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Cariogenic potential of cows', human and infant formula milks and effect of fluoride supplementation

Published online by Cambridge University Press:  25 June 2008

Regina Celia Rocha Peres
Affiliation:
Department of Pediatric Dentistry, Dental School of Piracicaba, State University of Campinas, Av. Limeira, 901 13414-903Piracicaba, Sao Paulo, Brazil
Luciane Cristina Coppi
Affiliation:
Physiological Sciences, Dental School of Piracicaba, State University of Campinas, Sao Paulo, Brazil
Maria Cristina Volpato
Affiliation:
Physiological Sciences, Dental School of Piracicaba, State University of Campinas, Sao Paulo, Brazil
Francisco Carlos Groppo
Affiliation:
Physiological Sciences, Dental School of Piracicaba, State University of Campinas, Sao Paulo, Brazil
Jaime Aparecido Cury
Affiliation:
Physiological Sciences, Dental School of Piracicaba, State University of Campinas, Sao Paulo, Brazil
Pedro Luiz Rosalen*
Affiliation:
Physiological Sciences, Dental School of Piracicaba, State University of Campinas, Sao Paulo, Brazil
*
*Corresponding author: Dr Pedro L. Rosalen, fax +55 19 2106 5218, email rosalen@fop.unicamp.br
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Abstract

The aim of the present study was to evaluate the cariogenicity of cows', human and infant formula milks, supplemented or not with fluoride, in rats. Sixty female Wistar rats were desalivated and infected with Streptococcus sobrinus 6715.Animals were divided into six groups: group 1, sterilised deionised distilled water (SDW; negative control); group 2, 5 % sucrose added to SDW (positive control); group 3, human milk; group 4, cows' milk; group 5, Ninho® formula reconstituted with SDW; group 6, Ninho® formula reconstituted with 10 parts per million F and SDW. At day 21 the animals were killed and their jaws removed to quantify total cultivable microbiota, Strep. sobrinus and dental caries. The concentration of carbohydrate and fluoride in the milks was analysed. The Kruskal–Wallis test (α = 5 %) was used to analyse the data. The caries score by the milk formula was as high as that provoked by sucrose. Regarding smooth-surface caries, human milk was statistically more cariogenic than cows' milk, which did not differ from the SDW and the Ninho® with fluoride (P>0·05). Groups 2–6 showed higher Strep. sobrinus counts when compared with the negative control group (P < 0·05) but no statistically significant difference was found among them (P>0·05). HPLC analysis showed that infant formula had 9·3 % sucrose and 3·6 % reducing sugars. The infant formula should be considered cariogenic due to the sugars found in it, but fluoride supplementation reduced its cariogenic effect. The human milk was more cariogenic than the cows' milk but not as much as the formula milk.

Type
Full Papers
Copyright
Copyright © The Authors 2008

Although it can be preventable, dental caries is considered a multi-factorial infectious and transmissible disease as well as one of the most common chronic diseases of early childhood(Reference Mouradian1, Reference Gussy, Waters, Walsh and Kilpatrick2). Sugar-containing solutions fed to infants before sleep time might lead to tooth decay(Reference Bowen, Pearson, Rosalen, Miguel and Shih3, Reference Gaffney, Farrar-Simpson, Claure and Davilla4). This practice seems to be one of the major causes of heavy infections on tooth surfaces by Streptococcus mutans, composing 60 % of the microbial population present in dental plaque(Reference Van Houte, Gibbs and Butera5). This condition associated with inappropriate feeding practices can be enhanced by the mechanical effects of a nipple or teat(Reference Bowen, Pearson, Rosalen, Miguel and Shih3) which is sometimes left in the infant's mouth for hours(Reference Chestnutt, Murdoch and Robson6).

Some researchers have assumed that cows' milk is a cariogenic agent and might induce early childhood caries(Reference Ripa7, Reference Kashket and De Paola8); however, others have reported it as a protective, anticariogenic agent due to its high concentration of Ca and phosphate(Reference Rugg-Gunn, Roberts and Wright9). Moreover, the buffering activity of proteins such as casein micelles present in this milk(Reference Bowen and Pearson10) might allow the formation of very stable complexes of calcium phosphate(Reference Aimitis11). Antibacterial enzymes, vitamin D and fluoride have also been found in cows' milk(Reference Grenby, Andrews, Mistry and Williams12).

There is controversy about the cariogenicity of human milk. Human milk has been related to a sort of caries which is like bottle caries, even though some studies have demonstrated its non-cariogenicity(Reference Erickson and Mazhari13). Others have shown that although it is possible for human milk to cause dental caries, the prevalence would appear to be very low and to be associated with breast-feeding that has continued until at least 2 years of age on many occasions during the day and night(Reference Valaitis, Hesch and Passarelli14). Furthermore, the cariogenic potential of human milk seems not to have been explored experimentally(Reference Thomson, Thomson and Chandler15) extensively in vivo. In a recent study using an animal model, human milk was significantly more cariogenic than cows' milk(Reference Bowen and Laurence16).

Infant formula milk has been the major nutritional supplementation method for feeding babies and children. To manufacture infant formulas, the composition of cows' milk is altered, and fluoridated water is usually added(Reference Marshall, Levy, Warren, Broffitt, Eichenberger-Gilmore and Stumbo17). A high potential for inducing caries could be expected for infant formulas due to their high carbohydrate variability(Reference Bowen, Pearson, Rosalen, Miguel and Shih3). Thus, it would be wise to add fluoridated water to the formulas in an attempt to reduce their cariogenic effect. The addition of small amounts of fluoride does not affect the appearance, texture and taste properties of this milk(Reference Bian, Wang, Wang, Rong and Lo18). The efficacy of fluoridated bovine milk in preventing dental caries has been studied in Scotland, Hungary, Chile, China, Russia, England and Bulgaria(Reference O'Mullane19, Reference Wainwright20).

Milk is widely consumed, especially by children, and thus the interaction between different kinds of milk consumed and caries development should be better understood and investigated. In normal conditions, the salivary flow is reduced during sleep and the contact of saliva with teeth can be restricted by bottle-feeding. Accordingly, even milk, which is considered non-cariogenic, might induce rampant caries(Reference Hackett, Rugg-Gunn, Murray and Roberts21).

Therefore, the purpose of the present study was to determine the cariogenic potential of infant formula milk reconstituted or not with 10 parts per million (ppm) fluoride compared with cows' and human milk in a desalivated rat cariogenic model, promoting a decrease in the salivary flow similar to that occurring in the mouth of a sleeping infant.

Materials and methods

Treatments

In the present study, sixty female Wistar rats, aged 19 d, SPF (specific pathogen free) from CEMIB/UNICAMP (Brazil) were used. The present study was approved by the Ethical Committee for Animal Research (CEEA/UNICAMP, approval no. 026/1).

The animals were screened for mutans streptococci as previous described(Reference Gold, Jordan and Van Houte22, Reference Rosalen, Bowen and Pearson23). The rats were infected with Streptococcus sobrinus 6715 at age 20 and 21 d, and received the diet 2000(Reference Keyes24) and sterilised deionised distilled water (SDW) with 10 % sucrose ad libitum for 7 d to establish infection(Reference Rosalen, Bowen and Pearson23). Plating of oral swabs revealed that all animals were successfully infected with the Streptococcus mutans group.

In an attempt to mimic the situation in infants who suck on the breast or the bottle nipple, the rats were surgically desalivated at age 25 d as previously described(Reference Bowen, Pearson, Young and Leach25). After desalivation, the animals were randomly placed in individual cages and assigned to six experimental groups: group 1, SDW; group 2, 5 % sucrose solution; group 3, human milk (pH 6·8); group 4, cows' whole milk (pH 6·7; 3·85 % fat); group 5, Ninho® (growth supporting, Nestlé do Brasil Ltda., Ituiutaba, Brazil) reconstituted with SDW (this milk was chosen in a first experiment where different brands were evaluated and it showed the most cariogenicity(Reference Peres, Coppi, Franco, Volpato, Groppo and Rosalen26)); group 6, Ninho® (growth supporting; Nestlé do Brasil Ltda.) reconstituted with 10 ppm F solution (NaF; Merck S.A., Rio de Janeiro, Brazil). All the animals were subjected to the treatments ad libitum but the rats from groups 1 and 2 additionally received a liquid diet (NCP#2; Ross Laboratories, Columbus, OH, USA (for Similac and Promod) and Cargill do Brasil, Sao Paulo, Brasil (Mazola corn oil)) twice per d (5 ml total), by oral administration, to meet their essential nutritional requirements(Reference Bowen, Pearson, Rosalen, Miguel and Shih3, Reference Bowen, Amsbaugh, Monnell-Torrens, Brunelle, Kuzmiak Jones and Cole27).

Human milk was obtained from the Clinical Hospital of the Medical School of Ribeirao Preto (Sao Paulo, Brazil) where it was collected and stored under freezing temperature until just before use. Milk was randomly mixed and submitted to gentle sonication twice daily to disperse fat globules.

The cows' milk and infant formulas were purchased from a local supermarket and immediately prepared with SDW according to the manufacturer's instructions. The amount of liquid consumed by each animal was recorded daily.

Animals

At day 21 (experiment completion), the animals were killed by CO2 asphyxiation followed by decapitation. The half-lower-left jaw of each animal was aseptically dissected, placed in 5 ml of 0·9 % NaCl solution and then sonicated for 30 s (VibraCell 400W; Sonics & Materials Inc., Danbury, CT, USA). The resulting suspension was used to inoculate blood (5 % sheep blood) agar plates (Difco Co., Detroit, MI, USA) using the Whitley Automatic Spiral Platter (DW Scientific, Shipley, West Yorks, England). Mitis salivarius agar (Difco Co.) plus streptomycin (Sigma Chemical Co., St Louis, MO, USA) plates were used to determine Strep. sobrinus counts(Reference Bowen, Pearson, Rosalen, Miguel and Shih3). Animal heads were defleshed, and caries scores were assessed by using the Keyes method(Reference Keyes28) modified by Larson(Reference Larson and Tanzer29), as follows. Considering unsliced and unstained tooth-smooth surfaces: ‘E’ for white opaque enamel; ‘Ds’ for dry and crumbly enamel surface; ‘Dm’ when dentine is exposed; and ‘Dx’ when dentine is soft or missing (may be dark in colour). Considering stained, sliced tooth-sulcal surfaces: ‘Ds-sulcal’ when the pink dye has penetrated into the dento-enamel junction and up to one-third of the depth of the dentine; ‘Dm-sulcal’ when the pink dye extends more than one-third of the depth of the dentine; ‘Dx-sulcal’ when the dye has penetrated through the dentine (may be soft or missing).

The carbohydrate concentration in the cows' milk, human milk and infant formula was assessed by the HPLC method(Reference Alpenfels, Mathews, Madden and Newsom30) by using Waters HPLC Model 480 E (Milford, MA, USA). The total fluoride in all solutions was determined (limit of detection 0·02 ppm F) according to the Taves method(Reference Taves31), by using a specific fluoride ion electrode (model 96-09; Orion Research, Inc., Boston, MA, USA) and a digital ionic analyser (model EA-940; Orion Research, Inc.).

Statistical analysis

The microbial data and caries scores were assessed separately. The results were statistically analysed using the Kruskal–Wallis test (Student–Newman–Keuls as a post hoc test) at the significance level of 5 % by using the Bioestat 4.0 statistical software (Bioestat 4.0; Mamiraua Institute, Belem, PA, Brazil).

Results

All animals survived and remained healthy during the 21 d experiment. The animal weight gain varied among the groups because the animals that received nutrition by oral administration gained less weight than the others (Fig. 1). A higher consumption of fluids was observed for groups 4, 5 and 6, without statistical difference among them; however, they were different when compared with the other groups (P < 0·05) (Fig. 2).

Fig. 1 Weight gain (g) by desalivated animals, after 21 d of experimentation. The central line is the median; the box represents the lower and upper quartiles; the whisker shows the maximum and minimum values; * outliers. SDW, sterile deionised distilled water; ppm, parts per million. a,b Median values with unlike letters were significantly different (P < 0·05; Kruskal–Wallis).

Fig. 2 Amount of fluid consumed (ml) daily by desalivated animals, after 21 d of experimentation. The central line is the median; the box represents the lower and upper quartiles; the whisker shows the maximum and minimum values. SDW, sterile deionised distilled water; ppm, parts per million. a,b,c Median values with unlike letters were significantly different (P < 0·05; Kruskal–Wallis).

Fig. 3 shows data concerning bacteria counts among all groups tested. The SDW group harboured the highest counts of bacteria (P < 0·05), while the cows' milk group presented the lowest counts (P < 0·05). No statistical difference (P>0·05) was observed among the other groups (5 % sucrose, and human, Ninho® and 10 ppm F Ninho®). All groups showed a high number or percentage of Strep. sobrinus recovered, without statistical difference (P>0·05), except for the SDW group (P < 0·05).

Fig. 3 Total number of bacteria ( × 106 colony-forming units (cfu)/ml; A), number of Streptococcus sobrinus ( × 106 cfu/ml; B) and Strep. sobrinus proportion (%; C) found in desalivated animals, after 21 d of experimentation. The central line is the median; the box represents the lower and upper quartiles; the whisker shows the maximum and minimum values. SDW, sterile deionised distilled water; ppm, parts per million. a,b,c Median values with unlike letters were significantly different (P < 0·05; Kruskal–Wallis) considering total number of bacteria, Strep. sobrinus number and Strep. sobrinus proportion separately.

Table 1 shows dental caries scores regarding sulcus and smooth surfaces. The cows', human and 10 ppm F Ninho® milks showed a reduction in total smooth-surface caries scores and did not differ from the SDW group; however, the cows' milk showed the lowest caries scores (P < 0·05). The total smooth-surface and sulcal caries scores observed for the Ninho® group did not differ statistically from the 5 % sucrose group. The total sulcal caries scores observed for the cows', human and 10 ppm F Ninho® milks were lower than those obtained for the 5 % sucrose and Ninho® groups and higher than that for the SDW group (P < 0·05). The Ds (lesion extended into dentin) and Dm (exposed dentin) severities in smooth-surface and sulcal caries scores basically followed the same profile of the respective total caries scores.

Table 1 Total and severity caries scores of smooth-surface and sulcal lesions

(Median values and lower and upper quartiles)

SDW, sterile deionised distilled water; ppm, parts per million; Ds, lesion extended into dentin; Dm, exposed dentin.

a,b,c Median values within a row with unlike superscript letters were significantly different (P < 0·05; Kruskal–Wallis).

Lactose was the only carbohydrate found in human and cows' milks and the fluoride amount was negligible (Fig. 4). However, Ninho® and 10 ppm F Ninho®, besides glucose and fructose, contained 9·3 % of sucrose and at least 3·5 times more lactose than the other milks; their fluoride concentration was 0·5 and 10·6 ppm, respectively.

Fig. 4 Percentage (w/v) of carbohydrate and total fluoride (parts per million; ppm) present in every milk tested (n 10/group). Values are means, with standard deviations represented by vertical bars. (), Human milk; (), Cows' milk; (), Ninho®; (), Ninho® 10 ppm F; –, no detected sugar or fluoride.

Discussion

The desalivated rat model, one of the most severe cariogenic challenges available(Reference Bowen and Laurence16), is a very suitable approach for reproducing oral conditions of a milk-bottle-fed infant during sleep, when salivary flow quickly decreases(Reference Bowen, Pearson, Rosalen, Miguel and Shih3).

In the present study, the fluid intake observed for the infant formulas and cows' milk groups was higher than that observed for the controls (5 % sucrose and SDW) and human milk group. This difference might have occurred because the control animals received additional liquid, i.e. an essential nutrition by oral administration twice daily. Although the infant formulas and cows' milk tested showed higher consumption levels when compared with the controls (SDW and 5 % sucrose), they were less cariogenic than 5 % sucrose(Reference Bowen and Pearson10). Human-milk-fed animals consumed similar amounts to those receiving 5 % sucrose and also showed lower levels of caries, even having the same level of Strep. sobrinus infection. It can be assumed that the different amounts consumed did not affect the number of bacteria and consequently caries score. As shown in previous studies(Reference Bowen, Pearson, Rosalen, Miguel and Shih3, Reference Bowen, Amsbaugh, Monnell-Torrens, Brunelle, Kuzmiak Jones and Cole27), a weak relationship between the amount of fluid consumed and caries score was also observed in the present study. All the milks and 5 % sucrose maintained the infection of Strep. sobrinus, which is in accordance with other reports(Reference Bowen, Pearson, Rosalen, Miguel and Shih3, Reference Bowen and Laurence16). In addition, 5 % sucrose is not the sole sugar able to maintain the infection; milks containing carbohydrates other than sucrose are more cariogenic than those containing just lactose.

Earlier studies reported good antibacterial activity for some substances and the protein casein found in milk against some oral micro-organisms(Reference Aimitis11). Evidence showed that milk composition (Ca, P, peptides) could chemically protect dental enamel against demineralisation(Reference Grenby, Andrews, Mistry and Williams12). This could also help to explain why 5 % sucrose was more cariogenic than formula milk which contains 9·3 % sucrose. In the present study, cows' milk showed a significant reduction in the number of total microbiota, except for Strep. sobrinus. This finding could be related to the antibacterial properties of some substance in cows' milk, such as protein casein(Reference Aimitis11). However, Bowen & Pearson(Reference Bowen and Pearson10) using the same animal model could not find any inhibitory effect of bovine milk on total bacteria, including Strep. sobrinus.

Milk was in the past reported as being cariogenic(Reference Ripa7, Reference Kashket and De Paola8), with a lack of proven evidence, since a distinction has not been drawn between the use of a bottle or nipple per se and the fluid content in the feeding bottle(Reference Bowen and Laurence16). If the bottle contains a caries-promoting substrate, then evidently the potential for damage is greatly enhanced.

Cows' milk is not a caries-promoting substrate, being consumed worldwide, especially by children. It is a natural and healthy beverage containing macro- and micronutrients, which could be beneficial for dental structures(Reference Bowen and Laurence16) and general health. The present results are in accord with those observed in previous studies reporting cows' milk as essentially non-cariogenic(Reference Bowen and Pearson10, Reference Bowen and Laurence16, Reference Bowen, Pearson, vanWuyckhuyse and Tabak32). Natural fluoride was found in the cows' milk tested, but its effect was considered irrelevant due to its low concentration (0·02 ppm F).

Epidemiological evidence indicates that breast-feeding for over 1 year during the night after tooth eruption might be associated with early childhood caries and with increased prevalence of dental decay(Reference Valaitis, Hesch and Passarelli14). However, other investigations showed no relationship between prevalence of caries and breast-feeding(Reference Alaluusua, Myllärniemi, Kallio, Salmenperä and Tainio33). In the present study, a significantly higher score concerning smooth-surface caries was observed for human-milk-fed animals when compared with cows' milk-fed ones; however, sulcal caries and its severity, concerning human milk, displayed similar scores to those found for cows' milk. Several factors might account for the higher scores of smooth-surface caries observed for the human-milk group. In the present study, human milk was found to contain more lactose (8·3 %) than that (4·9 %) observed for cows' milk. This higher concentration of lactose might reduce dental plaque pH values, but to a lesser extent than might be expected for sucrose. It is also possible that lactose fermentation in cows' milk is slower than that in human milk. Aqueous solutions of lactose have been reported as modestly cariogenic in rat models(Reference Bowen, Pearson, vanWuyckhuyse and Tabak32). It is assumable that other constituents, such as minerals and casein, in cows' milk might overcome the harmful effects of lactose(Reference Bowen and Pearson10).

There is little control over infant formulas regarding their caries potential. In addition, their stagnation inside the mouth due to the reduced salivary flow and the suckle–sleep–suckle cycle might contribute to the enzymic breakdown of their protective proteins, such as casein(Reference Erickson, McClintock, Green and LaFleur34). The present results, in accordance with previous findings(Reference Bowen, Pearson, Rosalen, Miguel and Shih3), showed cariogenic properties for the infant formula tested, showing a high concentration of sucrose (9·3 %), diversity in carbohydrate, and little amount of fluoride. These characteristics, combined with reduced salivary flow, might result in tooth decay(Reference Alaluusua, Myllärniemi, Kallio, Salmenperä and Tainio33).

Other components such as peptides, casein, ions and vitamins have been reported as reducing the cariogenicity of sugar(Reference Bowen, Amsbaugh, Monnell-Torrens, Brunelle, Kuzmiak Jones and Cole27). However, the efficacy of the formula milk compounds in reducing caries was not tested in the present study. The carbohydrate composition in the infant formula tested might be responsible for the differences in caries scores observed between the cows' and human milks. The present results are in accordance with those reported in previous studies using the same desalivated rat model, showing that infant formulas might have potential cariogenic activity(Reference Bowen, Pearson, Rosalen, Miguel and Shih3).

The addition of 10 ppm fluoride to Ninho® milk significantly reduced its cariogenicity, in accord with findings reported in previous studies(Reference O'Mullane19, Reference Wainwright20). The fluoride ion added to the formula milk tested showed a remarkable anticariogenic effect, even with one of the most severe cariogenic challenges, such as the desalivated animal model.

While the predominant beneficial effect of fluoride occurs in the oral cavity, its adverse effect, dental fluorosis, might result from fluoride intake during tooth development, or even in later mineralisation stages(Reference Fomon, Ekstrand and Ziegler35, Reference Levy36). In places where water is fluoridated, the risk of dental fluorosis development is high(Reference Paiva, Lima and Cury37). Fluoridated water added to powder milk could result in too high an intake of fluoride if infants are ingesting several doses of reconstituted formula per d(Reference Levy36, Reference Paiva, Lima and Cury37). Therefore, in areas with non-fluoridated water, milk supplemented with fluoride could help reduce caries prevalence, without risk of dental fluorosis.

The cariogenic potential of any product directly depends on its use. Ideally, children should not be allowed to sleep with a bottle containing any cariogenic substance and dental care professionals should actively discourage their use. Although our findings showed that the addition of fluoride to infant formula milk might significantly decrease its cariogenicity, further studies are needed before implementing the strategy suggested in the present study.

Our data showed that the infant formula milk was as cariogenic as sucrose. Its cariogenic potential was greatly reduced after fluoride addition. Cows' milk has negligible cariogenicity while human milk clearly has some potential for causing caries. The present results call attention to the importance of feeding infants on cows' and human milk, which were observed to be less cariogenic than the artificial milk formulas.

Acknowledgements

We are grateful to Nestlé for the HPLC assay on milks and to Juliana Bonetti Valerio for language review. This investigation was financially supported by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq; no. 300627/1992-0) and Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP; no. 98/04 779-0). We declare that we do not have any conflict of interest.

R. C. R. P. was responsible for the experimental procedures and manuscript writing; L. C. C. assisted in all the experimental procedures; M. C. V. assisted in all the experimental procedures; F. C. G. was responsible for the statistical analysis and graphic creation; J. A. C. was responsible for part of the laboratory analysis; P. L. R. advised, created and designed the study and also assisted in all the experimental procedures.

References

1Mouradian, WE (2001) The face of a child: children oral health and dental education. J Dent Educ 65, 821831.CrossRefGoogle ScholarPubMed
2Gussy, MG, Waters, EG, Walsh, O & Kilpatrick, NM (2006) Early childhood caries: current evidence for aetiology and prevention. J Paediatr Child Health 42, 3743.CrossRefGoogle ScholarPubMed
3Bowen, WH, Pearson, SK, Rosalen, PL, Miguel, JC & Shih, AY (1997) Assessing the cariogenic potential of some infant formulas, milk and sugar solutions. J Am Dent 128, 865871.CrossRefGoogle ScholarPubMed
4Gaffney, KE, Farrar-Simpson, MA, Claure, D & Davilla, G (2004) Prolonged baby bottle feeding: a health risk factor. Pediatr Nurs 30, 242245.Google ScholarPubMed
5Van Houte, J, Gibbs, G & Butera, C (1982) Oral flora of children with “nursing bottle caries”. J Dent Res 61, 382385.CrossRefGoogle ScholarPubMed
6Chestnutt, IG, Murdoch, C & Robson, KF (2003) Parents and carers' choice of drinks for infants and toddlers, in areas of social and economic disadvantage. Community Dent Health 20, 139145.Google ScholarPubMed
7Ripa, LW (1988) Nursing caries: a comprehensive review. Pediatr Dent 10, 427435.Google ScholarPubMed
8Kashket, S & De Paola, DP (2003) Cheese consumption and the development and progression of dental caries. Nutr Rev 60, 97103.CrossRefGoogle Scholar
9Rugg-Gunn, AJ, Roberts, GJ & Wright, WG (1985) Effect of human milk on plaque in situ and enamel dissolution in vitro compared with bovine milk, lactose and sucrose. Caries Res 19, 327334.CrossRefGoogle ScholarPubMed
10Bowen, WH & Pearson, SK (1993) Effect of milk on cariogenesis. Caries Res 27, 461466.CrossRefGoogle ScholarPubMed
11Aimitis, WR (2004) Bioactive properties of milk proteins with particular focus on anticariogenesis. J Nutr 134, 989S995S.CrossRefGoogle Scholar
12Grenby, TH, Andrews, AT, Mistry, M & Williams, RJ (2001) Dental caries-protective agents in milk and milk products: investigations in vitro. J Dent 29, 8392.CrossRefGoogle ScholarPubMed
13Erickson, PR & Mazhari, E (1999) Investigation of the role of human breast milk in caries development. Pediatr Dent 21, 8690.Google ScholarPubMed
14Valaitis, R, Hesch, R & Passarelli, C (2000) A systematic review of the relationship between breastfeeding and early childhood caries. Can J Public Health 91, 411417.CrossRefGoogle ScholarPubMed
15Thomson, ME, Thomson, CW & Chandler, NP (1996) In vitro and intra-oral investigations into the cariogenic potential of human milk. Caries Res 30, 434438.CrossRefGoogle ScholarPubMed
16Bowen, WH & Laurence, RA (2005) Comparison of the cariogenicity of cola, honey, cow milk, human milk, and sucrose. Pediatrics 116, 921926.CrossRefGoogle ScholarPubMed
17Marshall, TA, Levy, SM, Warren, JJ, Broffitt, B, Eichenberger-Gilmore, JM & Stumbo, PJ (2004) Associations between intakes of fluoride from beverages during infancy and dental fluorosis of primary teeth. J Am Coll Nutr 23, 108116.CrossRefGoogle ScholarPubMed
18Bian, JY, Wang, WH, Wang, WJ, Rong, WS & Lo, EC (2003) Effect of fluoridated milk on caries in primary teeth: 21-month results. Community Dent Oral 31, 241245.CrossRefGoogle ScholarPubMed
19O'Mullane, DM (1994) Systemic fluorides. Adv Dent Res 8, 181184.CrossRefGoogle ScholarPubMed
20Wainwright, WW (1987) Borrow Dental Milk Foundation: program to reduce dental caries in children. Odontostomatol Trop 10, 8596.Google ScholarPubMed
21Hackett, AF, Rugg-Gunn, AJ, Murray, JJ & Roberts, GJ (1984) Can breast feeding cause dental caries? Hum Nutr Appl Nutr 38, 2328.Google ScholarPubMed
22Gold, OG, Jordan, HV & Van Houte, JA (1973) A selective medium for Streptococcus mutans. Arch Oral Biol 18, 13571364.CrossRefGoogle ScholarPubMed
23Rosalen, PL, Bowen, WH & Pearson, SK (1997) Influence of fluoride co-crystallized with sugar on caries development in desalivated rats. Arch Oral Biol 42, 317322.CrossRefGoogle ScholarPubMed
24Keyes, PH (1959) Dental caries in the Syrian hamster. VIII. The induction of rampant caries activity in albino and golden animals. J Dent Res 38, 525533.CrossRefGoogle Scholar
25Bowen, WH, Pearson, SK & Young, DA (1986) The effect of partial desalivation on coronal and root surface caries in the rat. In Factors Relating to Demineralization and Remineralization of the Teeth, pp. 243250 [Leach, SA, editor]. Oxford: IRL Press.Google Scholar
26Peres, RC, Coppi, LC, Franco, EM, Volpato, MC, Groppo, FC & Rosalen, PL (2002) Cariogenicity of different types of milk: an experimental study using animal model. Braz Dent J 13, 2732.Google ScholarPubMed
27Bowen, WH, Amsbaugh, SM, Monnell-Torrens, S, Brunelle, J, Kuzmiak Jones, H & Cole, ME (1980) A method to assess cariogenic potential of foodstuffs. J Am Dent Assoc 100, 677681.CrossRefGoogle ScholarPubMed
28Keyes, PH (1958) Dental caries in the molar teeth of rats. II. A method for diagnosis and scoring several types of lesions simultaneously. J Dent Res 37, 10881099.CrossRefGoogle Scholar
29Larson, RW (1981) Merits and modifications of scoring rat dental caries by the Keyes's method. In Animal Models in Cariology, Microbiology Abstracts Special Supplement, pp. 195203 [Tanzer, JM, editor]. Washington, DC: IRL press.Google Scholar
30Alpenfels, WF, Mathews, RA, Madden, DE & Newsom, AE (1982) The rapid determination of neutral sugars in biological samples by high-performance liquid-chromatography. J Liq Chromatogr 9, 17111723.CrossRefGoogle Scholar
31Taves, DR (1968) Separation of fluoride by rapid diffusion using hexamethyldisiloxane. Talanta 15, 969974.CrossRefGoogle ScholarPubMed
32Bowen, WH, Pearson, SK, vanWuyckhuyse, BC & Tabak, L (1991) Influence of milk, lactose-reduced milk and lactose on caries in desalivated rats. Caries Res 25, 283286.CrossRefGoogle ScholarPubMed
33Alaluusua, S, Myllärniemi, S, Kallio, M, Salmenperä, L & Tainio, VM (1990) Prevalence of caries and salivary levels of mutans streptococci in 5-year-old children in relation to duration of breast feeding. Scand J Dent Res 98, 193196.Google ScholarPubMed
34Erickson, PR, McClintock, KL, Green, N & LaFleur, J (1998) Estimation of the caries-related risk associated with infant formulas. Pediatr Dent 20, 395403.Google ScholarPubMed
35Fomon, SJ, Ekstrand, J & Ziegler, EE (2000) Fluoride intake and prevalence of dental fluorosis: trends in fluoride intake with special attention to infants. J Public Health Dent 60, 131139.CrossRefGoogle ScholarPubMed
36Levy, SM (2003) An update on fluorides and fluorosis. J Can Dent Assoc 69, 286291.Google ScholarPubMed
37Paiva, SM, Lima, YB & Cury, JA (2003) Fluoride intake by Brazilian children from two communities with fluoridated water. Community Dent Oral Epidemiol 31, 184191.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1 Weight gain (g) by desalivated animals, after 21 d of experimentation. The central line is the median; the box represents the lower and upper quartiles; the whisker shows the maximum and minimum values; * outliers. SDW, sterile deionised distilled water; ppm, parts per million. a,b Median values with unlike letters were significantly different (P < 0·05; Kruskal–Wallis).

Figure 1

Fig. 2 Amount of fluid consumed (ml) daily by desalivated animals, after 21 d of experimentation. The central line is the median; the box represents the lower and upper quartiles; the whisker shows the maximum and minimum values. SDW, sterile deionised distilled water; ppm, parts per million. a,b,c Median values with unlike letters were significantly different (P < 0·05; Kruskal–Wallis).

Figure 2

Fig. 3 Total number of bacteria ( × 106 colony-forming units (cfu)/ml; A), number of Streptococcus sobrinus ( × 106 cfu/ml; B) and Strep. sobrinus proportion (%; C) found in desalivated animals, after 21 d of experimentation. The central line is the median; the box represents the lower and upper quartiles; the whisker shows the maximum and minimum values. SDW, sterile deionised distilled water; ppm, parts per million. a,b,c Median values with unlike letters were significantly different (P < 0·05; Kruskal–Wallis) considering total number of bacteria, Strep. sobrinus number and Strep. sobrinus proportion separately.

Figure 3

Table 1 Total and severity caries scores of smooth-surface and sulcal lesions(Median values and lower and upper quartiles)

Figure 4

Fig. 4 Percentage (w/v) of carbohydrate and total fluoride (parts per million; ppm) present in every milk tested (n 10/group). Values are means, with standard deviations represented by vertical bars. (), Human milk; (), Cows' milk; (), Ninho®; (), Ninho® 10 ppm F; –, no detected sugar or fluoride.