs2231142 allele G was 1.397 times higher in the Uygur patients compared with the Han. CONCLUSIONS ABCG2 gene rs2231137 with more allele C tends to be phlegm-block type and rs2725220 with more allele G tends to be non-phlegm-block type. In the Uygur hyperuricemia patients, ABCG2 gene rs2231142 with more allele G tends to be non-phlegm-block type. Allele C of rs2231137 and allele G of rs2231142 in ABCG2 gene are more likely to be found in the Uygur people.
背景 本研究旨在探讨中国新疆汉族和维吾尔族人群高尿酸血症(兼夹痰浊/非痰浊证)与 ABCG2 基因多态性的关系。
材料与方法 我们招募了 600 例兼夹痰浊/非痰浊证的高尿酸血症患者,提取其全血基因组 DNA,采用 SnaPshot 法进行基因多态性分型。
结果 ABCG2 基因的 SNP 位点 rs2725220 和 rs2231137,但并非 rs2231142,在非痰浊证和痰浊证患者之间存在显著差异(P<0.05)。在维吾尔族高尿酸血症患者中,rs2231142 等位基因 G 是保护因素。在汉族和高尿酸血症患者中,rs2725220 等位基因 G 是保护因素,rs2231137 等位基因 C 是危险因素。在非痰浊证高尿酸血症患者中,rs2231142 和 rs2231137 基因型在维吾尔族和汉族患者之间存在显著差异(P<0.05)。与汉族相比,维吾尔族 rs2231142 等位基因 G 高出 1.563 倍,rs2231137 等位基因 C 高出 1.673 倍。在痰浊证高尿酸血症患者中,维吾尔族 rs2231142 等位基因 G 高出汉族 1.397 倍。
结论 ABCG2 基因 rs2231137 携带更多等位基因 C 倾向于痰浊证型,rs2725220 携带更多等位基因 G 倾向于非痰浊证型。在维吾尔族高尿酸血症患者中,ABCG2 基因 rs2231142 携带更多等位基因 G 倾向于非痰浊证型。ABCG2 基因 rs2231137 的等位基因 C 和 rs2231142 的等位基因 G 在维吾尔族人群中更为常见。