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Expression of iron metabolism-related genes is altered in Familial Hypercholesterolemia patients

dc.contributor.authorMateus, Ana
dc.contributor.authorSilva, Bruno
dc.contributor.authorMarques, Liliana
dc.contributor.authorFaustino, Paula
dc.contributor.authorBourbon, Mafalda
dc.contributor.authorCosta, Luciana
dc.date.accessioned2013-06-25T11:21:15Z
dc.date.available2013-06-25T11:21:15Z
dc.date.issued2013-06
dc.description.abstractAtherosclerosis (ATH) is the major cause of cardiovascular diseases (CVD) causing great morbidity and mortality. Typically, ATH develops and progresses silently for years, without symptoms. Familial Hypercholesterolemia (FH) is an autosomal genetic disorder characterized by high levels of total and LDL cholesterol, a familial history of hypercholesterolemia and premature ATH. Atherogenesis is characterized by an early deposition of LDL in the artery walls, leading to the recruitment and activation of peripheral blood mononuclear cells (PBMC) to the plaque. In addition, monocyte-derived macrophages accumulate oxidized LDL and differentiate into foam cells, leading to the development of complex and unstable lesions. The oxidative modification of LDL, accelerated, or even initiated by transition metals as iron (Fe) has been implicated as an early step in the formation of atheromatous lesions.por
dc.description.sponsorshipThis work was supported by National Institute of Health Doutor Ricardo Jorge, I.P., Lisboa, Portugalpor
dc.identifier.urihttp://hdl.handle.net/10400.18/1633
dc.language.isoengpor
dc.publisherInstituto Nacional de Saúde Doutor Ricardo Jorge, IPpor
dc.subjectDeterminantes Imunológicos em Doenças Crónicaspor
dc.subjectDoenças Cardio e Cérebro-vascularespor
dc.subjectDoenças Genéticas
dc.titleExpression of iron metabolism-related genes is altered in Familial Hypercholesterolemia patientspor
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceLyon, Francepor
oaire.citation.title81st EAS-European Atherosclerosis Society Congress, 2-5 june 2013por
rcaap.rightsopenAccesspor
rcaap.typeconferenceObjectpor

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