XiaoYan Chen, XiongFeng Xie, XiaoYun Shi, XueJie Gao, Hong Ye, Rui Zhang, YouTao Chen
This study indicates that low fecal SIgA and butyrate are associated with CMPA, suggesting they may play a role in the disease. The SIgA-CoMiSS integrated workflow allows non-invasive diagnosis with improved accuracy, addressing some limitations of current OFC-based protocols.
OBJECTIVES: To investigate the clinical significance of fecal butyrate and SIgA as non-invasive biomarkers for CMPA diagnosis.
METHODS: 45 OFC-confirmed CMPA infants (0-24 months) and 45 healthy controls were enrolled. Fecal SIgA (ELISA/BCA) and butyrate (HPLC) were quantified. Analyses included: univariate and multivariable logistic regression (adjusting for age/weight/length), symptom correlation (Cow's Milk-related Symptom Score, CoMiSS), and ROC-based diagnostic validation.
RESULTS: CMPA infants showed lower SIgA (6.39 ± 2.79 vs. 11.31 ± 3.32 μg/mg; p<0.001) and butyrate (298.81 vs. 810.07 μg/g; p=0.009). Both were associated with CMPA risk and inversely correlated with symptom severity. SIgA combined with CoMiSS achieved superior diagnostic accuracy (AUC=0.909) vs. CoMiSS alone (ΔAUC=0.103, p=0.010). Butyrate with CoMiSS showed no significant improvement (ΔAUC=0.002, p=0.767).
CONCLUSIONS: This study indicates that low fecal SIgA and butyrate are associated with CMPA, suggesting they may play a role in the disease. The SIgA-CoMiSS integrated workflow allows non-invasive diagnosis with improved accuracy, addressing some limitations of current OFC-based protocols.