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ORIGINAL ARTICLE Whole cow’s milk in infancy Alexander KC Leung MBBS FRCPC FRCP (UK and Ireland) FRCPCH, Reginald S Sauve MD FRCPC AKC Leung, RS Sauve. Whole cow’s milk in infancy. Paediatr Child Health 2003;8(7):419-421. Early introduction of whole cow’s milk may lead to iron deficiency anemia. From a nutritional point of view, it is best to delay the introduction of whole cow’s milk until the infant is one year old. While there is no evidence to suggest adverse clinical sequelae associated with the increased renal solute load in healthy infants, feeding with whole cow’s milk would narrow the margin of safety in situations that may lead to dehydration. Early exposure to cow’s milk proteins increases the risk of developing allergy to milk proteins. Because of the possible association between early exposure to cow’s milk proteins and risk for type 1 diabetes mellitus, breast-feeding and avoidance of commercially available cow’s milk and products containing intact cow’s milk protein during the first year of life are strongly encouraged in families with a strong history of insulin dependent diabetes mellitus. The authors suggest that the optimal food in infancy is human breast milk. If human milk is not available, it is preferred that iron-fortified formulas rather than whole cow’s milk be used during the first year of life. Key words: whole cow’s milk; infancy n recent years, there has been a decline in the use of whole Icow’s milk in infant feeding (1). Nevertheless, many parents still make the transition from breast feeding or formula to whole cow’s milk when the infant is less than one year of age. In the United States (2) and the United Kingdom (3), it is recommended that whole cow’s milk should not be used before one year of age. In Denmark (4), it is recommended that whole cow’s milk can be introduced gradually from nine months of age and in Sweden (5) from 10 months of age. The Nutrition Committee of the Canadian Paediatric Society recommends that whole cow’s milk may be introduced at nine to 12 months of age (6). There are potential hazards associated with early introduction of whole cow’s milk. IRON DEFICIENCY ANEMIA The use of whole cow’s milk can be associated with occult loss of blood from the gastrointestinal tract, in both early and late infancy. Ziegler et al (7) randomly assigned 52 infants to receive either whole cow’s milk or a milk-based formula at 168 days of age. With the feeding of whole cow’s milk, the proportion of guaiac-positive stools increased from 3% at baseline to 30.3% during the first 28 days of the trial (P<0.01), whereas the proportion of guaiac-positive stools Le lait de vache entier pendant la première enfance L’adoption précoce de lait de vache entier chez les nourrissons peut entraîner une anémie ferriprive. D’un point de vue nutritionnel, il est préférable de retarder l’adoption du lait de vache entier jusqu’à ce que l’enfant ait un an. Bien qu’aucune donnée ne laisse supposer la possibilité de séquelles cliniques néfastes causées par la charge osmotique accrue des substances filtrées chez les nourrissons en santé, l’alimentation à l’aide de lait entier de vache réduit la marge de sécurité dans des cas qui peuvent provoquer une déshydratation. Une exposition précoce aux protéines du lait de vache accroît le risque que l’enfant développe une allergie aux protéines du lait. Étant donné l’association possible entre une exposition précoce aux protéines du lait de vache et le risque de diabète de type I, l’allaitement et l’évitement du lait de vache offert sur le marché et des produits contenant des protéines intactes de lait de vache au cours de la première année de vie sont fortement préconisés au sein des familles présentant des antécédents marqués de diabète de type I. Les auteurs indiquent que l’aliment optimal pendant la première enfance demeure le lait maternel. Si celui-ci n’est pas disponible, il est préférable de choisir un lait maternisé contenant des suppléments de fer plutôt que du lait de vache entier pendant la première année de vie. remained low (5%) with the feeding of formula. Although the proportion of guaiac-positive stools among infants fed whole cow’s milk declined later, it remained significantly elevated (P<0.01) for the entire trial. Stool hemoglobin concentration increased markedly with the introduction of whole cow’s milk from a mean (± SD) of 622±527 µg/g dry stool at baseline to 3598±10,479 µg/g dry stool during the first 28 days of ingestion of whole cow’s milk. Among infants fed formula, stool hemoglobin did not increase and was significantly (P<0.01) less than that in the group fed whole cow’s milk. Although normal infants lose measurable amounts of blood in the feces at all times, feeding with whole cow’s milk leads to increased enteric blood loss in a large proportion of normal infants (7,8). Because feeding with a heat processed cow’s milk proprietary formula would not result in increased enteric blood loss, it has been suggested that a heat labile protein such as bovine albumin in whole cow’s milk is responsible for intestinal bleeding (8). Cow’s milk-induced blood loss tends to occur only during infancy; even exquisitely sensitive infants tend to tolerate whole cow’s milk later in life without adverse effects (8). The levels of iron in both breast milk and whole cow’s milk are low, less than 0.3mg/L to 1 mg/L (9). Iron in breast Deparment of Paediatrics, University of Calgary and the Alberta Children’s Hospital, Calgary, Alberta Correspondence: Dr Alexander KC Leung, #200, 233-16th Avenue NW, Calgary, Alberta T2M 0H5. Telephone 403-230-3300, fax 403-230-3322, e-mail [email protected] Paediatr Child Health Vol 8 No 7 September 2003 ©2003 Pulsus Group Inc. All rights reserved 419 Leung et al milk is highly bioavailable, possibly because of the lower calcium and phosphorus content and the presence of lactoferrin (9). On the other hand, bovine milk proteins are potent inhibitors of iron absorption. Approximately 50% of the iron in the breast milk is absorbed compared with approximately 10% of that in whole cow’s milk (10). Several studies showed that feeding infants with whole cow’s milk instead of iron-fortified formula at six months of age resulted in an increased incidence of iron deficiency by one year of age (11,12). Supplemental foods may not always supply the necessary amounts of iron in the second six months of life (2,11). Iron deficiency anemia, especially during the first two years of life, can adversely affect behaviour and psychomotor development (13). NUTRITIONAL CONSIDERATIONS Protein provides approximately 7% of the calories in human milk and 20% of the calories in whole cow’s milk (14). Although the amounts of whey protein are similar, whole cow’s milk contains six to seven times as much casein as does human milk (14). The whey to casein ratio of human milk is approximately 35:65 whereas the whey to casein ratio of whole cow’s milk is 19:81 (14). The high casein content of whole cow’s milk is undesirable because casein forms a tough, hard to digest curd that is difficult for young infants to digest (15). The amino acids taurine and cystine are present in much higher concentrations in human milk than in whole cow’s milk (13). These amino acids may be essential for premature infants. Lipids provide 50% of the calories in both human and whole cow’s milk. Human milk contains a greater concentration of linoleic acid and polyunsaturated fatty acids than whole cow’s milk. Linoleic acid provides 4% of calories in human milk but only 1.8% in whole cow’s milk, the recommended level being 3% (2). The fatty acid profile in infant formulas simulates that of human milk. As such, fats in infant formulas are absorbed quite well by most infants and better than those in whole cow’s milk (14). Whole cow’s milk also has low contents of zinc, niacin, vitamin C and vitamin E (6). Whole cow’s milk contains approximately three times as much sodium and potassium, four times as much calcium and six times as much phosphorus as does human milk (14). The high phosphate load has been implicated as a cause of late hypocalcemic tetany of the neonate (14). For all the above reasons, it is best to delay the introduction of whole cow’s milk until the infant is one year old. HIGH RENAL SOLUTE LOAD A higher intake of protein, sodium, potassium, chloride and phosphorus associated with the use of whole cow’s milk inappropriately increases the renal solute load (6,16). The higher renal solute load of whole cow’s milk results in a urinary osmolality approximately twice that observed in breast fed infants (17). While there is no evidence to suggest adverse clinical sequelae associated with the increased renal solute load in healthy infants, feeding with whole cow’s milk would 420 narrow the margin of safety in situations that may lead to dehydration (16). Under circumstances in which water intake is reduced (eg, vomiting) or water loss is increased (eg, diarrhea, hot environment), whole cow’s milk may not supply enough free water. Dehydration may result unless additional water is offered. COW’S MILK ALLERGY Cow’s milk allergy affects 0.3% to 7.5% of infants (18). There is no evidence to suggest that whole cow’s milk is more allergenic than infant formulas that contain intact cow’s milk proteins. Infants with cow’s milk protein allergy should not be fed either whole cow’s milk or formulas containing intact whole cow’s milk proteins (2). Early exposure to cow’s milk proteins increases the risk of developing allergy to milk proteins. With increasing maturation, the intestinal epithelium becomes less permeable to macromolecules and there is less tendency toward allergic reactions. In normal infants without a known history of allergy to cow’s milk, the introduction of whole cow’s milk should be based on nutritional considerations, and not on the development of mucosal barrier to cow’s milk proteins (2). Several studies have reported the detection of cow’s milk antigen in human milk (19,20). Exposure to even minute amounts of cow’s milk protein in human milk may elicit allergic reactions (21). Several investigators found that the incidence of atopic dermatitis was significantly lower in the group of children whose lactating mothers had a diet free from cow’s milk whereas the incidences of all other atopic manifestations were similar compared with a control group of children whose mothers had no dietary restrictions (22,23). Other investigators found no preventive effect on the development of atopic diseases in children whose mothers avoided cow’s milk in the diet (24). It is premature, at the present stage, to advocate avoidance of whole cow’s milk during lactation to families with atopy. Further studies are necessary before a definitive recommendation can be made. Nevertheless, if the lactating mother notices that consumption of whole cow’s milk seems to cause an allergic reaction in her infant, it is reasonable to eliminate whole cow’s milk from her diet. DIABETES MELLITUS An association between early exposure to cow’s milk proteins and risk for type 1 diabetes mellitus has been reported in many (25-28) but not all (29) studies. Exposure to cow’s milk proteins elicits antibody formation to insulin in some children (25,26,28). Bovine serum albumin may provoke an immunological response in genetically susceptible individuals, which then cross reacts with a beta-cell surface protein, p 69 (25,26). The expression of this protein on the surface of beta cells is believed to mediate their destruction by exposing them to immune attack (26). Destruction of beta cells may lead to the development of diabetes mellitus. The American Academy of Pediatrics recommends that in families with a strong history of insulin-dependent diabetes mellitus, breastfeeding and avoidance of commercially available cow’s milk Paediatr Child Health Vol 8 No 7 September 2003 Whole cow’s milk in infancy and products containing intact cow’s milk proteins during the first year of life are strongly encouraged (30). Because the antigenicity of infant formulas and whole cow’s milk may be different and there is no evidence against the use of formulas for infants whose mothers do not breast-feed, commercial infant formulas using cow’s milk protein are an acceptable alternative (30). These recommendations should be followed until prospective well-designed randomized trials determine the relationship between cow’s milk proteins and diabetes mellitus. CONCLUSION The optimal food in infancy is human breast milk. If human milk is not available, it is preferred that iron-fortified formulas, rather than whole cow’s milk, be used during the first year of life. REFERENCES 1. Fomon SJ. Infant feeding in the 20th Century: Formula and beikost. J Nutr 2001;131:S409-20. 2. Committee on Nutrition, American Academy of Pediatrics. The use of whole cow’s milk in infancy. Pediatrics 1992;89:1105-9. 3. Department of Health. Report on Health and Social Subjects No.45. Weaning and the Weaning Diet. London: Her Majesty’s Stationery Office, 1994:1-15. 4. The National Board of Health (Denmark). Recommendations for the Nutrition of Infants: Recommendations for Health Personnel (in Danish). Copenhagen: The National Board of Health (Denmark), 1998:1-78. 5. Axelsson I, Gebre-Medhin M, Hernell O, et al. Vänta med Komjölk som dryck tills barnet är 10-12 månader! Läkartidningen 1999;96:22068. 6. Canadian Paediatric Society, Dietitians of Canada, and Health Canada. Nutrition for Healthy Term Infants. Ottawa: Ministry of Public Works and Government Services, 1998:1-50. 7. Ziegler EE, Fomon SJ, Nelson SE, et al. Cow milk feeding in infancy: Further observations on blood loss from the gastrointestinal tract. J Pediatr 1990;116:11-8. 8. Wilson JF, Lahey ME, Heiner DC. Studies on iron metabolism. V. Further observations on cow’s milk-induced gastrointestinal bleeding in infants with iron-deficiency anemia. J Pediatr 1974;84:335-44. 9. Leung AK, Chan KW. Iron deficiency anemia. Adv Pediatr (In press). 10. Oski FA. Iron deficiency in infancy and childhood. N Engl J Med 1993;329:190-3. Paediatr Child Health Vol 8 No 7 September 2003 11. Tunnessen WW Jr, Oski FA. Consequences of starting whole cow’s milk at 6 months of age. J Pediatr 1987;111:813-6. 12. Penrod JC, Anderson K, Acosta PB. Impact of iron status of introducing cow’s milk in the second six months of life. J Pediatr Gastroenterol Nutr 1990;10:462-7. 13. de Andraca I, Castillo M, Walter T. Psychomotor development and behavior in iron-deficiency anemic infants. Nutr Rev 1997;55:125-32. 14. Pipes PL. Infant feeding and nutrition. In: Trahms CM, Pipes PL, eds. Nutrition in Infancy and Childhood. New York: McGraw Hill, 1997:98129. 15. Anderson GH, Morson-Pasut LA, Bryan H, et al. Age of introduction of cow’s milk to infants. J Pediatr Gastroenterol Nutr 1985;4:692-8. 16. Ziegler EE. Milk and formulas for older infants. J Pediatr 1990;117:S769. 17. Fuchs GJ, Gastanaduy AS, Suskind RM. Comparative metabolic study of older infants fed infant formula, transition formula, or whole cow’s milk. Nutr Res 1992;12:1467-78. 18. Hide DW. Cow’s milk allergy. Clin Exp Allergy 1993;23:79-80. 19. Jacobsson I, Lindberg T, Benedictsson B, et al. Dietary bovine betalactoglobulin is transferred to human milk. Acta Paediatr Scand 1985;74:342-5. 20. Paganelli R, Cavangni G, Pallone F. The role of antigenic absorption and circulating immune complexes in food allergy. Ann allergy 1986;57:330-6. 21. Host A, Husby S, Osterballe O. A prospective study of cow’s milk allergy in exclusively breast-fed infants. Acta Paediatr Scand 1988;77:66370. 22. Hattevig G, Kjellman B, Sigurs N, et al. Effect of maternal avoidance of eggs, cow’s milk and fish during lactation upon allergic manifestations in infants. Clin Exp Allergy 1989;19:27-32. 23. Sigurs N, Hattevig G, Kjellman B. Maternal avoidance of eggs, cow’s milk and fish during lactation: Effect on allergic manifestations, skinprick tests, and specific IgE antibodies in children at age 4 years. Pediatrics 1992;89:735-9. 24. Lilja G, Dannaeus A, Foucard T, et al. Effect of maternal diet during late pregnancy and lactation on the development of atopic diseases in infants up to 18 months of age – in-vivo results. Clin Exp Allergy 1989;19:473-9. 25. Gerstein HC, VanderMeulen J. The relationship between cow’s milk exposure and type I diabetes. Diabetic Med 1996;13:230-9. 26. Sheard NF. Cow’s milk, diabetes, and infant feeding. Nutr Rev 1993;51:79-89. 27. Dahl-Jørgensen K, Joner G, Hanssen KF. Relationship between cow’s milk consumption and incidence of IDDM in childhood. Diabetes Care 1991;14:1081-3. 28. Varrala O, Knip M, Paronen J, et al. Cow’s milk formula feeding induces primary immunization to insulin in infants at genetic risk for type 1 diabetes. Diabetes 1999;48:1389-94. 29. Couper JJ, Steele C, Beresford S, et al. Lack of association between duration of breast-feeding or introduction of cow’s milk and development of islet autoimmunity. Diabetes 1999;48:2145-9. 30. American Academy of Pediatrics. Infant feeding practices and their possible relationship to the etiology of diabetes mellitus. Pediatrics 1994;94:752-4. 421