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Published on: January 16, 2015
Systemic vascular dysfunction is associated with emphysema burden in mild COPD
Joel T Zelt1, Joshua H Jones1, Daniel M Hirai1
1Laboratory of Clinical Exercise Physiology (LACEP), Division of Respiratory and Critical Care Medicine, Department of Medicine, Queen's University, Kingston, Canada.
Insights
Systemic vascular dysfunction is evident in early COPD, even in low-risk patients. Greater emphysema and reduced lung function correlate with poorer vascular health, suggesting a need for closer cardiovascular monitoring.
Area of Science:
- Pulmonary Medicine
- Cardiovascular Medicine
- Vascular Biology
Background:
- Cardiovascular diseases contribute significantly to morbidity and mortality in early stages of Chronic Obstructive Pulmonary Disease (COPD).
- Systemic vascular dysfunction is hypothesized to exist even in patients considered low-risk for cardiovascular outcomes (GOLD spirometric grade 1, clinical group A).
Purpose of the Study:
- To investigate the presence of systemic vascular dysfunction in patients with early-stage COPD.
- To determine the relationship between COPD-related structural lung changes (emphysema, airway disease) and vascular abnormalities.
Main Methods:
- 16 early-stage COPD patients and 16 controls underwent measurements of central arterial stiffness (pulse wave velocity), brachial flow-mediated dilation, and forearm muscle oxygenation (near-infrared spectroscopy).
- Computed tomography was used to quantify emphysema (percentage of low attenuation areas - LAA) and airway disease.
- Transfer factor for carbon monoxide (TLCO) was measured.
Main Results:
- COPD patients exhibited higher central arterial stiffness, lower normalized flow-mediated dilation, delayed dilation time, and poorer muscle oxygenation compared to controls (p < 0.05).
- Emphysema extent (LAA) was negatively related to TLCO (r = -0.63; p = 0.01).
- TLCO and emphysema, but not airway disease, were significantly associated with the observed vascular and muscle oxygenation abnormalities (r values 0.51–0.66; p < 0.05).
Conclusions:
- Systemic vascular dysfunction is present in early COPD, particularly in patients with higher emphysema burden and lower TLCO.
- These vascular and functional abnormalities, regardless of FEV1, may indicate a higher risk for adverse cardiovascular events.
- Patients with these findings warrant closer follow-up for early cardiovascular disease detection.
Background:
Cardiovascular diseases play a major role in morbidity and mortality in the earlier stages of COPD. We hypothesized that systemic vascular dysfunction would be present even in patients who are currently considered at "low-risk" for negative cardiovascular outcomes, i.e., those with largely preserved FEV1, few exacerbations and only mild burden of respiratory symptoms (GOLD spirometric grade 1, clinical group A).
Methods:
16 patients (FEV1 = 86 ± 13%) and 16 age- and gender-matched controls underwent measurements of: a) central arterial stiffness by pulse wave velocity, b) brachial flow-mediated dilation and c) forearm muscle oxygenation by near-infrared spectroscopy. Computed tomography quantified emphysema (% of low attenuation areas (LAA)) and airway disease.
Results:
Patients and controls were well matched for key clinical variables including co-morbidities burden. Thirteen patients presented with more than 5% LAA: emphysema extension was negatively related to transfer factor for carbon monoxide (TLCO) (r = -0.63; p = .01). Compared to controls, patients had higher central arterial stiffness, lower normalized (to shear stress) flow-mediated dilation, delayed time to peak flow-mediated dilation and poorer muscle oxygenation (p < .05). TLCO and emphysema, but not airway disease, were significantly related to each of these functional abnormalities (r values ranging from 0.51 to 0.66; p < .05).
Conclusion:
Systemic vascular dysfunction is present in the earlier stages of COPD, particularly in patients with greater emphysema burden and low TLCO. Regardless FEV1, patients showing those structural and functional abnormalities might be at higher risk of negative events thereby deserving closer follow-up for early detection of cardiovascular disease.
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