Low bone mineral density is not associated with angiographically determined coronary atherosclerosis in men
Summary This study for the first time investigates the association of bone mineral density (BMD) with angiographically determined coronary atherosclerosis in men. Our data show that the prevalence of low BMD is very high in men undergoing coronary angiography. However, neither osteopenia nor osteopo...
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| description | Summary This study for the first time investigates the association of bone mineral density (BMD) with angiographically determined coronary atherosclerosis in men. Our data show that the prevalence of low BMD is very high in men undergoing coronary angiography. However, neither osteopenia nor osteoporosis is associated with an increased prevalence of angiographically determined coronary atherosclerosis. Introduction The association of low BMD with angiographically determined coronary atherosclerosis in men is unknown. Methods We enrolled 623 consecutive men undergoing coronary angiography for the evaluation of established or suspected coronary artery disease (CAD). BMD was assessed by dual X-ray absorptiometry. CAD was diagnosed in the presence of any coronary artery lumen narrowing at angiography; coronary stenoses with lumen narrowing ≥50% were considered significant. Results From the total study cohort (mean age of 64 ± 11 years), 207 patients (33.2%) had osteopenia and 65 (10.4%) had osteoporosis; at angiography, CAD was diagnosed in 558 patients (89.6%) and 403 (64.7%) had significant coronary stenoses. In multivariate logistic regression analysis neither osteopenia nor osteoporosis was associated with an increased prevalence of CAD (adjusted odds ratios (ORs) = 0.71 [95% confidence interval 0.40-1.23]; p = 0.222 and 1.03 [0.38-2.80]; p = 0.955, respectively) or with significant coronary stenoses (OR 0.74 [0.52-1.07], p = 0.112 and 0.72 [0.41-1.26]; p = 0.251, respectively). Also, as a continuous variable, BMD was not associated with angiographically diagnosed CAD. Conclusions The prevalence of low BMD is very high in men undergoing coronary angiography. However, low BMD is not associated with angiographically determined coronary atherosclerosis in men. |
| doi_str_mv | 10.1007/s00198-009-1103-y |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_860388937</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>860388937</sourcerecordid><originalsourceid>FETCH-LOGICAL-c456t-dc00ad8b4782655924b91a34ca2ca7267a2b4736ba35ba6e39093a6b02f7223c3</originalsourceid><addsrcrecordid>eNqFkUuLFDEUhYMoTs_oD3CjQRhcleZVeSxl8AUNLnTAXbiVSnVnrE7apJqh_r0pqnHAhW6Sxf3OSe45CL2g5C0lRL0rhFCjG0JMQynhzfwIbajgvGFGto_RhhiuGiPojwt0WcodqRpj1FN0QY3hUiuyQT-36R53KXp8CNFnGHHvYwnTjEPBMU0YSkkuwOR7fB-mPYa4C2mX4bgPDsZxrvzk8yLusUs5RcgzhmnvcypuXM5qFCI--PgMPRlgLP75-b5Ctx8_fL_53Gy_fvpy837bONHKqekdIdDrTijNZNsaJjpDgQsHzIFiUgGrMy474G0H0nNT9wTZETYoxrjjV-jN6nvM6dfJl8keQnF-HCH6dCpWS8K1rtn8l1StqBFLJSr5-i_yLp1yrGtUiDCqWLtAdIVcXbtkP9hjDocaiKXELo3ZtTFbG7NLY3aumpdn41N38P2D4lxRBa7PAJSa-JAhulD-cIwzoVq9cGzlSh3Fnc8PP_zX669W0QDJwi5X49tvjFBOqNatYIL_Bgv7uCQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>750217254</pqid></control><display><type>article</type><title>Low bone mineral density is not associated with angiographically determined coronary atherosclerosis in men</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Beer, S ; Saely, C. H ; Hoefle, G ; Rein, P ; Vonbank, A ; Breuss, J ; Gaensbacher, B ; Muendlein, A ; Drexel, H</creator><creatorcontrib>Beer, S ; Saely, C. H ; Hoefle, G ; Rein, P ; Vonbank, A ; Breuss, J ; Gaensbacher, B ; Muendlein, A ; Drexel, H</creatorcontrib><description>Summary This study for the first time investigates the association of bone mineral density (BMD) with angiographically determined coronary atherosclerosis in men. Our data show that the prevalence of low BMD is very high in men undergoing coronary angiography. However, neither osteopenia nor osteoporosis is associated with an increased prevalence of angiographically determined coronary atherosclerosis. Introduction The association of low BMD with angiographically determined coronary atherosclerosis in men is unknown. Methods We enrolled 623 consecutive men undergoing coronary angiography for the evaluation of established or suspected coronary artery disease (CAD). BMD was assessed by dual X-ray absorptiometry. CAD was diagnosed in the presence of any coronary artery lumen narrowing at angiography; coronary stenoses with lumen narrowing ≥50% were considered significant. Results From the total study cohort (mean age of 64 ± 11 years), 207 patients (33.2%) had osteopenia and 65 (10.4%) had osteoporosis; at angiography, CAD was diagnosed in 558 patients (89.6%) and 403 (64.7%) had significant coronary stenoses. In multivariate logistic regression analysis neither osteopenia nor osteoporosis was associated with an increased prevalence of CAD (adjusted odds ratios (ORs) = 0.71 [95% confidence interval 0.40-1.23]; p = 0.222 and 1.03 [0.38-2.80]; p = 0.955, respectively) or with significant coronary stenoses (OR 0.74 [0.52-1.07], p = 0.112 and 0.72 [0.41-1.26]; p = 0.251, respectively). Also, as a continuous variable, BMD was not associated with angiographically diagnosed CAD. Conclusions The prevalence of low BMD is very high in men undergoing coronary angiography. However, low BMD is not associated with angiographically determined coronary atherosclerosis in men.</description><identifier>ISSN: 0937-941X</identifier><identifier>EISSN: 1433-2965</identifier><identifier>DOI: 10.1007/s00198-009-1103-y</identifier><identifier>PMID: 19936870</identifier><language>eng</language><publisher>London: London : Springer-Verlag</publisher><subject>Absorptiometry, Photon - methods ; Aged ; Atherosclerosis ; Atherosclerosis (general aspects, experimental research) ; Biological and medical sciences ; Blood and lymphatic vessels ; Bone Density ; Bone Diseases, Metabolic - complications ; Bone Diseases, Metabolic - physiopathology ; Cardiology. Vascular system ; Cardiovascular risk ; Coronary Angiography ; Coronary Artery Disease - complications ; Coronary Artery Disease - diagnostic imaging ; Coronary Artery Disease - physiopathology ; Diseases of the osteoarticular system ; Dual X-ray absorptiometry ; Endocrinology ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical imaging ; Medical sciences ; Medicine ; Medicine & Public Health ; Mens health ; Middle Aged ; Original Article ; Orthopedics ; Osteoarticular system. Muscles ; Osteoporosis - complications ; Osteoporosis - physiopathology ; Osteoporosis. Osteomalacia. Paget disease ; Radiodiagnosis. Nmr imagery. Nmr spectrometry ; Rheumatology ; Risk factors</subject><ispartof>Osteoporosis international, 2010-10, Vol.21 (10), p.1695-1701</ispartof><rights>International Osteoporosis Foundation and National Osteoporosis Foundation 2009</rights><rights>2015 INIST-CNRS</rights><rights>International Osteoporosis Foundation and National Osteoporosis Foundation 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c456t-dc00ad8b4782655924b91a34ca2ca7267a2b4736ba35ba6e39093a6b02f7223c3</citedby><cites>FETCH-LOGICAL-c456t-dc00ad8b4782655924b91a34ca2ca7267a2b4736ba35ba6e39093a6b02f7223c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00198-009-1103-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00198-009-1103-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23247580$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19936870$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Beer, S</creatorcontrib><creatorcontrib>Saely, C. H</creatorcontrib><creatorcontrib>Hoefle, G</creatorcontrib><creatorcontrib>Rein, P</creatorcontrib><creatorcontrib>Vonbank, A</creatorcontrib><creatorcontrib>Breuss, J</creatorcontrib><creatorcontrib>Gaensbacher, B</creatorcontrib><creatorcontrib>Muendlein, A</creatorcontrib><creatorcontrib>Drexel, H</creatorcontrib><title>Low bone mineral density is not associated with angiographically determined coronary atherosclerosis in men</title><title>Osteoporosis international</title><addtitle>Osteoporos Int</addtitle><addtitle>Osteoporos Int</addtitle><description>Summary This study for the first time investigates the association of bone mineral density (BMD) with angiographically determined coronary atherosclerosis in men. Our data show that the prevalence of low BMD is very high in men undergoing coronary angiography. However, neither osteopenia nor osteoporosis is associated with an increased prevalence of angiographically determined coronary atherosclerosis. Introduction The association of low BMD with angiographically determined coronary atherosclerosis in men is unknown. Methods We enrolled 623 consecutive men undergoing coronary angiography for the evaluation of established or suspected coronary artery disease (CAD). BMD was assessed by dual X-ray absorptiometry. CAD was diagnosed in the presence of any coronary artery lumen narrowing at angiography; coronary stenoses with lumen narrowing ≥50% were considered significant. Results From the total study cohort (mean age of 64 ± 11 years), 207 patients (33.2%) had osteopenia and 65 (10.4%) had osteoporosis; at angiography, CAD was diagnosed in 558 patients (89.6%) and 403 (64.7%) had significant coronary stenoses. In multivariate logistic regression analysis neither osteopenia nor osteoporosis was associated with an increased prevalence of CAD (adjusted odds ratios (ORs) = 0.71 [95% confidence interval 0.40-1.23]; p = 0.222 and 1.03 [0.38-2.80]; p = 0.955, respectively) or with significant coronary stenoses (OR 0.74 [0.52-1.07], p = 0.112 and 0.72 [0.41-1.26]; p = 0.251, respectively). Also, as a continuous variable, BMD was not associated with angiographically diagnosed CAD. Conclusions The prevalence of low BMD is very high in men undergoing coronary angiography. However, low BMD is not associated with angiographically determined coronary atherosclerosis in men.</description><subject>Absorptiometry, Photon - methods</subject><subject>Aged</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Bone Density</subject><subject>Bone Diseases, Metabolic - complications</subject><subject>Bone Diseases, Metabolic - physiopathology</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular risk</subject><subject>Coronary Angiography</subject><subject>Coronary Artery Disease - complications</subject><subject>Coronary Artery Disease - diagnostic imaging</subject><subject>Coronary Artery Disease - physiopathology</subject><subject>Diseases of the osteoarticular system</subject><subject>Dual X-ray absorptiometry</subject><subject>Endocrinology</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Medical sciences</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mens health</subject><subject>Middle Aged</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Osteoarticular system. Muscles</subject><subject>Osteoporosis - complications</subject><subject>Osteoporosis - physiopathology</subject><subject>Osteoporosis. Osteomalacia. Paget disease</subject><subject>Radiodiagnosis. Nmr imagery. Nmr spectrometry</subject><subject>Rheumatology</subject><subject>Risk factors</subject><issn>0937-941X</issn><issn>1433-2965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkUuLFDEUhYMoTs_oD3CjQRhcleZVeSxl8AUNLnTAXbiVSnVnrE7apJqh_r0pqnHAhW6Sxf3OSe45CL2g5C0lRL0rhFCjG0JMQynhzfwIbajgvGFGto_RhhiuGiPojwt0WcodqRpj1FN0QY3hUiuyQT-36R53KXp8CNFnGHHvYwnTjEPBMU0YSkkuwOR7fB-mPYa4C2mX4bgPDsZxrvzk8yLusUs5RcgzhmnvcypuXM5qFCI--PgMPRlgLP75-b5Ctx8_fL_53Gy_fvpy837bONHKqekdIdDrTijNZNsaJjpDgQsHzIFiUgGrMy474G0H0nNT9wTZETYoxrjjV-jN6nvM6dfJl8keQnF-HCH6dCpWS8K1rtn8l1StqBFLJSr5-i_yLp1yrGtUiDCqWLtAdIVcXbtkP9hjDocaiKXELo3ZtTFbG7NLY3aumpdn41N38P2D4lxRBa7PAJSa-JAhulD-cIwzoVq9cGzlSh3Fnc8PP_zX669W0QDJwi5X49tvjFBOqNatYIL_Bgv7uCQ</recordid><startdate>20101001</startdate><enddate>20101001</enddate><creator>Beer, S</creator><creator>Saely, C. H</creator><creator>Hoefle, G</creator><creator>Rein, P</creator><creator>Vonbank, A</creator><creator>Breuss, J</creator><creator>Gaensbacher, B</creator><creator>Muendlein, A</creator><creator>Drexel, H</creator><general>London : Springer-Verlag</general><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</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>7QP</scope><scope>7RV</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</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>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20101001</creationdate><title>Low bone mineral density is not associated with angiographically determined coronary atherosclerosis in men</title><author>Beer, S ; Saely, C. H ; Hoefle, G ; Rein, P ; Vonbank, A ; Breuss, J ; Gaensbacher, B ; Muendlein, A ; Drexel, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c456t-dc00ad8b4782655924b91a34ca2ca7267a2b4736ba35ba6e39093a6b02f7223c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Absorptiometry, Photon - methods</topic><topic>Aged</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis (general aspects, experimental research)</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Bone Density</topic><topic>Bone Diseases, Metabolic - complications</topic><topic>Bone Diseases, Metabolic - physiopathology</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular risk</topic><topic>Coronary Angiography</topic><topic>Coronary Artery Disease - complications</topic><topic>Coronary Artery Disease - diagnostic imaging</topic><topic>Coronary Artery Disease - physiopathology</topic><topic>Diseases of the osteoarticular system</topic><topic>Dual X-ray absorptiometry</topic><topic>Endocrinology</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Medical sciences</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mens health</topic><topic>Middle Aged</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Osteoarticular system. Muscles</topic><topic>Osteoporosis - complications</topic><topic>Osteoporosis - physiopathology</topic><topic>Osteoporosis. Osteomalacia. Paget disease</topic><topic>Radiodiagnosis. Nmr imagery. Nmr spectrometry</topic><topic>Rheumatology</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Beer, S</creatorcontrib><creatorcontrib>Saely, C. H</creatorcontrib><creatorcontrib>Hoefle, G</creatorcontrib><creatorcontrib>Rein, P</creatorcontrib><creatorcontrib>Vonbank, A</creatorcontrib><creatorcontrib>Breuss, J</creatorcontrib><creatorcontrib>Gaensbacher, B</creatorcontrib><creatorcontrib>Muendlein, A</creatorcontrib><creatorcontrib>Drexel, H</creatorcontrib><collection>AGRIS</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>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</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>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</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>Osteoporosis international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Beer, S</au><au>Saely, C. H</au><au>Hoefle, G</au><au>Rein, P</au><au>Vonbank, A</au><au>Breuss, J</au><au>Gaensbacher, B</au><au>Muendlein, A</au><au>Drexel, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low bone mineral density is not associated with angiographically determined coronary atherosclerosis in men</atitle><jtitle>Osteoporosis international</jtitle><stitle>Osteoporos Int</stitle><addtitle>Osteoporos Int</addtitle><date>2010-10-01</date><risdate>2010</risdate><volume>21</volume><issue>10</issue><spage>1695</spage><epage>1701</epage><pages>1695-1701</pages><issn>0937-941X</issn><eissn>1433-2965</eissn><abstract>Summary This study for the first time investigates the association of bone mineral density (BMD) with angiographically determined coronary atherosclerosis in men. Our data show that the prevalence of low BMD is very high in men undergoing coronary angiography. However, neither osteopenia nor osteoporosis is associated with an increased prevalence of angiographically determined coronary atherosclerosis. Introduction The association of low BMD with angiographically determined coronary atherosclerosis in men is unknown. Methods We enrolled 623 consecutive men undergoing coronary angiography for the evaluation of established or suspected coronary artery disease (CAD). BMD was assessed by dual X-ray absorptiometry. CAD was diagnosed in the presence of any coronary artery lumen narrowing at angiography; coronary stenoses with lumen narrowing ≥50% were considered significant. Results From the total study cohort (mean age of 64 ± 11 years), 207 patients (33.2%) had osteopenia and 65 (10.4%) had osteoporosis; at angiography, CAD was diagnosed in 558 patients (89.6%) and 403 (64.7%) had significant coronary stenoses. In multivariate logistic regression analysis neither osteopenia nor osteoporosis was associated with an increased prevalence of CAD (adjusted odds ratios (ORs) = 0.71 [95% confidence interval 0.40-1.23]; p = 0.222 and 1.03 [0.38-2.80]; p = 0.955, respectively) or with significant coronary stenoses (OR 0.74 [0.52-1.07], p = 0.112 and 0.72 [0.41-1.26]; p = 0.251, respectively). Also, as a continuous variable, BMD was not associated with angiographically diagnosed CAD. Conclusions The prevalence of low BMD is very high in men undergoing coronary angiography. However, low BMD is not associated with angiographically determined coronary atherosclerosis in men.</abstract><cop>London</cop><pub>London : Springer-Verlag</pub><pmid>19936870</pmid><doi>10.1007/s00198-009-1103-y</doi><tpages>7</tpages></addata></record> |
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| subjects | Absorptiometry, Photon - methods Aged Atherosclerosis Atherosclerosis (general aspects, experimental research) Biological and medical sciences Blood and lymphatic vessels Bone Density Bone Diseases, Metabolic - complications Bone Diseases, Metabolic - physiopathology Cardiology. Vascular system Cardiovascular risk Coronary Angiography Coronary Artery Disease - complications Coronary Artery Disease - diagnostic imaging Coronary Artery Disease - physiopathology Diseases of the osteoarticular system Dual X-ray absorptiometry Endocrinology Humans Investigative techniques, diagnostic techniques (general aspects) Male Medical imaging Medical sciences Medicine Medicine & Public Health Mens health Middle Aged Original Article Orthopedics Osteoarticular system. Muscles Osteoporosis - complications Osteoporosis - physiopathology Osteoporosis. Osteomalacia. Paget disease Radiodiagnosis. Nmr imagery. Nmr spectrometry Rheumatology Risk factors |
| title | Low bone mineral density is not associated with angiographically determined coronary atherosclerosis in men |
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