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Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus
Gout is a common disease resulting from hyperuricemia. Recently, a genome-wide association study identified an association between gout and a single nucleotide polymorphism (SNP) rs2188380, located on an intergenic region between MYL2 and CUX2 on chromosome 12. However, other genes around rs2188380...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867610/ https://www.ncbi.nlm.nih.gov/pubmed/27181629 http://dx.doi.org/10.1038/srep25360 |
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author | Sakiyama, Masayuki Matsuo, Hirotaka Nakaoka, Hirofumi Yamamoto, Ken Nakayama, Akiyoshi Nakamura, Takahiro Kawai, Sayo Okada, Rieko Ooyama, Hiroshi Shimizu, Toru Shinomiya, Nariyoshi |
author_facet | Sakiyama, Masayuki Matsuo, Hirotaka Nakaoka, Hirofumi Yamamoto, Ken Nakayama, Akiyoshi Nakamura, Takahiro Kawai, Sayo Okada, Rieko Ooyama, Hiroshi Shimizu, Toru Shinomiya, Nariyoshi |
author_sort | Sakiyama, Masayuki |
collection | PubMed |
description | Gout is a common disease resulting from hyperuricemia. Recently, a genome-wide association study identified an association between gout and a single nucleotide polymorphism (SNP) rs2188380, located on an intergenic region between MYL2 and CUX2 on chromosome 12. However, other genes around rs2188380 could possibly be gout susceptibility genes. Therefore, we performed a fine-mapping study of the MYL2-CUX2 region. From 8,595 SNPs in the MYL2-CUX2 region, 9 tag SNPs were selected, and genotyping of 1,048 male gout patients and 1,334 male controls was performed by TaqMan method. Eight SNPs showed significant associations with gout after Bonferroni correction. rs671 (Glu504Lys) of ALDH2 had the most significant association with gout (P = 1.7 × 10(−18), odds ratio = 0.53). After adjustment for rs671, the other 8 SNPs no longer showed a significant association with gout, while the significant association of rs671 remained. rs671 has been reportedly associated with alcohol drinking behavior, and it is well-known that alcohol drinking elevates serum uric acid levels. These data suggest that rs671, a common functional SNP of ALDH2, is a genuine gout-associated SNP in the MYL2-CUX2 locus and that “A” allele (Lys) of rs671 plays a protective role in the development of gout. |
format | Online Article Text |
id | pubmed-4867610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48676102016-05-31 Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus Sakiyama, Masayuki Matsuo, Hirotaka Nakaoka, Hirofumi Yamamoto, Ken Nakayama, Akiyoshi Nakamura, Takahiro Kawai, Sayo Okada, Rieko Ooyama, Hiroshi Shimizu, Toru Shinomiya, Nariyoshi Sci Rep Article Gout is a common disease resulting from hyperuricemia. Recently, a genome-wide association study identified an association between gout and a single nucleotide polymorphism (SNP) rs2188380, located on an intergenic region between MYL2 and CUX2 on chromosome 12. However, other genes around rs2188380 could possibly be gout susceptibility genes. Therefore, we performed a fine-mapping study of the MYL2-CUX2 region. From 8,595 SNPs in the MYL2-CUX2 region, 9 tag SNPs were selected, and genotyping of 1,048 male gout patients and 1,334 male controls was performed by TaqMan method. Eight SNPs showed significant associations with gout after Bonferroni correction. rs671 (Glu504Lys) of ALDH2 had the most significant association with gout (P = 1.7 × 10(−18), odds ratio = 0.53). After adjustment for rs671, the other 8 SNPs no longer showed a significant association with gout, while the significant association of rs671 remained. rs671 has been reportedly associated with alcohol drinking behavior, and it is well-known that alcohol drinking elevates serum uric acid levels. These data suggest that rs671, a common functional SNP of ALDH2, is a genuine gout-associated SNP in the MYL2-CUX2 locus and that “A” allele (Lys) of rs671 plays a protective role in the development of gout. Nature Publishing Group 2016-05-16 /pmc/articles/PMC4867610/ /pubmed/27181629 http://dx.doi.org/10.1038/srep25360 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Sakiyama, Masayuki Matsuo, Hirotaka Nakaoka, Hirofumi Yamamoto, Ken Nakayama, Akiyoshi Nakamura, Takahiro Kawai, Sayo Okada, Rieko Ooyama, Hiroshi Shimizu, Toru Shinomiya, Nariyoshi Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus |
title | Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus |
title_full | Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus |
title_fullStr | Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus |
title_full_unstemmed | Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus |
title_short | Identification of rs671, a common variant of ALDH2, as a gout susceptibility locus |
title_sort | identification of rs671, a common variant of aldh2, as a gout susceptibility locus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867610/ https://www.ncbi.nlm.nih.gov/pubmed/27181629 http://dx.doi.org/10.1038/srep25360 |
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