Body composition of children aged 1 to 12 years with biliary atresia or Alagille syndrome
- PMID: 15699687
- DOI: 10.1097/00005176-200502000-00012
Body composition of children aged 1 to 12 years with biliary atresia or Alagille syndrome
Abstract
Background: Growth and body composition have not been well described in older children with biliary atresia or Alagille syndrome living with their native liver. To optimize nutritional management of these conditions it is essential to understand the normal growth characteristics.
Objectives: The purpose of this study was to evaluate and compare the growth and body composition of children, particularly school-age children, with biliary atresia and Alagille syndrome.
Methods: A single observer measured height, weight, arm anthropometry and skin fold thickness in subjects aged 1 to 12 years with biliary atresia or Alagille syndrome who had not undergone liver transplantation.
Results: Forty-six subjects (10 biliary atresia/36 Alagille syndrome) were assessed. Biliary atresia subjects were below average in height for age with normal weight and elevated body mass index. Mean fat stores were mildly depressed. The z-scores for body mass index and weight for age were inversely correlated with age. Alagille subjects were stunted and had low body weight and reduced fat and muscle stores. Body mass index z-score was inversely correlated with age despite improved cholestasis.
Conclusions: Children with Alagille syndrome had significant growth deficits as measured by weight, height and upper arm anthropometry at all ages studied. In contrast, subjects with biliary atresia had normal weights and heights. However, body mass index and weight for age z-scores were lower in the older biliary atresia subjects. Few studies of anthropometry in biliary atresia or Alagille syndrome have included the school-aged child. This study addresses this gap in knowledge and provides baseline data for nutritional interventions in these patients.
Similar articles
-
Growth, nutritional status, body composition, and energy expenditure in prepubertal children with Alagille syndrome.J Pediatr. 1999 Feb;134(2):172-7. doi: 10.1016/s0022-3476(99)70411-7. J Pediatr. 1999. PMID: 9931525
-
Deficits in size-adjusted bone mass in children with Alagille syndrome.J Pediatr Gastroenterol Nutr. 2005 Jan;40(1):76-82. doi: 10.1097/00005176-200501000-00014. J Pediatr Gastroenterol Nutr. 2005. PMID: 15625431
-
Alagille Syndrome Mimicking Biliary Atresia in Early Infancy.PLoS One. 2015 Nov 30;10(11):e0143939. doi: 10.1371/journal.pone.0143939. eCollection 2015. PLoS One. 2015. PMID: 26618708 Free PMC article.
-
Factors affecting catch-up growth after liver transplantation in children with cholestatic liver diseases.Ann Transplant. 2010 Jan-Mar;15(1):72-6. Ann Transplant. 2010. PMID: 20305323 Review.
-
Biliary atresia and other cholestatic childhood diseases: Advances and future challenges.J Hepatol. 2016 Sep;65(3):631-42. doi: 10.1016/j.jhep.2016.04.032. Epub 2016 May 6. J Hepatol. 2016. PMID: 27164551 Review.
Cited by
-
Alagille Syndrome and the Liver: Current Insights.Euroasian J Hepatogastroenterol. 2018 Jul-Dec;8(2):140-147. doi: 10.5005/jp-journals-10018-1280. Epub 2019 Feb 1. Euroasian J Hepatogastroenterol. 2018. PMID: 30828556 Free PMC article. Review.
-
The liver plays a key role in whole body sterol accretion of the neonatal Golden Syrian hamster.Biochim Biophys Acta. 2007 Apr;1771(4):550-7. doi: 10.1016/j.bbalip.2007.01.017. Epub 2007 Feb 12. Biochim Biophys Acta. 2007. PMID: 17363324 Free PMC article.
-
Clinical and Genetic Characteristics of Alagille Syndrome in Adults.J Clin Transl Hepatol. 2023 Feb 28;11(1):156-162. doi: 10.14218/JCTH.2021.00313. Epub 2022 Mar 17. J Clin Transl Hepatol. 2023. PMID: 36406308 Free PMC article.
-
Instrumental variable analysis using offspring BMI in childhood as an indicator of parental BMI in relation to mortality.Sci Rep. 2021 Nov 17;11(1):22408. doi: 10.1038/s41598-021-01352-w. Sci Rep. 2021. PMID: 34789785 Free PMC article.
-
Alagille syndrome: pathogenesis, diagnosis and management.Eur J Hum Genet. 2012 Mar;20(3):251-7. doi: 10.1038/ejhg.2011.181. Epub 2011 Sep 21. Eur J Hum Genet. 2012. PMID: 21934706 Free PMC article. Review.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous