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Genetics of hyperuricemia and gout: Insights from recent genome-wide association studies and Mendelian randomization studies

Gout is the most common form of inflammatory arthritis in adults. Elevation serum uric acid (SUA) concentration is known to be the key to gout pathogenesis. Since the first genome-wide association study (GWAS) for SUA was performed in 2007, the number of gene loci known to be associated with hyperur...

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Autor principal: Ko, Yu-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9333104/
https://www.ncbi.nlm.nih.gov/pubmed/35912057
http://dx.doi.org/10.4103/tcmj.tcmj_117_21
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author Ko, Yu-Lin
author_facet Ko, Yu-Lin
author_sort Ko, Yu-Lin
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description Gout is the most common form of inflammatory arthritis in adults. Elevation serum uric acid (SUA) concentration is known to be the key to gout pathogenesis. Since the first genome-wide association study (GWAS) for SUA was performed in 2007, the number of gene loci known to be associated with hyperuricemia and gout has grown rapidly. GWASs and Mendelian randomization studies have also reported numerous novel results regarding the genetics of hyperuricemia and gout since 2018. We concisely review recent advances in scholarship on the effects of genetics on hyperuricemia and gout risk. We also review data from genetic association studies in Taiwan and perform GWASs of SUA levels among Taiwan Biobank participants.
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spelling pubmed-93331042022-07-29 Genetics of hyperuricemia and gout: Insights from recent genome-wide association studies and Mendelian randomization studies Ko, Yu-Lin Tzu Chi Med J Review Article Gout is the most common form of inflammatory arthritis in adults. Elevation serum uric acid (SUA) concentration is known to be the key to gout pathogenesis. Since the first genome-wide association study (GWAS) for SUA was performed in 2007, the number of gene loci known to be associated with hyperuricemia and gout has grown rapidly. GWASs and Mendelian randomization studies have also reported numerous novel results regarding the genetics of hyperuricemia and gout since 2018. We concisely review recent advances in scholarship on the effects of genetics on hyperuricemia and gout risk. We also review data from genetic association studies in Taiwan and perform GWASs of SUA levels among Taiwan Biobank participants. Wolters Kluwer - Medknow 2021-11-24 /pmc/articles/PMC9333104/ /pubmed/35912057 http://dx.doi.org/10.4103/tcmj.tcmj_117_21 Text en Copyright: © 2021 Tzu Chi Medical Journal https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Ko, Yu-Lin
Genetics of hyperuricemia and gout: Insights from recent genome-wide association studies and Mendelian randomization studies
title Genetics of hyperuricemia and gout: Insights from recent genome-wide association studies and Mendelian randomization studies
title_full Genetics of hyperuricemia and gout: Insights from recent genome-wide association studies and Mendelian randomization studies
title_fullStr Genetics of hyperuricemia and gout: Insights from recent genome-wide association studies and Mendelian randomization studies
title_full_unstemmed Genetics of hyperuricemia and gout: Insights from recent genome-wide association studies and Mendelian randomization studies
title_short Genetics of hyperuricemia and gout: Insights from recent genome-wide association studies and Mendelian randomization studies
title_sort genetics of hyperuricemia and gout: insights from recent genome-wide association studies and mendelian randomization studies
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9333104/
https://www.ncbi.nlm.nih.gov/pubmed/35912057
http://dx.doi.org/10.4103/tcmj.tcmj_117_21
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