Blood Pressure Control Determines Improvement in Diastolic Dysfunction in Early Hypertension
Background Diastolic dysfunction is common in early hypertension. We hypothesized that improvement in diastolic dysfunction is blood pressure (BP) dependent and may occur early with treatment in newly diagnosed untreated hypertensive patients. Methods Forty untreated hypertensive subjects (age 52 ±...
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description | Background Diastolic dysfunction is common in early hypertension. We hypothesized that improvement in diastolic dysfunction is blood pressure (BP) dependent and may occur early with treatment in newly diagnosed untreated hypertensive patients. Methods Forty untreated hypertensive subjects (age 52 ± 1.4 years, mean ± s.e.m.) with diastolic dysfunction based on Canadian Consensus Guidelines, received either bendroflumethiazide 2.5 mg (1.25 mg for the first month), or candesartan 16 mg (8 mg for the first month). Left ventricular (LV) structure and function, early diastolic velocity (E′) and systolic velocity, and systolic myocardial velocity (Sm) were assessed echocardiographically using M-mode, 2-dimensional, and tissue Doppler imaging (TDI) before and at 1 and 3 months following treatment. Results Antihypertensive treatment reduced BP significantly at 3 months (168 ± 2/97 ± 1–143 ± 2/86 ± 1 mm Hg, P < 0.0001). Both drugs had similar and significant effects on TDI E′ which increased from 7.8 ± 0.2 to 10 ± 0.3 cm/s (P < 0.001). The improvement in TDI E′ was independent of LV mass index (LVMI) regression but was significantly related to the improvement in Sm (r = 0.73, P < 0.0001) and the fall in systolic BP (R = 0.51, P < 0.001). Normalization of diastolic function was associated with better control of BP (130 ± 4/81 ± 2 mm Hg vs. 149 ± 2/88 ± 1 mm Hg, P < 0.05). In a stepwise regression model, reduction in systolic BP (P < 0.001) and TDI Sm (P < 0.0001) emerged as independent determinants of improvement in TDI E′ with no contribution from age, gender or change in relative wall thickness (RWT) (R2 = 0.68, P < 0.0001). Conclusions Achieving good BP control and enhancement in systolic function determines the improvement in diastolic function in early hypertension. American Journal of Hypertension 2009; 22:1227–1231 © 2009 American Journal of Hypertension, Ltd. |
doi_str_mv | 10.1038/ajh.2009.173 |
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We hypothesized that improvement in diastolic dysfunction is blood pressure (BP) dependent and may occur early with treatment in newly diagnosed untreated hypertensive patients. Methods Forty untreated hypertensive subjects (age 52 ± 1.4 years, mean ± s.e.m.) with diastolic dysfunction based on Canadian Consensus Guidelines, received either bendroflumethiazide 2.5 mg (1.25 mg for the first month), or candesartan 16 mg (8 mg for the first month). Left ventricular (LV) structure and function, early diastolic velocity (E′) and systolic velocity, and systolic myocardial velocity (Sm) were assessed echocardiographically using M-mode, 2-dimensional, and tissue Doppler imaging (TDI) before and at 1 and 3 months following treatment. Results Antihypertensive treatment reduced BP significantly at 3 months (168 ± 2/97 ± 1–143 ± 2/86 ± 1 mm Hg, P < 0.0001). Both drugs had similar and significant effects on TDI E′ which increased from 7.8 ± 0.2 to 10 ± 0.3 cm/s (P < 0.001). The improvement in TDI E′ was independent of LV mass index (LVMI) regression but was significantly related to the improvement in Sm (r = 0.73, P < 0.0001) and the fall in systolic BP (R = 0.51, P < 0.001). Normalization of diastolic function was associated with better control of BP (130 ± 4/81 ± 2 mm Hg vs. 149 ± 2/88 ± 1 mm Hg, P < 0.05). In a stepwise regression model, reduction in systolic BP (P < 0.001) and TDI Sm (P < 0.0001) emerged as independent determinants of improvement in TDI E′ with no contribution from age, gender or change in relative wall thickness (RWT) (R2 = 0.68, P < 0.0001). Conclusions Achieving good BP control and enhancement in systolic function determines the improvement in diastolic function in early hypertension. American Journal of Hypertension 2009; 22:1227–1231 © 2009 American Journal of Hypertension, Ltd.]]></description><identifier>ISSN: 0895-7061</identifier><identifier>EISSN: 1941-7225</identifier><identifier>EISSN: 1879-1905</identifier><identifier>DOI: 10.1038/ajh.2009.173</identifier><identifier>PMID: 19763121</identifier><identifier>CODEN: AJHYE6</identifier><language>eng</language><publisher>Basingstoke: Oxford University Press</publisher><subject>Antihypertensive Agents - therapeutic use ; Arterial hypertension. Arterial hypotension ; Bendroflumethiazide - therapeutic use ; Benzimidazoles - therapeutic use ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood Pressure - drug effects ; Cardiology. Vascular system ; Clinical manifestations. Epidemiology. Investigative techniques. Etiology ; Female ; Heart Ventricles - diagnostic imaging ; Heart Ventricles - physiopathology ; Hemodynamics - drug effects ; Humans ; Hypertension - complications ; Hypertension - drug therapy ; Hypertension - physiopathology ; Male ; Medical sciences ; Middle Aged ; Regression Analysis ; Tetrazoles - therapeutic use ; Ultrasonography ; Ventricular Dysfunction, Left - drug therapy ; Ventricular Dysfunction, Left - etiology ; Ventricular Dysfunction, Left - physiopathology</subject><ispartof>American journal of hypertension, 2009-11, Vol.22 (11), p.1227-1231</ispartof><rights>American Journal of Hypertension, Ltd. © 2009 by the American Journal of Hypertension, Ltd. 2009</rights><rights>2015 INIST-CNRS</rights><rights>Copyright Nature Publishing Group Nov 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-620626b5e0a8a73fe707a56d19e6574626a5410d7f621bff37784513ddf1a87f3</citedby><cites>FETCH-LOGICAL-c455t-620626b5e0a8a73fe707a56d19e6574626a5410d7f621bff37784513ddf1a87f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22184036$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19763121$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Almuntaser, Ibrahim</creatorcontrib><creatorcontrib>Mahmud, Azra</creatorcontrib><creatorcontrib>Brown, Angie</creatorcontrib><creatorcontrib>Murphy, Ross</creatorcontrib><creatorcontrib>King, Gerard</creatorcontrib><creatorcontrib>Crean, Peter</creatorcontrib><creatorcontrib>Feely, John</creatorcontrib><title>Blood Pressure Control Determines Improvement in Diastolic Dysfunction in Early Hypertension</title><title>American journal of hypertension</title><addtitle>AJH</addtitle><description><![CDATA[Background Diastolic dysfunction is common in early hypertension. We hypothesized that improvement in diastolic dysfunction is blood pressure (BP) dependent and may occur early with treatment in newly diagnosed untreated hypertensive patients. Methods Forty untreated hypertensive subjects (age 52 ± 1.4 years, mean ± s.e.m.) with diastolic dysfunction based on Canadian Consensus Guidelines, received either bendroflumethiazide 2.5 mg (1.25 mg for the first month), or candesartan 16 mg (8 mg for the first month). Left ventricular (LV) structure and function, early diastolic velocity (E′) and systolic velocity, and systolic myocardial velocity (Sm) were assessed echocardiographically using M-mode, 2-dimensional, and tissue Doppler imaging (TDI) before and at 1 and 3 months following treatment. Results Antihypertensive treatment reduced BP significantly at 3 months (168 ± 2/97 ± 1–143 ± 2/86 ± 1 mm Hg, P < 0.0001). Both drugs had similar and significant effects on TDI E′ which increased from 7.8 ± 0.2 to 10 ± 0.3 cm/s (P < 0.001). The improvement in TDI E′ was independent of LV mass index (LVMI) regression but was significantly related to the improvement in Sm (r = 0.73, P < 0.0001) and the fall in systolic BP (R = 0.51, P < 0.001). Normalization of diastolic function was associated with better control of BP (130 ± 4/81 ± 2 mm Hg vs. 149 ± 2/88 ± 1 mm Hg, P < 0.05). In a stepwise regression model, reduction in systolic BP (P < 0.001) and TDI Sm (P < 0.0001) emerged as independent determinants of improvement in TDI E′ with no contribution from age, gender or change in relative wall thickness (RWT) (R2 = 0.68, P < 0.0001). Conclusions Achieving good BP control and enhancement in systolic function determines the improvement in diastolic function in early hypertension. American Journal of Hypertension 2009; 22:1227–1231 © 2009 American Journal of Hypertension, Ltd.]]></description><subject>Antihypertensive Agents - therapeutic use</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Bendroflumethiazide - therapeutic use</subject><subject>Benzimidazoles - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Pressure - drug effects</subject><subject>Cardiology. Vascular system</subject><subject>Clinical manifestations. Epidemiology. Investigative techniques. Etiology</subject><subject>Female</subject><subject>Heart Ventricles - diagnostic imaging</subject><subject>Heart Ventricles - physiopathology</subject><subject>Hemodynamics - drug effects</subject><subject>Humans</subject><subject>Hypertension - complications</subject><subject>Hypertension - drug therapy</subject><subject>Hypertension - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Regression Analysis</subject><subject>Tetrazoles - therapeutic use</subject><subject>Ultrasonography</subject><subject>Ventricular Dysfunction, Left - drug therapy</subject><subject>Ventricular Dysfunction, Left - etiology</subject><subject>Ventricular Dysfunction, Left - physiopathology</subject><issn>0895-7061</issn><issn>1941-7225</issn><issn>1879-1905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqF0N9rFDEQB_BQlPasffNZFqT60j3zY5PsPta72itUVNqCiBByuxPMuZtck2zx_ntz3lGhLz4FZj5MZr4IvSJ4SjCr3-vVzynFuJkSyQ7QhDQVKSWl_Bma4LrhpcSCHKEXMa4wxpUQ5BAdkUYKRiiZoB8feu-74kuAGMcAxcy7FHxfzCFBGKyDWFwN6-AfYACXCuuKudUx-d62xXwTzejaZL3bNi506DfFYrOGkMDFXH2JnhvdRzjZv8fo7uPF7WxRXn--vJqdX5dtxXkqBcWCiiUHrGstmQGJpeaiIw0ILqvc07wiuJNGULI0hklZV5ywrjNE19KwY_R2Nzcvej9CTGqwsYW-1w78GJWQouG8phm-eQJXfgwu76a2WZJK4JpldbZTbfAxBjBqHeygwyajv07lzNU2c5Uzz_z1fui4HKD7h_chZ3C6Bzq2ujdBu9bGR0cpqSvMRHbvds6P6_99We6kjQl-P1odfuVbmeRq8e27oot8DP90o76yP6VFpEU</recordid><startdate>20091101</startdate><enddate>20091101</enddate><creator>Almuntaser, Ibrahim</creator><creator>Mahmud, Azra</creator><creator>Brown, Angie</creator><creator>Murphy, Ross</creator><creator>King, Gerard</creator><creator>Crean, Peter</creator><creator>Feely, John</creator><general>Oxford University Press</general><general>Nature Publishing Group</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20091101</creationdate><title>Blood Pressure Control Determines Improvement in Diastolic Dysfunction in Early Hypertension</title><author>Almuntaser, Ibrahim ; Mahmud, Azra ; Brown, Angie ; Murphy, Ross ; King, Gerard ; Crean, Peter ; Feely, John</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-620626b5e0a8a73fe707a56d19e6574626a5410d7f621bff37784513ddf1a87f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Antihypertensive Agents - therapeutic use</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Bendroflumethiazide - therapeutic use</topic><topic>Benzimidazoles - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood Pressure - drug effects</topic><topic>Cardiology. Vascular system</topic><topic>Clinical manifestations. Epidemiology. Investigative techniques. Etiology</topic><topic>Female</topic><topic>Heart Ventricles - diagnostic imaging</topic><topic>Heart Ventricles - physiopathology</topic><topic>Hemodynamics - drug effects</topic><topic>Humans</topic><topic>Hypertension - complications</topic><topic>Hypertension - drug therapy</topic><topic>Hypertension - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Regression Analysis</topic><topic>Tetrazoles - therapeutic use</topic><topic>Ultrasonography</topic><topic>Ventricular Dysfunction, Left - drug therapy</topic><topic>Ventricular Dysfunction, Left - etiology</topic><topic>Ventricular Dysfunction, Left - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Almuntaser, Ibrahim</creatorcontrib><creatorcontrib>Mahmud, Azra</creatorcontrib><creatorcontrib>Brown, Angie</creatorcontrib><creatorcontrib>Murphy, Ross</creatorcontrib><creatorcontrib>King, Gerard</creatorcontrib><creatorcontrib>Crean, Peter</creatorcontrib><creatorcontrib>Feely, John</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</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>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</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical 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>MEDLINE - Academic</collection><jtitle>American journal of hypertension</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Almuntaser, Ibrahim</au><au>Mahmud, Azra</au><au>Brown, Angie</au><au>Murphy, Ross</au><au>King, Gerard</au><au>Crean, Peter</au><au>Feely, John</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blood Pressure Control Determines Improvement in Diastolic Dysfunction in Early Hypertension</atitle><jtitle>American journal of hypertension</jtitle><addtitle>AJH</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>22</volume><issue>11</issue><spage>1227</spage><epage>1231</epage><pages>1227-1231</pages><issn>0895-7061</issn><eissn>1941-7225</eissn><eissn>1879-1905</eissn><coden>AJHYE6</coden><abstract><![CDATA[Background Diastolic dysfunction is common in early hypertension. We hypothesized that improvement in diastolic dysfunction is blood pressure (BP) dependent and may occur early with treatment in newly diagnosed untreated hypertensive patients. Methods Forty untreated hypertensive subjects (age 52 ± 1.4 years, mean ± s.e.m.) with diastolic dysfunction based on Canadian Consensus Guidelines, received either bendroflumethiazide 2.5 mg (1.25 mg for the first month), or candesartan 16 mg (8 mg for the first month). Left ventricular (LV) structure and function, early diastolic velocity (E′) and systolic velocity, and systolic myocardial velocity (Sm) were assessed echocardiographically using M-mode, 2-dimensional, and tissue Doppler imaging (TDI) before and at 1 and 3 months following treatment. Results Antihypertensive treatment reduced BP significantly at 3 months (168 ± 2/97 ± 1–143 ± 2/86 ± 1 mm Hg, P < 0.0001). Both drugs had similar and significant effects on TDI E′ which increased from 7.8 ± 0.2 to 10 ± 0.3 cm/s (P < 0.001). The improvement in TDI E′ was independent of LV mass index (LVMI) regression but was significantly related to the improvement in Sm (r = 0.73, P < 0.0001) and the fall in systolic BP (R = 0.51, P < 0.001). Normalization of diastolic function was associated with better control of BP (130 ± 4/81 ± 2 mm Hg vs. 149 ± 2/88 ± 1 mm Hg, P < 0.05). In a stepwise regression model, reduction in systolic BP (P < 0.001) and TDI Sm (P < 0.0001) emerged as independent determinants of improvement in TDI E′ with no contribution from age, gender or change in relative wall thickness (RWT) (R2 = 0.68, P < 0.0001). Conclusions Achieving good BP control and enhancement in systolic function determines the improvement in diastolic function in early hypertension. American Journal of Hypertension 2009; 22:1227–1231 © 2009 American Journal of Hypertension, Ltd.]]></abstract><cop>Basingstoke</cop><pub>Oxford University Press</pub><pmid>19763121</pmid><doi>10.1038/ajh.2009.173</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antihypertensive Agents - therapeutic use Arterial hypertension. Arterial hypotension Bendroflumethiazide - therapeutic use Benzimidazoles - therapeutic use Biological and medical sciences Blood and lymphatic vessels Blood Pressure - drug effects Cardiology. Vascular system Clinical manifestations. Epidemiology. Investigative techniques. Etiology Female Heart Ventricles - diagnostic imaging Heart Ventricles - physiopathology Hemodynamics - drug effects Humans Hypertension - complications Hypertension - drug therapy Hypertension - physiopathology Male Medical sciences Middle Aged Regression Analysis Tetrazoles - therapeutic use Ultrasonography Ventricular Dysfunction, Left - drug therapy Ventricular Dysfunction, Left - etiology Ventricular Dysfunction, Left - physiopathology |
title | Blood Pressure Control Determines Improvement in Diastolic Dysfunction in Early Hypertension |
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