Heterogeneity of peripheral blood monocytes, endothelial dysfunction and subclinical atherosclerosis in patients with Systemic Lupus Erythematosus

Autor: Tomasz Sliwa, Dominik Skiba, Bogdan Batko, M Krezelok, Tomasz Mikolajczyk, Tomasz J. Guzik, Juliusz Pryjma, Grzegorz Osmenda, Grzegorz Wilk
Jazyk: angličtina
Rok vydání: 2015
Předmět:
Carotid Artery Diseases
Male
Brachial Artery
SLE
Lipopolysaccharide Receptors
030204 cardiovascular system & hematology
Carotid Intima-Media Thickness
Monocytes
0302 clinical medicine
Risk Factors
Lupus Erythematosus
Systemic

flow-mediated dilation
Endothelial dysfunction
Brachial artery
Middle Aged
Flow Cytometry
Phenotype
Vasodilation
Carotid Arteries
Cardiology
Female
Adult
medicine.medical_specialty
CD14
CD16
GPI-Linked Proteins
Article
03 medical and health sciences
Young Adult
monocyte subsets
Rheumatology
Predictive Value of Tests
Internal medicine
medicine.artery
medicine
Humans
intima-media thickness
Aged
030203 arthritis & rheumatology
Lupus erythematosus
business.industry
Receptors
IgG

medicine.disease
Atherosclerosis
Intima-media thickness
Subclinical atherosclerosis
Case-Control Studies
Immunology
Asymptomatic Diseases
Endothelium
Vascular

business
Biomarkers
Popis: Background Systemic lupus erythematosus (SLE) is characterized by increased cardiovascular morbidity and mortality. SLE patients have increased prevalence of subclinical atherosclerosis, although the mechanisms of this observation remain unclear. Considering the emerging role of monocytes in atherosclerosis, we aimed to investigate the relationship between subclinical atherosclerosis, endothelial dysfunction and the phenotype of peripheral blood monocytes in SLE patients. Methods We characterized the phenotype of monocyte subsets defined by the expression of CD14 and CD16 in 42 patients with SLE and 42 non-SLE controls. Using ultrasonography, intima-media thickness (IMT) of carotid arteries and brachial artery flow-mediated dilation (FMD) as well as nitroglycerin-induced dilation (NMD) were assessed. Results Patients with SLE had significantly, but only modestly, increased IMT when compared with non-SLE controls (median (25th/75th percentile) 0.65 (0.60/0.71) mm vs 0.60 (0.56/0.68) mm; p Conclusions Our observations suggest that CD14dimCD16+monocytes are associated with subclinical atherosclerosis in SLE, although the mechanism appears to be independent of endothelial dysfunction.
Databáze: OpenAIRE