Creatine and guanidinoacetate content of human milk and infant formulas: implications for creatine deficiency syndromes and amino acid metabolism

被引:34
作者
Edison, Erica E. [1 ]
Brosnan, Margaret E. [1 ]
Aziz, Khalid [2 ]
Brosnan, John T. [1 ]
机构
[1] Mem Univ Newfoundland, Dept Biochem, St John, NF A1B 3X9, Canada
[2] Univ Alberta, DTC Royal Alexandra Hosp 5027, Dept Pediat, Edmonton, AB T5H 3V9, Canada
关键词
Methionine; Arginine; Methylation reactions; HUMAN MUSCLE; NEWBORN;
D O I
10.1017/S000711451300010X
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Creatine is essential for normal neural development; children with inborn errors of creatine synthesis or transport exhibit neurological symptoms such as mental retardation, speech delay and epilepsy. Creatine accretion may occur through dietary intake or de novo creatine synthesis. The objective of the present study was to determine how much creatine an infant must synthesise de novo. We have calculated how much creatine an infant needs to account for urinary creatinine excretion (creatine's breakdown product) and new muscle lay-down. To measure an infant's dietary creatine intake, we measured creatine in mother's milk and in various commercially available infant formulas. Knowing the amount of milk/formula ingested, we calculated the amount of creatine ingested. We have found that a breast-fed infant receives about 9% of the creatine needed in the diet and that infants fed cows' milk-based formula receive up to 36% of the creatine needed. However, infants fed a soya-based infant formula receive negligible dietary creatine and must rely solely on de novo creatine synthesis. This is the first time that it has been shown that neonatal creatine accretion is largely due to de novo synthesis and not through dietary intake of creatine. This has important implications both for infants suffering from creatine deficiency syndromes and for neonatal amino acid metabolism.
引用
收藏
页码:1075 / 1078
页数:4
相关论文
共 21 条
[1]   Arginine:glycine amidinotransferase (AGAT) deficiency in a newborn:: Early treatment can prevent phenotypic expression of the disease [J].
Battini, Roberta ;
Alessandri, Grazia ;
Leuzzi, Vincenzo ;
Moro, Francesca ;
Tosetti, Michela ;
Bianchi, Maria C. ;
Cioni, Giovanni .
JOURNAL OF PEDIATRICS, 2006, 148 (06) :828-830
[2]   Creatine deficiency syndromes and the importance of creatine synthesis in the brain [J].
Braissant, Olivier ;
Henry, Hugues ;
Beard, Elidie ;
Uldry, Josephine .
AMINO ACIDS, 2011, 40 (05) :1315-1324
[3]   Creatine: Endogenous metabolite, dietary, and therapeutic supplement [J].
Brosnan, John T. ;
Brosnan, Margaret E. .
ANNUAL REVIEW OF NUTRITION, 2007, 27 :241-261
[4]   Creatine Synthesis Is a Major Metabolic Process in Neonatal Piglets and Has Important Implications for Amino Acid Metabolism and Methyl Balance [J].
Brosnan, John T. ;
Wijekoon, Enoka P. ;
Warford-Woolgar, Lori ;
Trottier, Nathalie L. ;
Brosnan, Margaret E. ;
Brunton, Janet A. ;
Bertolo, Robert F. P. .
JOURNAL OF NUTRITION, 2009, 139 (07) :1292-1297
[5]   Automated high-performance liquid chromatographic method for the determination of guanidinoacetic acid in dried blood spots: a tool for early diagnosis of guanidinoacetate methyltransferase deficiency [J].
Carducci, C ;
Birarelli, M ;
Santagata, P ;
Leuzzi, V ;
Carducci, C ;
Antonozzi, I .
JOURNAL OF CHROMATOGRAPHY B, 2001, 755 (1-2) :343-348
[6]   Evaluating urinary flow and solute excretion from urinary creatinine in the first week of life [J].
Coulthard, MG ;
Hey, EN ;
Al-Dahhan, J ;
Haycock, GB .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 2000, 82 (03) :F257-F258
[7]   AMINO-ACID-COMPOSITION OF HUMAN-MILK IS NOT UNIQUE [J].
DAVIS, TA ;
NGUYEN, HV ;
GARCIABRAVO, R ;
FIOROTTO, ML ;
JACKSON, EM ;
LEWIS, DS ;
LEE, DR ;
REEDS, PJ .
JOURNAL OF NUTRITION, 1994, 124 (07) :1126-1132
[8]  
Denis W, 1916, J BIOL CHEM, V26, P379
[9]  
ERIKSSON BO, 1980, ACTA PAEDIATR SCAND, P20
[10]  
Graystone JE, 1968, HUMAN GROWTH, P182