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Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese

BACKGROUND: Serum uric acid (SUA), hyperuricemia (HUA) and gout are complex traits with relatively high heritability. This study aims to identify whether a candidate gene, SLC28A2, exerts susceptibility for SUA fluctuation and incidence of HUA and gout in the Han Chinese population. RESULTS: Three s...

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Autores principales: Zhou, Zhaowei, Li, Zhiqiang, Wang, Can, Li, Xinde, Cheng, Xiaoyu, Li, Changgui, Shi, Yongyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335706/
https://www.ncbi.nlm.nih.gov/pubmed/30679935
http://dx.doi.org/10.1186/s41065-018-0078-0
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author Zhou, Zhaowei
Li, Zhiqiang
Wang, Can
Li, Xinde
Cheng, Xiaoyu
Li, Changgui
Shi, Yongyong
author_facet Zhou, Zhaowei
Li, Zhiqiang
Wang, Can
Li, Xinde
Cheng, Xiaoyu
Li, Changgui
Shi, Yongyong
author_sort Zhou, Zhaowei
collection PubMed
description BACKGROUND: Serum uric acid (SUA), hyperuricemia (HUA) and gout are complex traits with relatively high heritability. This study aims to identify whether a candidate gene, SLC28A2, exerts susceptibility for SUA fluctuation and incidence of HUA and gout in the Han Chinese population. RESULTS: Three sample sets of 1376 gout patients, 1290 long-term HUA subjects (no gout attack) and 1349 normouricemic controls were recruited for this study. Eight polymorphisms in the SLC28A2 gene were genotyped using the ligase detection reaction-polymerase chain reaction (LDR-PCR) technology. Rs16941238 showed the most significant associations with SUA level (minor allele “A”, BETA = − 13.84 μmol/L, P = 0.0041, P(perm) = 0.0042) and HUA (OR = 0.7734, P = 0.0033, P(perm) = 0.0020), but not with gout (OR = 0.8801, P = 0.1315, P(perm) = 0.1491). Rs2271437 was significantly associated with gout (minor allele “G”, OR = 1.387, P = 0.0277, P(perm) = 0.0288), and was further confirmed in the meta-analysis with the previously published gout GWAS dataset (OR = 1.3221, P = 0.0089). Each variant basically conferred consistent OR direction on gout and HUA, compared with the normouricemic control. CONCLUSIONS: Our findings support the associations of the SLC28A2 gene with the SUA level, the HUA phenotype and gout in Han Chinese. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s41065-018-0078-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-63357062019-01-24 Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese Zhou, Zhaowei Li, Zhiqiang Wang, Can Li, Xinde Cheng, Xiaoyu Li, Changgui Shi, Yongyong Hereditas Research BACKGROUND: Serum uric acid (SUA), hyperuricemia (HUA) and gout are complex traits with relatively high heritability. This study aims to identify whether a candidate gene, SLC28A2, exerts susceptibility for SUA fluctuation and incidence of HUA and gout in the Han Chinese population. RESULTS: Three sample sets of 1376 gout patients, 1290 long-term HUA subjects (no gout attack) and 1349 normouricemic controls were recruited for this study. Eight polymorphisms in the SLC28A2 gene were genotyped using the ligase detection reaction-polymerase chain reaction (LDR-PCR) technology. Rs16941238 showed the most significant associations with SUA level (minor allele “A”, BETA = − 13.84 μmol/L, P = 0.0041, P(perm) = 0.0042) and HUA (OR = 0.7734, P = 0.0033, P(perm) = 0.0020), but not with gout (OR = 0.8801, P = 0.1315, P(perm) = 0.1491). Rs2271437 was significantly associated with gout (minor allele “G”, OR = 1.387, P = 0.0277, P(perm) = 0.0288), and was further confirmed in the meta-analysis with the previously published gout GWAS dataset (OR = 1.3221, P = 0.0089). Each variant basically conferred consistent OR direction on gout and HUA, compared with the normouricemic control. CONCLUSIONS: Our findings support the associations of the SLC28A2 gene with the SUA level, the HUA phenotype and gout in Han Chinese. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s41065-018-0078-0) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-16 /pmc/articles/PMC6335706/ /pubmed/30679935 http://dx.doi.org/10.1186/s41065-018-0078-0 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhou, Zhaowei
Li, Zhiqiang
Wang, Can
Li, Xinde
Cheng, Xiaoyu
Li, Changgui
Shi, Yongyong
Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese
title Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese
title_full Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese
title_fullStr Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese
title_full_unstemmed Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese
title_short Common variants in the SLC28A2 gene are associated with serum uric acid level and hyperuricemia and gout in Han Chinese
title_sort common variants in the slc28a2 gene are associated with serum uric acid level and hyperuricemia and gout in han chinese
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335706/
https://www.ncbi.nlm.nih.gov/pubmed/30679935
http://dx.doi.org/10.1186/s41065-018-0078-0
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