Abstract
Overweight (9%) and obesity (1%) in patients with cystic fibrosis homozygous for the deltaF508 mutation (CFdeltaF508) were non-trivial. Children with CFdeltaF508, in contrast to the general population, showed a positive association between body mass index and lung function for all body mass index z-scores.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adolescent
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Adult
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Body Mass Index
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Child
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Child, Preschool
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Cystic Fibrosis / complications*
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Cystic Fibrosis / genetics
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Cystic Fibrosis / physiopathology*
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Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
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Female
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Forced Expiratory Volume
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Homozygote
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Humans
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Infant
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Lung / physiopathology*
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Male
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Middle Aged
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Nutritional Status
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Obesity / complications*
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Obesity / physiopathology*
Substances
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CFTR protein, human
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cystic fibrosis transmembrane conductance regulator delta F508
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Cystic Fibrosis Transmembrane Conductance Regulator