THU0519 Xanthine Oxidase Gene Variants and Their Association with Blood Pressure and Incident Hypertension: A Population Study
BackgroundUric acid has been associated with blood pressure and hypertension. During the final stage of purine metabolism xanthine oxidoreductase (XOR) produces uric acid, while at the same time reactive oxygen species are formed. We hypothesized that uric acid production, as assessed indirectly fro...
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Veröffentlicht in: | Annals of the rheumatic diseases 2016-06, Vol.75 (Suppl 2), p.379-380 |
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creator | Scheepers, L.E. Wei, F. Stolarz-Skrzypek, K. Malyutina, S. Tikhonoff, V. Thijs, L. Salvi, E. Barlassina, C. Filipovský, J. Casiglia, E. Nikitin, Y.P. Kawecka-Jaszcz, K. Manunta, P. Cusi, D. Boonen, A. Staessen, J.A. Arts, I.C. |
description | BackgroundUric acid has been associated with blood pressure and hypertension. During the final stage of purine metabolism xanthine oxidoreductase (XOR) produces uric acid, while at the same time reactive oxygen species are formed. We hypothesized that uric acid production, as assessed indirectly from XOR variants, is associated with hypertension (figure 1).ObjectivesThe aim of the present study is to investigate the association of variants in the XOR gene with blood pressure and the development of hypertension.MethodsAnalyses were conducted in the prospective Flemish FLEMENGHO and European EPOGH study. Among 2769 participants (48.3% men; mean age 40.7 years) we genotyped 25 XOR SNPs and measured blood pressure at baseline and follow-up (median 8.8 years). The relation between variants of the XOR gene with changes in pulse pressure and mean arterial pressure over time; and incidence of hypertension, were analysed using multivariable mixed models and cox-regression, respectively.ResultsCompared with major allele homozygotes, pulse pressure increased approximately 2 mm Hg more in minor allele carriers of rs11904439 (P=value 0.01), whereas mean arterial pressure and diastolic blood pressure increased approximately 1 mm Hg less in minor allele carriers of rs2043013 (P=0.01). In 2050 participants normotensive at baseline, hazard ratios contrasting risk of hypertension in minor allele carriers vs. major allele homozygotes was 1.31 (95% confidence interval [CI] 1.03–1.68) for rs11904439 and 1.69 (95% CI 1.11–2.57) for rs148756340. With the false discovery rate set at 0.25, the aforementioned associations retained significance. The changes in systolic blood pressure from baseline to follow-up and the serum levels of uric acid at baseline (n=1949) were not associated with XOR.ConclusionsIn conclusion, pending confirmation in appropriately powered cohort studies, our findings suggest that variation in uric acid production, as captured by genetic variation in XOR, might be a predictor of changes in pulse pressure, mean arterial pressure and in the risk of hypertension.AcknowledgementThe authors gratefully acknowledge the clerical assistance of Mrs Renilde Wolfs.Disclosure of InterestNone declared |
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During the final stage of purine metabolism xanthine oxidoreductase (XOR) produces uric acid, while at the same time reactive oxygen species are formed. We hypothesized that uric acid production, as assessed indirectly from XOR variants, is associated with hypertension (figure 1).ObjectivesThe aim of the present study is to investigate the association of variants in the XOR gene with blood pressure and the development of hypertension.MethodsAnalyses were conducted in the prospective Flemish FLEMENGHO and European EPOGH study. Among 2769 participants (48.3% men; mean age 40.7 years) we genotyped 25 XOR SNPs and measured blood pressure at baseline and follow-up (median 8.8 years). The relation between variants of the XOR gene with changes in pulse pressure and mean arterial pressure over time; and incidence of hypertension, were analysed using multivariable mixed models and cox-regression, respectively.ResultsCompared with major allele homozygotes, pulse pressure increased approximately 2 mm Hg more in minor allele carriers of rs11904439 (P=value 0.01), whereas mean arterial pressure and diastolic blood pressure increased approximately 1 mm Hg less in minor allele carriers of rs2043013 (P=0.01). In 2050 participants normotensive at baseline, hazard ratios contrasting risk of hypertension in minor allele carriers vs. major allele homozygotes was 1.31 (95% confidence interval [CI] 1.03–1.68) for rs11904439 and 1.69 (95% CI 1.11–2.57) for rs148756340. With the false discovery rate set at 0.25, the aforementioned associations retained significance. The changes in systolic blood pressure from baseline to follow-up and the serum levels of uric acid at baseline (n=1949) were not associated with XOR.ConclusionsIn conclusion, pending confirmation in appropriately powered cohort studies, our findings suggest that variation in uric acid production, as captured by genetic variation in XOR, might be a predictor of changes in pulse pressure, mean arterial pressure and in the risk of hypertension.AcknowledgementThe authors gratefully acknowledge the clerical assistance of Mrs Renilde Wolfs.Disclosure of InterestNone declared</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/annrheumdis-2016-eular.2964</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><ispartof>Annals of the rheumatic diseases, 2016-06, Vol.75 (Suppl 2), p.379-380</ispartof><rights>2016, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2016 (c) 2016, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b1851-c17eb91449a504decab65dc4d24ca4930ce798f63a305bcee7026c6bb90697cf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://ard.bmj.com/content/75/Suppl_2/379.3.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://ard.bmj.com/content/75/Suppl_2/379.3.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,3196,23571,27924,27925,77600,77631</link.rule.ids></links><search><creatorcontrib>Scheepers, L.E.</creatorcontrib><creatorcontrib>Wei, F.</creatorcontrib><creatorcontrib>Stolarz-Skrzypek, K.</creatorcontrib><creatorcontrib>Malyutina, S.</creatorcontrib><creatorcontrib>Tikhonoff, V.</creatorcontrib><creatorcontrib>Thijs, L.</creatorcontrib><creatorcontrib>Salvi, E.</creatorcontrib><creatorcontrib>Barlassina, C.</creatorcontrib><creatorcontrib>Filipovský, J.</creatorcontrib><creatorcontrib>Casiglia, E.</creatorcontrib><creatorcontrib>Nikitin, Y.P.</creatorcontrib><creatorcontrib>Kawecka-Jaszcz, K.</creatorcontrib><creatorcontrib>Manunta, P.</creatorcontrib><creatorcontrib>Cusi, D.</creatorcontrib><creatorcontrib>Boonen, A.</creatorcontrib><creatorcontrib>Staessen, J.A.</creatorcontrib><creatorcontrib>Arts, I.C.</creatorcontrib><title>THU0519 Xanthine Oxidase Gene Variants and Their Association with Blood Pressure and Incident Hypertension: A Population Study</title><title>Annals of the rheumatic diseases</title><description>BackgroundUric acid has been associated with blood pressure and hypertension. During the final stage of purine metabolism xanthine oxidoreductase (XOR) produces uric acid, while at the same time reactive oxygen species are formed. We hypothesized that uric acid production, as assessed indirectly from XOR variants, is associated with hypertension (figure 1).ObjectivesThe aim of the present study is to investigate the association of variants in the XOR gene with blood pressure and the development of hypertension.MethodsAnalyses were conducted in the prospective Flemish FLEMENGHO and European EPOGH study. Among 2769 participants (48.3% men; mean age 40.7 years) we genotyped 25 XOR SNPs and measured blood pressure at baseline and follow-up (median 8.8 years). The relation between variants of the XOR gene with changes in pulse pressure and mean arterial pressure over time; and incidence of hypertension, were analysed using multivariable mixed models and cox-regression, respectively.ResultsCompared with major allele homozygotes, pulse pressure increased approximately 2 mm Hg more in minor allele carriers of rs11904439 (P=value 0.01), whereas mean arterial pressure and diastolic blood pressure increased approximately 1 mm Hg less in minor allele carriers of rs2043013 (P=0.01). In 2050 participants normotensive at baseline, hazard ratios contrasting risk of hypertension in minor allele carriers vs. major allele homozygotes was 1.31 (95% confidence interval [CI] 1.03–1.68) for rs11904439 and 1.69 (95% CI 1.11–2.57) for rs148756340. With the false discovery rate set at 0.25, the aforementioned associations retained significance. The changes in systolic blood pressure from baseline to follow-up and the serum levels of uric acid at baseline (n=1949) were not associated with XOR.ConclusionsIn conclusion, pending confirmation in appropriately powered cohort studies, our findings suggest that variation in uric acid production, as captured by genetic variation in XOR, might be a predictor of changes in pulse pressure, mean arterial pressure and in the risk of hypertension.AcknowledgementThe authors gratefully acknowledge the clerical assistance of Mrs Renilde Wolfs.Disclosure of InterestNone declared</description><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqVkMFOAjEQhhujiYi-QxPOiy3b7W71hESBhAQTwXhruu0QSqCL7W6UGxdf1CexgAevnib_zP_PTD6EOpR0KU35rXLOL6HZGBuSHqE8gWatfLcnODtDLcp4EducnKMWISRNmOD5JboKYRUlKWjRQvvZaE4yKr73X2_K1UvrAE8_rVEB8BCieFXexkHAyhk8W4L1uB9Cpa2qbeXwh62X-GFdVQY_ewih8XB0jp22BlyNR7st-BpciO473MfP1Tb-eMy-1I3ZXaOLhVoHuPmtbTR_epwNRslkOhwP-pOkpEVGE01zKAVlTKiMMANalTwzmpke04qJlGjIRbHgqUpJVmqAnPS45mUpCBe5XqRt1Dnt3frqvYFQy1XVeBdPSioILWiaERpd9yeX9lUIHhZy6-1G-Z2kRB6Qyz_I5QG5PCKXB-QxzU_pcrP6V_AHobKPTA</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Scheepers, L.E.</creator><creator>Wei, F.</creator><creator>Stolarz-Skrzypek, K.</creator><creator>Malyutina, S.</creator><creator>Tikhonoff, V.</creator><creator>Thijs, L.</creator><creator>Salvi, E.</creator><creator>Barlassina, C.</creator><creator>Filipovský, J.</creator><creator>Casiglia, E.</creator><creator>Nikitin, Y.P.</creator><creator>Kawecka-Jaszcz, K.</creator><creator>Manunta, P.</creator><creator>Cusi, D.</creator><creator>Boonen, A.</creator><creator>Staessen, J.A.</creator><creator>Arts, I.C.</creator><general>BMJ Publishing Group LTD</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>201606</creationdate><title>THU0519 Xanthine Oxidase Gene Variants and Their Association with Blood Pressure and Incident Hypertension: A Population Study</title><author>Scheepers, L.E. ; Wei, F. ; Stolarz-Skrzypek, K. ; Malyutina, S. ; Tikhonoff, V. ; Thijs, L. ; Salvi, E. ; Barlassina, C. ; Filipovský, J. ; Casiglia, E. ; Nikitin, Y.P. ; Kawecka-Jaszcz, K. ; Manunta, P. ; Cusi, D. ; Boonen, A. ; Staessen, J.A. ; Arts, I.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1851-c17eb91449a504decab65dc4d24ca4930ce798f63a305bcee7026c6bb90697cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scheepers, L.E.</creatorcontrib><creatorcontrib>Wei, F.</creatorcontrib><creatorcontrib>Stolarz-Skrzypek, K.</creatorcontrib><creatorcontrib>Malyutina, S.</creatorcontrib><creatorcontrib>Tikhonoff, V.</creatorcontrib><creatorcontrib>Thijs, L.</creatorcontrib><creatorcontrib>Salvi, E.</creatorcontrib><creatorcontrib>Barlassina, C.</creatorcontrib><creatorcontrib>Filipovský, J.</creatorcontrib><creatorcontrib>Casiglia, E.</creatorcontrib><creatorcontrib>Nikitin, Y.P.</creatorcontrib><creatorcontrib>Kawecka-Jaszcz, K.</creatorcontrib><creatorcontrib>Manunta, P.</creatorcontrib><creatorcontrib>Cusi, D.</creatorcontrib><creatorcontrib>Boonen, A.</creatorcontrib><creatorcontrib>Staessen, J.A.</creatorcontrib><creatorcontrib>Arts, I.C.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scheepers, L.E.</au><au>Wei, F.</au><au>Stolarz-Skrzypek, K.</au><au>Malyutina, S.</au><au>Tikhonoff, V.</au><au>Thijs, L.</au><au>Salvi, E.</au><au>Barlassina, C.</au><au>Filipovský, J.</au><au>Casiglia, E.</au><au>Nikitin, Y.P.</au><au>Kawecka-Jaszcz, K.</au><au>Manunta, P.</au><au>Cusi, D.</au><au>Boonen, A.</au><au>Staessen, J.A.</au><au>Arts, I.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>THU0519 Xanthine Oxidase Gene Variants and Their Association with Blood Pressure and Incident Hypertension: A Population Study</atitle><jtitle>Annals of the rheumatic diseases</jtitle><date>2016-06</date><risdate>2016</risdate><volume>75</volume><issue>Suppl 2</issue><spage>379</spage><epage>380</epage><pages>379-380</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>BackgroundUric acid has been associated with blood pressure and hypertension. During the final stage of purine metabolism xanthine oxidoreductase (XOR) produces uric acid, while at the same time reactive oxygen species are formed. We hypothesized that uric acid production, as assessed indirectly from XOR variants, is associated with hypertension (figure 1).ObjectivesThe aim of the present study is to investigate the association of variants in the XOR gene with blood pressure and the development of hypertension.MethodsAnalyses were conducted in the prospective Flemish FLEMENGHO and European EPOGH study. Among 2769 participants (48.3% men; mean age 40.7 years) we genotyped 25 XOR SNPs and measured blood pressure at baseline and follow-up (median 8.8 years). The relation between variants of the XOR gene with changes in pulse pressure and mean arterial pressure over time; and incidence of hypertension, were analysed using multivariable mixed models and cox-regression, respectively.ResultsCompared with major allele homozygotes, pulse pressure increased approximately 2 mm Hg more in minor allele carriers of rs11904439 (P=value 0.01), whereas mean arterial pressure and diastolic blood pressure increased approximately 1 mm Hg less in minor allele carriers of rs2043013 (P=0.01). In 2050 participants normotensive at baseline, hazard ratios contrasting risk of hypertension in minor allele carriers vs. major allele homozygotes was 1.31 (95% confidence interval [CI] 1.03–1.68) for rs11904439 and 1.69 (95% CI 1.11–2.57) for rs148756340. With the false discovery rate set at 0.25, the aforementioned associations retained significance. The changes in systolic blood pressure from baseline to follow-up and the serum levels of uric acid at baseline (n=1949) were not associated with XOR.ConclusionsIn conclusion, pending confirmation in appropriately powered cohort studies, our findings suggest that variation in uric acid production, as captured by genetic variation in XOR, might be a predictor of changes in pulse pressure, mean arterial pressure and in the risk of hypertension.AcknowledgementThe authors gratefully acknowledge the clerical assistance of Mrs Renilde Wolfs.Disclosure of InterestNone declared</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/annrheumdis-2016-eular.2964</doi><tpages>2</tpages></addata></record> |
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title | THU0519 Xanthine Oxidase Gene Variants and Their Association with Blood Pressure and Incident Hypertension: A Population Study |
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