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dc.contributor.authorEklund, Charlotte
dc.date.accessioned2014-03-14T13:59:39Z
dc.date.available2014-03-14T13:59:39Z
dc.date.issued2014-03-14
dc.identifier.isbn978-91-628-8898-5
dc.identifier.urihttp://hdl.handle.net/2077/34833
dc.description.abstractCardiovascular disease (CVD) is the major cause of death both in Sweden and globally. Atherosclerotic vascular changes are considered the major underlying pathology leading to clinical manifestations of CVD, e.g. myocardial infarction and stroke. Hyperlipidemia and chronic subclinical inflammation have been identified as major pathophysiological mechanisms driving atherosclerosis, which is a life-long vascular disease. Inflammatory diseases such as rheumatoid arthritis (RA) are known to be associated with increased risk of CVD. To be able to detect and follow atherosclerosis from its subclinical phase to its clinical stage, we are in great need of novel high-sensitive imaging tools to characterize functional and morphological vascular changes. Our group has successfully used very high frequency ultrasound to follow atherosclerosis in genetically modified mice models. In the current thesis, we adopted this technique to patients and evaluated biological relevance and prognostic significance of high-frequency ultrasound-measured radial artery intima-media thickness (rIMT) in patients with suspected myocardial ischemia. Further, rIMT and coronary flow reserve (CFR) in relationship to systemic inflammation were explored in a group of recent diagnosed RA patients. Clinical correlates and prognostic values of rIMT were evaluated in 416 patients with suspected myocardial ischemia undergoing myocardial perfusion imaging. Relationship between rIMT, CFR and systemic inflammatory status was explored in patients with recent-onset RA, immediately following diagnosis and four months after standard anti-rheumatic treatment. Radial artery IMT correlated with conventional cardiovascular (CV) risk factors. Presence of myocardial ischemia and significant coronary artery narrowing, as verified by myocardial perfusion scintigram respectively coronary angiogram, were associated with increased rIMT. Increased rIMT was seen in patients with CV events compared to those without events. Further, rIMT values above the median indicated an independent two-fold increased risk of CV events after multivariate adjustment. At RA onset, CFR correlated with rIMT, number of swollen joints and systemic inflammation. A reduced number of swollen joints after four months treatment were associated with improvement in CFR. In conclusion, rIMT can be accurately measured with good feasibility and reproducibility. Radial artery IMT is related to multiple CV risk factors and confers prognostic information in patients with suspected myocardial ischemia. Potential use of this vascular surrogate marker to follow atherosclerotic vascular changes and response to treatment warrants further studiessv
dc.language.isoengsv
dc.relation.haspartI. Eklund C et al. High-resolution radial artery intima-media thickness and cardiovascular risk factors in patients with suspected coronary artery disease – comparison with common carotid artery intima-media thickness. Atherosclerosis 2012; 221: 118-123 ::PMID::22265271sv
dc.relation.haspartII. Eklund C, et al. Radial artery intima-media thickness predicts major cardiovascular events in patients with suspected coronary artery disease. Eur Heart J Cardiovasc Imaging 2014 Jan 26. ::PMID:: 24469155sv
dc.relation.haspartIII. Eklund C, et al. Cardiovascular status in patients with recent-onset rheumatoid arthritis. In manuscriptsv
dc.subjectatherosclerosissv
dc.subjectintima-media thicknesssv
dc.subjectultrasoundsv
dc.subjectradial arterysv
dc.subjecthigh resolutionsv
dc.subjectcardiovascular diseasesv
dc.titleBiological relevance and prognostic significance of radial artery intima-media thicknesssv
dc.typetexteng
dc.type.svepDoctoral thesiseng
dc.gup.mailcharlotte.eklund@vgregion.sesv
dc.type.degreeDoctor of Philosophy (Medicine)sv
dc.gup.originUniversity of Gothenburg. Sahlgrenska Academysv
dc.gup.departmentInstitute of Medicine. Department of Molecular and Clinical Medicinesv
dc.gup.defenceplaceFredagen den 4 april 2014, kl.13.00, Hörsal Arvid Carlsson, Academicum, Medicinaregatan 3sv
dc.gup.defencedate2014-04-04
dc.gup.dissdb-fakultetSA


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