Variants of ALPK1 with ABCG2, SLC2A9, and SLC22A12 increased the positive predictive value for gout
Tu, Hung-Pin1,2; Ko, Albert Min-Shan3; Lee, Su-Shin4; Lee, Chi-Pin5; Kuo, Tzer-Min5; Huang, Chung-Ming6,7; Ko, Ying-Chin5
刊名JOURNAL OF HUMAN GENETICS
2018
卷号63期号:1页码:63-70
ISSN号1434-5161
DOI10.1038/s10038-017-0368-9
文献子类Article
英文摘要We investigated the interactions of ALPK1 variants and the loci of ABCG2, SLC2A9, and SLC22A12 on gout risk. We conducted two case-control studies. Participants were recruited from hospitals (n = 410; 104 gout cases and 306 controls) and communities (n = 678; 373 gout cases and 305 controls) in Taiwan. The genotypes of ALPK1 (rs11726117 M861T, rs231247 R1084R, and rs231253 3' UTR), ABCG2 (rs2231142 Q141K and rs2231137 V12M), SLC2A9 (rs3733591 R265H and rs1014290), and SLC22A12 (rs3825016 H86H, rs11231825 H142H, and rs475688) were genotyped. Under a recessive model, the joint effects of ALPK1 variants and the SNPs rs2231142 of ABCG2, rs1014290 of SLC2A9, or rs475688 and rs3825016 of SLC22A12 were associated with gout. The rs11726117 [CC] of ALPK1 and rs2231142 [TT] of ABCG2 with the sequential addition of the rs1014290 [AA] of SLC2A9 and rs3825016 [CC] of SLC22A12 were associated with gout risk (odds ratio (OR): 13.01, 15.11, and 55.00 and positive predictive value (PPV): 56%, 69%, and 99% in the Han group, respectively; OR: 3.76, 5.78, and 12.30 and PPV: 74%, 80%, and 81% in the aboriginal group, respectively). Combined exposure to the four high-risk genotypes of ALPK1 and the uric-acid-related loci of ABCG2, SLC2A9, and SLC22A12 was associated with an increased gout risk and a high PPV for gout.
WOS关键词GENOME-WIDE ASSOCIATION ; URIC-ACID ; MOLECULAR PHYSIOLOGY ; HYPERURICEMIA ; RISK ; POPULATION ; IDENTIFICATION ; EXCRETION ; ARTHRITIS ; LOCI
WOS研究方向Genetics & Heredity
语种英语
出版者NATURE PUBLISHING GROUP
WOS记录号WOS:000419977800008
资助机构Ministry of Science and Technology(MOST 105-2632-B-039-001 ; China Medical University(CMU105-S-01 ; Kaohsiung Medical University Research Foundation(KMU-M106006) ; MOST 106-2314-B-037-034) ; CMU105-S-03 ; CMU105-S-04 ; CMU105-S-06 ; DMR-106-115)
内容类型期刊论文
源URL[http://119.78.100.205/handle/311034/8713]  
专题中国科学院古脊椎动物与古人类研究所
通讯作者Ko, Ying-Chin
作者单位1.Kaohsiung Med Univ, Coll Med, Sch Med, Dept Publ Hlth & Environm Med, Kaohsiung, Taiwan
2.Kaohsiung Med Univ Hosp, Dept Med Res, Kaohsiung, Taiwan
3.Chinese Acad Sci, IVPP, Key Lab Vertebrate Evolut & Human Origins, Beijing 100044, Peoples R China
4.Kaohsiung Med Univ Hosp, Dept Surg, Div Plast Surg, Kaohsiung, Taiwan
5.China Med Univ, China Med Univ Hosp, Environment Omics Dis Res Ctr, Taichung 40402, Taiwan
6.China Med Univ Hosp, Dept Internal Med, Div Rheumatol & Immunol, Taichung 404, Taiwan
7.China Med Univ, Grad Inst Integrated Med, Taichung, Taiwan
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GB/T 7714
Tu, Hung-Pin,Ko, Albert Min-Shan,Lee, Su-Shin,et al. Variants of ALPK1 with ABCG2, SLC2A9, and SLC22A12 increased the positive predictive value for gout[J]. JOURNAL OF HUMAN GENETICS,2018,63(1):63-70.
APA Tu, Hung-Pin.,Ko, Albert Min-Shan.,Lee, Su-Shin.,Lee, Chi-Pin.,Kuo, Tzer-Min.,...&Ko, Ying-Chin.(2018).Variants of ALPK1 with ABCG2, SLC2A9, and SLC22A12 increased the positive predictive value for gout.JOURNAL OF HUMAN GENETICS,63(1),63-70.
MLA Tu, Hung-Pin,et al."Variants of ALPK1 with ABCG2, SLC2A9, and SLC22A12 increased the positive predictive value for gout".JOURNAL OF HUMAN GENETICS 63.1(2018):63-70.
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