Improvements of hypertriglyceridemia and hyperlacticemia in Japanese children with glycogen storage disease type Ia by medium-chain triglyceride milk

被引:28
作者
Nagasaka, Hironori
Hirano, Ken-ichi
Ohtake, Akira
Miida, Takashi
Takatani, Tomozumi
Murayama, Kei
Yorifuji, Tohru
Kobayashi, Kunihiko
Kanazawa, Masaki
Ogawa, Atsushi
Takayanagi, Masaki
机构
[1] Chiba Childrens Hosp, Div Metab, Midori Ku, Chiba, Japan
[2] Osaka Univ, Grad Sch Med, Dept Cardiovasc Med, Osaka, Japan
[3] Saitama Med Sch, Dept Pediat, Saitama, Japan
[4] Niigata Univ, Grad Sch Med & Dent Sci, Div Clin Prevent Med, Niigata, Japan
[5] Chiba Univ, Sch Med, Dept Pediat, Chiba, Japan
[6] Kyoto Univ, Grad Sch Med, Dept Pediat, Kyoto, Japan
[7] Hokkaido Univ, Grad Sch Med, Dept Pediat, Sapporo, Hokkaido 060, Japan
关键词
glycogen storage disease type Ia; medium-chain triglyceride milk; hypoglycemia; hyperlacticemia; hypertriglyceridemia; fatty acid beta-oxidation; LIPOPROTEIN-LIPASE; DIAGNOSIS; KETOGENESIS; DEFICIENCY; OXIDATION;
D O I
10.1007/s00431-006-0372-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Besides profound hypoglycemia with hyperlacticemia, glycogen storage disease type Ia (GSD Ia) presents hypertriglyceridemia that is often resistant to dietary treatment with cornstarch. The present study aimed to evaluate the effects of medium-chain triglycerides (MCT)-which are absorbed via the portal vein without being incorporated into chylomicrons-on hypertriglyceridemia and to explore otherwise metabolic changes in children with GSD Ia. A 13-year-old boy with GSD Ia who received a dietary treatment with MCT milk after cornstarch administration and two infants also with GSD Ia, ages 6 and 7 months, who received MCT milk after carbohydrate-rich, lipid-poor milk were enrolled. In addition to serum glucose and lactate levels, serum levels of total cholesterol, triglycerides, and high-density lipoprotein (HDL) cholesterol were serially determined. Simultaneously, serum levels of total carnitine, free carnitine, acylcarnitine, and ketone bodies were determined to evaluate fatty acid beta-oxidation. Mean glucose level (mmol/l) of patient 1 remained stable, the value being around 4.5, while those of patients 2 and 3 increased to this level from 4.00 and 3.72, respectively. Lactate levels were significantly decreased in all patients. Mean triglyceride levels (mM) of patient 1 decreased from 3.00 to 2.05. Also, triglyceride levels of patients 2 and 3 decreased from 2.74 and 3.15 to 2.13 and 2.70, respectively. HDL cholesterol, acylcarnitine, and ketone body levels increased in all patients after MCT administration, while total and free carnitine levels decreased. We describe here the beneficial effects on lipid and carbohydrate metabolisms in three Japanese children with GSD Ia. In light of the unfavorable influence of lipid restriction on growth and development in infancy, dietary treatment with MCT milk may be a better treatment for infants with GSD Ia. Further investigation should be required to confirm the efficacy of MCT milk in GSD Ia.
引用
收藏
页码:1009 / 1016
页数:8
相关论文
共 20 条
[1]  
Akanuma J, 2000, AM J MED GENET, V91, P107, DOI 10.1002/(SICI)1096-8628(20000313)91:2<107::AID-AJMG5>3.3.CO
[2]  
2-P
[3]   Disturbed lipid metabolism in glycogen storage disease type 1 [J].
Bandsma, RHJ ;
Smit, GPA ;
Kuipers, F .
EUROPEAN JOURNAL OF PEDIATRICS, 2002, 161 (Suppl 1) :S65-S69
[4]   DECREASED KETOGENESIS IN VONGIERKES DISEASE (TYPE-I GLYCOGENOSIS) [J].
BINKIEWICZ, A ;
SENIOR, B .
JOURNAL OF PEDIATRICS, 1973, 83 (06) :973-978
[5]  
Chen Y.-T., 2001, METABOLIC MOL BASIS, VI, P1521
[6]   Familial lipoprotein lipase deficiency in infancy:: Clinical, biochemical, and molecular study [J].
Feoli-Fonseca, JC ;
Lévy, E ;
Godard, M ;
Lambert, M .
JOURNAL OF PEDIATRICS, 1998, 133 (03) :417-423
[7]  
Fingerhut R, 2001, CLIN CHEM, V47, P1763
[8]  
FOSTER DW, 2004, ANN NY ACAD SCI, V6, P402
[9]   HYPERLIPIDEMIA AND FATTY-ACID COMPOSITION IN PATIENTS TREATED FOR TYPE-IA GLYCOGEN-STORAGE-DISEASE [J].
GREENE, HL ;
SWIFT, LL ;
KNAPP, HR .
JOURNAL OF PEDIATRICS, 1991, 119 (03) :398-403
[10]   Glycogen storage disease type I: diagnosis and phenotype/genotype correlation [J].
Matern, D ;
Seydewitz, HH ;
Bali, D ;
Lang, C ;
Chen, YT .
EUROPEAN JOURNAL OF PEDIATRICS, 2002, 161 (Suppl 1) :S10-S19