Literature DB >> 8929828

Blood lipids and rheological modifications in glycogen storage disease.

K Keddad1, S M Razavian, C Baussan, J Chalas, A Abella, J Levenson, A Simon, N Moatti, A Legrand.   

Abstract

OBJECTIVES: Hyperlipidemia is a feature of liver glycogen storage disease (GSD). Recent studies have suggested that rheological mechanisms such as elevated erythrocyte aggregation may be involved in the pathogenesis of ischemic syndromes associated with hyperlipidemia. DESIGN AND METHODS: We investigated erythrocyte aggregation, lipids, and circulatory proteins in the blood of 24 patients affected with GSD, aged from 1 to 23 years (mean = 8) and 26 controls aged from 1 to 28 years (mean = 9).
RESULTS: The aggregation results were much higher in patients than controls. The lipid data showed a mixed hyperlipidemia with predominant hypertriglyceridemia, low HDL-C, apoA-I and LpA-I/A-II, and high apoB as compared with controls. However, the LpA-I was not significantly different from controls.
CONCLUSIONS: In conclusion, patients with GSD presented hyperlipidemia and elevated erythrocyte aggregation such that they are at long-term risk of ischemic complications.

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Year:  1996        PMID: 8929828     DOI: 10.1016/0009-9120(95)02014-4

Source DB:  PubMed          Journal:  Clin Biochem        ISSN: 0009-9120            Impact factor:   3.281


  2 in total

1.  Apolipoprotein E polymorphism and serum concentrations in patients with glycogen storage disease type Ia.

Authors:  P Trioche; J Francoual; L Capel; M Odièvre; A Lindenbaum; P Labrune
Journal:  J Inherit Metab Dis       Date:  2000-03       Impact factor: 4.982

2.  Blood lipids and endothelial function in glycogen storage disease type III.

Authors:  E Hershkovitz; A Donald; M Mullen; P J Lee; J V Leonard
Journal:  J Inherit Metab Dis       Date:  1999-12       Impact factor: 4.982

  2 in total

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