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<dc:title>Bone mineral density, bone remodeling and osteoprotegerin in patients with acute coronary syndrome</dc:title>
<dc:creator>Pérez Castrillon, José Luis</dc:creator>
<dc:creator>Abad Manteca, Laura</dc:creator>
<dc:creator>Vega, Gemma</dc:creator>
<dc:creator>Sanz Cantalapiedra, Alberto</dc:creator>
<dc:creator>San Miguel, Ángel</dc:creator>
<dc:creator>Mazón Ramos, María de los Ángeles</dc:creator>
<dc:creator>Luis Román, Daniel Antonio de</dc:creator>
<dc:creator>Dueñas Laita, Antonio</dc:creator>
<dc:subject>Osteoporosis</dc:subject>
<dcterms:abstract>The objective of this study was to evaluate the relationship between coronary disease and osteoporosis and determine the effect of&#xd;
osteoprotegerin (OPG) on bone remodeling and bone mineral density (BMD) in a group of patients with acute coronary syndrome. Eightythree&#xd;
patients (52 males and 31 women) with acute coronary syndrome (75 patients with acute myocardial infarction and 8 with unstable&#xd;
angina) with an average age of 61±10 years were studied. Levels of osteocalcin, urinarydeoxypyridinoline, OPG and the receptor activator of&#xd;
nuclear factor-κB ligand (RANKL) were determined during the hospital stay. Femoral neck, trochanter and lumbar spine densitometry was&#xd;
carried out using a DXA densitometer. Thirty percent of patients presented osteoporosis (39% of females and 26% of males). Osteoporotic&#xd;
patients were older and had a lower weight and height and elevated serum levels of osteocalcin (3.6±2.25 2.63 versus ±1.55, p=0.05).&#xd;
Levels of OPG and RANKL were similar in both groups and showed no relationship with BMD. In conclusion, no relationship was observed&#xd;
between the OPG/RANKL system and BMD in these patients.</dcterms:abstract>
<dcterms:dateAccepted>2014-09-09T10:56:29Z</dcterms:dateAccepted>
<dcterms:available>2014-09-09T10:56:29Z</dcterms:available>
<dcterms:created>2014-09-09T10:56:29Z</dcterms:created>
<dcterms:issued>2008</dcterms:issued>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>International Journal of Cardiology, 2008, vol. 129, p. 144-145</dc:identifier>
<dc:identifier>0167-5273</dc:identifier>
<dc:identifier>http://uvadoc.uva.es/handle/10324/5881</dc:identifier>
<dc:identifier>10.1016/j.ijcard.2007.06.035</dc:identifier>
<dc:identifier>144</dc:identifier>
<dc:identifier>145</dc:identifier>
<dc:identifier>International Journal of Cardiology</dc:identifier>
<dc:identifier>129</dc:identifier>
<dc:language>eng</dc:language>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
<dc:publisher>Elsevier Ireland Ltd.</dc:publisher>
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