Department of Radiology, University of Washington, 1959 NE Pacific St, Box 357115, Seattle, WA, 98195, USA.
Center for Interstitial Lung Diseases, Department of Medicine, University of Washington, Seattle, WA, USA.
Eur Radiol. 2023 Jul;33(7):4746-4757. doi: 10.1007/s00330-023-09439-w. Epub 2023 Feb 14.
Interstitial lung disease (ILD) impacts mortality in antisynthetase syndrome (ASyS). Computed tomographic (CT) patterns and evolution in ASyS ILD are not well described. We report longitudinal CT patterns in ASyS-ILD and their impact on survival.
This is a monocentric retrospective study of 47 patients with ASyS-ILD. Longitudinal CT patterns and fibrosis severity (severity of radiographic features indicating fibrosis) were analyzed by two radiologists in consensus. The association between imaging features and survival was examined using univariate Cox regression analysis.
In total, 211 CT scans were analyzed with an average of 4 ± 2 CT scans/patient with a median follow-up of 79 months in 47 patients. Non-fibrotic patterns were present initially in 63.8% (n = 30) of patients, while fibrotic patterns occurred in 36.2% (n = 17). The initial non-fibrotic patterns/abnormalities resolved in 23.3% (n = 7), evolved in 6.7% (n = 2), persisted in 13.3% (n = 4), and progressed in 56.7% (n = 17), while initial fibrotic patterns persisted in 82.4% (n = 14) and progressed in 17.6% (n = 3). Radiographic progression of ILD (progression in CT pattern or increased fibrosis severity) occurred in 53.2% (n = 25) of patients. Advanced age and radiographic progression were associated with decreased survival (all p < 0.05). The presence of ground-glass opacities (GGO) and predominant lower lung distribution of abnormalities on initial CTs were associated with increased survival (all p < 0.05).
Progression occurred in 56.7% of ASyS-ILD patients presenting with non-fibrotic patterns. Fibrotic patterns tended to persist. Age and radiographic progression were associated with reduced survival while the initial presence of GGO and predominant lower lobe distribution were associated with increased survival.
• In ASyS-ILD, initial non-fibrotic patterns such as OP, cNSIP, or OP-cNSIP tended to progress to fNSIP. • Fibrotic patterns such as fNSIP or UIP in ASyS-ILD tended to persist without pattern changes. • GGO and lower lung predominance on initial CT were associated with better survival while advanced baseline age and radiographic ILD progression during follow-up were associated with decreased survival.
间质性肺病(ILD)会影响抗合成酶综合征(ASyS)患者的死亡率。ASyS 患者的 CT 表现和演变尚不清楚。我们报告 ASyS-ILD 的纵向 CT 表现及其对生存的影响。
这是一项单中心回顾性研究,纳入了 47 例 ASyS-ILD 患者。两位放射科医生通过共识分析了纵向 CT 模式和纤维化严重程度(指示纤维化的放射特征严重程度)。使用单因素 Cox 回归分析评估影像学特征与生存之间的关系。
共分析了 211 次 CT 扫描,每位患者平均进行 4±2 次 CT 扫描,47 例患者的中位随访时间为 79 个月。63.8%(n=30)的患者最初表现为非纤维化模式,36.2%(n=17)的患者表现为纤维化模式。23.3%(n=7)的初始非纤维化模式/异常消失,6.7%(n=2)的模式进展,13.3%(n=4)的模式持续存在,56.7%(n=17)的模式进展,而初始纤维化模式持续存在于 82.4%(n=14)的患者中,进展于 17.6%(n=3)的患者中。ILD 的影像学进展(CT 模式进展或纤维化严重程度增加)发生在 53.2%(n=25)的患者中。高龄和影像学进展与生存率降低相关(均 p<0.05)。初始 CT 上存在磨玻璃影(GGO)和异常主要分布于下肺与生存率增加相关(均 p<0.05)。
56.7%的 ASyS-ILD 患者出现非纤维化表现,进展为纤维化。纤维化模式倾向于持续存在。年龄和影像学进展与生存率降低相关,而初始 GGO 和主要分布于下叶与生存率增加相关。