Key result
Impaired right ventricular global longitudinal strain (>−18%) in COPD conferred a 3.4-fold increased risk of adverse cardiopulmonary outcomes (HR 3.4; 95% CI 1.8–6.2; p<0.001).
Why the study?
Subclinical right ventricular contractile failure in COPD is often undetected by conventional echocardiography. This study evaluated whether right ventricular global longitudinal strain (RV-GLS) identifies early subclinical dysfunction and independently predicts adverse outcomes in patients with COPD.
Does right ventricular global longitudinal strain (RV-GLS) identify early subclinical dysfunction and independently predict adverse outcomes in patients with stable COPD (GOLD II–IV)?
Cohort (n=146)
Does right ventricular global longitudinal strain (RV-GLS) identify early subclinical dysfunction and independently predict adverse outcomes in patients with stable COPD (GOLD II–IV)?
Right ventricular global longitudinal strain (RV-GLS) detects early subclinical cardiac dysfunction missed by conventional echocardiography and independently predicts adverse clinical outcomes in stable COPD patients.
Abstract Right ventricular (RV) dysfunction may drive clinical deterioration in chronic pulmonary disease more than airflow limitation. Persistent pulmonary vascular load induces maladaptive RV remodeling, impaired RV–pulmonary arterial coupling, and subclinical contractile failure, often undetected by conventional echocardiography. The aim of this study was to determine whether RV myocardial deformation, assessed by global longitudinal strain (RV-GLS), identifies early subclinical dysfunction and independently predicts adverse outcomes in patients with COPD, thereby establishing the right ventricle as a central determinant of disease progression. Methods In this prospective study, 146 patients with stable COPD (GOLD II–IV) underwent spirometry, NT-proBNP measurement, 6-minute walk testing (6MWT), and transthoracic echocardiography with RV-GLS. Standard RV functional indices—tricuspid annular plane systolic excursion, fractional area change, and tricuspid regurgitation velocity—were assessed. Patients were followed for 18 months. The primary endpoint was a composite of severe exacerbation, COPD-related hospitalization, or major cardiovascular event. Independent predictors were evaluated using multivariable Cox regression. Results Impaired RV-GLS (>−18%) was observed in 32% of patients and frequently preceded abnormalities in conventional systolic indices, which remained preserved in 58% of these cases. RV-GLS correlated with FEV₁, NT-proBNP, and 6MWT distance. During follow-up, 27% of patients experienced the primary endpoint. Impaired RV-GLS conferred a 3.4-fold increased risk of adverse outcomes (HR 3.4; 95% CI 1.8–6.2; p<0.001) and remained independently predictive after adjustment for pulmonary severity and standard echocardiographic measures. Conclusions Right ventricular myocardial deformation emerges as a central prognostic axis in COPD. RV-GLS detects early cardiac maladaptation invisible to conventional indices and independently stratifies risk. These findings challenge the lung-centric paradigm, positioning the right ventricle as the principal determinant of outcome. COPD should be reconceptualized as a cardiopulmonary syndrome in which right ventricular dysfunction ultimately dictates clinical trajectory.
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Noniashvili et al. (2026) conducted a cohort in Stable COPD (GOLD II-IV) (n=146). Impaired right ventricular global longitudinal strain (RV-GLS >-18%) vs. Preserved RV-GLS (≤-18%) was evaluated on Composite of severe exacerbation, COPD-related hospitalization, or major cardiovascular event (HR 3.4, 95% CI 1.8-6.2, p=<0.001). Impaired right ventricular global longitudinal strain (>−18%) in COPD conferred a 3.4-fold increased risk of adverse cardiopulmonary outcomes (HR 3.4; 95% CI 1.8–6.2; p<0.001).
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