Literature DB >> 16641581

Fractional calcium absorption is increased in girls with Rett syndrome.

Kathleen J Motil1, Rebecca J Schultz, Steven Abrams, Kenneth J Ellis, Daniel G Glaze.   

Abstract

BACKGROUND: Rett syndrome (RTT), an X-linked neurodevelopmental disorder primarilyaffecting girls, is characterized in part by osteopenia and increased risk of skeletal fractures. We hypothesized that decreased intestinal calcium (Ca) absorption relative to dietary Ca intake and increased renal Ca excretion might cause these problems in RTT.
OBJECTIVE: We measured fractional Ca absorption, urinary Ca loss, dietary Ca intake, and the hormonal factors regulating Ca metabolism to determine whether abnormalities in Ca balance might relate to poor bone mineralization in RTT girls and to evaluate the contribution of these factors to the overall dietary Ca needs of RTT girls. STUDY
DESIGN: Ten RTT girls and 10 controls, matched for age, sex, and pubertal status, were given a 3 day constant Ca diet that mimicked their habitual intakes. At the end of each dietary period, girls received single doses of Ca (intravenous) and Ca (oral). Fractional urinary excretion of Ca, Ca, 24 hour urinary Ca, and urinary cortisol excretion were determined. Serum Ca, phosphorous, alkaline phosphatase, vitamin D metabolites, parathyroid hormone (PTH), and osteocalcin were measured in the postabsorptive state. Bone mineral content (BMC) was measured by dual-energy x-ray absorptiometry.
RESULTS: Fractional Ca absorption was significantly higher in RTT than in control girls (mean +/- SDp, 52 vs. 33 +/- 13%). Dietary Ca intake (mean +/- SDp, 1,100 vs. 1,446 +/- 440 g/d) and net Ca absorption (mean +/- SDp, 513 vs. 362 +/- 306 mg/d) did not differ significantly between RTT and controls, respectively. Although urinary Ca excretion did not differ between groups, the increased urinary Ca:creatinine ratio (mean +/- SDp, 0.39 vs. 0.23 +/- 0.38) was consistent with clinical hypercalcuria and paralleled the significantly increased urinary cortisol excretion (mean +/- SDp, 3.1 vs. 1.7 +/- 1.1 mg/kg lean body mass per day) in the RTT girls. BMC was significantly lower in RTT than in controls (mean +/- SDp, 527 vs. 860 +/- 275 g). Serum Ca, P, alkaline phosphatase, vitamin D metabolites, PTH, and osteocalcin concentrations did not differ between the groups.
CONCLUSION: Fractional Ca absorption showed a compensatory increase in the presence of adequate dietary Ca intakes, mild hypercalcuria, and pronounced bone mineral deficits in RTT girls. Whether supplemental dietary Ca could enhance fractional Ca absorption and improve bone mineralization in RTT girls is unknown.

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Year:  2006        PMID: 16641581     DOI: 10.1097/01.mpg.0000189370.22288.0c

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


  12 in total

1.  Vitamin D deficiency is prevalent in girls and women with Rett syndrome.

Authors:  Kathleen J Motil; Judy O Barrish; Jane Lane; Suzanne P Geerts; Fran Annese; Lauren McNair; Alan K Percy; Steven A Skinner; Jeffrey L Neul; Daniel G Glaze
Journal:  J Pediatr Gastroenterol Nutr       Date:  2011-11       Impact factor: 2.839

2.  Low bone mineral mass is associated with decreased bone formation and diet in girls with Rett syndrome.

Authors:  Kathleen J Motil; Judy O Barrish; Jeffrey L Neul; Daniel G Glaze
Journal:  J Pediatr Gastroenterol Nutr       Date:  2014-09       Impact factor: 2.839

3.  Bone mineral content and density in Rett syndrome and their contributing factors.

Authors:  Amanda L Jefferson; Helen J Woodhead; Sue Fyfe; Julie Briody; Ami Bebbington; Boyd J Strauss; Peter Jacoby; Helen Leonard
Journal:  Pediatr Res       Date:  2011-04       Impact factor: 3.756

4.  Osteoporosis in Rett syndrome: a case study presenting a novel management intervention for severe osteoporosis.

Authors:  M Lotan; R Reves-Siesel; R S Eliav-Shalev; J Merrick
Journal:  Osteoporos Int       Date:  2013-07-05       Impact factor: 4.507

5.  Enhanced anxiety and stress-induced corticosterone release are associated with increased Crh expression in a mouse model of Rett syndrome.

Authors:  Bryan E McGill; Sharyl F Bundle; Murat B Yaylaoglu; James P Carson; Christina Thaller; Huda Y Zoghbi
Journal:  Proc Natl Acad Sci U S A       Date:  2006-11-15       Impact factor: 11.205

6.  Bone mineral content and bone mineral density are lower in older than in younger females with Rett syndrome.

Authors:  Kathleen J Motil; Kenneth J Ellis; Judy O Barrish; Erwin Caeg; Daniel G Glaze
Journal:  Pediatr Res       Date:  2008-10       Impact factor: 3.756

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
Journal:  J Pediatr Gastroenterol Nutr       Date:  2012-09       Impact factor: 2.839

8.  Mecp2 deficiency decreases bone formation and reduces bone volume in a rodent model of Rett syndrome.

Authors:  R D O'Connor; M Zayzafoon; M C Farach-Carson; N C Schanen
Journal:  Bone       Date:  2009-05-03       Impact factor: 4.398

9.  Biomechanical properties of bone in a mouse model of Rett syndrome.

Authors:  Bushra Kamal; David Russell; Anthony Payne; Diogo Constante; K Elizabeth Tanner; Hanna Isaksson; Neashan Mathavan; Stuart R Cobb
Journal:  Bone       Date:  2014-10-24       Impact factor: 4.398

10.  Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.

Authors:  Sharyl L Fyffe; Jeff L Neul; Rodney C Samaco; Hsiao-Tuan Chao; Shay Ben-Shachar; Paolo Moretti; Bryan E McGill; Evan H Goulding; Elinor Sullivan; Laurence H Tecott; Huda Y Zoghbi
Journal:  Neuron       Date:  2008-09-25       Impact factor: 17.173

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