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Upregulated expression of FFAR2 and SOC3 genes is associated with gout

OBJECTIVE: To examine the expression of Free fatty acid receptor 2 (FFAR2) and Suppressor of cytokine signalling 3 (SOCS3) genes in asymptomatic hyperuricaemia (AH), AH with MSU crystal deposition, inter-critical gout and gout flare. METHODS: Study participants (n = 120) comprised 34 people with ser...

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Autores principales: Orji, Oliver C, López-Domínguez, Maria B, Sandoval-Plata, Gabriela, Guetta-Baranes, Tamar, Valdes, Ana M, Doherty, Michael, Morgan, Kevin, Abhishek, Abhishek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891400/
https://www.ncbi.nlm.nih.gov/pubmed/35731142
http://dx.doi.org/10.1093/rheumatology/keac360
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author Orji, Oliver C
López-Domínguez, Maria B
Sandoval-Plata, Gabriela
Guetta-Baranes, Tamar
Valdes, Ana M
Doherty, Michael
Morgan, Kevin
Abhishek, Abhishek
author_facet Orji, Oliver C
López-Domínguez, Maria B
Sandoval-Plata, Gabriela
Guetta-Baranes, Tamar
Valdes, Ana M
Doherty, Michael
Morgan, Kevin
Abhishek, Abhishek
author_sort Orji, Oliver C
collection PubMed
description OBJECTIVE: To examine the expression of Free fatty acid receptor 2 (FFAR2) and Suppressor of cytokine signalling 3 (SOCS3) genes in asymptomatic hyperuricaemia (AH), AH with MSU crystal deposition, inter-critical gout and gout flare. METHODS: Study participants (n = 120) comprised 34 people with serum urate (SU) <360 μmol/l, 69 with AH ± MSU crystal deposition and 17 with a gout flare. Sixteen of the 17 patients with a gout flare attended a second visit 6–12 weeks later. Gene expression levels were assessed using RT-qPCR and results computed as fold changes (FC) after normalization to the reference gene. RESULTS: FFAR2 was significantly upregulated during gout flares (FC = 2.9) compared with normal SU, AH, and AH + MSU crystal deposition (FC = 1.1, P < 0.0001 for each comparison). FFAR2 was also significantly upregulated during inter-critical gout (FC = 1.8) compared with normal SU, AH and AH + MSU (FC = 1.1, P < 0.001 for each comparison). SOCS3 was significantly upregulated during gout flares (FC = 3.4) compared with normal SU, AH, and AH + MSU crystal deposition (FC = 1.1, 1.1 and 1.2, respectively, P < 0.0001 for each comparison). SOCS3 was also upregulated during inter-critical gout (FC = 2.1) compared with normal SU (P = 0.02) and AH (P = 0.006) (FC = 1.1 and 1.2, respectively). FFAR2 expression was upregulated during gout flare compared with inter-critical gout and SOCS3 expression showed negative correlation with flare duration (r = –0.49, P < 0.05). CONCLUSION: FFAR2 upregulation is associated with gout and may trigger gout flares. SOCS3 may have a role in amelioration of gout flares.
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spelling pubmed-98914002023-02-02 Upregulated expression of FFAR2 and SOC3 genes is associated with gout Orji, Oliver C López-Domínguez, Maria B Sandoval-Plata, Gabriela Guetta-Baranes, Tamar Valdes, Ana M Doherty, Michael Morgan, Kevin Abhishek, Abhishek Rheumatology (Oxford) Basic Science OBJECTIVE: To examine the expression of Free fatty acid receptor 2 (FFAR2) and Suppressor of cytokine signalling 3 (SOCS3) genes in asymptomatic hyperuricaemia (AH), AH with MSU crystal deposition, inter-critical gout and gout flare. METHODS: Study participants (n = 120) comprised 34 people with serum urate (SU) <360 μmol/l, 69 with AH ± MSU crystal deposition and 17 with a gout flare. Sixteen of the 17 patients with a gout flare attended a second visit 6–12 weeks later. Gene expression levels were assessed using RT-qPCR and results computed as fold changes (FC) after normalization to the reference gene. RESULTS: FFAR2 was significantly upregulated during gout flares (FC = 2.9) compared with normal SU, AH, and AH + MSU crystal deposition (FC = 1.1, P < 0.0001 for each comparison). FFAR2 was also significantly upregulated during inter-critical gout (FC = 1.8) compared with normal SU, AH and AH + MSU (FC = 1.1, P < 0.001 for each comparison). SOCS3 was significantly upregulated during gout flares (FC = 3.4) compared with normal SU, AH, and AH + MSU crystal deposition (FC = 1.1, 1.1 and 1.2, respectively, P < 0.0001 for each comparison). SOCS3 was also upregulated during inter-critical gout (FC = 2.1) compared with normal SU (P = 0.02) and AH (P = 0.006) (FC = 1.1 and 1.2, respectively). FFAR2 expression was upregulated during gout flare compared with inter-critical gout and SOCS3 expression showed negative correlation with flare duration (r = –0.49, P < 0.05). CONCLUSION: FFAR2 upregulation is associated with gout and may trigger gout flares. SOCS3 may have a role in amelioration of gout flares. Oxford University Press 2022-06-22 /pmc/articles/PMC9891400/ /pubmed/35731142 http://dx.doi.org/10.1093/rheumatology/keac360 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Science
Orji, Oliver C
López-Domínguez, Maria B
Sandoval-Plata, Gabriela
Guetta-Baranes, Tamar
Valdes, Ana M
Doherty, Michael
Morgan, Kevin
Abhishek, Abhishek
Upregulated expression of FFAR2 and SOC3 genes is associated with gout
title Upregulated expression of FFAR2 and SOC3 genes is associated with gout
title_full Upregulated expression of FFAR2 and SOC3 genes is associated with gout
title_fullStr Upregulated expression of FFAR2 and SOC3 genes is associated with gout
title_full_unstemmed Upregulated expression of FFAR2 and SOC3 genes is associated with gout
title_short Upregulated expression of FFAR2 and SOC3 genes is associated with gout
title_sort upregulated expression of ffar2 and soc3 genes is associated with gout
topic Basic Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9891400/
https://www.ncbi.nlm.nih.gov/pubmed/35731142
http://dx.doi.org/10.1093/rheumatology/keac360
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