Functional non-synonymous variants of ABCG2 and gout risk
- PMID: 28968913
- DOI: 10.1093/rheumatology/kex295
Functional non-synonymous variants of ABCG2 and gout risk
Abstract
Objectives: Common dysfunctional variants of ATP binding cassette subfamily G member 2 (Junior blood group) (ABCG2), a high-capacity urate transporter gene, that result in decreased urate excretion are major causes of hyperuricemia and gout. In the present study, our objective was to determine the frequency and effect on gout of common and rare non-synonymous and other functional allelic variants in the ABCG2 gene.
Methods: The main cohort recruited from the Czech Republic consisted of 145 gout patients; 115 normouricaemic controls were used for comparison. We amplified, directly sequenced and analysed 15 ABCG2 exons. The associations between genetic variants and clinical phenotype were analysed using the t-test, Fisher's exact test and a logistic and linear regression approach. Data from a New Zealand Polynesian sample set and the UK Biobank were included for the p.V12M analysis.
Results: In the ABCG2 gene, 18 intronic (one dysfunctional splicing) and 11 exonic variants were detected: 9 were non-synonymous (2 common, 7 rare including 1 novel), namely p.V12M, p.Q141K, p.R147W, p.T153M, p.F373C, p.T434M, p.S476P, p.D620N and p.K360del. The p.Q141K (rs2231142) variant had a significantly higher minor allele frequency (0.23) in the gout patients compared with the European-origin population (0.09) and was significantly more common among gout patients than among normouricaemic controls (odds ratio = 3.26, P < 0.0001). Patients with non-synonymous allelic variants had an earlier onset of gout (42 vs 48 years, P = 0.0143) and a greater likelihood of a familial history of gout (41% vs 27%, odds ratio = 1.96, P = 0.053). In a meta-analysis p.V12M exerted a protective effect from gout (P < 0.0001).
Conclusion: Genetic variants of ABCG2, common and rare, increased the risk of gout. Non-synonymous allelic variants of ABCG2 had a significant effect on earlier onset of gout and the presence of a familial gout history. ABCG2 should thus be considered a common and significant risk factor for gout.
Keywords: ABCG2; gout; urate transport.
© The Author 2017. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For Permissions, please email: journals.permissions@oup.com
Similar articles
-
The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients.Arthritis Res Ther. 2019 Mar 20;21(1):77. doi: 10.1186/s13075-019-1860-8. Arthritis Res Ther. 2019. PMID: 30894219 Free PMC article.
-
Functional Characterization of Clinically-Relevant Rare Variants in ABCG2 Identified in a Gout and Hyperuricemia Cohort.Cells. 2019 Apr 18;8(4):363. doi: 10.3390/cells8040363. Cells. 2019. PMID: 31003562 Free PMC article.
-
Pleiotropic effect of the ABCG2 gene in gout: involvement in serum urate levels and progression from hyperuricemia to gout.Arthritis Res Ther. 2020 Mar 12;22(1):45. doi: 10.1186/s13075-020-2136-z. Arthritis Res Ther. 2020. PMID: 32164793 Free PMC article.
-
The association between genetic polymorphisms in ABCG2 and SLC2A9 and urate: an updated systematic review and meta-analysis.BMC Med Genet. 2020 Oct 21;21(1):210. doi: 10.1186/s12881-020-01147-2. BMC Med Genet. 2020. PMID: 33087043 Free PMC article.
-
[ROLE OF SLC2A9 AND ABCG2 GENE POLYMORPHISMS IN ORIGIN OF HYPERURICEMIA AND GOUT].Georgian Med News. 2016 Mar;(252):79-83. Georgian Med News. 2016. PMID: 27119840 Review. Russian.
Cited by
-
Susceptibility genes of hyperuricemia and gout.Hereditas. 2022 Aug 4;159(1):30. doi: 10.1186/s41065-022-00243-y. Hereditas. 2022. PMID: 35922835 Free PMC article. Review.
-
Examining an Association of Single Nucleotide Polymorphisms with Hyperuricemia in Chinese Flight Attendants.Pharmgenomics Pers Med. 2022 Jun 8;15:589-602. doi: 10.2147/PGPM.S364206. eCollection 2022. Pharmgenomics Pers Med. 2022. PMID: 35702613 Free PMC article.
-
Update on the epidemiology, genetics, and therapeutic options of hyperuricemia.Am J Transl Res. 2020 Jul 15;12(7):3167-3181. eCollection 2020. Am J Transl Res. 2020. PMID: 32774692 Free PMC article. Review.
-
The impact of dysfunctional variants of ABCG2 on hyperuricemia and gout in pediatric-onset patients.Arthritis Res Ther. 2019 Mar 20;21(1):77. doi: 10.1186/s13075-019-1860-8. Arthritis Res Ther. 2019. PMID: 30894219 Free PMC article.
-
Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels.Nat Commun. 2018 Oct 12;9(1):4228. doi: 10.1038/s41467-018-06620-4. Nat Commun. 2018. PMID: 30315176 Free PMC article.
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical