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Growth in children with cystic fibrosis-related diabetes
M S Cheung1, N A Bridges, S A Prasad
1Chelsea & Westminster Hospital, London, UK.
Insights
Cystic fibrosis-related diabetes (CFRD) in children significantly impairs height velocity for years before and after diagnosis. Reduced growth may indicate underlying glucose metabolism issues in CF patients.
Area of Science:
- Pediatric Endocrinology
- Pulmonology
- Metabolic Disorders
Background:
- Cystic fibrosis-related diabetes (CFRD) is linked to poorer health outcomes in cystic fibrosis (CF) patients.
- Limited data exist on CFRD's impact on childhood growth.
- Understanding growth patterns is crucial for managing CFRD in pediatric populations.
Purpose of the Study:
- To investigate the effects of CFRD on growth and lung function in children.
- To compare growth velocity and lung function in children with and without CFRD.
- To identify potential early indicators of impaired glucose metabolism in pediatric CF patients.
Main Methods:
- Retrospective case-controlled study involving 34 children with CFRD from London specialist centers.
- Analysis of height velocity and FEV(1) (Forced Expiratory Volume in 1 second) in the 2 years preceding and following CFRD diagnosis.
- Comparison with age-matched control groups without CFRD.
Main Results:
- Children with CFRD exhibited significantly reduced mean height velocity in the 2 years before CFRD diagnosis (4.9 cm/year vs. 6.0 cm/year).
- Height velocity remained significantly lower in the 2 years post-diagnosis (3.4 cm/year vs. 4.4 cm/year).
- Mean FEV(1) was reduced at diagnosis but normalized with controls 2 years later.
Conclusions:
- Compromised height velocity and lung function occur before CFRD diagnosis in children with CF.
- Reduced height velocity should be considered an indicator of impaired glucose metabolism in pediatric CF.
- Further research is needed to determine if early insulin therapy can promote catch-up growth in these children.
Abstract:
Cystic fibrosis-related diabetes (CFRD) is associated with a shortened life expectancy and greater deterioration in lung function than in CF patients with normal glucose metabolism. There are few published data on how CFRD affects growth in childhood. We carried out a retrospective case controlled study of growth and lung function in 34 children with CFRD attending three specialist centers in London. We found that for the 2 years leading to CFRD diagnosis (at a mean age of 13.1 years), the mean height velocity was significantly less compared to controls: 4.9 (standard deviation-SD 1.6) cm/year vs. 6.0 (SD 1.9) cm/year (P = 0.005). For the 2 years following diagnosis, height velocity remained significantly lower (3.4 (SD 2.2) cm/year vs. 4.4 (SD 2.2) cm/year, P = 0.02). Mean FEV(1) was reduced prior to diagnosis and at diagnosis, but was similar to controls 2 years after diagnosis. This study highlights the compromise in height velocity and lung function that occurs prior to diagnosis of CFRD in children with CF, and a reduction in height velocity should be considered an indicator of impaired glucose metabolism. It would be useful to know whether early treatment with insulin can help promote catch up growth.
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