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摘要:
Background: More and more chronic kidney disease (CKD) patients are accompanied with hyperuricaemia. As is known, hyperuricaemia is an independent hazard of both cardiovascular diseases (CVD) and chronic kidney diseases. We aim at identifying Single Nucleotide Polymorphism (SNP) difference of hURAT1 (rs7932775) and ABCG2 (rs3825016) on CKD patient with hyperuricemia and/or gout. Methods: All forty-two CKD patients were divided into two groups: hyperuricemia, and control group. 24 hours urine sample and serum were prepared for testing biochemistry parameters. The polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method is used to analyze hURAT1 and ABCG2 single nucleotide polymorphisms in different groups. Results: 17 patients have CT SNP of hURAT1 (rs7932775) and 13 patients have CT SNP of ABCG2 (rs3825016) in hyperuricemia group, while only 5 persons and 6 persons have the same mutations in control group respectively. 7 patients have CT SNP of both hURAT1 (rs7932775) and ABCG2 (rs3825016) in hyperuricemia group, while only 2 persons have the same mutations in control group. CT mutation rates of hURAT1 (rs7932775) and ABCG2 (rs3825016) in hyperuricemia group were 60.7% (17/28) and 50% (13/28) respectively, higher than that of control group (35.7% (5/14) and 42.8% (6/14)). What is more, Double SNP mutations in both hURAT1 (rs7932775) and ABCG2 (rs3825016) in hyperuricemia group were 25% (7/28), higher than that of control group (14.2%, 2/14). Conclusion: There are higher mutation rates of CT SNP in hURAT1 (rs7932775) and/or ABCG2 (rs3825016) in hyperuricemia group. We can conclude that hyperuricemia is a high risk factor in progress of CKD, which is necessary to take measures of decreasing serum uric acid to delay CKD progress.
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篇名 Single Nucleotide Polymorphisms (SNPs) of URAT1 (rs7932775) and ABCG2 (rs3825016) on Chronic Kidney Disease Patients with Hyperuricemia
来源期刊 中医(英文) 学科 医学
关键词 HYPERURICEMIA Chronic Kidney Disease (CKD) Single NUCLEOTIDE Polymorphisms (SNP) Human URATE Transport Protein (Hurat1) ATP Binding TRANSPORTER G Super Family (ABCG2)
年,卷(期) zyyw_2018,(3) 所属期刊栏目
研究方向 页码范围 118-125
页数 8页 分类号 R5
字数 语种
DOI
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研究主题发展历程
节点文献
HYPERURICEMIA
Chronic
Kidney
Disease
(CKD)
Single
NUCLEOTIDE
Polymorphisms
(SNP)
Human
URATE
Transport
Protein
(Hurat1)
ATP
Binding
TRANSPORTER
G
Super
Family
(ABCG2)
研究起点
研究来源
研究分支
研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
中医(英文)
季刊
2151-1918
武汉市江夏区汤逊湖北路38号光谷总部空间
出版文献量(篇)
35
总下载数(次)
0
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