Literature DB >> 19525868

Gastrostomy placement improves height and weight gain in girls with Rett syndrome.

Kathleen J Motil1, Matthew Morrissey, Erwin Caeg, Judy O Barrish, Daniel G Glaze.   

Abstract

BACKGROUND: Growth failure and undernutrition complicate the clinical course of girls with Rett syndrome (RTT). These abnormalities are, in part, the consequence of oral motor dysfunction and inadequate dietary intake.
OBJECTIVE: To determine whether gastrostomy placement for nutritional therapy alters the natural history of growth failure and undernutrition in RTT. HYPOTHESIS: We hypothesized that gastrostomy placement for nutritional therapy reverses the decline in height, weight, and body mass index (BMI) z scores in RTT.
METHODS: Standard stadiometric and anthropometric measures were obtained to derive height, weight, and BMI z scores and estimates of fat-free mass (FFM) and body fat in a cohort of girls (n = 92) with RTT before and after gastrostomy placement. Methyl-CpG-binding protein 2 (MECP2) mutations and the presence or absence of a fundoplication were recorded.
RESULTS: The differences in height (n = 73), weight (n = 81), and BMI (n = 81) z score slopes before and after gastrostomy placement were 1.31 + 2.06 (P < 0.001), 2.38 +/- 3.18 (P < 0.001), and 3.25 +/- 3.32 (P < 0.001), respectively. FFM and body fat (n = 43) increased after gastrostomy by 41 +/- 27 g/cm height (P < 0.001) and 7.5% +/- 5.7% body weight (P < 0.001), respectively. The differences in height, weight, and BMI z score slopes were similar regardless of the age at which the gastrostomy was placed. The differences in height, weight, and BMI z score slopes, as well as the change in FFM and body fat deposition after gastrostomy placement, did not differ between those who did or did not have a fundoplication and among the classes of MECP2 mutations.
CONCLUSION: Gastrostomy placement for aggressive nutritional therapy favorably altered the natural history of growth failure and undernutrition in RTT, but did not restore height and weight z scores to birth values, regardless of the age at which surgery occurred and in the presence or absence of a fundoplication.

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Year:  2009        PMID: 19525868     DOI: 10.1097/MPG.0b013e31818f61fd

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  12 in total

1.  The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders.

Authors:  Daniel C Tarquinio; Wei Hou; Jeffrey L Neul; Walter E Kaufmann; Daniel G Glaze; Kathleen J Motil; Steven A Skinner; Hye-Seung Lee; Alan K Percy
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2.  Longitudinal course of epilepsy in Rett syndrome and related disorders.

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4.  Surgical correction of scoliosis in Rett syndrome: cord monitoring and complications.

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Authors:  Daniel C Tarquinio; Wei Hou; Jeffrey L Neul; Jane B Lane; Katherine V Barnes; Heather M O'Leary; Natalie M Bruck; Walter E Kaufmann; Kathleen J Motil; Daniel G Glaze; Steven A Skinner; Fran Annese; Lauren Baggett; Judy O Barrish; Suzanne P Geerts; Alan K Percy
Journal:  Pediatr Neurol       Date:  2015-02-16       Impact factor: 3.372

6.  Growth failure and outcome in Rett syndrome: specific growth references.

Authors:  Daniel Charles Tarquinio; Kathleen J Motil; Wei Hou; Hye-Seung Lee; Daniel G Glaze; Steven A Skinner; Jeff L Neul; Fran Annese; Lauren McNair; Judy O Barrish; Suzanne P Geerts; Jane B Lane; Alan K Percy
Journal:  Neurology       Date:  2012-10-03       Impact factor: 9.910

7.  Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome.

Authors:  Kathleen J Motil; Erwin Caeg; Judy O Barrish; Suzanne Geerts; Jane B Lane; Alan K Percy; Fran Annese; Lauren McNair; Steven A Skinner; Hye-Seung Lee; Jeffrey L Neul; Daniel G Glaze
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Authors:  Helen Leonard; Madhur Ravikumara; Gordon Baikie; Nusrat Naseem; Carolyn Ellaway; Alan Percy; Suzanne Abraham; Suzanne Geerts; Jane Lane; Mary Jones; Katherine Bathgate; Jenny Downs
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9.  Experience of gastrostomy using a quality care framework: the example of rett syndrome.

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10.  Progress in Rett Syndrome: from discovery to clinical trials.

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