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Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals.

Authors :
Nakatochi M
Kanai M
Nakayama A
Hishida A
Kawamura Y
Ichihara S
Akiyama M
Ikezaki H
Furusyo N
Shimizu S
Yamamoto K
Hirata M
Okada R
Kawai S
Kawaguchi M
Nishida Y
Shimanoe C
Ibusuki R
Takezaki T
Nakajima M
Takao M
Ozaki E
Matsui D
Nishiyama T
Suzuki S
Takashima N
Kita Y
Endoh K
Kuriki K
Uemura H
Arisawa K
Oze I
Matsuo K
Nakamura Y
Mikami H
Tamura T
Nakashima H
Nakamura T
Kato N
Matsuda K
Murakami Y
Matsubara T
Naito M
Kubo M
Kamatani Y
Shinomiya N
Yokota M
Wakai K
Okada Y
Matsuo H
Source :
Communications biology [Commun Biol] 2019 Apr 08; Vol. 2, pp. 115. Date of Electronic Publication: 2019 Apr 08 (Print Publication: 2019).
Publication Year :
2019

Abstract

Gout is a common arthritis caused by elevated serum uric acid (SUA) levels. Here we investigated loci influencing SUA in a genome-wide meta-analysis with 121,745 Japanese subjects. We identified 8948 variants at 36 genomic loci ( P <5 × 10 <superscript>-8</superscript> ) including eight novel loci. Of these, missense variants of SESN2 and PNPLA3 were predicted to be damaging to the function of these proteins; another five loci- TMEM18 , TM4SF4 , MXD3-LMAN2 , PSORS1C1-PSORS1C2 , and HNF4A -are related to cell metabolism, proliferation, or oxidative stress; and the remaining locus, LINC01578 , is unknown. We also identified 132 correlated genes whose expression levels are associated with SUA-increasing alleles. These genes are enriched for the UniProt transport term, suggesting the importance of transport-related genes in SUA regulation. Furthermore, trans-ethnic meta-analysis across our own meta-analysis and the Global Urate Genetics Consortium has revealed 15 more novel loci associated with SUA. Our findings provide insight into the pathogenesis, treatment, and prevention of hyperuricemia/gout.<br />Competing Interests: The authors declare no competing interests.

Details

Language :
English
ISSN :
2399-3642
Volume :
2
Database :
MEDLINE
Journal :
Communications biology
Publication Type :
Academic Journal
Accession number :
30993211
Full Text :
https://doi.org/10.1038/s42003-019-0339-0