Department of Respiratory and Critical Care Medicine, Peking University First Hospital, Beijing, China.
Department of Nephrology, Peking University First Hospital, Beijing, China.
Respiration. 2023;102(4):257-273. doi: 10.1159/000529085. Epub 2023 Jan 24.
Interstitial lung disease (ILD) is a common pulmonary manifestation of antineutrophil cytoplasmic antibody-associated vasculitis (AAV).
We aimed to clarify the clinical predictors of mortality in a cohort of patients with AAV-related ILD (AAV-ILD).
We retrospectively identified AAV-ILD patients seen at Peking University First Hospital from January 2010 to June 2020 and manually screened for study inclusion. Baseline computed tomography (CT) images were further classified as nonspecific interstitial pneumonia (NSIP), usual interstitial pneumonia (UIP), organizing pneumonia (OP), and unclassified ILD. Disease characteristics and other pulmonary findings including pulmonary function test and bronchoalveolar lavage (BAL) were also evaluated. Multivariable Cox regression analysis was performed to identify clinical predictors of mortality.
The cohort included 204 patients with AAV-ILD, 152 had UIP on CT (AAV-UIP), 39 had NSIP on CT (AAV-NSIP), 3 had OP, and 10 had unclassified ILD. Microscopic polyangiitis was more prevalent in patients with UIP, while granulomatosis with polyangiitis was more common in the NSIP and OP groups, and eosinophilic granulomatosis with polyangiitis was more frequent in patients with unclassified ILD. ILD diagnosis before AAV was more common in patients with either UIP or NSIP patterns. During the median follow-up of 40 months, 44 (21.6%) patients died. One- and 5-year overall survival rates were 88.2% (95% CI, 83.7-92.7%) and 81.0% (95% CI, 74.9-87.1%) for the entire cohort. Patients with UIP patterns had the worst prognosis, while those with NSIP patterns had the best long-term outcome. Specifically, patients with UIP patterns had an approximately 5-fold risk of death compared to those with NSIP. After controlling for potential confounding factors, we observed that each 10% increase in the BAL fluid neutrophil percentage was associated with nearly a 20% increased risk of death (HR 1.195, 95% CI 1.018-1.404).
Clinical characteristics and survival differ between subgroups defined by CT patterns. BAL fluid neutrophilia is an independent predictor of mortality among AAV-ILD patients, and therefore, the clinical utility of BAL at the time of AAV diagnosis should be considered.
间质性肺疾病(ILD)是抗中性粒细胞胞质抗体相关性血管炎(AAV)的常见肺部表现。
我们旨在明确抗中性粒细胞胞质抗体相关性血管炎相关间质性肺病(AAV-ILD)患者队列的死亡率预测因素。
我们回顾性地确定了 2010 年 1 月至 2020 年 6 月期间在北京大学第一医院就诊的 AAV-ILD 患者,并进行了手工筛选以纳入研究。进一步将基线计算机断层扫描(CT)图像分类为非特异性间质性肺炎(NSIP)、寻常间质性肺炎(UIP)、机化性肺炎(OP)和未分类的 ILD。还评估了疾病特征和其他肺部发现,包括肺功能检查和支气管肺泡灌洗(BAL)。采用多变量 Cox 回归分析确定死亡率的预测因素。
该队列包括 204 例 AAV-ILD 患者,其中 152 例 CT 表现为 UIP(AAV-UIP),39 例 CT 表现为 NSIP(AAV-NSIP),3 例表现为 OP,10 例表现为未分类的 ILD。UIP 患者中显微镜下多血管炎更为常见,而 NSIP 和 OP 组中肉芽肿性多血管炎更为常见,未分类的 ILD 患者中嗜酸性肉芽肿性多血管炎更为常见。ILD 在 AAV 之前的诊断在 UIP 或 NSIP 模式的患者中更为常见。在中位随访 40 个月期间,44(21.6%)例患者死亡。整个队列的 1 年和 5 年总生存率分别为 88.2%(95%CI,83.7%-92.7%)和 81.0%(95%CI,74.9%-87.1%)。UIP 模式患者的预后最差,而 NSIP 模式患者的长期预后最好。具体而言,UIP 模式患者的死亡风险约为 NSIP 模式患者的 5 倍。在控制潜在混杂因素后,我们发现 BAL 液中性粒细胞百分比每增加 10%,死亡风险增加近 20%(HR 1.195,95%CI 1.018-1.404)。
根据 CT 模式定义的亚组之间存在临床特征和生存差异。BAL 液中性粒细胞增多是 AAV-ILD 患者死亡的独立预测因素,因此应考虑在 AAV 诊断时进行 BAL 的临床应用。