University Hospital Zurich, Zurich, Switzerland, and Assiut University Hospital, Assiut, Egypt.
University Hospital Zurich, Zurich, Switzerland, and Dr. I. Cantacuzino Hospital and Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
Arthritis Rheumatol. 2015 Dec;67(12):3256-61. doi: 10.1002/art.39405.
Validated methods for the screening and early diagnosis of systemic sclerosis (SSc; scleroderma)-related interstitial lung disease (ILD) are needed. The aim of this study was to evaluate the performance of pulmonary function tests (PFTs) compared with that of high-resolution computed tomography (HRCT) of the chest for the detection of SSc-related ILD in clinical practice, and to identify predictors of lung involvement that is functionally occult but significant on HRCT.
Prospectively enrolled patients with SSc were assessed according to the European League Against Rheumatism (EULAR)/EULAR Scleroderma Trial and Research standards. The assessment included PFTs and HRCT. The HRCT images were evaluated in a blinded manner by 2 experienced radiologists. The performance parameters of PFTs for the diagnosis of SSc-related ILD were calculated. Predictors of significant ILD as determined by HRCT in patients with normal forced vital capacity (FVC) values were identified through logistic regression.
Among the 102 patients, 64 (63.0%) showed significant ILD on HRCT, while only 27 (26.0%) had an FVC <80% of predicted, and 54 (53.0%) had a decrease in the results of at least 1 PFT. Forty (62.5%) of 64 patients with significant ILD on HRCT had a normal FVC value, translating into a high false-negative rate. Notably, 5 of 40 patients with a normal FVC value had severe, functionally occult lung fibrosis; in 2 of these patients, the results of all of the PFTs were within normal limits. Patients with normal FVC values despite evidence of fibrosis on HRCT more frequently had anti-Scl-70 antibodies and diffuse SSc and less frequently had anticentromere antibodies (ACAs) compared with patients with both normal FVC values and normal HRCT results.
The derived evidence-based data reveal a high risk of missing significant SSc-related ILD when relying solely on PFTs. More comprehensive screening algorithms for early detection are warranted. In particular, additional imaging investigations for the early detection of SSc-related ILD should be considered in ACA-negative patients with normal FVC values.
需要验证用于筛查和早期诊断系统性硬化症(SSc;硬皮病)相关间质性肺病(ILD)的方法。本研究旨在评估肺功能检查(PFTs)与胸部高分辨率计算机断层扫描(HRCT)在临床实践中检测 SSc 相关 ILD 的性能,并确定在 HRCT 上功能隐匿但显著的肺受累的预测因子。
根据欧洲抗风湿病联盟(EULAR)/EULAR 硬皮病试验和研究标准,前瞻性评估 SSc 患者。评估包括 PFTs 和 HRCT。由 2 名经验丰富的放射科医生对 HRCT 图像进行盲法评估。计算 PFTs 对 SSc 相关 ILD 的诊断性能参数。通过逻辑回归确定在 FVC 值正常的患者中,由 HRCT 确定的有意义的 ILD 的预测因子。
在 102 例患者中,64 例(63.0%)HRCT 显示有显著的 ILD,而仅有 27 例(26.0%)FVC<预计值的 80%,54 例(53.0%)至少有 1 项 PFT 结果下降。64 例 HRCT 显示有显著 ILD 的患者中有 40 例(62.5%)FVC 值正常,这导致了高假阴性率。值得注意的是,40 例 FVC 值正常的患者中有 5 例有严重的、功能隐匿性肺纤维化;其中 2 例患者的所有 PFT 结果均在正常范围内。与 FVC 值正常且 HRCT 结果正常的患者相比,尽管 HRCT 显示有纤维化,但 FVC 值正常的患者更常具有抗 Scl-70 抗体和弥漫性 SSc,而较少具有抗着丝点抗体(ACA)。
这些基于证据的数据揭示了仅依靠 PFTs 时,漏诊严重 SSc 相关 ILD 的风险很高。需要制定更全面的早期检测筛查算法。特别是,在 FVC 值正常且 ACA 阴性的患者中,应考虑额外的影像学检查以早期发现 SSc 相关 ILD。