Chaudhary Muhammad F A, Awan Hira A, Gerard Sarah E, Bodduluri Sandeep, Comellas Alejandro P, Barjaktarevic Igor, Barr R Graham, Cooper Christopher B, Galban Craig J, Han MeiLan, Curtis Jeffrey L, Hansel Nadia N, Krishnan Jerry A, Menchaca Martha G, Martinez Fernando J, Ohar Jill, Vargas Buonfiglio Luis G, Paine Robert, Bhatt Surya P, Hoffman Eric A, Reinhardt Joseph M
The University of Iowa, Iowa City, Iowa, United States.
The University of Iowa, The Roy J. Carver Department of Biomedical Engineering, Iowa City, Iowa, United States.
Am J Respir Crit Care Med. 2025 Mar 12. doi: 10.1164/rccm.202409-1847OC.
Quantifying functional small airways disease (fSAD) requires additional expiratory computed tomography (CT) scan, limiting clinical applicability. Artificial intelligence (AI) could enable fSAD quantification from chest CT scan at total lung capacity (TLC) alone (fSAD).
To evaluate an AI model for estimating fSAD, compare it with dual-volume parametric response mapping fSAD (fSAD), and assess its clinical associations and repeatability in chronic obstructive pulmonary disease (COPD).
We analyzed 2513 participants from the SubPopulations and InteRmediate Outcome Measures in COPD Study (SPIROMICS). Using a randomly sampled subset ( = 1055), we developed a generative model to produce virtual expiratory CTs for estimating fSAD in the remaining 1458 SPIROMICS participants. We compared fSAD with dual volume, parametric response mapping fSAD. We investigated univariate and multivariable associations of fSAD with FEV, FEV/FVC, six-minute walk distance (6MWD), St. George's Respiratory Questionnaire (SGRQ), and FEV decline. The results were validated in a subset ( = 458) from COPDGene study. Multivariable models were adjusted for age, race, sex, BMI, baseline FEV, smoking pack years, smoking status, and percent emphysema.
Inspiratory fSAD showed a strong correlation with fSAD in both SPIROMICS (Pearson's R = 0.895) and COPDGene (R = 0.897) cohorts. Higher fSAD levels were significantly associated with lower lung function, including lower postbronchodilator FEV (L) and FEV/FVC ratio, and poorer quality of life reflected by higher total SGRQ scores, independent of percent CT emphysema. In SPIROMICS, individuals with higher fSAD experienced an annual decline in FEV of 1.156 mL (relative decrease; 95% CI: 0.613, 1.699; < 0.001) per year for every 1% increase in fSAD. The rate of decline in COPDGene was slightly lower at 0.866 mL / year (relative decrease; 95% CI: 0.345, 1.386; < 0.001) for percent increase in fSAD. Inspiratory fSAD demonstrated greater consistency between repeated measurements with a higher intraclass correlation coefficient (ICC) of 0.99 (95% CI: 0.98, 0.99) compared to fSAD [ICC: 0.83 (95% CI: 0.76, 0.88)].
Small airways disease can be reliably assessed from a single inspiratory CT scan using generative AI, eliminating the need for an additional expiratory CT scan. fSAD estimation from inspiratory CT correlates strongly with fSAD, demonstrates a significant association with FEV decline, and offers greater repeatability.
量化功能性小气道疾病(fSAD)需要额外的呼气计算机断层扫描(CT),限制了其临床应用。人工智能(AI)能够仅根据全肺容量(TLC)时的胸部CT扫描来量化fSAD(fSAD)。
评估一种用于估计fSAD的AI模型,将其与双容积参数反应映射fSAD(fSAD)进行比较,并评估其在慢性阻塞性肺疾病(COPD)中的临床相关性和可重复性。
我们分析了慢性阻塞性肺疾病研究中的亚组和中间结局指标(SPIROMICS)的2513名参与者。使用随机抽样子集(=1055),我们开发了一个生成模型,为其余1458名SPIROMICS参与者生成虚拟呼气CT以估计fSAD。我们将fSAD与双容积、参数反应映射fSAD进行比较。我们研究了fSAD与FEV、FEV/FVC、六分钟步行距离(6MWD)、圣乔治呼吸问卷(SGRQ)和FEV下降的单变量和多变量关联。结果在慢性阻塞性肺疾病基因(COPDGene)研究的一个子集(=458)中得到验证。多变量模型针对年龄、种族、性别、体重指数、基线FEV、吸烟包年数、吸烟状态和肺气肿百分比进行了调整。
吸气fSAD在SPIROMICS(Pearson相关系数R=0.895)和COPDGene(R=0.897)队列中均与fSAD显示出强相关性。较高的fSAD水平与较低的肺功能显著相关,包括支气管扩张剂后较低的FEV(L)和FEV/FVC比值,以及较高的SGRQ总分所反映的较差生活质量,与CT肺气肿百分比无关。在SPIROMICS中,fSAD每增加1%,fSAD较高的个体每年FEV下降1.156 mL(相对下降;95%置信区间:0.613,1.699;P<0.001)。COPDGene中的下降率略低,fSAD每增加1%为0.866 mL/年(相对下降;95%置信区间:0.345,1.386;P<0.001)。与fSAD相比,吸气fSAD在重复测量之间表现出更高的一致性,组内相关系数(ICC)更高,为0.99(95%置信区间:0.98,0.99)[fSAD的ICC:0.83(95%置信区间:0.76,0.88)]。
使用生成式AI可从单次吸气CT扫描可靠地评估小气道疾病,无需额外的呼气CT扫描。吸气CT估计的fSAD与fSAD密切相关,与FEV下降显著相关,且具有更高的可重复性。