The Effect of Trandolapril and Its Fixed-Dose Combination with Verapamil on Circulating Adhesion Molecules Levels in Hypertensive Patients with Type 2 Diabetes

Background and Aim. Endothelial dysfunction in hypertensive type-2 diabetic patients is associated with increased levels of circulating soluble adhesion molecules (SAM). SAM participate in the development of diabetic macroangiopathy and microangiopathy. The aim of this study was to compare the effec...

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Veröffentlicht in:Clinical and experimental hypertension (1993) 2008-01, Vol.30 (7), p.682-688
Hauptverfasser: Rubio-Guerra, Alberto Francisco, Vargas-Robles, Hilda, Vargas-Ayala, German, Rodriguez-Lopez, Leticia, Escalante-Acosta, Bruno Alfonso
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container_end_page 688
container_issue 7
container_start_page 682
container_title Clinical and experimental hypertension (1993)
container_volume 30
creator Rubio-Guerra, Alberto Francisco
Vargas-Robles, Hilda
Vargas-Ayala, German
Rodriguez-Lopez, Leticia
Escalante-Acosta, Bruno Alfonso
description Background and Aim. Endothelial dysfunction in hypertensive type-2 diabetic patients is associated with increased levels of circulating soluble adhesion molecules (SAM). SAM participate in the development of diabetic macroangiopathy and microangiopathy. The aim of this study was to compare the effect of trandolapril (T) and its fixed-dose combination with verapamil (FDTV) on SAM levels in hypertensive type-2 diabetic patients. Methods. Forty type-2 diabetic patients with never-treated hypertension were randomly assigned to two groups. One group (FDTV) received 2 180 mg once a day; the other group received T 2 mg once a day. Study drugs were administered for three months in both groups. VCAM-1, ICAM, and E-selectin were measured by ELISA at the beginning and end of the study. Patients were evaluated monthly for blood pressure, fasting serum glucose, and adverse events. Statistical analysis was performed with ANOVA. Results. Both therapeutics regimens reduced significantly the levels of the SAM tested. When both groups were compared, we did not find a significant difference in ICAM and E-selectin reduction. However, VCAM-1 presented a significantly greater reduction (p = 0.022) in the trandolapril-verapamil group. No patient suffered adverse events. Conclusion. Our results show that FDTV produces a greater reduction of VCAM-1 circulating levels than trandolapril alone. This may explain some of the beneficial effects of this fixed dosed combination that are non-related to its antihypertensive effects.
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Endothelial dysfunction in hypertensive type-2 diabetic patients is associated with increased levels of circulating soluble adhesion molecules (SAM). SAM participate in the development of diabetic macroangiopathy and microangiopathy. The aim of this study was to compare the effect of trandolapril (T) and its fixed-dose combination with verapamil (FDTV) on SAM levels in hypertensive type-2 diabetic patients. Methods. Forty type-2 diabetic patients with never-treated hypertension were randomly assigned to two groups. One group (FDTV) received 2 180 mg once a day; the other group received T 2 mg once a day. Study drugs were administered for three months in both groups. VCAM-1, ICAM, and E-selectin were measured by ELISA at the beginning and end of the study. Patients were evaluated monthly for blood pressure, fasting serum glucose, and adverse events. Statistical analysis was performed with ANOVA. Results. Both therapeutics regimens reduced significantly the levels of the SAM tested. When both groups were compared, we did not find a significant difference in ICAM and E-selectin reduction. However, VCAM-1 presented a significantly greater reduction (p = 0.022) in the trandolapril-verapamil group. No patient suffered adverse events. Conclusion. Our results show that FDTV produces a greater reduction of VCAM-1 circulating levels than trandolapril alone. This may explain some of the beneficial effects of this fixed dosed combination that are non-related to its antihypertensive effects.</description><identifier>ISSN: 1064-1963</identifier><identifier>EISSN: 1525-6006</identifier><identifier>DOI: 10.1080/10641960802251941</identifier><identifier>PMID: 18855271</identifier><identifier>CODEN: CEHYER</identifier><language>eng</language><publisher>Colchester: Informa UK Ltd</publisher><subject>Aged ; Angiotensin-Converting Enzyme Inhibitors - administration &amp; dosage ; Antihypertensive agents ; Antihypertensive Agents - administration &amp; dosage ; Arterial hypertension. Arterial hypotension ; Biological and medical sciences ; Blood and lymphatic vessels ; Calcium Channel Blockers - administration &amp; dosage ; Cardiology. Vascular system ; Cardiovascular system ; Cell Adhesion Molecules - blood ; Diabetes Complications - blood ; Diabetes Complications - drug therapy ; Diabetes Mellitus, Type 2 - blood ; Diabetes Mellitus, Type 2 - complications ; Diabetes Mellitus, Type 2 - drug therapy ; Drug Combinations ; E-Selectin - blood ; Female ; fixed-dose combination ; Humans ; Hypertension - blood ; Hypertension - complications ; Hypertension - drug therapy ; Indoles - administration &amp; dosage ; Intercellular Adhesion Molecule-1 - blood ; Male ; Medical sciences ; Middle Aged ; Pharmacology. 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Endothelial dysfunction in hypertensive type-2 diabetic patients is associated with increased levels of circulating soluble adhesion molecules (SAM). SAM participate in the development of diabetic macroangiopathy and microangiopathy. The aim of this study was to compare the effect of trandolapril (T) and its fixed-dose combination with verapamil (FDTV) on SAM levels in hypertensive type-2 diabetic patients. Methods. Forty type-2 diabetic patients with never-treated hypertension were randomly assigned to two groups. One group (FDTV) received 2 180 mg once a day; the other group received T 2 mg once a day. Study drugs were administered for three months in both groups. VCAM-1, ICAM, and E-selectin were measured by ELISA at the beginning and end of the study. Patients were evaluated monthly for blood pressure, fasting serum glucose, and adverse events. Statistical analysis was performed with ANOVA. Results. Both therapeutics regimens reduced significantly the levels of the SAM tested. When both groups were compared, we did not find a significant difference in ICAM and E-selectin reduction. However, VCAM-1 presented a significantly greater reduction (p = 0.022) in the trandolapril-verapamil group. No patient suffered adverse events. Conclusion. Our results show that FDTV produces a greater reduction of VCAM-1 circulating levels than trandolapril alone. This may explain some of the beneficial effects of this fixed dosed combination that are non-related to its antihypertensive effects.</description><subject>Aged</subject><subject>Angiotensin-Converting Enzyme Inhibitors - administration &amp; dosage</subject><subject>Antihypertensive agents</subject><subject>Antihypertensive Agents - administration &amp; dosage</subject><subject>Arterial hypertension. Arterial hypotension</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Calcium Channel Blockers - administration &amp; dosage</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular system</subject><subject>Cell Adhesion Molecules - blood</subject><subject>Diabetes Complications - blood</subject><subject>Diabetes Complications - drug therapy</subject><subject>Diabetes Mellitus, Type 2 - blood</subject><subject>Diabetes Mellitus, Type 2 - complications</subject><subject>Diabetes Mellitus, Type 2 - drug therapy</subject><subject>Drug Combinations</subject><subject>E-Selectin - blood</subject><subject>Female</subject><subject>fixed-dose combination</subject><subject>Humans</subject><subject>Hypertension - blood</subject><subject>Hypertension - complications</subject><subject>Hypertension - drug therapy</subject><subject>Indoles - administration &amp; dosage</subject><subject>Intercellular Adhesion Molecule-1 - blood</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>soluble adhesion molecules</subject><subject>trandolapril</subject><subject>type-2 diabetes mellitus</subject><subject>Vascular Cell Adhesion Molecule-1 - blood</subject><subject>verapamil</subject><subject>Verapamil - administration &amp; dosage</subject><issn>1064-1963</issn><issn>1525-6006</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFu1DAQhiMEoqXwAFyQL3AL2F7bmwgu1ballRbBYeEaOc6YuHLsxXZa9ml4VabsAkJIPXk0__eP7fmr6jmjrxlt6BtGlWCtwpJzyVrBHlTHTHJZK0rVQ6xRrxFYHFVPcr6mlAklm8fVEWsaKfmSHVc_NiOQc2vBFBIt2SQdhuj1NjlPsCRXJZML9x2G-ixmIKs49S7o4mIgt66M5AskvdUT0thZuWRmj2r4Sk6HEfId9iF6wC5ksoYb8Jm4QC53W0gFQnY3QD6hAQLe82vgBiXCyZnTPRTIT6tHVvsMzw7nSfX54nyzuqzXH99frU7XtRELUWqlRSuH3i4tCKkUY3bguh1AWsqXduiNbhttoAEhmJRtz5serOG0WTKFul2cVK_2c7cpfpshl25y2YD3OkCcc6da3JxQLYJsD5oUc05gO9zVpNOuY7S7S6X7LxX0vDgMn_sJhr-OQwwIvDwAOhvtLaZgXP7DcdoyJBVy7_acCzamSd_G5Ieu6J2P6bdpcd873v5jH0H7MhqdoLuOcwq44Ht-8RPs9byT</recordid><startdate>20080101</startdate><enddate>20080101</enddate><creator>Rubio-Guerra, Alberto Francisco</creator><creator>Vargas-Robles, Hilda</creator><creator>Vargas-Ayala, German</creator><creator>Rodriguez-Lopez, Leticia</creator><creator>Escalante-Acosta, Bruno Alfonso</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</general><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>7X8</scope></search><sort><creationdate>20080101</creationdate><title>The Effect of Trandolapril and Its Fixed-Dose Combination with Verapamil on Circulating Adhesion Molecules Levels in Hypertensive Patients with Type 2 Diabetes</title><author>Rubio-Guerra, Alberto Francisco ; Vargas-Robles, Hilda ; Vargas-Ayala, German ; Rodriguez-Lopez, Leticia ; Escalante-Acosta, Bruno Alfonso</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-6a495dbf7fe456611fd2a9de5f027fdbca98ace8e441559b28befc2087167fdf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aged</topic><topic>Angiotensin-Converting Enzyme Inhibitors - administration &amp; dosage</topic><topic>Antihypertensive agents</topic><topic>Antihypertensive Agents - administration &amp; dosage</topic><topic>Arterial hypertension. Arterial hypotension</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Calcium Channel Blockers - administration &amp; dosage</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular system</topic><topic>Cell Adhesion Molecules - blood</topic><topic>Diabetes Complications - blood</topic><topic>Diabetes Complications - drug therapy</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - drug therapy</topic><topic>Drug Combinations</topic><topic>E-Selectin - blood</topic><topic>Female</topic><topic>fixed-dose combination</topic><topic>Humans</topic><topic>Hypertension - blood</topic><topic>Hypertension - complications</topic><topic>Hypertension - drug therapy</topic><topic>Indoles - administration &amp; dosage</topic><topic>Intercellular Adhesion Molecule-1 - blood</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>soluble adhesion molecules</topic><topic>trandolapril</topic><topic>type-2 diabetes mellitus</topic><topic>Vascular Cell Adhesion Molecule-1 - blood</topic><topic>verapamil</topic><topic>Verapamil - administration &amp; dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rubio-Guerra, Alberto Francisco</creatorcontrib><creatorcontrib>Vargas-Robles, Hilda</creatorcontrib><creatorcontrib>Vargas-Ayala, German</creatorcontrib><creatorcontrib>Rodriguez-Lopez, Leticia</creatorcontrib><creatorcontrib>Escalante-Acosta, Bruno Alfonso</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Clinical and experimental hypertension (1993)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rubio-Guerra, Alberto Francisco</au><au>Vargas-Robles, Hilda</au><au>Vargas-Ayala, German</au><au>Rodriguez-Lopez, Leticia</au><au>Escalante-Acosta, Bruno Alfonso</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Effect of Trandolapril and Its Fixed-Dose Combination with Verapamil on Circulating Adhesion Molecules Levels in Hypertensive Patients with Type 2 Diabetes</atitle><jtitle>Clinical and experimental hypertension (1993)</jtitle><addtitle>Clin Exp Hypertens</addtitle><date>2008-01-01</date><risdate>2008</risdate><volume>30</volume><issue>7</issue><spage>682</spage><epage>688</epage><pages>682-688</pages><issn>1064-1963</issn><eissn>1525-6006</eissn><coden>CEHYER</coden><abstract>Background and Aim. Endothelial dysfunction in hypertensive type-2 diabetic patients is associated with increased levels of circulating soluble adhesion molecules (SAM). SAM participate in the development of diabetic macroangiopathy and microangiopathy. The aim of this study was to compare the effect of trandolapril (T) and its fixed-dose combination with verapamil (FDTV) on SAM levels in hypertensive type-2 diabetic patients. Methods. Forty type-2 diabetic patients with never-treated hypertension were randomly assigned to two groups. One group (FDTV) received 2 180 mg once a day; the other group received T 2 mg once a day. Study drugs were administered for three months in both groups. VCAM-1, ICAM, and E-selectin were measured by ELISA at the beginning and end of the study. Patients were evaluated monthly for blood pressure, fasting serum glucose, and adverse events. Statistical analysis was performed with ANOVA. Results. Both therapeutics regimens reduced significantly the levels of the SAM tested. When both groups were compared, we did not find a significant difference in ICAM and E-selectin reduction. However, VCAM-1 presented a significantly greater reduction (p = 0.022) in the trandolapril-verapamil group. No patient suffered adverse events. Conclusion. Our results show that FDTV produces a greater reduction of VCAM-1 circulating levels than trandolapril alone. This may explain some of the beneficial effects of this fixed dosed combination that are non-related to its antihypertensive effects.</abstract><cop>Colchester</cop><pub>Informa UK Ltd</pub><pmid>18855271</pmid><doi>10.1080/10641960802251941</doi><tpages>7</tpages></addata></record>
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source MEDLINE; Taylor & Francis Journals Complete
subjects Aged
Angiotensin-Converting Enzyme Inhibitors - administration & dosage
Antihypertensive agents
Antihypertensive Agents - administration & dosage
Arterial hypertension. Arterial hypotension
Biological and medical sciences
Blood and lymphatic vessels
Calcium Channel Blockers - administration & dosage
Cardiology. Vascular system
Cardiovascular system
Cell Adhesion Molecules - blood
Diabetes Complications - blood
Diabetes Complications - drug therapy
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - complications
Diabetes Mellitus, Type 2 - drug therapy
Drug Combinations
E-Selectin - blood
Female
fixed-dose combination
Humans
Hypertension - blood
Hypertension - complications
Hypertension - drug therapy
Indoles - administration & dosage
Intercellular Adhesion Molecule-1 - blood
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
soluble adhesion molecules
trandolapril
type-2 diabetes mellitus
Vascular Cell Adhesion Molecule-1 - blood
verapamil
Verapamil - administration & dosage
title The Effect of Trandolapril and Its Fixed-Dose Combination with Verapamil on Circulating Adhesion Molecules Levels in Hypertensive Patients with Type 2 Diabetes
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