Publication:
Subclinical atherosclerosis in young Thai adults with juvenile-onset systemic lupus erythematosus

dc.contributor.authorNalinee Pattrakornkulen_US
dc.contributor.authorPatamakom Pruangpraserten_US
dc.contributor.authorPrakul Chanthongen_US
dc.contributor.authorRatana Chawanasuntorapojen_US
dc.contributor.authorAnirut Pattaragarnen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-12-11T02:17:02Z
dc.date.accessioned2019-03-14T08:04:08Z
dc.date.available2018-12-11T02:17:02Z
dc.date.available2019-03-14T08:04:08Z
dc.date.issued2016-04-01en_US
dc.description.abstractBackground: Cardiovascular disease (CVD) is a leading cause of morbidity and mortality in adult patients with systemic lupus erythematosus (SLE). Increased risk of CVD and atherosclerosis has been demonstrated in children with SLE. However, evidence of atherosclerosis in adults with juvenile-onset SLE is limited and their additional CVD risk factors unclear. Objectives: To investigate the presence of subclinical atherosclerosis in young Thai adults with juvenile-onset SLE, and evaluate atherosclerotic risk factors. Methods: We recruited a cohort of patients aged 18-40 years who had been diagnosed SLE before the age of 18 years for this observational study. Patients with chronic kidney disease stage IV or V, alcoholism, chronic liver disease, or life threatening illness were excluded. Common carotid intima-media thickness (CCIMT) was measured. Clinical and laboratory parameters, treatment, and SLE-related factors, which could be risk factors for atherosclerosis and classic risk factors were obtained. Results: We enrolled 29 patients (24 female). Their mean age was 25.1 years and mean disease duration 11.3 years. The age of participants, persistent proteinuria and use of cyclosporin correlated with increased CCIMT by multivariable analysis (P = 0.02, 0.02, and 0.03, respectively). These patients had significantly abnormal CCIMT when compared with a healthy population (mean 690 (SD 150) μm versus mean 447 (SD 76) μm, respectively; P < 0.001). Conclusions: Subclinical atherosclerosis, identified by abnormal CCIMT, appears in young adults with juvenile-onset SLE. The CCIMT abnormality progresses with increasing age, and persistent proteinuria and use of cyclosporin appears to increase the risk for atherosclerosis.en_US
dc.identifier.citationAsian Biomedicine. Vol.10, No.2 (2016), 139-146en_US
dc.identifier.doi10.5372/1905-7415.1002.475en_US
dc.identifier.issn1875855Xen_US
dc.identifier.issn19057415en_US
dc.identifier.other2-s2.0-84982908695en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/43075
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84982908695&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleSubclinical atherosclerosis in young Thai adults with juvenile-onset systemic lupus erythematosusen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84982908695&origin=inwarden_US

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