Food science & nutrition
Nutrient-, Food-Group-, and Food-Item-Level Dietary Signatures of Psoriasis Comorbidity Among Adults With Anxiety Disorder: An Explainable Machine Learning Study
Par Gao C, Duan X, Luan M et 3 autres.
Contenu en anglais
Résumé
Psoriasis and anxiety disorders frequently co-occur, yet the dietary features associated with this comorbidity remain poorly characterized. This cross-sectional study compared nutrient-, food-group-, and food-item-level dietary representations among adults with medication-defined anxiety disorder using linked National Health and Nutrition Examination Survey (NHANES), Food Patterns Equivalents Database/MyPyramid Equivalents Database (FPED/MPED), and What We Eat in America (WWEIA) data. Three analytic datasets were constructed at the nutrient level (n = 1016; 37 psoriasis-comorbidity cases), food-group level (n = 1215; 46 cases), and food-item level (n = 1257; 46 cases). Each dataset was divided using a fixed stratified 7:3 training-validation split. Correlation filtering, shadow-feature selection, scaling, class-imbalance handling, and hyperparameter tuning were confined to the training workflow, with five-fold stratified cross-validation and an untouched validation set. Seven models, including conventional multivariable logistic regression, were compared. In locked validation, the nutrient-level logistic regression model showed the strongest validation signal (area under the receiver operating characteristic curve [AUC-ROC] 0.645, 95% confidence interval [CI] 0.464-0.811; area under the precision-recall curve [AUC-PR] 0.063; Brier score 0.176). The food-group logistic regression model (AUC-ROC 0.396, 95% CI 0.256-0.539) and the food-item extreme gradient boosting (XGBoost) model (AUC-ROC 0.401, 95% CI 0.273-0.537) provided more limited validation signals in the present sample. SHapley Additive exPlanations (SHAP) analyses of the cross-validation-selected models identified niacin, carbohydrate intake, β-cryptoxanthin, fat-related variables, hypertension, body mass index, and selected food categories as influential model features. These contributions are best interpreted as model-derived signals that prioritize candidate dietary and clinical features for further study. Together, the findings highlight nutrient-level dietary information as the most promising representation for subsequent development of nutrition-informed risk assessment in adults with anxiety. Larger prospective cohorts and external validation may further strengthen the clinical applicability of these signals.



