Department of Cardiology, Oslo University Hospital, Oslo, Norway.
Department of Pulmonary Medicine, Oslo University Hospital, Oslo, Norway.
J Am Coll Cardiol. 2013 Sep 17;62(12):1103-1111. doi: 10.1016/j.jacc.2013.04.091. Epub 2013 Jul 10.
The aim of the present study was to elucidate right ventricular (RV) function and structure in patients with chronic obstructive pulmonary disease (COPD) without pulmonary hypertension (PH).
There is little knowledge of RV function and remodeling in COPD without PH.
Thirty-four controls and 98 patients with COPD were included. The study patients were divided into 2 groups by right heart catheterization: no PH (mean pulmonary artery pressure [mPAP] <25 mm Hg) and PH (mPAP ≥25 mm Hg). The echocardiographic tissue Doppler imaging variables of RV isovolumic acceleration, peak systolic strain, and RV myocardial performance index were measured at the basal free wall, and RV wall thickness and RV internal dimension were measured in the RV outflow tract.
The increases in RV wall thickness and RV dimension were more evident when comparing controls with the no PH group (3.5 ± 0.5 mm to 5.5 ± 1.0 mm [p < 0.01] and 1.5 cm ± 0.2 to 2.0 ± 0.5 cm [p < 0.01]) than comparing the no PH group with the PH group (5.5 ± 1.0 mm to 6.6 ± 1.1 mm [p < 0.01] and 2.0 cm ± 0.5 to 2.1 ± 0.3 cm [p = NS]), respectively. Similarly, RV isovolumic acceleration, performance index, and strain deteriorated significantly when comparing controls with the no PH group and comparing the no PH group with the PH group (p < 0.01). Significant correlations were observed between mPAP and RV isovolumic acceleration, performance index, strain, and RV wall thickness (p < 0.01). RV impairment and increased RV wall thickness and RV dimensions were present even at slight elevations of mPAP (18 ± 3 mm Hg) in the no PH group.
The present study showed that impaired RV systolic function, hypertrophy, and dilation were present even at a slight increase of mPAP, which indicates an early impact on RV function and structure in patients with COPD. RV isovolumic acceleration, performance index, and strain could detect subclinical disease and separate controls from those with no PH.
本研究旨在阐明无肺动脉高压(PH)的慢性阻塞性肺疾病(COPD)患者的右心室(RV)功能和结构。
对于无 PH 的 COPD 患者的 RV 功能和重塑,人们知之甚少。
纳入 34 名对照者和 98 名 COPD 患者。根据右心导管检查结果,将研究患者分为两组:无 PH(平均肺动脉压 [mPAP] <25mmHg)和 PH(mPAP ≥25mmHg)。在基底游离壁测量 RV 等容加速、收缩期峰值应变和 RV 心肌运动指数的组织多普勒成像变量,并在 RV 流出道测量 RV 壁厚度和 RV 内径。
与无 PH 组相比,对照组 RV 壁厚度和 RV 内径的增加更为明显(3.5 ± 0.5mm 至 5.5 ± 1.0mm [p<0.01]和 1.5cm ± 0.2cm 至 2.0 ± 0.5cm [p<0.01]),而与 PH 组相比,无 PH 组的增加更为明显(5.5 ± 1.0mm 至 6.6 ± 1.1mm [p<0.01]和 2.0cm ± 0.5cm 至 2.1 ± 0.3cm [p=NS])。同样,与对照组相比,与无 PH 组相比,RV 等容加速、性能指数和应变显著恶化(p<0.01)。mPAP 与 RV 等容加速、性能指数、应变和 RV 壁厚度呈显著相关(p<0.01)。即使在无 PH 组 mPAP 轻度升高(18 ± 3mmHg)时,也存在 RV 收缩功能障碍、RV 肥厚和扩张。
本研究表明,即使 mPAP 略有升高,也存在 RV 收缩功能障碍、心肌肥厚和扩张,这表明 COPD 患者的 RV 功能和结构很早就受到影响。RV 等容加速、性能指数和应变可以检测亚临床疾病,并将对照者与无 PH 者区分开来。