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Genetic association and functional analysis of rs7903456 in FAM35A gene and hyperuricemia: a population based study
Recent studies have identified SNP rs7903456 of FAM35A to be associated with gout. Because of the close connections between hyperuricemia and gout, we hypothesized that the effect of rs7903456 on gout might be mediated by hyperuricemia or its related quantitative trait, uric acid level. We investiga...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018507/ https://www.ncbi.nlm.nih.gov/pubmed/29942023 http://dx.doi.org/10.1038/s41598-018-27956-3 |
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author | Yan, Feng Sun, Peng Zhao, Huishou Zhao, Changhai Zhang, Nana Dai, Yujie |
author_facet | Yan, Feng Sun, Peng Zhao, Huishou Zhao, Changhai Zhang, Nana Dai, Yujie |
author_sort | Yan, Feng |
collection | PubMed |
description | Recent studies have identified SNP rs7903456 of FAM35A to be associated with gout. Because of the close connections between hyperuricemia and gout, we hypothesized that the effect of rs7903456 on gout might be mediated by hyperuricemia or its related quantitative trait, uric acid level. We investigated the association between 31 SNPs of FAM35A, including rs7903456, and hyperuricemia based on 2,773 hyperuricemia patients and controls. We fitted a simple model for each of these 31 SNPs to screen the candidate SNP for further analyses. Moreover, we selected potential confounders and fitted a multivariate model to investigate the adjusted effects of the targeted SNPs. Both disease status of hyperuricemia and blood uric acid level were considered as the main phenotype. We have identified rs7903456 to be associated with hyperuricemia and uric acid level. The significant signal was identified between rs7903456 and uric acid level after adjusted by several potential confounders. Our findings showed that the T allele of rs7903456 could increase the uric acid level by ~10 mmol/L on average after adjusting several biochemical and clinical variables. Our findings indicated that the previously identified effects of rs7903456 on gout might partly be mediated by its effect on uric acid levels. |
format | Online Article Text |
id | pubmed-6018507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60185072018-07-06 Genetic association and functional analysis of rs7903456 in FAM35A gene and hyperuricemia: a population based study Yan, Feng Sun, Peng Zhao, Huishou Zhao, Changhai Zhang, Nana Dai, Yujie Sci Rep Article Recent studies have identified SNP rs7903456 of FAM35A to be associated with gout. Because of the close connections between hyperuricemia and gout, we hypothesized that the effect of rs7903456 on gout might be mediated by hyperuricemia or its related quantitative trait, uric acid level. We investigated the association between 31 SNPs of FAM35A, including rs7903456, and hyperuricemia based on 2,773 hyperuricemia patients and controls. We fitted a simple model for each of these 31 SNPs to screen the candidate SNP for further analyses. Moreover, we selected potential confounders and fitted a multivariate model to investigate the adjusted effects of the targeted SNPs. Both disease status of hyperuricemia and blood uric acid level were considered as the main phenotype. We have identified rs7903456 to be associated with hyperuricemia and uric acid level. The significant signal was identified between rs7903456 and uric acid level after adjusted by several potential confounders. Our findings showed that the T allele of rs7903456 could increase the uric acid level by ~10 mmol/L on average after adjusting several biochemical and clinical variables. Our findings indicated that the previously identified effects of rs7903456 on gout might partly be mediated by its effect on uric acid levels. Nature Publishing Group UK 2018-06-25 /pmc/articles/PMC6018507/ /pubmed/29942023 http://dx.doi.org/10.1038/s41598-018-27956-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yan, Feng Sun, Peng Zhao, Huishou Zhao, Changhai Zhang, Nana Dai, Yujie Genetic association and functional analysis of rs7903456 in FAM35A gene and hyperuricemia: a population based study |
title | Genetic association and functional analysis of rs7903456 in FAM35A gene and hyperuricemia: a population based study |
title_full | Genetic association and functional analysis of rs7903456 in FAM35A gene and hyperuricemia: a population based study |
title_fullStr | Genetic association and functional analysis of rs7903456 in FAM35A gene and hyperuricemia: a population based study |
title_full_unstemmed | Genetic association and functional analysis of rs7903456 in FAM35A gene and hyperuricemia: a population based study |
title_short | Genetic association and functional analysis of rs7903456 in FAM35A gene and hyperuricemia: a population based study |
title_sort | genetic association and functional analysis of rs7903456 in fam35a gene and hyperuricemia: a population based study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018507/ https://www.ncbi.nlm.nih.gov/pubmed/29942023 http://dx.doi.org/10.1038/s41598-018-27956-3 |
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