Division of Rheumatology, Columbia University Irving Medical Center, New York, NY.
Division of Pulmonary and Critical Care, Johns Hopkins University, Baltimore, MD.
Rheumatology (Oxford). 2022 Jul 6;61(7):2792-2804. doi: 10.1093/rheumatology/keab828.
To assess predictors of subclinical RA-associated interstitial lung disease (RA-ILD) using quantitative lung densitometry (qLD).
RA patients underwent multi-detector row CT scanning at baseline and after an average of 39 months. Scans were analysed with qLD for the percentage of lung parenchyma with high attenuation areas (%HAA: the percentage of voxels of -600 to -250 Hounsfield units). Additionally, a pulmonary radiologist calculated an expert radiologist scoring (ERS) for RA-ILD features. Generalized linear models were used to identify indicators of baseline %HAA and predictors of %HAA change.
Baseline %HAA was assessed in 193 RA patients and 106 had repeat qLD assessment. %HAA was correlated with ERS (Spearman's rho = 0.261; P < 0.001). Significant indicators of high baseline %HAA (>10% of lung parenchyma with high attenuation) included female sex, higher pack-years of smoking, higher BMI and anti-CCP ≥200 units, collectively contributing an area under the receiver operator curve of 0.88 (95% CI 0.81, 0.95). Predictors of %HAA increase, occurring in 49% with repeat qLD, included higher baseline %HAA, presence of mucin 5B (MUC5B) minor allele and absence of HLA-DRB1 shared epitope (area under the receiver operator curve = 0.69; 95% CI 0.58, 0.79). The association of the MUC5B minor allele with %HAA change was higher among men and those with higher cumulative smoking. Within the group with increased %HAA, anti-CCP level was significantly associated with a greater increase in %HAA.
%HAA, assessed with qLD, was linked to several known risk factors for RA-ILD and may represent a more quantitative method to identify RA-ILD and track progression than expert radiologist interpretation.
使用定量肺密度(qLD)评估亚临床类风湿关节炎相关间质性肺病(RA-ILD)的预测因子。
RA 患者在基线和平均 39 个月后进行多排 CT 扫描。使用 qLD 分析肺实质高衰减区的百分比(%HAA:-600 至-250 亨氏单位的体素百分比)。此外,一名肺部放射科医生计算了 RA-ILD 特征的专家放射学评分(ERS)。使用广义线性模型确定基线 %HAA 的指标和 %HAA 变化的预测因子。
评估了 193 例 RA 患者的基线 %HAA,其中 106 例进行了重复 qLD 评估。%HAA 与 ERS 呈正相关(Spearman rho=0.261;P<0.001)。基线 %HAA 较高(>10%的肺实质存在高衰减)的显著指标包括女性、吸烟包年数较高、BMI 较高和抗 CCP≥200 单位,联合贡献了 0.88(95%CI 0.81,0.95)的接收器操作特征曲线下面积。重复 qLD 检查时出现 49%的 %HAA 增加的预测因子包括较高的基线 %HAA、MUC5B 次要等位基因的存在和 HLA-DRB1 共享表位的缺失(接收器操作特征曲线下面积=0.69;95%CI 0.58,0.79)。在 %HAA 增加的患者中,MUC5B 次要等位基因与 %HAA 变化的相关性在男性和累积吸烟量较高的患者中更高。在 %HAA 增加的患者中,抗 CCP 水平与 %HAA 增加显著相关。
qLD 评估的 %HAA 与 RA-ILD 的几个已知危险因素相关,可能代表一种比专家放射学解释更定量的方法来识别 RA-ILD 并跟踪其进展。