Literature DB >> 22481133

Bone mineral density in glycogen storage disease type Ia and Ib.

Laurie A Minarich1, Alexander Kirpich, Laurie M Fiske, David A Weinstein.   

Abstract

Purpose:The aim of this study was to characterize the pathogenesis of low bone mineral density in glycogen storage disease type Ia and Ib.
Methods: A retrospective chart review performed at the University of Florida Glycogen Storage Disease Program included patients with glycogen storage disease type Ia and Ib for whom dual-energy X-ray absorptiometry analysis was performed. A Z-score less than -2 SD was considered low. Analysis for association of bone mineral density with age, gender, presence of complications, mean triglyceride and 25-hydroxyvitamin D concentrations, erythrocyte sedimentation rate, duration of granulocyte colony-stimulating factor therapy, and history of corticosteroid use was performed.
Results: In glycogen storage disease Ia, 23/42 patients (55%) had low bone mineral density. Low bone mineral density was associated with other disease complications (P = 0.02) and lower mean serum 25-hydroxyvitamin D concentration (P = 0.03). There was a nonsignificant trend toward lower mean triglyceride concentration in the normal bone mineral density group (P = 0.1).In patients with glycogen storage disease type Ib, 8/12 (66.7%) had low bone mineral density. We did not detect an association with duration of granulocyte colony-stimulating factor therapy (P = 0.68), mean triglyceride level (P = 0.267), erythrocyte sedimentation rate (P = 0.3), or 25-hydroxyvitamin D (P = 0.63) concentration, and there was no evidence that corticosteroid therapy was associated with lower bone mineral density (P = 1).
Conclusion: In glycogen storage disease type Ia, bone mineral density is associated with other complications and 25-hydroxyvitamin D status. In glycogen storage disease type Ib, bone mineral density was not associated with any covariates analyzed, suggesting multifactorial etiology or reflecting a small sample.Genet Med advance online publication 5 April 2012.

Entities:  

Year:  2012        PMID: 22481133      PMCID: PMC3884026          DOI: 10.1038/gim.2012.36

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  15 in total

Review 1.  Glycogen storage diseases.

Authors:  Joseph I Wolfsdorf; David A Weinstein
Journal:  Rev Endocr Metab Disord       Date:  2003-03       Impact factor: 6.514

2.  Inhibition of osteoblastogenesis and promotion of apoptosis of osteoblasts and osteocytes by glucocorticoids. Potential mechanisms of their deleterious effects on bone.

Authors:  R S Weinstein; R L Jilka; A M Parfitt; S C Manolagas
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3.  Glucocorticoids act directly on osteoclasts to increase their life span and reduce bone density.

Authors:  D Jia; C A O'Brien; S A Stewart; S C Manolagas; R S Weinstein
Journal:  Endocrinology       Date:  2006-08-24       Impact factor: 4.736

4.  Acidosis inhibits osteoblastic and stimulates osteoclastic activity in vitro.

Authors:  N S Krieger; N E Sessler; D A Bushinsky
Journal:  Am J Physiol       Date:  1992-03

5.  Effect of continuous glucose therapy with uncooked cornstarch on the long-term clinical course of type 1a glycogen storage disease.

Authors:  David A Weinstein; Joseph I Wolfsdorf
Journal:  Eur J Pediatr       Date:  2002-07-31       Impact factor: 3.183

6.  Neutropenia and impaired neutrophil migration in type IB glycogen storage disease.

Authors:  A L Beaudet; D C Anderson; V V Michels; W J Arion; A J Lange
Journal:  J Pediatr       Date:  1980-12       Impact factor: 4.406

7.  Hypovitaminosis D in glycogen storage disease type I.

Authors:  Suhrad G Banugaria; Stephanie L Austin; Anne Boney; Thomas J Weber; Priya S Kishnani
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Authors:  T F Roe; D W Thomas; V Gilsanz; H Isaacs; J B Atkinson
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9.  Low bone mass in glycogen storage disease type 1 is associated with reduced muscle force and poor metabolic control.

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Authors:  Daniëlle H J Martens; Jan Peter Rake; Gerjan Navis; Vaclav Fidler; Catharina M L van Dael; G Peter A Smit
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  9 in total

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Authors:  Gyongyi O Okechuku; Lawrence R Shoemaker; Monika Dambska; Laurie M Brown; Justin Mathew; David A Weinstein
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2.  High Incidence of Serologic Markers of Inflammatory Bowel Disease in Asymptomatic Patients with Glycogen Storage Disease Type Ia.

Authors:  Nicole T Lawrence; Tayoot Chengsupanimit; Laurie M Brown; David A Weinstein
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4.  Glycogen Storage Disease type 1a - a secondary cause for hyperlipidemia: report of five cases.

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5.  Long-term complications of glycogen storage disease type Ia in the canine model treated with gene replacement therapy.

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6.  Aggressive therapy improves cirrhosis in glycogen storage disease type IX.

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Journal:  Mol Genet Metab       Date:  2013-03-21       Impact factor: 4.797

Review 7.  Glycogen Storage Disease Type Ia: Current Management Options, Burden and Unmet Needs.

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Review 8.  Bone health in patients with inborn errors of metabolism.

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9.  A preliminary study of telemedicine for patients with hepatic glycogen storage disease and their healthcare providers: from bedside to home site monitoring.

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  9 in total

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