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Effects of azelnidipine on the autonomic functions and its influence on arterial stiffness and endothelial functions

Summary Background The present study was conducted to clarify whether azelnidipine might have beneficial effects on autonomic functions, and whether such beneficial effects might affect the vascular functions (i.e., arterial stiffness and endothelial function). Methods and results This study with a...

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Published in:Journal of cardiology 2008-04, Vol.51 (2), p.114-120
Main Authors: Yamada, Jiko, Tomiyama, Hirofumi, Matsumoto, Chisa, Yoshida, Masanobu, Shiina, Kazuki, Yamashina, Akira
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container_title Journal of cardiology
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description Summary Background The present study was conducted to clarify whether azelnidipine might have beneficial effects on autonomic functions, and whether such beneficial effects might affect the vascular functions (i.e., arterial stiffness and endothelial function). Methods and results This study with a cross-over design was conducted in 21 hypertensive patients (65 ± 9 years old) being treated with calcium channel blockers (CCBs) other than azelnidipine or benidipine (i.e., during the study period, the CCB was switched to either azelnidipine 16 mg/day or benidipine 4 mg/day, administered alternately for 8 weeks each). Blood examinations were conducted and the heart rate variability, baro-receptor sensitivity (BRS), brachial-ankle pulse wave velocity (baPWV) and flow-mediated vasodilatation (FMD) in the brachial artery were measured after treatment with each of the two drugs. While the blood pressure levels decreased to a similar degree after both treatments, the BRS (8.8 ± 5.5 ms/mmHg vs. 6.4 ± 2.9 ms/mmHg, p < 0.01) and high-frequency power component (HF: 139 ±152 ms2 /Hz vs. 88 ± 97 ms2 /Hz) were higher after treatment with azelnidipine than after treatment with benidipine ( p < 0.05). However, the baPWV, FMD and plasma levels of malonyldialdehyde low-density lipoprotein cholesterol and nitric oxides were similar after treatment with both drugs. Conclusion Azelnidipine has greater beneficial effects on the autonomic functions than benidipine although the degree of reduction of blood pressure induced by the two drugs was similar. However, this greater beneficial effect of azelnidipine on the autonomic functions did not produce any distinguishable differences in effects of azelnidipine and benidipine on the arterial stiffness and endothelial functions.
doi_str_mv 10.1016/j.jjcc.2008.01.005
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Methods and results This study with a cross-over design was conducted in 21 hypertensive patients (65 ± 9 years old) being treated with calcium channel blockers (CCBs) other than azelnidipine or benidipine (i.e., during the study period, the CCB was switched to either azelnidipine 16 mg/day or benidipine 4 mg/day, administered alternately for 8 weeks each). Blood examinations were conducted and the heart rate variability, baro-receptor sensitivity (BRS), brachial-ankle pulse wave velocity (baPWV) and flow-mediated vasodilatation (FMD) in the brachial artery were measured after treatment with each of the two drugs. While the blood pressure levels decreased to a similar degree after both treatments, the BRS (8.8 ± 5.5 ms/mmHg vs. 6.4 ± 2.9 ms/mmHg, p &lt; 0.01) and high-frequency power component (HF: 139 ±152 ms2 /Hz vs. 88 ± 97 ms2 /Hz) were higher after treatment with azelnidipine than after treatment with benidipine ( p &lt; 0.05). However, the baPWV, FMD and plasma levels of malonyldialdehyde low-density lipoprotein cholesterol and nitric oxides were similar after treatment with both drugs. Conclusion Azelnidipine has greater beneficial effects on the autonomic functions than benidipine although the degree of reduction of blood pressure induced by the two drugs was similar. However, this greater beneficial effect of azelnidipine on the autonomic functions did not produce any distinguishable differences in effects of azelnidipine and benidipine on the arterial stiffness and endothelial functions.</description><identifier>ISSN: 0914-5087</identifier><identifier>EISSN: 1876-4738</identifier><identifier>DOI: 10.1016/j.jjcc.2008.01.005</identifier><identifier>PMID: 18522784</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Aged ; Arteries - physiopathology ; Autonomic function ; Autonomic Pathways - physiopathology ; Azetidinecarboxylic Acid - administration &amp; dosage ; Azetidinecarboxylic Acid - analogs &amp; derivatives ; Baro-receptor sensitivity ; Brachial Artery - physiopathology ; Calcium channel blocker ; Calcium Channel Blockers - administration &amp; dosage ; Cardiovascular ; Cross-Over Studies ; Dihydropyridines - administration &amp; dosage ; Double-Blind Method ; Endothelial function ; Endothelium, Vascular - physiopathology ; Female ; Heart Rate ; Humans ; Hypertension - drug therapy ; Hypertension - physiopathology ; Male ; Middle Aged ; Pulse ; Pulse wave velocity ; Vasodilation</subject><ispartof>Journal of cardiology, 2008-04, Vol.51 (2), p.114-120</ispartof><rights>Japanese College of Cardiology</rights><rights>2008 Japanese College of Cardiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c572t-262a3c49dafe2e616206a7346674721d93e4f8da7a422376279fc249009b0bbc3</citedby><cites>FETCH-LOGICAL-c572t-262a3c49dafe2e616206a7346674721d93e4f8da7a422376279fc249009b0bbc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18522784$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamada, Jiko</creatorcontrib><creatorcontrib>Tomiyama, Hirofumi</creatorcontrib><creatorcontrib>Matsumoto, Chisa</creatorcontrib><creatorcontrib>Yoshida, Masanobu</creatorcontrib><creatorcontrib>Shiina, Kazuki</creatorcontrib><creatorcontrib>Yamashina, Akira</creatorcontrib><title>Effects of azelnidipine on the autonomic functions and its influence on arterial stiffness and endothelial functions</title><title>Journal of cardiology</title><addtitle>J Cardiol</addtitle><description>Summary Background The present study was conducted to clarify whether azelnidipine might have beneficial effects on autonomic functions, and whether such beneficial effects might affect the vascular functions (i.e., arterial stiffness and endothelial function). Methods and results This study with a cross-over design was conducted in 21 hypertensive patients (65 ± 9 years old) being treated with calcium channel blockers (CCBs) other than azelnidipine or benidipine (i.e., during the study period, the CCB was switched to either azelnidipine 16 mg/day or benidipine 4 mg/day, administered alternately for 8 weeks each). Blood examinations were conducted and the heart rate variability, baro-receptor sensitivity (BRS), brachial-ankle pulse wave velocity (baPWV) and flow-mediated vasodilatation (FMD) in the brachial artery were measured after treatment with each of the two drugs. While the blood pressure levels decreased to a similar degree after both treatments, the BRS (8.8 ± 5.5 ms/mmHg vs. 6.4 ± 2.9 ms/mmHg, p &lt; 0.01) and high-frequency power component (HF: 139 ±152 ms2 /Hz vs. 88 ± 97 ms2 /Hz) were higher after treatment with azelnidipine than after treatment with benidipine ( p &lt; 0.05). However, the baPWV, FMD and plasma levels of malonyldialdehyde low-density lipoprotein cholesterol and nitric oxides were similar after treatment with both drugs. Conclusion Azelnidipine has greater beneficial effects on the autonomic functions than benidipine although the degree of reduction of blood pressure induced by the two drugs was similar. However, this greater beneficial effect of azelnidipine on the autonomic functions did not produce any distinguishable differences in effects of azelnidipine and benidipine on the arterial stiffness and endothelial functions.</description><subject>Aged</subject><subject>Arteries - physiopathology</subject><subject>Autonomic function</subject><subject>Autonomic Pathways - physiopathology</subject><subject>Azetidinecarboxylic Acid - administration &amp; dosage</subject><subject>Azetidinecarboxylic Acid - analogs &amp; derivatives</subject><subject>Baro-receptor sensitivity</subject><subject>Brachial Artery - physiopathology</subject><subject>Calcium channel blocker</subject><subject>Calcium Channel Blockers - administration &amp; dosage</subject><subject>Cardiovascular</subject><subject>Cross-Over Studies</subject><subject>Dihydropyridines - administration &amp; dosage</subject><subject>Double-Blind Method</subject><subject>Endothelial function</subject><subject>Endothelium, Vascular - physiopathology</subject><subject>Female</subject><subject>Heart Rate</subject><subject>Humans</subject><subject>Hypertension - drug therapy</subject><subject>Hypertension - physiopathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pulse</subject><subject>Pulse wave velocity</subject><subject>Vasodilation</subject><issn>0914-5087</issn><issn>1876-4738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp9kUFrFDEUx4NY7Lb6BTzInLzN-JLJJjMggpRahUIP6jlkkxfMOJusSabQfvpm3EXBg6d3eL__H97vEfKaQkeBindTN03GdAxg6IB2ANtnZEMHKVou--E52cBIebuFQZ6Ti5wnAAHjIF6QczpsGZMD35By7RyakpvoGv2Ic_DWH3zAJoam_MBGLyWGuPemcUswxceQGx1s42vEBzcvGMxvWKeCyeu5ycU7FzAfOQw21p553fxpeEnOnJ4zvjrNS_L90_W3q8_t7d3Nl6uPt63ZSlZaJpjuDR-tdshQUMFAaNlzISSXjNqxR-4Gq6XmjPVSMDk6w_gIMO5gtzP9JXl77D2k-GvBXNTeZ4PzrAPGJStJBed0ZBVkR9CkmHNCpw7J73V6UBTU6lpNanWtVtcKqKqua-jNqX3Z7dH-jZzkVuD9EcB6473HpLLxqy_rU3WubPT_7__wT9zMPnij55_4gHmKSwrVnqIqMwXq6_rt9dkwAEBPWf8Ed0SmQw</recordid><startdate>20080401</startdate><enddate>20080401</enddate><creator>Yamada, Jiko</creator><creator>Tomiyama, Hirofumi</creator><creator>Matsumoto, Chisa</creator><creator>Yoshida, Masanobu</creator><creator>Shiina, Kazuki</creator><creator>Yamashina, Akira</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</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>20080401</creationdate><title>Effects of azelnidipine on the autonomic functions and its influence on arterial stiffness and endothelial functions</title><author>Yamada, Jiko ; Tomiyama, Hirofumi ; Matsumoto, Chisa ; Yoshida, Masanobu ; Shiina, Kazuki ; Yamashina, Akira</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c572t-262a3c49dafe2e616206a7346674721d93e4f8da7a422376279fc249009b0bbc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Aged</topic><topic>Arteries - physiopathology</topic><topic>Autonomic function</topic><topic>Autonomic Pathways - physiopathology</topic><topic>Azetidinecarboxylic Acid - administration &amp; dosage</topic><topic>Azetidinecarboxylic Acid - analogs &amp; derivatives</topic><topic>Baro-receptor sensitivity</topic><topic>Brachial Artery - physiopathology</topic><topic>Calcium channel blocker</topic><topic>Calcium Channel Blockers - administration &amp; dosage</topic><topic>Cardiovascular</topic><topic>Cross-Over Studies</topic><topic>Dihydropyridines - administration &amp; dosage</topic><topic>Double-Blind Method</topic><topic>Endothelial function</topic><topic>Endothelium, Vascular - physiopathology</topic><topic>Female</topic><topic>Heart Rate</topic><topic>Humans</topic><topic>Hypertension - drug therapy</topic><topic>Hypertension - physiopathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pulse</topic><topic>Pulse wave velocity</topic><topic>Vasodilation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamada, Jiko</creatorcontrib><creatorcontrib>Tomiyama, Hirofumi</creatorcontrib><creatorcontrib>Matsumoto, Chisa</creatorcontrib><creatorcontrib>Yoshida, Masanobu</creatorcontrib><creatorcontrib>Shiina, Kazuki</creatorcontrib><creatorcontrib>Yamashina, Akira</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamada, Jiko</au><au>Tomiyama, Hirofumi</au><au>Matsumoto, Chisa</au><au>Yoshida, Masanobu</au><au>Shiina, Kazuki</au><au>Yamashina, Akira</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of azelnidipine on the autonomic functions and its influence on arterial stiffness and endothelial functions</atitle><jtitle>Journal of cardiology</jtitle><addtitle>J Cardiol</addtitle><date>2008-04-01</date><risdate>2008</risdate><volume>51</volume><issue>2</issue><spage>114</spage><epage>120</epage><pages>114-120</pages><issn>0914-5087</issn><eissn>1876-4738</eissn><abstract>Summary Background The present study was conducted to clarify whether azelnidipine might have beneficial effects on autonomic functions, and whether such beneficial effects might affect the vascular functions (i.e., arterial stiffness and endothelial function). Methods and results This study with a cross-over design was conducted in 21 hypertensive patients (65 ± 9 years old) being treated with calcium channel blockers (CCBs) other than azelnidipine or benidipine (i.e., during the study period, the CCB was switched to either azelnidipine 16 mg/day or benidipine 4 mg/day, administered alternately for 8 weeks each). Blood examinations were conducted and the heart rate variability, baro-receptor sensitivity (BRS), brachial-ankle pulse wave velocity (baPWV) and flow-mediated vasodilatation (FMD) in the brachial artery were measured after treatment with each of the two drugs. While the blood pressure levels decreased to a similar degree after both treatments, the BRS (8.8 ± 5.5 ms/mmHg vs. 6.4 ± 2.9 ms/mmHg, p &lt; 0.01) and high-frequency power component (HF: 139 ±152 ms2 /Hz vs. 88 ± 97 ms2 /Hz) were higher after treatment with azelnidipine than after treatment with benidipine ( p &lt; 0.05). However, the baPWV, FMD and plasma levels of malonyldialdehyde low-density lipoprotein cholesterol and nitric oxides were similar after treatment with both drugs. Conclusion Azelnidipine has greater beneficial effects on the autonomic functions than benidipine although the degree of reduction of blood pressure induced by the two drugs was similar. However, this greater beneficial effect of azelnidipine on the autonomic functions did not produce any distinguishable differences in effects of azelnidipine and benidipine on the arterial stiffness and endothelial functions.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>18522784</pmid><doi>10.1016/j.jjcc.2008.01.005</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0914-5087
ispartof Journal of cardiology, 2008-04, Vol.51 (2), p.114-120
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1876-4738
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subjects Aged
Arteries - physiopathology
Autonomic function
Autonomic Pathways - physiopathology
Azetidinecarboxylic Acid - administration & dosage
Azetidinecarboxylic Acid - analogs & derivatives
Baro-receptor sensitivity
Brachial Artery - physiopathology
Calcium channel blocker
Calcium Channel Blockers - administration & dosage
Cardiovascular
Cross-Over Studies
Dihydropyridines - administration & dosage
Double-Blind Method
Endothelial function
Endothelium, Vascular - physiopathology
Female
Heart Rate
Humans
Hypertension - drug therapy
Hypertension - physiopathology
Male
Middle Aged
Pulse
Pulse wave velocity
Vasodilation
title Effects of azelnidipine on the autonomic functions and its influence on arterial stiffness and endothelial functions
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