Carotid artery disease (CAD) as a comorbidity in COPD patients

We investigated the association between chronic obstructive pulmonary disease (COPD) and carotid artery disease (CAD), as well as the relation to airflow limitation severity and serum C-reactive protein (CRP) levels. This cross-sectional study included 220 newly diagnosed patients with stable COPD as Investigated Group (IG), aged 40–75 years, and 58 non-COPD subjects as Control Group (CG), matched by gender, age, BMI, and smoking status. All participants underwent lung function tests, Doppler ultrasound of the carotid arteries, and serum CRP measurement. Results showed a higher frequency of CAD in the COPD group compared to the control group 21(9.55%) vs. 1(1.72%), P=0.0052. In COPD patients, CAD was present in 8(16.33%) of GOLD4 cases, 5(9.62%) of GOLD3, 6(9.68%) of GOLD2, and 2(3.51%) of GOLD1. Doppler findings were classified as normal, intima-media thickening (IMT), mild stenosis (1%-39%), moderate stenosis (40%-59%), and severe stenosis (60%-79%). No patients had critical stenosis (80%-99%). IMT was more common in the COPD group than in the control group 106(48.2%) vs. 15(25.9%), P=0.0023. The mean IMT value in COPD patients with CAD was significantly higher than in the control group with CAD (0.8±0.2 vs. 0.6±0.1, P=0.0043). IMT in COPD patients was strongly linked to lower FEV1 (P=0.000) and higher CRP levels (P=0.001). COPD patients had a 2.66 times higher risk of IMT compared to the control group (OR=2.66, 95% CI: 1.39–5.08). The study found that vascular changes in COPD patients were strongly associated with disease severity and inflammation levels. The presence of CAD, even in early COPD stages, highlights the need for prevention, screening, and early treatment.

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Published
2025-09-27
DOI
https://doi.org/10.1183/13993003.congress-2025.pa1395
Primary Topic
Chronic Obstructive Pulmonary Disease (COPD) Research
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article
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Carotid artery disease (CAD) as a comorbidity in COPD patients

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Carotid artery disease (CAD) as a comorbidity in COPD patients

Ivica Stojanoski, Radmila Milosheska, Јордан Минов, Ivana Mickovski, Bozidar Poposki, Daniela Buklioska Ilievska, Adriana Buklioska, Vesna Trajkova
article en

Abstract

We investigated the association between chronic obstructive pulmonary disease (COPD) and carotid artery disease (CAD), as well as the relation to airflow limitation severity and serum C-reactive protein (CRP) levels. This cross-sectional study included 220 newly diagnosed patients with stable COPD as Investigated Group (IG), aged 40–75 years, and 58 non-COPD subjects as Control Group (CG), matched by gender, age, BMI, and smoking status. All participants underwent lung function tests, Doppler ultrasound of the carotid arteries, and serum CRP measurement. Results showed a higher frequency of CAD in the COPD group compared to the control group 21(9.55%) vs. 1(1.72%), P=0.0052. In COPD patients, CAD was present in 8(16.33%) of GOLD4 cases, 5(9.62%) of GOLD3, 6(9.68%) of GOLD2, and 2(3.51%) of GOLD1. Doppler findings were classified as normal, intima-media thickening (IMT), mild stenosis (1%-39%), moderate stenosis (40%-59%), and severe stenosis (60%-79%). No patients had critical stenosis (80%-99%). IMT was more common in the COPD group than in the control group 106(48.2%) vs. 15(25.9%), P=0.0023. The mean IMT value in COPD patients with CAD was significantly higher than in the control group with CAD (0.8±0.2 vs. 0.6±0.1, P=0.0043). IMT in COPD patients was strongly linked to lower FEV1 (P=0.000) and higher CRP levels (P=0.001). COPD patients had a 2.66 times higher risk of IMT compared to the control group (OR=2.66, 95% CI: 1.39–5.08). The study found that vascular changes in COPD patients were strongly associated with disease severity and inflammation levels. The presence of CAD, even in early COPD stages, highlights the need for prevention, screening, and early treatment.

PHI University Psychiatric Clinic - Skopje (MK), Goce Delcev University (MK), Ss. Cyril and Methodius University in Skopje (MK)
Openalex Percentile: Top 48%
Chronic Obstructive Pulmonary Disease (COPD) Research
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