Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/18489
Title: COPD as a risk factor for carotid artery disease (CAD) and low-extremity artery disease (LEAD)
Authors: Buklioska Ilievska, Daniela 
Minov, Jordan 
Kochovska Kamchevska, Nade
Baloski, Marjan
Poposki, Bozidar
Keywords: COPD
COPD - management
Comorbidities
Issue Date: 7-Sep-2020
Publisher: European Respiratory Society
Source: Buklioska Ilievska D, Minov J, Kochovska Kamchevska N, Baloski M, Poposki B. COPD as a risk factor for carotid artery disease (CAD) and low-extremity artery disease (LEAD). European Respiratory Journal 2020; 56: Suppl. 64, 5118.
Journal: European respiratory Journal
Conference: 2020 ERS International Congress, in session “Respiratory viruses in the "pre COVID-19" era”
Abstract: We aimed to investigate the association between COPD and peripheral artery disease (PAD), the relation to the severity of airflow limitation and the level of serum C-reactive protein (CRP). Cross-sectional study including 120 patients with initially diagnosed COPD, aged 40 to 75 years and 60 non-COPD subjects matched by age, smoking status, body mass index, as controls. All study participants underwent pulmonary evaluation (dyspnea severity assessment, baseline and post-bronchodilator spirometry, gas analyses, chest X-ray), Doppler ultrasonography and measurement of serum CRP. Results presented statistically significant difference in presence of LEAD in COPD patients compared to controls (78.3% vs 38.3%; P<0.001). According to the Fontaine classification, COPD patients with LEAD were categorized in stages I, IIA and IIB (60%, 30% and 15%, respectively), whereas all controls with LEAD were in the Fontaine stage I. COPD patients with LEAD presented significant association between disease severity and clinical manifestations due to the vascular changes (P=0.001) and CRP (P<0.05). Comparison between presence of CAD in COPD and controls showed statistical significance (70% vs 36%; P < 0.0001). The mean value of intima-media thickness (IMT) in COPD patients with CAD was significantly higher than its mean value in controls (0.8 ± 0.2 vs. 0.6 ± 0.1; P=0.0043). IMT value in COPD patients with CAD was significantly related to FEV1 decline (P=0.000) and CRP (P=0.001). We found higher prevalence and severity of PAD in COPD patients compared to non-COPD and significant relation to FEV1 decline and serum CRP. Our findings suggest a need for early screening for PAD in COPD and an integrated-care approach.
URI: http://hdl.handle.net/20.500.12188/18489
DOI: 10.1183/13993003.congress-2020.5118
Appears in Collections:Faculty of Medicine: Conference papers

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