Improved early growth in Danish children with cystic fibrosis from 2000-2022

•Growth has improved between 2000 and 2022 in children with cystic fibrosis.•The occurrence of stunting in children with CF decreased over the period.•During the same time, the occurrence of overweight children increased.•Individualized nutrition care throughout early childhood remains imperative. Improved growth in children with CF may have resulted from advances in treatment for cystic fibrosis (CF) over the past two decades, including the implementation of newborn screening in Denmark in 2016. This observational cohort study focuses on changes in early growth in Danish children with CF born between 2000 and January 2022. Age, length/height, and weight data of children 0–5 years old were obtained from the Danish CF Cohort. Data were stratified to four birth cohorts born between 2000 and 2022. Weight-for-age (WAZ), length-for-age (LAZ), height-for-age (HAZ) and body-mass-index (BMZ) z-scores were computed using WHO growth curves. Cubic spline mixed effects models were used to evaluate growth over 5 years between birth cohorts. We included 255 children in the analyses. Cubic spline mixed effects models show that catch-up growth improved in birth cohorts over time, with the 2016–2022 birth cohort achieving growth reference curve values in WAZ, LAZ/HAZ and BMZ the earliest. The proportion of underweight and stunting observations among children born 2000–2004 decreased by the 2016–2022 birth cohort, while the proportion of overweight, low BMZ and high BMZ observations increased. Advances in care for young children with CF have led to improvements in growth – with the 2016–2022 birth cohort approaching potential for overweight. Nonetheless, low BMZ remains. Immediate, individualized nutrition care throughout early childhood remain crucial in mitigating malnutrition.