Effects of Losartan and Simvastatin on Monocyte-Derived Microparticles in Hypertensive Patients With and Without Type 2 Diabetes Mellitus
Monocyte-derived microparticles play an important role in the pathogenesis of diabetic vasculopathy, and angiotensin II receptor blocker and statin have been shown to have a beneficial effect on the angiopathies of hypertension and hyperglycemia in patients with type 2 diabetes mellitus. However, th...
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Veröffentlicht in: | Clinical and applied thrombosis/hemostasis 2004-04, Vol.10 (2), p.133-141 |
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description | Monocyte-derived microparticles play an important role in the pathogenesis of diabetic vasculopathy, and angiotensin II receptor blocker and statin have been shown to have a beneficial effect on the angiopathies of hypertension and hyperglycemia in patients with type 2 diabetes mellitus. However, the interaction between angiotensin II receptor blocker and statin, and monocyte-derived microparticles in atherosclerosis is poorly understood. The effects of losartan and simvastatin on circulating concentrations of monocyte-derived microparticles, chemokines, and soluble adhesion markers were studied in hypertensive patients with or without type 2 diabetes mellitus. Monocyte-derived microparticles were measured by flow cytometry, and levels of serum chemokines (MCP-1 and RANTES) and soluble adhesion markers (sP-selectin and sVCAM-1) were measured by enzyme-linked immunosorbent assay. Losartan decreased both the systolic and diastolic blood pressure in hypertensive patients with and without type 2 diabetes mellitus. The concentrations of monocyte-derived microparticles, chemokines, and soluble adhesion molecules were higher in hypertensive patients who also had type 2 diabetes mellitus vs. those who did not. The administration of angiotensin II receptor blocker decreased the circulating concentration of all these markers. In addition, all markers were decreased by combination therapy, and monocyte-derived microparticles were decreased more with combination therapy with losartan and simvastatin than monotherapy with losartan. The administration of angiotensin II receptor blocker inhibited monocyte-derived microparticle generation and suggests that angiotensin II is intimately related to vascular changes that occur in type 2 diabetes mellitus. Combination therapy with a statin and angiotensin II receptor blocker might be valuable as anti-atherosclerotic therapy in patients with type 2 diabetes mellitus and nephropathy. |
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However, the interaction between angiotensin II receptor blocker and statin, and monocyte-derived microparticles in atherosclerosis is poorly understood. The effects of losartan and simvastatin on circulating concentrations of monocyte-derived microparticles, chemokines, and soluble adhesion markers were studied in hypertensive patients with or without type 2 diabetes mellitus. Monocyte-derived microparticles were measured by flow cytometry, and levels of serum chemokines (MCP-1 and RANTES) and soluble adhesion markers (sP-selectin and sVCAM-1) were measured by enzyme-linked immunosorbent assay. Losartan decreased both the systolic and diastolic blood pressure in hypertensive patients with and without type 2 diabetes mellitus. The concentrations of monocyte-derived microparticles, chemokines, and soluble adhesion molecules were higher in hypertensive patients who also had type 2 diabetes mellitus vs. those who did not. The administration of angiotensin II receptor blocker decreased the circulating concentration of all these markers. In addition, all markers were decreased by combination therapy, and monocyte-derived microparticles were decreased more with combination therapy with losartan and simvastatin than monotherapy with losartan. The administration of angiotensin II receptor blocker inhibited monocyte-derived microparticle generation and suggests that angiotensin II is intimately related to vascular changes that occur in type 2 diabetes mellitus. Combination therapy with a statin and angiotensin II receptor blocker might be valuable as anti-atherosclerotic therapy in patients with type 2 diabetes mellitus and nephropathy.</description><identifier>ISSN: 1076-0296</identifier><identifier>EISSN: 1938-2723</identifier><identifier>DOI: 10.1177/107602960401000203</identifier><identifier>PMID: 15094933</identifier><language>eng</language><publisher>Thousand Oaks, CA: SAGE Publications</publisher><subject>Aged ; Angiotensin Receptor Antagonists ; Biomarkers - analysis ; Biomarkers - blood ; Blood Pressure - drug effects ; Chemokines ; Chemokines - blood ; Diabetes ; Diabetes Complications ; Diabetes Mellitus - drug therapy ; Female ; Glucose ; Humans ; Hypertension ; Hypertension - complications ; Hypertension - drug therapy ; Losartan - administration & dosage ; Losartan - pharmacology ; Male ; Middle Aged ; Monocytes - drug effects ; Monocytes - metabolism ; Receptors, Angiotensin - metabolism ; Simvastatin - administration & dosage ; Simvastatin - pharmacology</subject><ispartof>Clinical and applied thrombosis/hemostasis, 2004-04, Vol.10 (2), p.133-141</ispartof><rights>Copyright SAGE PUBLICATIONS, INC. 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The administration of angiotensin II receptor blocker decreased the circulating concentration of all these markers. In addition, all markers were decreased by combination therapy, and monocyte-derived microparticles were decreased more with combination therapy with losartan and simvastatin than monotherapy with losartan. The administration of angiotensin II receptor blocker inhibited monocyte-derived microparticle generation and suggests that angiotensin II is intimately related to vascular changes that occur in type 2 diabetes mellitus. Combination therapy with a statin and angiotensin II receptor blocker might be valuable as anti-atherosclerotic therapy in patients with type 2 diabetes mellitus and nephropathy.</description><subject>Aged</subject><subject>Angiotensin Receptor Antagonists</subject><subject>Biomarkers - analysis</subject><subject>Biomarkers - blood</subject><subject>Blood Pressure - drug effects</subject><subject>Chemokines</subject><subject>Chemokines - blood</subject><subject>Diabetes</subject><subject>Diabetes Complications</subject><subject>Diabetes Mellitus - drug therapy</subject><subject>Female</subject><subject>Glucose</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Hypertension - complications</subject><subject>Hypertension - drug therapy</subject><subject>Losartan - administration & dosage</subject><subject>Losartan - pharmacology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Monocytes - drug effects</subject><subject>Monocytes - metabolism</subject><subject>Receptors, Angiotensin - metabolism</subject><subject>Simvastatin - administration & dosage</subject><subject>Simvastatin - pharmacology</subject><issn>1076-0296</issn><issn>1938-2723</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqFkd9qFDEUxoMotlZfwAsJCL0be_JnJpNLaasVdmnBipdDJpNoym6yJpnCPoJv7Vl3odCCXuWE_L7v5JyPkLcMPjCm1BkD1QHXHUhgAMBBPCPHTIu-4YqL51gj0OyII_KqlDsApjvdvSRHrAUttRDH5Pel987WQpOni1RMriZSEyf6NazvTammhkhTpMsUk91W11y4HO7dRJfB5rRBPtiVKxSpq-3G5epiwXd6g0IX0fd7qD__Gu6KNFd6ixjl9CKY0VVULt1qFepcXpMX3qyKe3M4T8i3T5e351fN4vrzl_OPi8YK3dfGaNvpcVS8lcq2eDF-EpPGqaXn3CqLKxk1F1q6Xvh-7GHq7CTYCEKAEl6ckNO97yanX7MrdViHYvETJro0l0GxXnLV6v-CHKCXTLUIvn8E3qU5Rxxi4EIiwiXrkOJ7CvdWSnZ-2OSwNnk7MBh2eQ5P80TRu4P1PK7d9CA5BIjA2R4o5od76PsPyz9fK6g-</recordid><startdate>200404</startdate><enddate>200404</enddate><creator>Nomura, Shosaku</creator><creator>Shouzu, Akira</creator><creator>Omoto, Seitaro</creator><creator>Nishikawa, Mitsushige</creator><creator>Iwasaka, Toshiji</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><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>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200404</creationdate><title>Effects of Losartan and Simvastatin on Monocyte-Derived Microparticles in Hypertensive Patients With and Without Type 2 Diabetes Mellitus</title><author>Nomura, Shosaku ; Shouzu, Akira ; Omoto, Seitaro ; Nishikawa, Mitsushige ; Iwasaka, Toshiji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-a9c69bb72547c59c6afd3d99384f22c7c602b92394e83f8b80d6cd31b033073f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Aged</topic><topic>Angiotensin Receptor Antagonists</topic><topic>Biomarkers - analysis</topic><topic>Biomarkers - blood</topic><topic>Blood Pressure - drug effects</topic><topic>Chemokines</topic><topic>Chemokines - blood</topic><topic>Diabetes</topic><topic>Diabetes Complications</topic><topic>Diabetes Mellitus - drug therapy</topic><topic>Female</topic><topic>Glucose</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Hypertension - complications</topic><topic>Hypertension - drug therapy</topic><topic>Losartan - administration & dosage</topic><topic>Losartan - pharmacology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Monocytes - drug effects</topic><topic>Monocytes - metabolism</topic><topic>Receptors, Angiotensin - metabolism</topic><topic>Simvastatin - administration & dosage</topic><topic>Simvastatin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nomura, Shosaku</creatorcontrib><creatorcontrib>Shouzu, Akira</creatorcontrib><creatorcontrib>Omoto, Seitaro</creatorcontrib><creatorcontrib>Nishikawa, Mitsushige</creatorcontrib><creatorcontrib>Iwasaka, Toshiji</creatorcontrib><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>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>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 Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content 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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and applied thrombosis/hemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Nomura, Shosaku</au><au>Shouzu, Akira</au><au>Omoto, Seitaro</au><au>Nishikawa, Mitsushige</au><au>Iwasaka, Toshiji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Losartan and Simvastatin on Monocyte-Derived Microparticles in Hypertensive Patients With and Without Type 2 Diabetes Mellitus</atitle><jtitle>Clinical and applied thrombosis/hemostasis</jtitle><addtitle>Clin Appl Thromb Hemost</addtitle><date>2004-04</date><risdate>2004</risdate><volume>10</volume><issue>2</issue><spage>133</spage><epage>141</epage><pages>133-141</pages><issn>1076-0296</issn><eissn>1938-2723</eissn><abstract>Monocyte-derived microparticles play an important role in the pathogenesis of diabetic vasculopathy, and angiotensin II receptor blocker and statin have been shown to have a beneficial effect on the angiopathies of hypertension and hyperglycemia in patients with type 2 diabetes mellitus. However, the interaction between angiotensin II receptor blocker and statin, and monocyte-derived microparticles in atherosclerosis is poorly understood. The effects of losartan and simvastatin on circulating concentrations of monocyte-derived microparticles, chemokines, and soluble adhesion markers were studied in hypertensive patients with or without type 2 diabetes mellitus. Monocyte-derived microparticles were measured by flow cytometry, and levels of serum chemokines (MCP-1 and RANTES) and soluble adhesion markers (sP-selectin and sVCAM-1) were measured by enzyme-linked immunosorbent assay. Losartan decreased both the systolic and diastolic blood pressure in hypertensive patients with and without type 2 diabetes mellitus. The concentrations of monocyte-derived microparticles, chemokines, and soluble adhesion molecules were higher in hypertensive patients who also had type 2 diabetes mellitus vs. those who did not. The administration of angiotensin II receptor blocker decreased the circulating concentration of all these markers. In addition, all markers were decreased by combination therapy, and monocyte-derived microparticles were decreased more with combination therapy with losartan and simvastatin than monotherapy with losartan. The administration of angiotensin II receptor blocker inhibited monocyte-derived microparticle generation and suggests that angiotensin II is intimately related to vascular changes that occur in type 2 diabetes mellitus. Combination therapy with a statin and angiotensin II receptor blocker might be valuable as anti-atherosclerotic therapy in patients with type 2 diabetes mellitus and nephropathy.</abstract><cop>Thousand Oaks, CA</cop><pub>SAGE Publications</pub><pmid>15094933</pmid><doi>10.1177/107602960401000203</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Angiotensin Receptor Antagonists Biomarkers - analysis Biomarkers - blood Blood Pressure - drug effects Chemokines Chemokines - blood Diabetes Diabetes Complications Diabetes Mellitus - drug therapy Female Glucose Humans Hypertension Hypertension - complications Hypertension - drug therapy Losartan - administration & dosage Losartan - pharmacology Male Middle Aged Monocytes - drug effects Monocytes - metabolism Receptors, Angiotensin - metabolism Simvastatin - administration & dosage Simvastatin - pharmacology |
title | Effects of Losartan and Simvastatin on Monocyte-Derived Microparticles in Hypertensive Patients With and Without Type 2 Diabetes Mellitus |
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