A PRETERM INFANT WITH SECONDARY CARNITINE DEFICIENCY DUE TO MCT FORMULA - EFFECTIVE TREATMENT OF L-CARNITINE

被引:4
作者
ISHIDA, A
GOTO, A
TAKAHASHI, Y
NAKAJIMA, W
ARAI, H
TAZAWA, Y
TAKADA, G
机构
[1] Department of Pediatrics, Akita University School of Medicine, Akita, 1-1-1 Hondo
关键词
PRETERM INFANT; CARNITINE DEFICIENCY; L-CARNITINE; MCT;
D O I
10.1620/tjem.172.59
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report a preterm infant who was prescribed an MCT formula and subsequently developed carnitine deficiency with liver dysfunction and an elevation of serum CK level. A male infant who had been born at 24 weeks' gestation with birth weight 799 g, was fed with an MCT formula containing 76.8% of all kinds of lipids, because of his steatorrhea after the 30th day. On the 100th day, he was noted hepatomegaly and elevation of serum levels of AST, ALT and CK. The needle biopsy of the liver indicated the existence of the liver damage. He showed low serum carnitine with high urinary loss of acylcarnitine and dicarboxylic aciduria. Administration of L-carnitine was an effective treatment. The carnitine deficiency might be exaggerated by an increased urinary loss of acylcarnitine. We should be cautious of the risk of carnitine deficiency in preterm infants during prolonged use of MCT formula.
引用
收藏
页码:59 / 64
页数:6
相关论文
共 16 条
  • [1] THE INFLUENCE OF INTRAVENOUS MEDIUM-CHAIN AND LONG-CHAIN TRIGLYCERIDES AND CARNITINE ON THE EXCRETION OF DICARBOXYLIC-ACIDS
    BOHLES, H
    AKCETIN, Z
    LEHNERT, W
    [J]. JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 1987, 11 (01) : 46 - 48
  • [2] MEDIUM-CHAIN TRIGLYCERIDES IN FORMULA FOR PRETERM NEONATES - IMPLICATIONS FOR HEPATIC AND EXTRAHEPATIC METABOLISM
    BORUM, PR
    [J]. JOURNAL OF PEDIATRICS, 1992, 120 (04) : S139 - S145
  • [3] URINARY-EXCRETION OF L-CARNITINE AND ACYLCARNITINES BY PATIENTS WITH DISORDERS OF ORGANIC-ACID METABOLISM - EVIDENCE FOR SECONDARY INSUFFICIENCY OF L-CARNITINE
    CHALMERS, RA
    ROE, CR
    STACEY, TE
    HOPPEL, CL
    [J]. PEDIATRIC RESEARCH, 1984, 18 (12) : 1325 - 1328
  • [4] ENGEL AG, 1986, MYOLOGY, V2, P1663
  • [5] TRANSIENT 5-OXOPROLINURIA IN A VERY-LOW-BIRTH-WEIGHT INFANT
    GOTO, A
    ISHIDA, A
    GOTO, R
    HAYASAKA, K
    NANAO, K
    YAMASHITA, A
    YAMAGUCHI, S
    TAKADA, G
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1992, 15 (02) : 284 - 285
  • [6] SYNDROME OF SYSTEMIC CARNITINE DEFICIENCY - CLINICAL, MORPHOLOGIC, BIOCHEMICAL, AND PATHOPHYSIOLOGIC FEATURES
    KARPATI, G
    CARPENTER, S
    ENGEL, AG
    WATTERS, G
    ALLEN, J
    ROTHMAN, S
    KLASSEN, G
    MAMER, OA
    [J]. NEUROLOGY, 1975, 25 (01) : 16 - 24
  • [7] MATSUO M, 1989, Acta Paediatrica Japonica, V31, P211
  • [8] LOW CARNITINE INTAKE AND ALTERED LIPID-METABOLISM IN INFANTS
    OLSON, AL
    NELSON, SE
    REBOUCHE, CJ
    [J]. AMERICAN JOURNAL OF CLINICAL NUTRITION, 1989, 49 (04) : 624 - 628
  • [9] PARVIN R, 1977, ANAL BIOCHEM, V79, P191
  • [10] DECREASED TISSUE CARNITINE CONCENTRATIONS IN NEWBORN-INFANTS RECEIVING TOTAL PARENTERAL-NUTRITION
    PENN, D
    SCHMIDTSOMMERFELD, E
    PASCU, F
    [J]. JOURNAL OF PEDIATRICS, 1981, 98 (06) : 976 - 978