The Journal of asthma : official journal of the Association for the Care of Asthma · 2026
Inflammatory biomarker score and asthma risk: Longitudinal evidence from Chinese and English aging cohorts.
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Yang Zhe, Liu Lulu, Shi Yitong, Zhang Meihui, Ning Haoyong
Аннотация
UNLABELLED: Asthma is a prevalent airway disease influenced by various factors. Despite the known association between inflammation and asthma, no study has systematically investigated the relationship between inflammatory scores (INS) and asthma risk. This study aimed to explore this longitudinal relationship using two prospective cohorts: the China Health and Retirement Longitudinal Study (CHARLS) and the English Longitudinal Study of Ageing (ELSA). This study included 8,541 CHARLS and 5,701 ELSA participants. A multivariate-adjusted logistic regression model was used to determine the association between INS and risk of developing asthma. Restricted cubic spline (RCS) methods were employed to explore potential nonlinear relationships. Stratification and interaction tests were performed . After performing multiple imputations for the missing data, a sensitivity analysis was conducted to verify the robustness of the conclusions.
RESULTS: In the fully adjusted model, INS were associated positively with asthma risk (OR = 1.087, 95% CI: 1.010-1.157). The fully adjusted ELSA model also showed a positive association (OR = 1.055, 95% CI: 1.004-1.108). RCS analyses revealed no significant nonlinear relationship between the INS and asthma. Subgroup analysis of the CHARLS cohort identified interaction effects between INS and asthma risk, particularly when stratified by age and smoking status.
UNLABELLED: Higher baseline INS was modestly associated with greater odds of subsequent asthma in both CHARLS and ELSA. These findings suggest a possible role of systemic inflammatory burden in asthma development, although further studies are required to establish causality and clinical relevance.
RESULTS: In the fully adjusted model, INS were associated positively with asthma risk (OR = 1.087, 95% CI: 1.010-1.157). The fully adjusted ELSA model also showed a positive association (OR = 1.055, 95% CI: 1.004-1.108). RCS analyses revealed no significant nonlinear relationship between the INS and asthma. Subgroup analysis of the CHARLS cohort identified interaction effects between INS and asthma risk, particularly when stratified by age and smoking status.
UNLABELLED: Higher baseline INS was modestly associated with greater odds of subsequent asthma in both CHARLS and ELSA. These findings suggest a possible role of systemic inflammatory burden in asthma development, although further studies are required to establish causality and clinical relevance.