Literature DB >> 14517523

Decreased energy expenditure is caused by abnormal body composition in infants with Prader-Willi Syndrome.

M Tracy Bekx1, Aaron L Carrel, Timothy C Shriver, Zhanhai Li, David B Allen.   

Abstract

OBJECTIVE: Infants with Prader-Willi syndrome (PWS) are hypotonic and underweight before the onset of childhood obesity. This study evaluates body composition in the PWS infant and its relationship to energy expenditure. STUDY
DESIGN: Sixteen infants and toddlers with PWS (mean age, 12.4+/-6 months; eight female subjects) underwent analysis of body composition with dual-energy x-ray absorptiometry and deuterium dilution, and energy expenditure with both doubly labeled water and indirect calorimetry.
RESULTS: Percent body fat was significantly increased (male subjects, P<.001; female subjects, P<.001) and fat-free mass (FFM) was significantly decreased (male subjects, P<.001; female subjects, P=.04) in infants with PWS when compared with age-matched published data for normal infants. Meanwhile, total energy expenditure was significantly decreased (male subjects, P=.025; female subjects, P<.001) in infants with PWS when compared with published normative data. There was a normal relationship between FFM and total energy expenditure in infants with PWS.
CONCLUSION: Compared with published data for infants without PWS, infants with PWS demonstrate increased percent body fat, decreased FFM, and decreased energy expenditure. Importantly, total energy expenditure per kilogram of FFM appears similar in infants with and without PWS. We conclude that lower energy expenditure in infants with PWS is caused by decreased FFM.

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Year:  2003        PMID: 14517523     DOI: 10.1067/S0022-3476(03)00386-X

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  25 in total

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4.  Energy expenditure and physical activity in Prader-Willi syndrome: comparison with obese subjects.

Authors:  Merlin G Butler; Mariana F Theodoro; Douglas C Bittel; Joseph E Donnelly
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5.  Systematic review of the clinical and genetic aspects of Prader-Willi syndrome.

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Authors:  Gregory A Hollman; David B Allen; Jens C Eickhoff; Aaron L Carrel
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8.  Long-term growth hormone therapy changes the natural history of body composition and motor function in children with prader-willi syndrome.

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Review 10.  Prader Willi Syndrome: Genetics, Metabolomics, Hormonal Function, and New Approaches to Therapy.

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