N | ΔFEV1 (mL) | ΔFVC (mL) | ΔFEV1/FVC (%) | ΔFEF25–75% (mL/s) | |
---|---|---|---|---|---|
β (95% CI)† | β (95% CI)† | β (95% CI)† | β (95% CI)† | ||
▵PM10 (per 10 μg/m3 increase in 10 years) | |||||
PiMZ | 97 | −6 (−15 to 4) | −2 (−18 to 15) | −0.2 (−0.4 to 0.0) | −24 (−52 to 4) |
PiMM | 3642 | −3 (−7 to 0) | −0 (−5 to 5) | −0.0 (−0.1 to 0.0) | −12 (−21 to −3) |
High-level VGDF exposure | |||||
PiMZ | 97 | −8 (−27 to 11) | 10 (−16 to 35) | −0.3 (−0.6 to 0.0)‡ | −82 (−125 to 39)‡ |
PiMM | 3642 | 1 (−2 to 4) | −2 (−7 to 2) | 0.1 (0.0 to 0.1) | 6 (−1 to 13) |
*Annual change in lung function was modelled in linear mixed regression with random intercept for area consisting of the following baseline covariates: age, age squared, sex, foreign status, height, body mass index, early respiratory infection, parental asthma, high-level education, cumulative VGDF exposure, and outdoor PM10; additional covariates included smoking status through follow-up, cumulative pack-years through follow-up, daily environmental tobacco smoke exposure at follow-up, difference in body mass index over follow-up period, seasonality, ▵PM10, high-level VGDF exposure during follow-up, and two-way interaction terms between environmental tobacco smoke exposure at follow-up and SERPINA1 genotype (PiMZ, PiMM as reference), and smoking status through follow-up and SERPINA1 genotype; we estimated the effect of ▵PM10 and high-level VGDF exposure during follow-up in PiMZ and PiMM carriers by adding interaction terms in the model.
†Negative signs indicate acceleration of decline in the lung function parameter with higher levels of exposure to the inhalants.
‡p<0.0001 and p=0.03 for interactions between SERPINA1 genotype and high-level VGDF exposure on ▵FEF25–75% and ▵FEV1/FVC, respectively.
FVC, forced vital capacity; FEF, forced expiratory flow; FEV, forced expiratory volume; VGDF, vapours, dusts, gases and fumes.