TY - JOUR
T1 - Association Between Pulmonary Vascular Volume and Cardiac Structure and Function in Patients With Atrial Fibrillation
AU - Nielsen, Anne Bjerg
AU - Skaarup, Kristoffer Grundtvig
AU - Djernæs, Kasper
AU - Duus, Lisa Steen
AU - Espersen, Caroline
AU - Sørensen, Samuel Kiil
AU - Ruwald, Martin Huth
AU - Hansen, Morten Lock
AU - Worck, René Husted
AU - Johannessen, Arne
AU - Hansen, Jim
AU - Nardelli, Pietro
AU - San José Estépar, Rubén
AU - San José Estépar, Raúl
AU - Biering-Sørensen, Tor
N1 - Publisher Copyright:
© 2023 The Author(s)
PY - 2023/10/15
Y1 - 2023/10/15
N2 - Pulmonary vascular abnormalities, quantified from computed tomography scans, have frequently been observed in patients with pulmonary diseases. However, little is known about pulmonary vascular changes in patients with cardiac disease. Thus, we aimed to examine the cardiopulmonary relation in patients with atrial fibrillation (AF) by comparing pulmonary vascular volume (PVV) to echocardiographic measures and AF severity. A total of 742 patients (median age 63 years, 70% men) who underwent ablation for AF were included. Preprocedural cardiac computed tomography was used to measure the total and small-vessel PVV, along with the pulmonary artery to aorta ratio and the degree of emphysema. The association between PVV and echocardiographic parameters was evaluated using a multivariable linear regression analysis. Lower total and small-vessel PVV were associated with more impaired measures of cardiac structure and function, including but not limited to left ventricular ejection fraction and peak atrial longitudinal strain. Patients with reduced total and small-vessel PVV had higher odds of having persistent AF than paroxysmal AF in the unadjusted logistic regression analyses. However, after clinical and echocardiographic adjustments, only reduced small-vessel PVV remained independently associated with persistent AF (odds ratio 1.90, 95% confidence interval 1.26 to 2.87, p = 0.002). In conclusion, pulmonary vascular remodeling is associated with persistent AF and with more impaired measures of cardiac structure and function, providing further insights into heart-lung interactions in this patient group.
AB - Pulmonary vascular abnormalities, quantified from computed tomography scans, have frequently been observed in patients with pulmonary diseases. However, little is known about pulmonary vascular changes in patients with cardiac disease. Thus, we aimed to examine the cardiopulmonary relation in patients with atrial fibrillation (AF) by comparing pulmonary vascular volume (PVV) to echocardiographic measures and AF severity. A total of 742 patients (median age 63 years, 70% men) who underwent ablation for AF were included. Preprocedural cardiac computed tomography was used to measure the total and small-vessel PVV, along with the pulmonary artery to aorta ratio and the degree of emphysema. The association between PVV and echocardiographic parameters was evaluated using a multivariable linear regression analysis. Lower total and small-vessel PVV were associated with more impaired measures of cardiac structure and function, including but not limited to left ventricular ejection fraction and peak atrial longitudinal strain. Patients with reduced total and small-vessel PVV had higher odds of having persistent AF than paroxysmal AF in the unadjusted logistic regression analyses. However, after clinical and echocardiographic adjustments, only reduced small-vessel PVV remained independently associated with persistent AF (odds ratio 1.90, 95% confidence interval 1.26 to 2.87, p = 0.002). In conclusion, pulmonary vascular remodeling is associated with persistent AF and with more impaired measures of cardiac structure and function, providing further insights into heart-lung interactions in this patient group.
KW - atrial fibrillation
KW - computed tomography
KW - pulmonary vascular volume
KW - transthoracic echocardiography
UR - http://www.scopus.com/inward/record.url?scp=85168525692&partnerID=8YFLogxK
U2 - 10.1016/j.amjcard.2023.07.119
DO - 10.1016/j.amjcard.2023.07.119
M3 - Journal article
C2 - 37604065
AN - SCOPUS:85168525692
SN - 0002-9149
VL - 205
SP - 182
EP - 189
JO - American Journal of Cardiology
JF - American Journal of Cardiology
ER -