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Common variant of ALPK1 is not associated with gout: a replication study

Gout is one of the most kinds of common inflammatory arthritis as a consequence of hyperuricemia. Alpha-protein kinase 1 (ALPK1) gene locates in a gout-susceptibility locus on chromosome 4q21–31, and encodes ALPK1 protein which plays a pivotal role in the phosphorylation of myosin 1. In the previous...

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Autores principales: Chiba, Toshinori, Matsuo, Hirotaka, Sakiyama, Masayuki, Nakayama, Akiyoshi, Shimizu, Seiko, Wakai, Kenji, Suma, Shino, Nakashima, Hiroshi, Sakurai, Yutaka, Shimizu, Toru, Ichida, Kimiyoshi, Shinomiya, Nariyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286131/
https://www.ncbi.nlm.nih.gov/pubmed/25326865
http://dx.doi.org/10.1007/s13577-014-0103-1
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author Chiba, Toshinori
Matsuo, Hirotaka
Sakiyama, Masayuki
Nakayama, Akiyoshi
Shimizu, Seiko
Wakai, Kenji
Suma, Shino
Nakashima, Hiroshi
Sakurai, Yutaka
Shimizu, Toru
Ichida, Kimiyoshi
Shinomiya, Nariyoshi
author_facet Chiba, Toshinori
Matsuo, Hirotaka
Sakiyama, Masayuki
Nakayama, Akiyoshi
Shimizu, Seiko
Wakai, Kenji
Suma, Shino
Nakashima, Hiroshi
Sakurai, Yutaka
Shimizu, Toru
Ichida, Kimiyoshi
Shinomiya, Nariyoshi
author_sort Chiba, Toshinori
collection PubMed
description Gout is one of the most kinds of common inflammatory arthritis as a consequence of hyperuricemia. Alpha-protein kinase 1 (ALPK1) gene locates in a gout-susceptibility locus on chromosome 4q21–31, and encodes ALPK1 protein which plays a pivotal role in the phosphorylation of myosin 1. In the previous genetic study of Taiwanese populations, 3 single nucleotide polymorphisms (SNPs), rs11726117, rs231247 and rs231253, in ALPK1 gene were reported to have a significant association with gout. However, no replication study has been performed to confirm this association. Therefore, we first conducted a replication study with clinically defined gout patients in a different population. Linkage disequilibrium (LD) analyzes of the 3 SNPs in ALPK1 revealed that these SNPs are in strong LD in a Japanese population. Among the 3 SNPs of ALPK1, rs11726117 (M861T) is the only missense SNP. Therefore, rs11726117 was genotyped in a Japanese population of 903 clinically defined gout cases and 1,302 controls, and was evaluated for a possible association with gout. The minor allele frequencies of rs11726117 were 0.26 and 0.25 in the case and control groups, respectively. The association analysis has not detected a significant association between rs11726117 and gout susceptibility in a Japanese population (p = 0.44). Because ABCG2, a major causative gene for gout, also locates in the gout-susceptibility locus on chromosome 4q, these findings suggest that among genes in a gout-susceptibility locus, not ALPK1 but ABCG2 could be important as a gout-susceptible gene.
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spelling pubmed-42861312015-01-12 Common variant of ALPK1 is not associated with gout: a replication study Chiba, Toshinori Matsuo, Hirotaka Sakiyama, Masayuki Nakayama, Akiyoshi Shimizu, Seiko Wakai, Kenji Suma, Shino Nakashima, Hiroshi Sakurai, Yutaka Shimizu, Toru Ichida, Kimiyoshi Shinomiya, Nariyoshi Hum Cell Rapid Communication Gout is one of the most kinds of common inflammatory arthritis as a consequence of hyperuricemia. Alpha-protein kinase 1 (ALPK1) gene locates in a gout-susceptibility locus on chromosome 4q21–31, and encodes ALPK1 protein which plays a pivotal role in the phosphorylation of myosin 1. In the previous genetic study of Taiwanese populations, 3 single nucleotide polymorphisms (SNPs), rs11726117, rs231247 and rs231253, in ALPK1 gene were reported to have a significant association with gout. However, no replication study has been performed to confirm this association. Therefore, we first conducted a replication study with clinically defined gout patients in a different population. Linkage disequilibrium (LD) analyzes of the 3 SNPs in ALPK1 revealed that these SNPs are in strong LD in a Japanese population. Among the 3 SNPs of ALPK1, rs11726117 (M861T) is the only missense SNP. Therefore, rs11726117 was genotyped in a Japanese population of 903 clinically defined gout cases and 1,302 controls, and was evaluated for a possible association with gout. The minor allele frequencies of rs11726117 were 0.26 and 0.25 in the case and control groups, respectively. The association analysis has not detected a significant association between rs11726117 and gout susceptibility in a Japanese population (p = 0.44). Because ABCG2, a major causative gene for gout, also locates in the gout-susceptibility locus on chromosome 4q, these findings suggest that among genes in a gout-susceptibility locus, not ALPK1 but ABCG2 could be important as a gout-susceptible gene. Springer Japan 2014-10-19 2015 /pmc/articles/PMC4286131/ /pubmed/25326865 http://dx.doi.org/10.1007/s13577-014-0103-1 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Rapid Communication
Chiba, Toshinori
Matsuo, Hirotaka
Sakiyama, Masayuki
Nakayama, Akiyoshi
Shimizu, Seiko
Wakai, Kenji
Suma, Shino
Nakashima, Hiroshi
Sakurai, Yutaka
Shimizu, Toru
Ichida, Kimiyoshi
Shinomiya, Nariyoshi
Common variant of ALPK1 is not associated with gout: a replication study
title Common variant of ALPK1 is not associated with gout: a replication study
title_full Common variant of ALPK1 is not associated with gout: a replication study
title_fullStr Common variant of ALPK1 is not associated with gout: a replication study
title_full_unstemmed Common variant of ALPK1 is not associated with gout: a replication study
title_short Common variant of ALPK1 is not associated with gout: a replication study
title_sort common variant of alpk1 is not associated with gout: a replication study
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4286131/
https://www.ncbi.nlm.nih.gov/pubmed/25326865
http://dx.doi.org/10.1007/s13577-014-0103-1
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