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Review Article
variation chiefly during the first 2 years of life.[8] The initial Table 1: History of the development of milk formulas
colonizers are facultatively anaerobic in genera, such as Year Constituents added to infant formula
streptococci and Actinomyces. These are succeeded by Cow’s milk‑based formulas
more strictly anaerobic genera, such as Bifidobaterium in 1867 Formula contained wheat flour, cow’s milk, malt
the gut and Veillonella in the mouth.[4] flour, and potassium bicarbonate
1915 Formula contained cow’s milk, lactose, oleo oils,
Infant Formula and vegetable oils in a powdered form
It is an alternative to breast milk for feeding the child 1935 Protein content of formula was taken into
consideration
and is obtained from other human (surrogate mothers) or
1959 Formula fortified with iron
another mammal. The most frequently used sources include
1960 Formula was concentrated to reduce the renal load
the cow, sheep, and goat.[9]
1962 Whey: Casein ratio was made similar to human’s
Numerous health organizations, including the World milk
Health Organization (2002), the American Academy 1984 Taurine fortification introduced
of Pediatrics (1997), the American Academy of Late 90s Nucleotide fortification was done
Family Physicians (2003), and various others, promote Early 2000s Long‑chain polyunsaturated fatty‑acid fortification
breastfeeding as the ideal form of nutrition for infants introduced
during the 1st year of life. Even so, a vast majority of Noncow’s milk‑based formulas
infants in various parts of the world are fed human’s milk 1929 Introduction of commercially available soy
formula (soy flour)
substitutes since the age of 6 months.[9] Even though these
Mid 1960s Isolated soy protein introduced
food sources are inferior to human’s milk in multiple
respects, it promotes more efficient growth, development,
and nutrient balance than commercially available cow’s of energy.[9] The composition of infant formulas includes
milk. It is recommended that infants who are not breastfed protein, lipid, carbohydrate, linoleic acid, vitamins, and
should consume iron‑fortified infant formulas rather minerals in standardized ranges. When prepared according
than cow’s or goat’s milk until 12 months of age by the to the label directions for use, the product should be free
American Academy of Pediatrics.[8] of lumps and of large coarse particles and suitable for
adequate feeding of young infants. The ingredients should
Infant formulas can be used as substitutes or supplements be clean, of good quality, safe and suitable for ingestion by
for human’s milk. Infant formulas are commonly infants. Furthermore, the normal quality requirements, such
recommended in low birth weight babies, cases of as color, flavor, and odor, are assessed. Various thickeners
malnutrition, emergency situations such as famines, and acidity regulators are also added to it. The product and
vulnerable groups, HIV‑positive mother, and lactose its component should not have been treated by ionizing
intolerant babies.[8] irradiation. Thus, the nutritional safety and adequacy of the
Infant formulas are of two types: cow’s milk‑based formula should be scientifically demonstrated to support
formulas and noncow’s milk‑based formulas. Table 1 shows growth and development of infants.[9]
the history and development of infant formula.[8] The carbohydrate content in infant formula is
predominantly distributed among lactose, sucrose, maltose,
By the early 20th century, it was clear that cow’s milk was
or glucose. Formulas highest in sucrose are alternatives
most likely the best animal‑milk base to work with but
to lactose‑containing milk‑based formulas. The grams of
that certain modifications were needed to make it safe and
total sugars per serving ranged from 1.28 to 11.16 g. Some
palatable for human infants. These modifications included
products are found to be containing 12 g of sugar per
removing animal fat and substituting vegetable oils,
serving.[10]
diluting the protein content for the newborn’s relatively
immature renal tubular system, and adding or balancing Various in vitro studies conducted on rat teeth [Table 2] and
minerals and vitamins (e.g., adding iron, adjusting the human teeth [Table 3] have tried to evaluate the cariogenic
calcium:phosphorus ratio).[8] potential of infant formulas. Some in vivo studies [Table 4]
have also tried to compare the cariogenic potential of
Essential Composition commercially available infant formulas.
Infant formula is a milk‑based product obtained from cows Breast milk provides nutrition for the infant and
or other animals or a mixture of other ingredients which is a source of lactobacilli, Bifidobacteria, and
have been proven to be suitable for infant feeding. All streptococci.[21,22] However, components of breast
ingredients and food additives should be gluten free. Infant milk inhibit growth and attachment of the cariogenic
formula prepared ready for consumption in accordance bacteria, S. mutans in particular.[22] A study conducted by
with instructions of the manufacturer should contain per Holgerson et al.[23] revealed that the Lactobacillus counts
100 ml not <60 kcal (250 kJ) and not >70 kcal (295 kJ) in the oral cavity were higher in breastfed as compared to
formula‑fed infants. They also concluded that lactobacilli that formula‑fed infants were at higher risk of developing
species had an inhibitory effect on MS. This suggested dental caries. A systematic review compared various
an experimental study using animal model. Braz Dent J to host ligand‑coated hydroxyapatite in vitro. Caries Res
2002;13:27-32. 2009;43:171‑8.
15. Bowen WH, Lawrence RA. Comparison of the cariogenicity 23. Holgerson PL, Vestman NR, Claesson R, Ohman C, Domellöf M,
of cola, honey, cow milk, human milk, and sucrose. Pediatrics Tanner AC, et al. Oral microbial profile discriminates breast‑fed
2005;116:921‑6. from formula‑fed infants. J Pediatr Gastroenterol Nutr
16. Peres RC, Coppi LC, Volpato MC, Groppo FC, Cury JA, 2013;56:127‑36.
Rosalen PL. Cariogenic potential of cows', human and infant 24. Tan SF, Tong HJ, Lin XY, Mok B, Hong CH. The cariogenicity
formula milks and effect of fluoride supplementation. British J of commercial infant formulas: A systematic review. Eur Arch
Nutr 2008;101:376-82. Paediatr Dent 2016;17:145‑56.
17. Hinds LM, Moser EAS, Eckert G, Gregory RL. Effect of Infant 25. Silva M, Reynolds EC. Fluoride content of infant formulae in
Formula on Streptococcus Mutans Biofilm Formation. J Clin Australia. Aust Dent J 1996;41:37‑42.
Pediatr Dent 2016;40:178-85. 26. Nagata ME, Delbem AC, Kondo KY, de Castro LP, Hall KB,
18. Munshi AK, Kavita H, Santhi KP. Acidogenic potential of the Percinoto C, et al. Fluoride concentrations of milk, infant
infant milk formulas marketed in India. J Indian Soc Pedo Prev formulae, and soy‑based products commercially available in
Dent 2001:1-8. Brazil. J Public Health Dent 2016;76:129‑35.
19. Masih U, Prabhakar M, Joshi JL, Mahay P. A comparative 27. Do LG, Levy SM, Spencer AJ. Association between infant
study of acidogenic potential of milk and commonly used milk formula feeding and dental fluorosis and caries in Australian
formulae. Int J Dent Clin 2010;2:30‑2. children. J Public Health Dent 2012;72:112‑21.
20. Raju AS, Hirehal M, Manjunath PG, Reddy VV, Natraj CG. The 28. Hujoel PP, Zina LG, Moimaz SA, Cunha‑Cruz J. Infant formula
acidogenic potential of different milk formulas on dental plaque and enamel fluorosis: A systematic review. J Am Dent Assoc
pH. Oral Health Prev Dent 2012;10:225‑30. 2009;140:841‑54.
21. Martín R, Heilig GH, Zoetendal EG, Smidt H, Rodríguez JM. 29. Rahul P, Hegde AM, Munshi AK. Estimation of the fluoride
Diversity of the Lactobacillus group in breast milk and vagina concentrations in human breast milk, cow’s milk and infant
of healthy women and potential role in the colonization of the formulae. J Clin Pediatr Dent 2003;27:257‑60.
infant gut. J Appl Microbiol 2007;103:2638‑44. 30. Aarthi J, Muthu MS, Sujatha S. Cariogenic potential of milk and
22. Danielsson Niemi L, Hernell O, Johansson I. Human milk infant formulas: A systematic review. Eur Arch Paediatr Dent
compounds inhibiting adhesion of mutans streptococci 2013;14:289‑300.