<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-14T15:32:34Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/5943" metadataPrefix="mods">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/5943</identifier><datestamp>2025-02-10T13:15:07Z</datestamp><setSpec>com_10324_1179</setSpec><setSpec>com_10324_931</setSpec><setSpec>com_10324_894</setSpec><setSpec>col_10324_1306</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
<mods:name>
<mods:namePart>Pérez Castrillon, José Luis</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Vega, Gemma</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Abad Manteca, Laura</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Sanz Cantalapiedra, Alberto</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>González Sagrado, Manuel</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Luis Román, Daniel Antonio de</mods:namePart>
</mods:name>
<mods:name>
<mods:namePart>Dueñas Laita, Antonio</mods:namePart>
</mods:name>
<mods:extension>
<mods:dateAvailable encoding="iso8601">2014-09-15T08:20:24Z</mods:dateAvailable>
</mods:extension>
<mods:extension>
<mods:dateAccessioned encoding="iso8601">2014-09-15T08:20:24Z</mods:dateAccessioned>
</mods:extension>
<mods:originInfo>
<mods:dateIssued encoding="iso8601">2008</mods:dateIssued>
</mods:originInfo>
<mods:identifier type="citation">Annals of Nutrition and Metabolism, 2008, vol. 53, p. 117-121</mods:identifier>
<mods:identifier type="issn">0250-6807</mods:identifier>
<mods:identifier type="uri">http://uvadoc.uva.es/handle/10324/5943</mods:identifier>
<mods:identifier type="doi">10.1159/000170886</mods:identifier>
<mods:identifier type="publicationfirstpage">117</mods:identifier>
<mods:identifier type="publicationlastpage">121</mods:identifier>
<mods:identifier type="publicationtitle">Annals of Nutrition and Metabolism</mods:identifier>
<mods:identifier type="publicationvolume">53</mods:identifier>
<mods:abstract>Aims: To evaluate the effect of atorvastatin on bone mass&#xd;
and markers of bone remodeling in patients with acute coronary&#xd;
syndrome depending on the tumor necrosis factor-  &#xd;
(TNF   )-308 G/A polymorphism. Methods: Sixty-two patients&#xd;
with acute coronary syndrome (35 males and 27 females),&#xd;
average age 60 8 10 years, were included. Patients&#xd;
were given low (10–20 mg) and high doses (40–80 mg) atorvastatin&#xd;
according to their baseline levels of cholesterol and&#xd;
triglycerides and their index of vascular risk. Patients were&#xd;
studied during hospital admission (baseline) and at 12&#xd;
months of follow-up. Cholesterol, triglycerides, total calcium,&#xd;
phosphorus, magnesium, osteocalcin and urinary deoxypyridinoline&#xd;
were determined in all patients at baseline&#xd;
and at 12 months of follow-up. Densitometric studies were&#xd;
conducted in the lumbar spine (L 2 –L 4 ), femoral neck and&#xd;
trochanter using an X-ray densitometer. The TNF   -308 G/A&#xd;
polymorphism was determined by the polymerase chain reaction.&#xd;
Results: Forty-five patients were homozygous for&#xd;
G/G (72.5%) and 17 were heterozygous for G/A (27.5%). The&#xd;
prevalence of osteoporosis (T score ^ 2.5 in the lumbar spineand/or hip) was 33% for the G/G genotype and 35% for the&#xd;
G/A genotype, with no statistically significant differences&#xd;
between groups. There was a statistically significant increase&#xd;
in bone mineral density (BMD) in the lumbar spine (1.107 8&#xd;
0.32 vs. 1.129 8 0.23; p = 0.0001) in patients with the G/G&#xd;
genotype. No changes were observed in patients with the&#xd;
G/A genotype. Conclusion: In patients with acute coronary&#xd;
syndrome, atorvastatin increases lumbar spine BMD solely&#xd;
in patients with the G/G genotype of the TNF   -308 G/A polymorphism.</mods:abstract>
<mods:language>
<mods:languageTerm>eng</mods:languageTerm>
</mods:language>
<mods:accessCondition type="useAndReproduction">info:eu-repo/semantics/openAccess</mods:accessCondition>
<mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by-nc-nd/4.0/</mods:accessCondition>
<mods:accessCondition type="useAndReproduction">Attribution-NonCommercial-NoDerivatives 4.0 International</mods:accessCondition>
<mods:subject>
<mods:topic>Huesos - Enfermedades</mods:topic>
</mods:subject>
<mods:subject>
<mods:topic>Cardiovascular, Aparato - Enfermedades</mods:topic>
</mods:subject>
<mods:titleInfo>
<mods:title>Effect of the TNF   -308 G/A Polymorphism on the Changes Produced by Atorvastatin in Bone Mineral Density in Patients with Acute Coronary Syndrome</mods:title>
</mods:titleInfo>
<mods:genre>info:eu-repo/semantics/article</mods:genre>
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