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Clin Nutr ; 24(5): 737-45, 2005 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-16182037

RESUMO

BACKGROUND AND AIMS: Poor nutrition and growth status are common in people with cystic fibrosis (CF), and females often have a worse clinical course. Relationships between sexual maturity, nutrition, resting energy expenditure (REE), and pulmonary status in females with CF and pancreatic insufficiency (PI) were evaluated. METHODS: Pre- and post-menarcheal females with CF and PI (8-29 yr) were compared to healthy females. Z-scores for growth and body composition, anthropometry and DEXA were assessed. REE was measured in all subjects and pulmonary function in CF. RESULTS: Compared to healthy females (n=28, 14.6+/-4.1 yr), females with CF (n=16, 14.7+/-4.4 yr) had lower height Z (-0.1+/-0.9 versus -0.9+/-0.9, P=0.009) and muscle area Z (0.8+/-1.3 versus -0.4+/-1.2, P=0.007), and higher REE (100+/-10 versus 110+/-11% predicted, P=0.008). Difference in REE was more pronounced for post-menarcheal girls. REE adjusted for fat and fat-free mass was significantly higher with CF (+110 calories/day), and declined with menarcheal age in all subjects. FEV1 was positively associated with BMI Z score, and negatively associated with age at menarche. CONCLUSIONS: Height and muscle stores were reduced and REE elevated in subjects with CF compared to healthy controls. Poorer growth and nutritional status and delayed menarche were associated with poorer pulmonary function in CF and were likely related to the cumulative effect of energy imbalance on growth and body composition.


Assuntos
Fibrose Cística/fisiopatologia , Metabolismo Energético/fisiologia , Insuficiência Pancreática Exócrina/fisiopatologia , Estado Nutricional , Maturidade Sexual/fisiologia , Adolescente , Adulto , Metabolismo Basal/fisiologia , Composição Corporal/fisiologia , Estatura/fisiologia , Peso Corporal/fisiologia , Calorimetria Indireta , Estudos de Casos e Controles , Criança , Fibrose Cística/metabolismo , Feminino , Humanos , Absorção Intestinal , Menarca/fisiologia , Testes de Função Respiratória
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