Key result
Chest CT body composition combined with clinical data identifies coronary atherosclerosis with ~0.81 AUC.
Why the study?
Does combining non-contrast chest CT-derived body composition phenotypes with clinical information improve the opportunistic identification of coronary atherosclerosis risk in middle-aged and older adults?
Cohort (n=1,249)
Yes
Does combining non-contrast chest CT-derived body composition phenotypes with clinical information improve the opportunistic identification of coronary atherosclerosis risk in middle-aged and older adults?
Opportunistic screening using non-contrast chest CT-derived body composition phenotypes combined with clinical information can effectively identify coronary atherosclerosis risk in middle-aged and older adults.
May support opportunistic CT-based atherosclerosis screening; leaves open need for prospective outcome trials before clinical use.
Non-contrast chest computed tomography (CT) scans contain a large amount of background redundant information, but their clinical utilization is currently insufficient. This study aimed to assess whether non-contrast CT-derived body composition phenotypes combined with clinical information could opportunistically identify coronary atherosclerosis (CA) risk in middle-aged and older adults. This retrospective study included 1,196 adults who underwent non-contrast chest CT and were divided into a training set ( n = 837) and a validation set ( n = 359). An external cohort ( n = 53) also served as validation. Body composition phenotypes were automatically extracted from chest CT and selected by least absolute shrinkage and selection operator (LASSO) regression. Clinical variables, including demographics, medical history, and laboratory parameters before imaging, were collected and screened by logistic regression. Models were developed using generalized linear model (GLM), support vector machine (SVM), random forest (RF), and extreme gradient boosting (XGBoost). Performance was evaluated by area under the receiver operating characteristic curve (AUC), accuracy, sensitivity, and specificity. Among all models, the combined GLM achieved AUCs of 0.817 (95% confidence interval [CI], 0.788–0.845), 0.810 (95% CI, 0.760–0.852), and 0.726 (95% CI, 0.562–0.851) in the internal training, internal validation, and external validation sets, respectively. SHapley Additive exPlanations (SHAP) analysis identified skeletal muscle mean attenuation as the strongest contributor in image model. Features derived from non-contrast chest CT, combined with clinical information, can opportunistically identify CA risk in middle-aged and older adults, extending the utility of chest CT beyond its primary diagnostic purpose.
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Liang et al. (2026) conducted a cohort in Coronary atherosclerosis (n=1,249). Non-contrast chest CT-derived body composition phenotypes combined with clinical information was evaluated on Identification of coronary atherosclerosis (AUC in internal validation) (AUC 0.810, 95% CI 0.760-0.852). A combined model integrating clinical variables and non-contrast chest CT-derived body composition phenotypes opportunistically identified coronary atherosclerosis with an AUC of 0.810 in internal validation and 0.726 in external validation.
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