Literature DB >> 24343108

Assessment of Basal Metabolic Rate and Nutritional Status in Patients with Gaucher Disease Type III.

Divair Doneda1, Filippo P Vairo, André L Lopes, Alvaro Reischak-Oliveira, Pedro Schestatsky, Marino M Bianchin, Cileide C Moulin, Ida V D Schwartz.   

Abstract

UNLABELLED: Gaucher disease type III (GD III) is a rare form of GD characterized by neurological involvement and severe systemic disease. The objective of this study was to assess the nutritional status and energy metabolism of patients with GD III.
METHODS: The basal metabolic rate (BMR, measured by indirect calorimetry) and anthropometric parameters (height, weight, body mass index (BMI), and arm circumference) of three patients with GD III (p.L444P/L444P genotype) were assessed at different time points. The clinical severity of GD was assessed by means of physical examination, laboratory tests, imaging findings, and the severity scores proposed by Zimran (SSI) and Davies (SSNI).
RESULTS: The measured BMR of patients 1 (age 14 years, not on enzyme replacement therapy (ERT), SSI score 33, SSNI score 14.5), 2 (age 17 years, on ERT, SSI score 33, SSNI score 16), and 3 (age 20 years, on ERT, SSI score 33, SSNI score 7.5) was, respectively, 47%, 72%, and 15% higher than that estimated by the Harris-Benedict equation. Patients with a more severe phenotype had more marked hypermetabolism. Patients 1 and 2 had BMI-for-age z scores of -1.09 and -1.39, respectively, and height-for-age z scores of -4.27 and -3.02, respectively; patient 3 had a BMI of 24.7 kg/m(2).
CONCLUSION: All three patients showed hypermetabolism; however, the two patients with the highest BMR had more severe GD and were malnourished. Additional studies are warranted to assess whether hypermetabolism may be a biomarker of disease severity in GD.

Entities:  

Year:  2013        PMID: 24343108      PMCID: PMC4213328          DOI: 10.1007/8904_2013_281

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  22 in total

1.  The efficacy of enzyme replacement therapy in patients with chronic neuronopathic Gaucher's disease.

Authors:  G Altarescu; S Hill; E Wiggs; N Jeffries; C Kreps; C C Parker; R O Brady; N W Barton; R Schiffmann
Journal:  J Pediatr       Date:  2001-04       Impact factor: 4.406

2.  Enzyme replacement therapy in type III Gaucher disease.

Authors:  A Tylki-Szymańska; B Czartoryska
Journal:  J Inherit Metab Dis       Date:  1999-04       Impact factor: 4.982

Review 3.  Best practice methods to apply to measurement of resting metabolic rate in adults: a systematic review.

Authors:  Charlene Compher; David Frankenfield; Nancy Keim; Lori Roth-Yousey
Journal:  J Am Diet Assoc       Date:  2006-06

4.  A French experience of type 3 Gaucher disease: Phenotypic diversity and neurological outcome of 10 patients.

Authors:  Ichraf Kraoua; Frédéric Sedel; Catherine Caillaud; Roseline Froissart; Jérôme Stirnemann; Guy Chaurand; Hugues Flodrops; Saliha Tari; Isabelle Gourfinkel-An; Sophie Mathieu; Nadia Belmatoug; Thierry Billette de Villemeur; Cyril Mignot
Journal:  Brain Dev       Date:  2010-03-21       Impact factor: 1.961

5.  Gaucher's disease variant characterised by progressive calcification of heart valves and unique genotype.

Authors:  A Abrahamov; D Elstein; V Gross-Tsur; B Farber; Y Glaser; I Hadas-Halpern; S Ronen; M Tafakjdi; M Horowitz; A Zimran
Journal:  Lancet       Date:  1995-10-14       Impact factor: 79.321

Review 6.  A severity scoring tool to assess the neurological features of neuronopathic Gaucher disease.

Authors:  E H Davies; R Surtees; C DeVile; I Schoon; A Vellodi
Journal:  J Inherit Metab Dis       Date:  2007-09-16       Impact factor: 4.982

7.  Potential efficacy of enzyme replacement and substrate reduction therapy in three siblings with Gaucher disease type III.

Authors:  J Cox-Brinkman; M J van Breemen; B T van Maldegem; L Bour; W E Donker; C E M Hollak; F A Wijburg; J M F G Aerts
Journal:  J Inherit Metab Dis       Date:  2008-10-15       Impact factor: 4.982

8.  Enzyme infusion therapy of the Norrbottnian (type 3) Gaucher disease.

Authors:  A Erikson; M Aström; J E Månsson
Journal:  Neuropediatrics       Date:  1995-08       Impact factor: 1.947

9.  Isolated horizontal supranuclear gaze palsy as a marker of severe systemic involvement in Gaucher's disease.

Authors:  M C Patterson; M Horowitz; R B Abel; J N Currie; K T Yu; C Kaneski; J J Higgins; R R O'Neill; P Fedio; A Pikus
Journal:  Neurology       Date:  1993-10       Impact factor: 9.910

10.  Increased basal glucose production in type 1 Gaucher's disease.

Authors:  E P Corssmit; C E Hollak; E Endert; M H van Oers; H P Sauerwein; J A Romijn
Journal:  J Clin Endocrinol Metab       Date:  1995-09       Impact factor: 5.958

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