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Cardiovascular risk profile in systemic lupus erythematosus and rheumatoid arthritis: a comparative study of female patients

dc.contributor.authorSantos, MJ
dc.contributor.authorVinagre, F
dc.contributor.authorSilva, J
dc.contributor.authorGil, V
dc.contributor.authorFonseca, J
dc.date.accessioned2011-09-01T11:09:46Z
dc.date.available2011-09-01T11:09:46Z
dc.date.issued2010
dc.description.abstractOBJECTIVE: Premature atherosclerosis is well-documented both in Systemic Lupus Erythematosus (SLE) and in Rheumatoid Arthritis (RA) patients, but cardiovascular (CV) risk is particularly high in lupus women. Although conventional CV risk factors do not fully explain the excessive risk in inflammatory diseases, they remain major contributors to atherosclerosis. The aim of the present study was to investigate whether CV risk factors are differentially associated with SLE and RA. METHODS: One hundred women with SLE, 98 with RA and 102 controls matched on age and without overt CV or renal disease were assessed for the presence of Framingham (hypertension, hypercholesterolemia, low HDL, diabetes, smoking) and other CV risks (atherogenic index of plasma (AIP), insulin resistance, obesity, central obesity, metabolic syndrome, uric acid, sedentarism, hypothyroidism and family history of premature CV disease). RESULTS: Modifiable CV risk factors are highly prevalent and occur more frequently in SLE and RA than in age-matched controls. Some differences in Framingham risk factors were found between SLE and RA, with hypertension being more common in young lupus women, hypercholesterolemia more frequent in RA and low HDL-C more frequent in SLE. However, the estimated 10-year Framingham CHD risk or the Reynolds Risk Score was comparable in both diseases. Although hypercholesterolemia was more frequent in RA, lupus women display a more atherogenic lipid profile, with significantly lower HDL-C levels (56.5±16 mg/dl versus 63.7±18; p=0.005), and more cases above the high risk cutpoints for cholesterol/HDL-C (14% versus 4.1%; p=0.01) and for AIP (15% versus 6.1%; p=0.03). Also, uric acid levels are higher in SLE women (4.8±1.5 mg/dl) than in RA (4.1±1.1 mg/dl), p=0.001. On the other hand, insulin resistance is significantly higher in women with RA as compared with SLE (median HOMA-IR 3.5 [6.4]) versus 0.72 [2.5]; p<0.0001) and the difference remained significant after adjustment for BMI and corticosteroids. CONCLUSIONS: Cardiovascular risk profile is distinct in SLE and RA women and the contribution of traditional CV risk factors to atherogenesis may be different in these two diseases. Prospective studies are necessary to understand how the control of modifiable risks can improve CV outcome in different inflammatory settings.por
dc.identifier.citationActa Reumatol Port. 2010 Jul-Sep;35(3):325-32por
dc.identifier.issn0303-464X
dc.identifier.urihttp://hdl.handle.net/10400.10/424
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherSociedade Portuguesa de Reumatologiapor
dc.subjectArterite reumatóidepor
dc.subjectDoenças cardiovascularespor
dc.subjectLúpus eritematoso sistémicopor
dc.subjectRheumatoid arthritispor
dc.subjectSystemic lupus erythematosuspor
dc.titleCardiovascular risk profile in systemic lupus erythematosus and rheumatoid arthritis: a comparative study of female patientspor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.conferencePlaceLisboapor
oaire.citation.endPage332por
oaire.citation.startPage325por
oaire.citation.titleActa Reumatológica Portuguesapor
rcaap.rightsopenAccesspor
rcaap.typearticlepor

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