scholarly journals P316 Nutritional status, body composition and pulmonary function in cystic fibrosis children and adolescents - age and gender relationship

2019 ◽  
Vol 18 ◽  
pp. S147
Author(s):  
M. Mielus ◽  
M. Lurzynska ◽  
P. Barloga ◽  
U. Borawska-Kowalczyk ◽  
M. Oltarzewski ◽  
...  
2018 ◽  
Vol 16 (1) ◽  
Author(s):  
Renata Ongaratto ◽  
Katiana Murieli da Rosa ◽  
Juliana Cristina Eloi ◽  
Matias Epifanio ◽  
Paulo Marostica ◽  
...  

Abstract Objective We evaluated the association between vitamin D levels and nutritional status, pulmonary function and pulmonary exacerbations in children and adolescents with cystic fibrosis. Methods 25-hydroxyvitamin D (25(OH)D) levels of 37 children and adolescents were retrospectively evaluated. Pulmonary function, body mass index, height for age, and pulmonary exacerbations episodes were associated with vitamin D levels divided into two groups: sufficient (≥30ng/mL) and hypovitaminosis (<30ng/mL). Results Hypovitaminosis D (25(OH)D <30ng/mL) was observed in 54% of subjects. The mean level of 25(OH)D was 30.53±12.14ng/mL. Pulmonary function and nutritional status were not associated with vitamin D levels. Pulmonary exacerbations over a 2-year period (p=0.007) and the period from measurement up to the end of the follow-up period (p=0.002) were significantly associated with vitamin D levels. Conclusion Hypovitaminosis D was associated with higher rates of pulmonary exacerbations in this sample of children and adolescents with cystic fibrosis. Hypovitaminosis D should be further studied as a marker of disease severity in cystic fibrosis. Further prospective and randomized studies are necessary to investigate causality of this association.


2006 ◽  
Vol 5 ◽  
pp. S52
Author(s):  
E. Hatziagorou ◽  
P. Anagnostopoulou ◽  
E. Kirvasilis ◽  
P. Savopoulou ◽  
J. Kioumis ◽  
...  

2007 ◽  
Vol 115 (2) ◽  
pp. 211-220 ◽  
Author(s):  
E. Fliers ◽  
N. Rommelse ◽  
S. H. H. M. Vermeulen ◽  
M. Altink ◽  
C. J. M. Buschgens ◽  
...  

2012 ◽  
Vol 5 (2) ◽  
pp. 115-120 ◽  
Author(s):  
Mireia Orgilés ◽  
Xavier Méndez ◽  
José Pedro Espada ◽  
Jose Luis Carballo ◽  
José Antonio Piqueras

PEDIATRICS ◽  
1990 ◽  
Vol 86 (3) ◽  
pp. 374-377
Author(s):  
J. Reisman ◽  
M. Corey ◽  
G. Canny ◽  
H. Levison

Patient data obtained from the cystic fibrosis clinic of the Hospital for Sick Children (Toronto, Canada) over the period 1977 to 1988 were analyzed to compare the diabetic and nondiabetic cystic fibrosis patients. The pulmonary function, nutritional status, and survival data for 713 patients who attended the clinic over the 11-year period are reported. Insulin-dependent diabetes was found to exist in 37 (5.2%) of 713 patients. The patient age at time of diabetes diagnosis ranged from 2 to 34 years, with a mean ± SD of 20.0 ± 7.4 years. Patients who died in both the diabetic and nondiabetic groups had worse pulmonary and nutritional status than the surviving patients, but there were no significant differences between the diabetic and nondiabetic groups in those who died or in those who remained alive. Survival analysis showed a similar prognosis in the diabetic and nondiabetic groups. It is concluded that cystic fibrosis patients with diabetes are, for their age, not different from patients without diabetes with respect to pulmonary function, nutritional status, and survival.


2008 ◽  
Vol 7 ◽  
pp. S63
Author(s):  
S. Lubovich ◽  
V. Rodriguez ◽  
S. Zaragoza ◽  
C. Kofman ◽  
L. Galanternik ◽  
...  

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