Hepatocellular adenoma and metabolic balance in patients with type Ia glycogen storage disease

被引:29
作者
Di Rocco, Maia [1 ]
Calevo, Maria Grazia [2 ]
Taro, Marina [1 ]
Melis, Daniela [3 ]
Allegri, Anna Elsa Maria [1 ]
Parenti, Giancarlo [3 ]
机构
[1] Gaslini Inst, Pediat Div 2, Unit Rare Dis, I-16147 Genoa, Italy
[2] Gaslini Inst, Serv Epidemiol & Stat, I-16147 Genoa, Italy
[3] Univ Naples Federico 2, Pediat Clin, Naples, Italy
关键词
glycogen storage disease type I; hepatocellular adenoma; metabolic balance;
D O I
10.1016/j.ymgme.2007.10.134
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Glycogen storage disease type I (GSD I) is a metabolic disorder resulting from defects in the glucose-6-phosphatase system. Approximately 75% of adolescent and adult patients develop hepatocellular adenomas, which can lead to considerable morbidity and mortality. The pathogenesis of adenomas is unclear and the risk of developing adenomas in treated patients is uncertain. The objective of this study was to determine whether metabolic imbalance was related to the occurrence of adenomas in patients with GSD I, and to determine what specific biochemical pathways were involved. We performed a 1: 1 case-control retrospective study; cases were GSD I patients with adenomas and controls were GSD I patients without adenomas. Controls and cases were matched according to age at diagnosis, age at adenoma detection, and gender. We investigated biochemical abnormalities indicative of metabolic balance and exogenous factors potentially related to the onset of adenomas in the two groups. We detected no significant differences in dietetic treatment, compliance to treatment, or biochemical parameters related to metabolic balance between the two groups. In conclusion, we were unable to identify any significant differences in metabolic balance between GSD I patients who developed adenomas and those who did not. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:398 / 402
页数:5
相关论文
共 15 条
[1]
BIANCHI L, 1993, EUR J PEDIATR, V152, pS63
[2]
Hepatocellular adenoma subtype classification using molecular markers and lmmunohistochemistry [J].
Bioulac-Sage, Paulette ;
Rebouissou, Sandra ;
Thomas, Cristel ;
Blanc, Jean-Frederic ;
Saric, Jean ;
Cunha, Antonio Sa ;
Ruiller, Anne ;
Cubel, Gaeelle ;
Couchy, Gabrielle ;
Imbeaud, Sandrine ;
Balabaud, Charles ;
Zucman-Rossi, Jessica .
HEPATOLOGY, 2007, 46 (03) :740-748
[3]
Chen Y.-T., 2001, METABOLIC MOL BASIS, VI, P1521
[4]
Type I glycogen storage disease: favourable outcome on a strict management regimen avoiding increased lactate production during childhood and adolescence [J].
Gerhard Däublin ;
Bernd Schwahn ;
Udo Wendel .
European Journal of Pediatrics, 2002, 161 (1) :S40-S45
[5]
GLYCOGEN-STORAGE DISEASE - RECOMMENDATIONS FOR TREATMENT [J].
FERNANDES, J ;
LEONARD, JV ;
MOSES, SW ;
ODIEVRE, M ;
DIROCCO, M ;
SCHAUB, J ;
SMIT, GPA ;
ULLRICH, K ;
DURAND, P .
EUROPEAN JOURNAL OF PEDIATRICS, 1988, 147 (03) :226-228
[6]
Lee PJ, 2002, EUR J PEDIATR, V161, pS46
[7]
OCKNER RK, 1993, HEPATOLOGY, V18, P669, DOI 10.1016/0270-9139(93)90369-X
[8]
PARKER P, 1981, GASTROENTEROLOGY, V81, P534
[9]
Rake JP, 2002, EUR J PEDIATR, V161, pS20, DOI [10.1007/BF02679990, 10.1007/s00431-002-0999-4]
[10]
Resection of hepatocellular adenoma in patients with glycogen storage disease type Ia [J].
Reddy, Srinevas K. ;
Kishnani, Priya S. ;
Sullivan, Jennifer A. ;
Koeberl, Dwight D. ;
Desai, Dev M. ;
Skinner, Michael A. ;
Rice, Henry E. ;
Clary, Bryan M. .
JOURNAL OF HEPATOLOGY, 2007, 47 (05) :658-663