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特发性肺纤维化患者运动时的肺血管反应模式。

Pulmonary vascular response patterns during exercise in interstitial lung disease.

机构信息

Respiratory Division, Paulista School of Medicine, Federal University of São Paulo, São Paulo, Brazil Pulmonary and Critical Care Unit, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.

Pulmonary and Critical Care Unit, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.

出版信息

Eur Respir J. 2015 Sep;46(3):738-49. doi: 10.1183/09031936.00191014. Epub 2015 May 14.

Abstract

When overt pulmonary hypertension arises in interstitial lung disease (ILD), it contributes to exercise intolerance. We sought to determine the functional significance of abnormal pulmonary arterial pressure (PAP) responses to exercise in ILD.27 ILD patients and 11 age-matched controls underwent invasive cardiopulmonary exercise testing (iCPET). Mean PAP (mPAP) was indexed to cardiac output (Q'T) during exercise, with a mPAP-Q'T slope ≥3 mmHg·min·L(-1) defined as an abnormal pulmonary vascular response.All control subjects had mPAP-Q'T slopes <3 mmHg·min·L(-1) (mean±sem 1.5±0.1 mmHg·min·L(-1)). 15 ILD patients had mPAP-Q'T slopes ≥3 mmHg·min·L(-1) (4.1±0.2 mmHg·min·L(-1)) and were labelled as having ILD plus pulmonary vascular dysfunction (PVD). Subjects without pulmonary hypertension and with mPAP-Q´T slopes <3 mmHg·min·L(-1) (1.9±0. 2 mmHg·min·L(-1)) were labelled as ILD minus PVD (n=12). ILD+PVD and ILD-PVD patients did not differ in terms of age, sex, body mass index, pulmonary function testing or degree of exercise oxygen desaturation. Peak oxygen consumption was lower in ILD+PVD than in ILD-PVD (13.0±0.9 versus 17±1.1 mL·kg(-1)·min(-1), p=0.012) and controls (19.8±1.7 mL·kg(-1)·min(-1), p=0.003). ILD+PVD patients had increased dead space volume (VD)/tidal volume (VT) and minute ventilation/carbon dioxide production at the anaerobic threshold.In ILD, mPAP-Q'T slope ≥3 mmHg·min·L(-1) is associated with lower peak oxygen consumption, increased VD/VT and inefficient ventilation. While noninvasive parameters were unable to predict those with abnormal pulmonary vascular responses to exercise, iCPET-derived mPAP-Q'T slope may aid in identifying physiologically significant, early pulmonary vascular disease in ILD.

摘要

当特发性肺纤维化(ILD)出现显性肺动脉高压时,会导致运动不耐受。我们旨在确定ILD 患者运动时肺动脉压(PAP)异常反应的功能意义。27 例ILD 患者和 11 名年龄匹配的对照者接受了有创心肺运动测试(iCPET)。运动时以心输出量(Q'T)为指标对平均 PAP(mPAP)进行指数化,mPAP-Q'T 斜率≥3mmHg·min·L(-1)定义为肺血管反应异常。所有对照者的 mPAP-Q'T 斜率均<3mmHg·min·L(-1)(均值±SEM 1.5±0.1mmHg·min·L(-1))。15 例ILD 患者的 mPAP-Q'T 斜率≥3mmHg·min·L(-1)(4.1±0.2mmHg·min·L(-1)),被标记为患有ILD 合并肺血管功能障碍(PVD)。无肺动脉高压且 mPAP-Q´T 斜率<3mmHg·min·L(-1)(1.9±0.2mmHg·min·L(-1))的患者被标记为ILD 合并 PVD(n=12)。ILD+PVD 和ILD-PVD 患者在年龄、性别、体重指数、肺功能检查或运动时氧饱和度下降程度方面无差异。ILD+PVD 患者的峰值摄氧量低于 ILD-PVD(13.0±0.9 与 17±1.1mL·kg(-1)·min(-1),p=0.012)和对照组(19.8±1.7mL·kg(-1)·min(-1),p=0.003)。ILD+PVD 患者在无氧阈时的死腔量(VD)/潮气量(VT)和分钟通气量/二氧化碳产量增加。在 ILD 中,mPAP-Q'T 斜率≥3mmHg·min·L(-1)与峰值摄氧量降低、VD/VT 增加和通气效率降低相关。虽然无创参数无法预测运动时肺动脉压异常反应的患者,但 iCPET 衍生的 mPAP-Q'T 斜率可能有助于识别ILD 中具有生理意义的早期肺血管疾病。

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