159 ALLOPURINOL REDUCES LEFT VENTRICULAR MASS IN PATIENTS WITH TYPE 2 DIABETES AND LEFT VENTRICULAR HYPERTROPHY
Introduction Left Ventricular Hypertrophy (LVH) is common in Type 2 Diabetes (T2DM) and contributes to their high cardiovascular (CV) event rate. LVH can be related to oxidative stress (OS) and allopurinol reduces OS. We therefore investigated whether allopurinol regresses LVH in patients with T2DM....
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Veröffentlicht in: | Heart (British Cardiac Society) 2013-05, Vol.99 (suppl 2), p.A93-A93 |
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description | Introduction Left Ventricular Hypertrophy (LVH) is common in Type 2 Diabetes (T2DM) and contributes to their high cardiovascular (CV) event rate. LVH can be related to oxidative stress (OS) and allopurinol reduces OS. We therefore investigated whether allopurinol regresses LVH in patients with T2DM. Methods We conducted a randomised, double blind, placebo controlled study in 66 T2DM patients with echocardiographic evidence of LVH. Allopurinol 600 mg/day or placebo was given for 9 months over the study period. The primary outcome was reduction in left ventricular mass (LVM) as calculated by cardiac MRI at baseline and at 9 months follow-up. The secondary end-points were change in flow mediated dilatation (FMD) and augmentation index (AIx). Results Allopurinol significantly reduced absolute LVM (−2.65±5.91 g and placebo group +1.21±5.10 g (p=0.012)) and LVM indexed to body surface area (−1.32±2.84 g/m2 and placebo group +0.65±3.07 g/m2 (p=0.017)). No significant change was seen in both FMD and AIx. Figure 1 Conclusions Allopurinol regresses LVM in patients with T2DM and LVH. Regressing LVH has been shown previously to improve CV mortality and morbidity. Therefore allopurinol may be a useful therapy to reduce CV events in T2DM patients with LVH. |
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LVH can be related to oxidative stress (OS) and allopurinol reduces OS. We therefore investigated whether allopurinol regresses LVH in patients with T2DM. Methods We conducted a randomised, double blind, placebo controlled study in 66 T2DM patients with echocardiographic evidence of LVH. Allopurinol 600 mg/day or placebo was given for 9 months over the study period. The primary outcome was reduction in left ventricular mass (LVM) as calculated by cardiac MRI at baseline and at 9 months follow-up. The secondary end-points were change in flow mediated dilatation (FMD) and augmentation index (AIx). Results Allopurinol significantly reduced absolute LVM (−2.65±5.91 g and placebo group +1.21±5.10 g (p=0.012)) and LVM indexed to body surface area (−1.32±2.84 g/m2 and placebo group +0.65±3.07 g/m2 (p=0.017)). No significant change was seen in both FMD and AIx. Figure 1 Conclusions Allopurinol regresses LVM in patients with T2DM and LVH. Regressing LVH has been shown previously to improve CV mortality and morbidity. Therefore allopurinol may be a useful therapy to reduce CV events in T2DM patients with LVH.</description><identifier>ISSN: 1355-6037</identifier><identifier>EISSN: 1468-201X</identifier><identifier>DOI: 10.1136/heartjnl-2013-304019.159</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and British Cardiovascular Society</publisher><ispartof>Heart (British Cardiac Society), 2013-05, Vol.99 (suppl 2), p.A93-A93</ispartof><rights>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: 2013 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><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://heart.bmj.com/content/99/suppl_2/A93.1.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://heart.bmj.com/content/99/suppl_2/A93.1.full$$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>Szwejkowski, B R S</creatorcontrib><creatorcontrib>Gandy, S G</creatorcontrib><creatorcontrib>Rekhraj, S R</creatorcontrib><creatorcontrib>Houston, G H</creatorcontrib><creatorcontrib>Lang, C C L</creatorcontrib><creatorcontrib>George, J G</creatorcontrib><creatorcontrib>Morris, A D M</creatorcontrib><creatorcontrib>Struthers, A D S</creatorcontrib><title>159 ALLOPURINOL REDUCES LEFT VENTRICULAR MASS IN PATIENTS WITH TYPE 2 DIABETES AND LEFT VENTRICULAR HYPERTROPHY</title><title>Heart (British Cardiac Society)</title><addtitle>Heart</addtitle><description>Introduction Left Ventricular Hypertrophy (LVH) is common in Type 2 Diabetes (T2DM) and contributes to their high cardiovascular (CV) event rate. LVH can be related to oxidative stress (OS) and allopurinol reduces OS. We therefore investigated whether allopurinol regresses LVH in patients with T2DM. Methods We conducted a randomised, double blind, placebo controlled study in 66 T2DM patients with echocardiographic evidence of LVH. Allopurinol 600 mg/day or placebo was given for 9 months over the study period. The primary outcome was reduction in left ventricular mass (LVM) as calculated by cardiac MRI at baseline and at 9 months follow-up. The secondary end-points were change in flow mediated dilatation (FMD) and augmentation index (AIx). Results Allopurinol significantly reduced absolute LVM (−2.65±5.91 g and placebo group +1.21±5.10 g (p=0.012)) and LVM indexed to body surface area (−1.32±2.84 g/m2 and placebo group +0.65±3.07 g/m2 (p=0.017)). No significant change was seen in both FMD and AIx. Figure 1 Conclusions Allopurinol regresses LVM in patients with T2DM and LVH. Regressing LVH has been shown previously to improve CV mortality and morbidity. Therefore allopurinol may be a useful therapy to reduce CV events in T2DM patients with LVH.</description><issn>1355-6037</issn><issn>1468-201X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</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>eNqNkF1PwjAUhhejiYj-hyZeD_uxdu3lHMMtzg3HAOGmKVuJIDDcINF_b8nUG2-8Os3J85y3eS0LINhDiLC7V63qw3q3sTFExCbQgUj0EBVnVgc5jJ_WL-fmTSi1GSTupXXVNGsIoSM461iVQYEXx-lwnEVJGoMs6I_9YATiYJCDSZDkWeSPYy8DT95oBKIEDL08MusRmEZ5CPLZMAAY9CPvPsiN5iX9v2pooCzP0mE4u7YulmrT6Jvv2bXGgyD3QztOHyLfi-0FhkLYrqakwEIopQlx1JLoJXSpLjVzBETcfBqiouRFqaiDuVOWWHFWMI0YLyjDmHSt2_buvq7ej7o5yHV1rHcmUiKXQ5dgRwhD8ZYq6qppar2U-3q1VfWnRFCe6pU_9cpTvbKtV5p4o9qtumoO-uPXU_WbZC5xqUwmvpzPn_tT-pjJzPCk5Rfb9f9TvgAjSYXw</recordid><startdate>201305</startdate><enddate>201305</enddate><creator>Szwejkowski, B R S</creator><creator>Gandy, S G</creator><creator>Rekhraj, S R</creator><creator>Houston, G H</creator><creator>Lang, C C L</creator><creator>George, J G</creator><creator>Morris, A D M</creator><creator>Struthers, A D S</creator><general>BMJ Publishing Group Ltd and British Cardiovascular Society</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><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>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</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>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope></search><sort><creationdate>201305</creationdate><title>159 ALLOPURINOL REDUCES LEFT VENTRICULAR MASS IN PATIENTS WITH TYPE 2 DIABETES AND LEFT VENTRICULAR HYPERTROPHY</title><author>Szwejkowski, B R S ; Gandy, S G ; Rekhraj, S R ; Houston, G H ; Lang, C C L ; George, J G ; Morris, A D M ; Struthers, A D S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b2099-7e53c299aae334af3ef075ede64901815901cd8cda54284dd2a86c6e168c56223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Szwejkowski, B R S</creatorcontrib><creatorcontrib>Gandy, S G</creatorcontrib><creatorcontrib>Rekhraj, S R</creatorcontrib><creatorcontrib>Houston, G H</creatorcontrib><creatorcontrib>Lang, C C L</creatorcontrib><creatorcontrib>George, J G</creatorcontrib><creatorcontrib>Morris, A D M</creatorcontrib><creatorcontrib>Struthers, A D S</creatorcontrib><collection>Istex</collection><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>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>ProQuest Central</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>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>Heart (British Cardiac Society)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Szwejkowski, B R S</au><au>Gandy, S G</au><au>Rekhraj, S R</au><au>Houston, G H</au><au>Lang, C C L</au><au>George, J G</au><au>Morris, A D M</au><au>Struthers, A D S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>159 ALLOPURINOL REDUCES LEFT VENTRICULAR MASS IN PATIENTS WITH TYPE 2 DIABETES AND LEFT VENTRICULAR HYPERTROPHY</atitle><jtitle>Heart (British Cardiac Society)</jtitle><addtitle>Heart</addtitle><date>2013-05</date><risdate>2013</risdate><volume>99</volume><issue>suppl 2</issue><spage>A93</spage><epage>A93</epage><pages>A93-A93</pages><issn>1355-6037</issn><eissn>1468-201X</eissn><abstract>Introduction Left Ventricular Hypertrophy (LVH) is common in Type 2 Diabetes (T2DM) and contributes to their high cardiovascular (CV) event rate. LVH can be related to oxidative stress (OS) and allopurinol reduces OS. We therefore investigated whether allopurinol regresses LVH in patients with T2DM. Methods We conducted a randomised, double blind, placebo controlled study in 66 T2DM patients with echocardiographic evidence of LVH. Allopurinol 600 mg/day or placebo was given for 9 months over the study period. The primary outcome was reduction in left ventricular mass (LVM) as calculated by cardiac MRI at baseline and at 9 months follow-up. The secondary end-points were change in flow mediated dilatation (FMD) and augmentation index (AIx). Results Allopurinol significantly reduced absolute LVM (−2.65±5.91 g and placebo group +1.21±5.10 g (p=0.012)) and LVM indexed to body surface area (−1.32±2.84 g/m2 and placebo group +0.65±3.07 g/m2 (p=0.017)). No significant change was seen in both FMD and AIx. Figure 1 Conclusions Allopurinol regresses LVM in patients with T2DM and LVH. Regressing LVH has been shown previously to improve CV mortality and morbidity. Therefore allopurinol may be a useful therapy to reduce CV events in T2DM patients with LVH.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and British Cardiovascular Society</pub><doi>10.1136/heartjnl-2013-304019.159</doi><oa>free_for_read</oa></addata></record> |
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title | 159 ALLOPURINOL REDUCES LEFT VENTRICULAR MASS IN PATIENTS WITH TYPE 2 DIABETES AND LEFT VENTRICULAR HYPERTROPHY |
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