Clinical characteristics associated with small airways disease in systemic sclerosis.

Sanskriti Varma, Jae Hee Yun, John S Kim, Anna J Podolanczuk, Nina M Patel, Elana J Bernstein
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Abstract

Objective: Pulmonary manifestations of systemic sclerosis are a major cause of morbidity and mortality. Small airways disease can cause dyspnea and pulmonary function test abnormalities. We aimed to determine the prevalence of small airways disease and describe the characteristics associated with small airways disease in a cohort of systemic sclerosis patients.

Methods: We performed a retrospective cohort study of adults with systemic sclerosis who met American College of Rheumatology/European League Against Rheumatism 2013 classification criteria and were evaluated at our institution between November 2000 and November 2015. Patients with prior lung transplantation were excluded. Small airways disease was defined as the presence of one or more of the following: airway-centered fibrosis on surgical lung biopsy, forced expiratory volume at 25-75% ⩽ 50% on pulmonary function tests, and/or high-resolution computed tomography scan of the chest with bronchiolitis, mosaic attenuation, or air trapping on expiratory views. The primary outcome was small airways disease diagnosis. We performed multivariable logistic regression to determine the association of clinical variables with small airways disease.

Results: One-hundred thirty-six systemic sclerosis patients were included; 55 (40%) had small airways disease. Compared to those without small airways disease, a significantly greater proportion of those with small airways disease had interstitial lung disease, chronic obstructive pulmonary disease, pulmonary hypertension, and gastroesophageal reflux disease. On multivariable analysis, pulmonary hypertension (odds ratio = 2.91, 95% confidence interval = 1.11-7.65, p-value = 0.03), gastroesophageal reflux disease (odds ratio = 2.70, 95% confidence interval = 1.08-6.79, p-value = 0.034), and anti-topoisomerase I (anti-Scl-70) antibody positivity (odds ratio = 0.42, 95% confidence interval = 0.19-0.93, p-value = 0.033) were associated with diagnosis of small airways disease.

Conclusion: Small airways disease is prevalent among systemic sclerosis patients; those with pulmonary hypertension or gastroesophageal reflux disease may have a higher risk of small airways disease.

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系统性硬化症小气道病变的临床特征
目的:系统性硬化症的肺部表现是发病和死亡的主要原因。小气道疾病可引起呼吸困难和肺功能检查异常。我们旨在确定系统性硬化症患者中小气道疾病的患病率,并描述与小气道疾病相关的特征。方法:我们对符合美国风湿病学会/欧洲抗风湿病联盟2013年分类标准的成人系统性硬化症患者进行了回顾性队列研究,并于2000年11月至2015年11月在我们的机构进行了评估。排除既往有肺移植史的患者。小气道疾病被定义为存在以下一种或多种情况:手术肺活检显示气道中心纤维化,肺功能检查显示用力呼气体积在25-75%≤50%,和/或高分辨率胸部计算机断层扫描显示有细支气管炎、马赛克衰减或呼气视图显示空气困住。主要转归是小气道疾病的诊断。我们采用多变量逻辑回归来确定临床变量与小气道疾病的关系。结果:纳入136例系统性硬化症患者;55例(40%)有小气道疾病。与没有小气道疾病的患者相比,小气道疾病患者发生间质性肺疾病、慢性阻塞性肺疾病、肺动脉高压和胃食管反流疾病的比例明显更高。在多变量分析中,肺动脉高压(优势比= 2.91,95%可信区间= 1.11-7.65,p值= 0.03)、胃食管反流病(优势比= 2.70,95%可信区间= 1.08-6.79,p值= 0.034)、抗拓扑异构酶I(抗scl -70)抗体阳性(优势比= 0.42,95%可信区间= 0.19-0.93,p值= 0.033)与小气道疾病的诊断相关。结论:小气道病变在系统性硬化症患者中普遍存在;那些患有肺动脉高压或胃食管反流疾病的人可能有更高的小气道疾病风险。
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CiteScore
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0.00%
发文量
31
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