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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1161/01.atv.19.7.1734</dc:identifier><dc:language>eng</dc:language><dc:creator>Acton, S.</dc:creator><dc:creator>Osgood, D.</dc:creator><dc:creator>Donoghue, M.</dc:creator><dc:creator>Corella, D.</dc:creator><dc:creator>Pocovi, M.</dc:creator><dc:creator>Cenarro, A.</dc:creator><dc:creator>Mozas, P.</dc:creator><dc:creator>Keilty, J.</dc:creator><dc:creator>Squazzo, S.</dc:creator><dc:creator>Woolf, E. A.</dc:creator><dc:creator>Ordovas, J. M.</dc:creator><dc:title>Association of polymorphisms at the SR-BI gene locus with plasma lipid levels and body mass index in a white population</dc:title><dc:identifier>ART-1999-176</dc:identifier><dc:description>The scavenger receptor class B type I (SR-BI) is a lipoprotein receptor that has been shown to be important in high density lipoprotein cholesterol (HDL-C) metabolism in mice. To determine its role in humans, we have characterized the human SR-BI gene and investigated its genetic variation in 489 white men and women. Five variants were demonstrated: 2 in introns (3 and 5) and 3 in exons (1, 8, and 11). Three variants at exons 1 and 8 and intron 5 with allele frequencies &gt;0.1 were used to examine associations with lipid or anthropometric variables. The exon 1 variant was significantly (P&lt;0.05) associated with increased HDL-C and lower low density lipoprotein cholesterol (LDL-C) values in men, but no associations were observed in women. The exon 8 variant was associated in women with lower LDL-C concentrations (3.05±0.98 mmol/L and 3.00±0.93 mmol/L for heterozygotes and homozygotes, respectively) compared with women homozygous for the common allele (3.39±1.09 mmol/L, P=0.043). No associations for this variant were observed in men. Women carriers of the intron 5 variant showed a higher body mass index (23.8±3.8 kg/m2, P=0.031) than those women homozygous for the common allele (22.4±3.4 kg/m2). Similar results were observed after haplotype analysis. Multiple regression analysis using HDL-C, LDL-C, and body mass index as dependent variables and age, sex, and each of the genetic variants as predictors also provided similar results. The associations found with both LDL-C and HDL-C suggest that SR-BI may play a role in the metabolism of both lipoprotein classes in humans.</dc:description><dc:date>1999</dc:date><dc:source>http://zaguan.unizar.es/record/168694</dc:source><dc:doi>10.1161/01.atv.19.7.1734</dc:doi><dc:identifier>http://zaguan.unizar.es/record/168694</dc:identifier><dc:identifier>oai:zaguan.unizar.es:168694</dc:identifier><dc:identifier.citation>Arteriosclerosis, Thrombosis, and Vascular Biology 19, 7 (1999), 1734-1743</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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