Testosterone and Coronary Artery Disease
The strongest independent risk factors for coronary artery disease (CAD) are increasing age and male gender. Whilst a wide variation in CAD mortality exists between countries, a male to female ratio of approximately 2:1 is consistently observed. These observations have led to the assumption that tes...
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Veröffentlicht in: | Advances in the Management of Testosterone Deficiency 2009-01, Vol.37, p.91-107 |
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description | The strongest independent risk factors for coronary artery disease (CAD) are increasing age and male gender. Whilst a wide variation in CAD mortality exists between countries, a male to female ratio of approximately 2:1 is consistently observed. These observations have led to the assumption that testosterone may exert a detrimental influence on the cardiovascular system. Despite this, coronary atherosclerosis increases with age, whilst a marked fall in serum bioavailable testosterone levels is observed. Similarly, low testosterone levels are also associated with other cardiovascular risk factors and increased expression of mediators of the atherosclerotic process. This in itself suggests that testosterone does not promote atheroma formation. Moreover, epidemiological studies show an inverse relationship between testosterone levels and surrogate markers of atherosclerosis, which suggests that it may be a testosterone deficient state, rather than male sex which is associated with CAD. In cholesterol-fed animal models, atherosclerosis is accelerated by castration and reduced after testosterone replacement therapy. Testosterone has also been shown to improve myocardial ischemia in men with angina pectoris. Consequently, increasing evidence suggests that the process of atherosclerosis is beneficially modulated by testosterone. These studies are the focus of this chapter. |
doi_str_mv | 10.1159/000176047 |
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(Barnsley/Sheffield) ; Jones, T. H</contributor><creatorcontrib>Nettleship, J. ; Jones, R. ; Channer, K. ; Jones, T. ; Jones ; T.H. (Barnsley/Sheffield) ; Jones, T. H</creatorcontrib><description>The strongest independent risk factors for coronary artery disease (CAD) are increasing age and male gender. Whilst a wide variation in CAD mortality exists between countries, a male to female ratio of approximately 2:1 is consistently observed. These observations have led to the assumption that testosterone may exert a detrimental influence on the cardiovascular system. Despite this, coronary atherosclerosis increases with age, whilst a marked fall in serum bioavailable testosterone levels is observed. Similarly, low testosterone levels are also associated with other cardiovascular risk factors and increased expression of mediators of the atherosclerotic process. This in itself suggests that testosterone does not promote atheroma formation. Moreover, epidemiological studies show an inverse relationship between testosterone levels and surrogate markers of atherosclerosis, which suggests that it may be a testosterone deficient state, rather than male sex which is associated with CAD. In cholesterol-fed animal models, atherosclerosis is accelerated by castration and reduced after testosterone replacement therapy. Testosterone has also been shown to improve myocardial ischemia in men with angina pectoris. Consequently, increasing evidence suggests that the process of atherosclerosis is beneficially modulated by testosterone. These studies are the focus of this chapter.</description><identifier>ISSN: 0301-3073</identifier><identifier>ISBN: 3805586221</identifier><identifier>ISBN: 9783805586221</identifier><identifier>EISSN: 1662-3762</identifier><identifier>EISBN: 9783805586238</identifier><identifier>EISBN: 380558623X</identifier><identifier>DOI: 10.1159/000176047</identifier><identifier>OCLC: 923648421</identifier><identifier>PMID: 19011291</identifier><identifier>LCCallNum: RC898 -- .A38 2009eb</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Angina Pectoris - drug therapy ; Animals ; Atherosclerosis - drug therapy ; Chapter ; Cholesterol, HDL - blood ; Coronary Artery Disease - blood ; Coronary Artery Disease - etiology ; Hormone Replacement Therapy ; Humans ; Hypogonadism - complications ; Hypogonadism - drug therapy ; Insulin Resistance ; Interleukin-1beta - blood ; Intra-Abdominal Fat - metabolism ; Male ; Risk Factors ; Testosterone - blood ; Testosterone - therapeutic use ; Vascular Cell Adhesion Molecule-1 - blood</subject><ispartof>Advances in the Management of Testosterone Deficiency, 2009-01, Vol.37, p.91-107</ispartof><rights>2009 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-fa56dd3edbeaf260189690ae8c3b2594712d3a5c403d2eed837b950a5ee14f853</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttps://ebookcentral.proquest.com/covers/3016446-l.jpg</thumbnail><link.rule.ids>779,780,784,793,26081,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19011291$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Jones</contributor><contributor>T.H. (Barnsley/Sheffield)</contributor><contributor>Jones, T. H</contributor><creatorcontrib>Nettleship, J.</creatorcontrib><creatorcontrib>Jones, R.</creatorcontrib><creatorcontrib>Channer, K.</creatorcontrib><creatorcontrib>Jones, T.</creatorcontrib><title>Testosterone and Coronary Artery Disease</title><title>Advances in the Management of Testosterone Deficiency</title><addtitle>Front Horm Res</addtitle><description>The strongest independent risk factors for coronary artery disease (CAD) are increasing age and male gender. Whilst a wide variation in CAD mortality exists between countries, a male to female ratio of approximately 2:1 is consistently observed. These observations have led to the assumption that testosterone may exert a detrimental influence on the cardiovascular system. Despite this, coronary atherosclerosis increases with age, whilst a marked fall in serum bioavailable testosterone levels is observed. Similarly, low testosterone levels are also associated with other cardiovascular risk factors and increased expression of mediators of the atherosclerotic process. This in itself suggests that testosterone does not promote atheroma formation. Moreover, epidemiological studies show an inverse relationship between testosterone levels and surrogate markers of atherosclerosis, which suggests that it may be a testosterone deficient state, rather than male sex which is associated with CAD. In cholesterol-fed animal models, atherosclerosis is accelerated by castration and reduced after testosterone replacement therapy. Testosterone has also been shown to improve myocardial ischemia in men with angina pectoris. Consequently, increasing evidence suggests that the process of atherosclerosis is beneficially modulated by testosterone. These studies are the focus of this chapter.</description><subject>Angina Pectoris - drug therapy</subject><subject>Animals</subject><subject>Atherosclerosis - drug therapy</subject><subject>Chapter</subject><subject>Cholesterol, HDL - blood</subject><subject>Coronary Artery Disease - blood</subject><subject>Coronary Artery Disease - etiology</subject><subject>Hormone Replacement Therapy</subject><subject>Humans</subject><subject>Hypogonadism - complications</subject><subject>Hypogonadism - drug therapy</subject><subject>Insulin Resistance</subject><subject>Interleukin-1beta - blood</subject><subject>Intra-Abdominal Fat - metabolism</subject><subject>Male</subject><subject>Risk Factors</subject><subject>Testosterone - blood</subject><subject>Testosterone - therapeutic use</subject><subject>Vascular Cell Adhesion Molecule-1 - blood</subject><issn>0301-3073</issn><issn>1662-3762</issn><isbn>3805586221</isbn><isbn>9783805586221</isbn><isbn>9783805586238</isbn><isbn>380558623X</isbn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdUbtOA0EMXN65hBT8AAoNojmw17evMgpPKRJNqE97dw6EPC7sJkX-npUSGipb9sxoxhbiCuEeUbkHAECjoTBHou-MJQtKWS3JHosMtZY5GS1PRPdvIfFUZECAOYGhc5E5SbqwhcSO6Mb4DaCcA30hOugAUTrMxN2E46aNGw7tigd-1QxGbWp92A2GIU13g8dZZB_5UpxN_SJy_1B74uP5aTJ6zcfvL2-j4TivCd0mn3qlm4a4qdhPpQa0TjvwbGuqpHKFQdmQV3UB1EjmxpKpnAKvmLGYWkU9cbvXXYf2Z5vMlctZrHmx8Ctut7HU2kiUkhLw-gDcVktuynWYLZPt8i9bAtA_Ja7adl7zahP8ov7y65Qvluleuih0qU2JIBPrZs-a-_DJYc-JkcOMY7l_B_0C9XFyGw</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Nettleship, J.</creator><creator>Jones, R.</creator><creator>Channer, K.</creator><creator>Jones, T.</creator><general>S. Karger AG</general><scope>FFUUA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20090101</creationdate><title>Testosterone and Coronary Artery Disease</title><author>Nettleship, J. ; Jones, R. ; Channer, K. ; Jones, T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-fa56dd3edbeaf260189690ae8c3b2594712d3a5c403d2eed837b950a5ee14f853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Angina Pectoris - drug therapy</topic><topic>Animals</topic><topic>Atherosclerosis - drug therapy</topic><topic>Chapter</topic><topic>Cholesterol, HDL - blood</topic><topic>Coronary Artery Disease - blood</topic><topic>Coronary Artery Disease - etiology</topic><topic>Hormone Replacement Therapy</topic><topic>Humans</topic><topic>Hypogonadism - complications</topic><topic>Hypogonadism - drug therapy</topic><topic>Insulin Resistance</topic><topic>Interleukin-1beta - blood</topic><topic>Intra-Abdominal Fat - metabolism</topic><topic>Male</topic><topic>Risk Factors</topic><topic>Testosterone - blood</topic><topic>Testosterone - therapeutic use</topic><topic>Vascular Cell Adhesion Molecule-1 - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nettleship, J.</creatorcontrib><creatorcontrib>Jones, R.</creatorcontrib><creatorcontrib>Channer, K.</creatorcontrib><creatorcontrib>Jones, T.</creatorcontrib><collection>ProQuest Ebook Central - Book Chapters - Demo use only</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Advances in the Management of Testosterone Deficiency</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nettleship, J.</au><au>Jones, R.</au><au>Channer, K.</au><au>Jones, T.</au><au>Jones</au><au>T.H. (Barnsley/Sheffield)</au><au>Jones, T. H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Testosterone and Coronary Artery Disease</atitle><jtitle>Advances in the Management of Testosterone Deficiency</jtitle><addtitle>Front Horm Res</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>37</volume><spage>91</spage><epage>107</epage><pages>91-107</pages><issn>0301-3073</issn><eissn>1662-3762</eissn><isbn>3805586221</isbn><isbn>9783805586221</isbn><eisbn>9783805586238</eisbn><eisbn>380558623X</eisbn><abstract>The strongest independent risk factors for coronary artery disease (CAD) are increasing age and male gender. Whilst a wide variation in CAD mortality exists between countries, a male to female ratio of approximately 2:1 is consistently observed. These observations have led to the assumption that testosterone may exert a detrimental influence on the cardiovascular system. Despite this, coronary atherosclerosis increases with age, whilst a marked fall in serum bioavailable testosterone levels is observed. Similarly, low testosterone levels are also associated with other cardiovascular risk factors and increased expression of mediators of the atherosclerotic process. This in itself suggests that testosterone does not promote atheroma formation. Moreover, epidemiological studies show an inverse relationship between testosterone levels and surrogate markers of atherosclerosis, which suggests that it may be a testosterone deficient state, rather than male sex which is associated with CAD. In cholesterol-fed animal models, atherosclerosis is accelerated by castration and reduced after testosterone replacement therapy. Testosterone has also been shown to improve myocardial ischemia in men with angina pectoris. Consequently, increasing evidence suggests that the process of atherosclerosis is beneficially modulated by testosterone. These studies are the focus of this chapter.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>19011291</pmid><doi>10.1159/000176047</doi><oclcid>923648421</oclcid><tpages>17</tpages></addata></record> |
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source | Karger eBooks Collection Archiv (DFG Nationallizenzen); MEDLINE; Karger Book Series |
subjects | Angina Pectoris - drug therapy Animals Atherosclerosis - drug therapy Chapter Cholesterol, HDL - blood Coronary Artery Disease - blood Coronary Artery Disease - etiology Hormone Replacement Therapy Humans Hypogonadism - complications Hypogonadism - drug therapy Insulin Resistance Interleukin-1beta - blood Intra-Abdominal Fat - metabolism Male Risk Factors Testosterone - blood Testosterone - therapeutic use Vascular Cell Adhesion Molecule-1 - blood |
title | Testosterone and Coronary Artery Disease |
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