Abstract Rationale Interstitial lung abnormalities (ILA) are incidental CT findings that often represent early, subclinical interstitial lung disease. Their prevalence and progression rates vary widely across studies, emphasizing the need to understand the impact of age, sex, and smoking for better risk stratification and management. Objectives To evaluate the prevalence and progression rates of ILA by age, sex, and smoking intensity using individual patient-level data from global cohorts, and to analyze progression-free survival (PFS). Methods Systematic searches in OVID-MEDLINE and Embase identified eligible original articles reporting ILA prevalence or progression, confirmed through radiologist-reviewed CT scans. Random-effects models were used to pool estimates stratified by age, sex, and smoking intensity. Risk of bias was assessed using the Newcastle-Ottawa Scale (NOS). Progression-free survival (PFS) probabilities were calculated using Kaplan-Meier analysis. Measurements and Main Results Data from 14 studies comprising 31,739 individual subjects showed a pooled ILA prevalence of 5.6% (95% CI, 4.3-7.3%), increasing with age from 2.5% (55 years) to 14.6% (≥80 years). Age was the most influential factor, and it was further amplified in males and heavy smokers. The overall pooled progression was 34%, with fibrotic ILAs exhibiting higher progression, and age did not affect progression. PFS was evaluated in 202 individuals with ILA, with estimated rates of 76% at 3 years and 55% at 5 years. Conclusions Age is the strongest determinant of ILA prevalence. ILAs show significant progression on imaging over time, and progression is mainly driven by fibrotic features rather than age once ILA is established. Given the higher prevalence in older adults, targeted screening in aging populations remains appropriate, while follow-up strategies should be guided by fibrotic burden rather than age.
Chae et al. (Mon,) studied this question.