Overbury Rebecca S, Murtaugh Maureen A, Frech Tracy M, Steen Virginia D
Division of Rheumatology, Department of Internal Medicine, The University of Utah, Salt Lake City, UT, USA.
George E. Wahlen Department of Veterans Affairs Medical Center, Salt Lake City, UT, USA.
J Scleroderma Relat Disord. 2018 Oct;3(3):237-241. doi: 10.1177/2397198318778818. Epub 2018 Jun 1.
Our purpose was to determine the frequency of normal diffusing capacity for carbon monoxide defined as ⩾70% predicted, in those diagnosed with pulmonary arterial hypertension in the Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma cohort. We compared those with normal diffusing capacity for carbon monoxide to those with reduced diffusing capacity for carbon monoxide <70% in order to better clarify the role of pulmonary function testing as a screening test for pulmonary arterial hypertension and to better understand this population.
Entry criteria included a right heart catheterization with mean pulmonary artery pressure ⩾25 mm Hg and pulmonary capillary wedge pressure ⩽15 mm Hg. Demographics, echocardiogram variables, B-type natriuretic peptide levels, right heart catheterization findings, and survival were described for both groups.
Of (n = 202), 11 (5.4%) had a diffusing capacity for carbon monoxide of ⩾70% versus 191 (94.6%) who had a diffusing capacity for carbon monoxide <70%. There were no identified statistical differences between the groups. Left atrium size was 4.1 cm in the normal diffusing capacity for carbon monoxide patients compared to 3.7 cm in the low diffusing capacity for carbon monoxide group but did not reach statistical significance. There were no statistically significant differences in survival. On repeat testing, seven patients subsequently developed a diffusing capacity for carbon monoxide <70%.
Pulmonary Hypertension Assessment and Recognition of Outcomes in Scleroderma data suggest that it is very rare for a patient to develop pulmonary arterial hypertension with a preserved diffusing capacity for carbon monoxide. The data support the importance of obtaining diffusing capacity for carbon monoxide and that a patient with a normal diffusing capacity for carbon monoxide while suspected to have systemic sclerosis-pulmonary arterial hypertension should be considered critically. Diffusing capacity for carbon monoxide >70% was present in too few patients to find significant differences in B-type natriuretic peptide and atrium size. Future research should seek to confirm abnormal B-type natriuretic peptide, increased left atrium size, and other evidence of myocardial involvement on diffusing capacity for carbon monoxide.
我们的目的是确定在硬皮病队列中肺动脉高压评估与结局识别研究中,一氧化碳弥散能力正常(定义为预测值的⩾70%)在被诊断为肺动脉高压患者中的频率。我们将一氧化碳弥散能力正常的患者与一氧化碳弥散能力降低(<70%)的患者进行比较,以便更好地阐明肺功能测试作为肺动脉高压筛查试验的作用,并更好地了解这一人群。
纳入标准包括右心导管检查,平均肺动脉压⩾25 mmHg且肺毛细血管楔压⩽15 mmHg。描述了两组患者的人口统计学特征、超声心动图变量、B型利钠肽水平、右心导管检查结果和生存率。
在(n = 202)例患者中,11例(5.4%)一氧化碳弥散能力⩾70%,而191例(94.6%)一氧化碳弥散能力<70%。两组之间未发现统计学差异。一氧化碳弥散能力正常组患者的左心房大小为4.1 cm,而一氧化碳弥散能力低的组为3.7 cm,但未达到统计学意义。生存率无统计学显著差异。在重复检测时,7例患者随后一氧化碳弥散能力降至<70%。
硬皮病队列中肺动脉高压评估与结局识别研究的数据表明,一氧化碳弥散能力保留的患者发生肺动脉高压非常罕见。这些数据支持获取一氧化碳弥散能力的重要性,对于疑似患有系统性硬化症相关肺动脉高压但一氧化碳弥散能力正常的患者应进行严格评估。一氧化碳弥散能力>70%的患者太少,无法在B型利钠肽和心房大小方面发现显著差异。未来的研究应寻求证实B型利钠肽异常、左心房增大以及其他心肌受累对一氧化碳弥散能力影响的证据。