Association of SLC22A12 and SLC2A9 genetic polymorphisms with hypouricemia in Ningxia population
- VernacularTitle:SLC22A12及SLC2A9基因多态性与宁夏地区人群低尿酸血症的相关性
- Author:
Yi-Cong YIN
1
;
Chao-Chao MA
;
Jie WU
;
Song-Lin YU
;
Xiu-Zhi GUO
;
Li-An HOU
;
Ting-Ting YOU
;
Dan-Chen WANG
;
Hong-Lei LI
;
Tao XU
;
Ling QIU
Author Information
1. 中国医学科学院北京协和医学院北京协和医院检验科
- Keywords:
hyporuricemia;
Ningxia population;
single nucleotide polymorphisms
- From:
Basic & Clinical Medicine
2018;38(5):638-642
- CountryChina
- Language:Chinese
-
Abstract:
Objective To study the relationship among rs505802 in SLC22A12,rs6855911,rs737267,rs12498742, rs7442295, rs734553, rs16890979 in SLC2A9 genetic polymorphisms and hypouricemia in Ningxia.Methods 6 056 subjects were collected by multistage,stratified random cluster sampling method in October and November in 2011 in Ningxia Hui autonomous region, 98 subjects with hypouricemia were selected.According to gender and age,84 controls were selected.Physical examination and laboratory biochemical index test were conducted for the study population.T test was used to compare general clinical data and biochemical indexs between two groups. SNPs were detected by Sequenom Mass ARRAY technology.By x2test,we compared the frequencies of the geno-type and allele in each group.Samples representativeness was confirmed through the Hardy-Weinberg inspection. Results The levels of TC, LDLC, and Cr in the patients were lower than those in the control group(P<0.05). There were significant differences in the distribution of A,G allele frequencies of SLC2A9 gene rs7442295 between two groups.The risk of hypouricemia in patients with A/A genotype was lower than that of A/G genotype(Pc<0.05),indicating that A>G mutation was associated with hypouricemia.Conclusions Polymorphisms of SLC2A9 gene rs7442295 are significantly correlated with hyporuricemia in Ningxia.
