|Year : 2023 | Volume
| Issue : 1 | Page : 101-107
Breastfeeding effect on primary teeth emergence in relation to craniofacial growth among Iraqi infants
Shaimaa Thabit Salih, Ban Sahib Diab
Department of Pediatric and Preventive Dentistry, College of Dentistry, University of Baghdad, Baghdad, Iraq
|Date of Submission||14-Nov-2022|
|Date of Acceptance||14-Dec-2022|
|Date of Web Publication||29-Apr-2023|
Shaimaa Thabit Salih
Department of Pediatric and Preventive Dentistry, College of Dentistry, University of Baghdad, Baghdad
Source of Support: None, Conflict of Interest: None
Background: Breastfeeding is more than just nutrition; it can be viewed as a natural orthotic device for the harmonious development of the face. Sucking has an impact on a child’s premaxillary region’s growth, and mandibular movements encourage mandibular growth. Along with the advantages for general health, breastfeeding also helps with the right development of teeth, face muscles, and occlusion. Hence symmetric, well-proportioned face and appropriate occlusion depend on balanced facial growth. Objectives: This study aims to evaluate the effect of breastfeeding on the timing of teething in relation to craniofacial development. Materials and Methods: This study is a cross sectional comparative study concerning craniofacial growth assessment, with prospective view concerning timing of eruption. Sample was composed of 100 breastfed infants compared with 100 infants depending on formula milk. Clinical examinations and follow-up for teeth emergence was done for whole sample. Results: Breastfeeding was found to be associated with early teeth emergence. Additionally, although, there were no significant differences between facial growth and feeding pattern there was a significant correlation between delay eruption time of primary dentition and facial growth parameters (mandible and maxilla depths) among bottle-feeding group. Conclusion: The current study confirms the effect of breastfeeding on the early teething emergence of primary dentition; however, there were no significant differences between type of feeding and facial growth parameters. While a significant relation between delay eruption time and facial growth parameters (mandible and maxilla depths) was found among bottle-feeding infants.
Keywords: Breastfeeding, craniofacial growth, primary teeth emergence
|How to cite this article:|
Salih ST, Diab BS. Breastfeeding effect on primary teeth emergence in relation to craniofacial growth among Iraqi infants. Med J Babylon 2023;20:101-7
| Introduction|| |
Human milk is the recommended diet for infants and is known as the “gold” standard for baby nutrition because of its nutritious balance, immunological protection, and other growth-promoting ingredients., In addition to breastfeeding’s positive effects on general growth, it also plays a crucial role in establishing proper craniofacial development because it encourages vigorous orofacial exercise, which enhances the development of the functions of breathing, swallowing, chewing, and phonation. Breastfeeding, according to some schools of thought, is beneficial for the oral cavity’s growth. Among them is better hard palate contouring, which leads to the deciduous dentition being aligned correctly and less malocclusion issues. According to reports, breastfeeding is a habitual nutritive sucking strategy that guards against malocclusion in the primary dentition. Infants’ sucking methods for nursing and bottle feeding may differ, and the sucking mechanism utilized for bottle feeding may increase the risk of a newborn developing a malocclusion., Admittedly, human breasts can alter shape to resemble the oral cavity because they are soft and flexible. On the nipple-squeezing movements, there is agreement that they encourage appropriate lip closure during repose and the correction of physiological mandibular retrognathism. Additionally, because of the tonicity acquired from the high tongue muscle activity, these movements encourage proper tongue alignment in the central incisor palatine region.
Facial growth, which refers to the expansion of the face and cranium bones as well as the general process of postnatal facial development, is crucial for the plastic surgeon. Numerous genetic and craniomaxillofacial illnesses can be diagnosed with the use of facial morphology, a crucial phenotypic trait. When a newborn infant’s skull is proportionally compared to that of an adult, it is clear that the infant has a relatively much larger cranium and a considerably smaller face; this transition is a key component of the pattern of facial growth. The face is one of the more intricate parts of the skull. It consists of about a dozen separate bones and combines a variety of anatomical and functional areas. Simple soft tissue points that lie on top of these bone landmarks can be used to measure the skull. Although soft tissue provides fluctuation, anthropometry nevertheless enables one to directly monitor an individual’s growth. However, variations in skeletal dimensions, muscular development, and environmental factors including diet, health, and climatic effects, which are significant determinants of growth and development, all affect face proportion. For the detection of facial morphological malformations, facial width and height are helpful. Undoubtedly, a short, wide face is mirrored by a subnormal index, whereas a long, narrow face is reflected by a supernormal index. Both Class III and Class II malocclusions are characterized by an unbalanced ratio of the height and width of the face, which affects the occlusion between the dental arches and the patient’s esthetics. In order to achieve a harmonic soft tissue relationship, the underlying dental, skeletal, and neuromuscular systems must be in harmony because they are all interrelated. According to academics and scholars, symmetry is the most important factor in beauty and appeal. Perfect symmetry can be seen on a perfect face. Larger eyes, a narrower nose, and a proportional face overall. There are early indications that people like attractive faces, even at youthful children. According to research, certain infants’ facial symmetry made them appear more appealing than others. Planning for cosmetic and reconstructive facial surgery requires a facial anthropometric analysis. For a quantitative evaluation of the face, there are two anthropometric techniques:
Manual anthropometry: Typically, anthropometric measures are acquired directly from the patient using calipers, necessitating close proximity to the person. Inevitably, the operator’s expertise and experience will determine how accurate the measurements are.
Digital anthropometry: Since the development of stereophotography, it has become feasible to obtain a realistic 3D image of the face with true color and texture. These stereophotographic systems are made up of multiple pairs of similar cameras that are angled at particular angles to collect 3D surface data using specialized software.
Breast milk composition affects mother nutrition and environment., Therefore, considering breastfeeding status is a possible source of variation in the teeth’s emergence time., Human milk contains necessary nutrients for healthy teeth development such as phosphate, calcium, and vitamins A, C, and D. For hydroxyapatite crystals to form properly, calcium and phosphorus are necessary. So, deficiency in the previous nutrients can have an effect on tooth development., The eruption of teeth is a constant biological process by which evolving teeth emerge across jaws and the overlying mucosa into the oral cavity. Tooth eruption also reflects the body’s growth in general. Thus, when tooth eruption is delayed, the body’s growth in general can be said to be constrained. It is a complex and tightly regulated process; hence many factors can influence tooth eruption, for instance: genetics, ethnical, racial, geographical differences, hormones, gender, and nutritional differences.,
As far as there were no previous Iraqi studies concerning the breastfeeding effect on primary teeth emergence in relation to craniofacial growth among infants, therefore, this study was conducted in order to evaluate the effect of breastfeeding on the timing of teething in relation to craniofacial development.
| Materials and Methods|| |
Cross-sectional comparative study is the study’s methodology, concerning craniofacial growth assessment, with longitudinal prospective concern for timing of eruption. The selected sample consisted of (100) breastfed infants compared with (100) infants depending on formula milk. All infants examined and followed for timing of teeth emergence. Both groups examined when they attended the health centers of Baghdad during primary health care. Infants aged between 4 and 9 months were selected in the study. The time of primary teeth emergence in infants was examined through the intraoral examination by using the index finger, feel the incisal edge or tooth cusp tip on the alveolar ridge. When the tooth’s crown edge was clearly visible in the oral cavity, it was regarded to have erupted. Early and delayed teething were taken into consideration when dividing the eruption time into monthly intervals (5–6, 7–8, 9–10, and +11). The infant was placed in the mother’s lap during the intraoral examination, which was done knee to knee position. A mouth mirror was used to inspect the mouth without the use of radiographs. Infants with no teeth emerged at monthly intervals, until the precise eruption time was recorded. Parents were instructed to consider a tooth erupted as soon as any part of the crown emerged through the gingival surface, and to record the date at which this occurred. Craniofacial growth was measured throughout the manual anthropometric measurements of the infants’ face. Measurements were taken directly from the infant using standard spreading caliper and measuring tape according to standard anthropometric methods. Many of these landmarks are easily recognizable visually and measured with a measuring tape, but a few of them require palpation to be located. These landmarks are marked with a face painting marker pen to aid in precise measurement; the tips of a caliper are then placed on the landmarks after inspection and/or palpation. A measurement was deemed asymmetrical if there was a 2 mm or more disparity between the two sides., During measurement, the infants were tried to sit at a rest position on their mother’s lap. The anthropometric landmarks referenced in this study: endocanthion (en); exocanthion (ex); gnathion (gn); nasion (n); subnasale (sn); zygion (zy); tragus (t); cheilion (ch). However, the main distances in the face were measured in this study are: interchanthal distance (en-en); exterchanthal distance (ex-ex); face height (n- gn); face width (zy-zy); and both left and right measurements for all the maxillary depth (t-sn); mandibular depth (t-gn); palpebral fissure length (en-ex); oropalpebral distance (ex-ch). These facial characteristics were measured using the approach outlined by Hall et al. with the child’s head in the Frankfurt horizontal position as shown in [Figure 1]. This study also assesses the facial index, which describes the ratio between the interzygomatic widths to facial height., Additionally, Farkas proportion index (Farkas ratios) to evaluate the growth of maxilla in relation to mandible for both sides, and the differences between right and left were also calculated.
Infants with malnutrition, chronic illness or systemic diseases were excluded. Infants with mixed feeding also were excluded.
Apparently healthy infants, which are absent of systemic congenital abnormalities. Only the Iraqi Arab infants aged between 4 and 9 months were included in this study; at this age the infants depend mainly on breastfeeding as essential nutrition, with taking in consideration the matching in complementary food intake.
The ethical committee of the College of Dentistry/University of Baghdad approved this study at the date of: 2021-4-4, and number: 325. Legal permission was obtained from the Ministry of health to perform clinical examinations at health centers. Also, a special informed consent in accordance with the College of Dentistry in University of Baghdad prepared and distributed to mothers to obtain permission to participate in this study. The Declaration of Helsinki, the World Medical Association’s code of ethics for studies involving humans, guided the conduct of this work.
Statistical analysis using Statistical Package for social Science (SPSS version 22, Chicago, IL), mean and standard error (SE), inferential statistics are: Student ttest, one way analysis of variance (ANOVA), and Pearson correlation, level of significance is at 0.05.
| Results|| |
Infants’ eruption time for primary teeth in relation to feeding pattern is shown in [Table 1]. The data show that the eruption time was significantly higher among bottle feeding infants. Moreover, the relation between facial growth and feeding pattern is shown in [Table 2]. This result reveals that all parameters were lower among breastfeeding than bottle-feeding group, although all differences were not significant. In addition, the result illustrates that the facial proportion indices variability by feeding pattern, were no consistent differences, as well as no significant differences occurred bilaterally as can be seen in [Table 3].
|Table 3: Facial index and Farkas proportion index (Farkas ratios) (mean ± SE) according to feeding pattern|
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The correlation between eruption time of primary dentition and facial anthropometric measurements by feeding pattern is shown in [Table 4]. This result showed that although there were no significant correlations in both groups, there was a highly significant correlation in bilateral facial measurements (maxillary depth (t-sn); mandibular depth (t-gn)) and teething time among bottle-feeding groups. Additionally, [Table 5] shows the facial index mean values according to the eruption time by feeding pattern. Data analyses in each feeding group showed that there was no significant difference in facial index among different eruption time intervals. Moreover, data analyses in each feeding group also indicated that there was no difference that was meaningful in Farkas ratios (bilaterally) among different eruption time periods as shown in [Table 6].
|Table 4: The correlation between eruption time of primary dentition and facial anthropometric measurements by feeding pattern|
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|Table 5: Facial index (FI) (mean ± SE) according to the eruption time by feeding pattern|
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|Table 6: Bi-lateral Farkas proportion index (Farkas ratios) (mean ± SE) by eruption time according to feeding pattern|
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| Discussion|| |
This study was performed to assess how breastfeeding affects the timing of teething in relation to craniofacial growth, and because of no previous Iraqi research works studied these relationships, this study was conducted. The findings of the current study indicate that the breastfed infants have earlier eruption time in comparison with those depending on bottle feeding. This finding is confirmed by many previous studies., This could be attributed to the fact that breast milk contains nutrients in nearly optimum amounts., In addition to other components that aid in the absorption of essential nutrients such as calcium, phosphorus, and vitamins A, C, and D. To create hydroxyapatite crystals successfully, calcium and phosphorus are needed., Also the optimum stimulus for the physiological development of the skeletal and muscular components of the orofacial complex, as well as the emergence of teeth, has been suggested to be breastfeeding. However, the present results were disagreed with several studies who did not show the effect of breastfeeding on the timing and pattern of tooth emergence within the first 12 months of children’s life., This study revealed no significant differences of all facial parameters and facial proportion indices by feeding pattern, and this may confirm the actual impact of breastfeeding on early primary teeth emergence. This is parallel with studies that found no relation between the child’s growth and teething period., Therefore, it is recommended to evaluate the impact of feeding practices on orofacial growth using more retrospective research with older age children and larger sample sizes. However, there was a highly significant correlation in bilateral facial measurements (maxillary depth (t-sn); mandibular depth (t-gn)) and teething time among bottle-feeding groups. This result may confirm delay teething time associated with facial growth gain, especially with mandibular and maxillary depths according to the bottle-feeding group. This is parallel with studies that found positive correlation between bottle-feeding and the craniofacial growth or malocclusion, and concluded that breastfeeding has a positive impact on dental occlusion, and this impact may be greater if breastfeeding lasts for at least six months. Conversely, insufficient breastfeeding and excessive bottle feeding can result in an increase in the frequency of these nonnutritive sucking habits, which are linked to a risk for developing malocclusions.,, Although there was no more evidence available for the relation between facial anthropometric measurements and teething time according to feeding pattern. Therefore, more longitudinal studies need to evaluate the occlusion growth in relation to teething emergence by feeding pattern.
Infants’ age restricts the use of manual method for easily identifiable facial landmarks, despite the disadvantages of this direct method, such as variations in tension and thickness as well as the compressibility of soft tissues are major sources of mistake with this technique. Difficult to achieve the meeting interview (on the infants follow up) due to presence of coronavirus at the time of the study, only calling follow-up interview for assessment teeth emergence.
| Conclusion|| |
The current study confirms the effect of breastfeeding on the early teething emergence of primary dentition; there were no significant differences between type of feeding and facial growth parameters. Moreover, there was a significant correlation among bottle-feeding infants between delay eruption time and facial growth parameters (mandible and maxilla depths); however, they were not significant among breast-feeding groups. Furthermore, no facial symmetrical differences by feeding pattern were found in this study. More longitudinal studies recommended confirming this evidence.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
Data availability statements
The data are original and available online.
| References|| |
Al-Assadi AH Dental caries in relation to oral infections and feeding types among children aged 2–5 years. J Bagh Coll Dent 2012;24:104-8.
Hendricks G, Guo M Human Milk Biochemistry and Infant Formula Manufacturing Technology. Cambridge, United Kingdom: Woodhead Publishing; 2020.
Kefah A Majhool KA, Diab BS The impact of feeding pattern and mother’s oral health on infant’s growth parameters. J Res Med Dent Sci 2022;10:8-11.
Viggiano D, Fasano D, Monaco G, Strohmenger L Breast feeding, bottle feeding, and non-nutritive sucking; effects on occlusion in deciduous dentition. Arch Dis Child 2004;89:1121-3.
Boronat-Catalá M, Montiel-Company JM, Bellot-Arcís C, Almerich-Silla JM, Catalá-Pizarro M Association between duration of breastfeeding and malocclusions in primary and mixed dentition: A systematic review and meta-analysis. Sci Rep 2017;7:1-11.
Hermont AP, Martins CC, Zina LG, Auad SM, Paiva SM, Pordeus IA Breastfeeding, bottle feeding practices and malocclusion in the primary dentition: A systematic review of cohort studies. Int J Environ Res Public Health 2015;12:3133-51.
Al-kinane SM, Al-Dahan ZA The effects of thumb sucking habit on the development of malocclusions in preschool age children in Hilla city. J Baghdad Coll Dent 2019;31:44-9.
Thomaz EBAF, Alves CMC, Gomes e Silva LF, Ribeiro de Almeida CCC, Soares de Britto e Alves MTS, Hilgert J, et al
. Breastfeeding versus bottle feeding on malocclusion in children: A meta-analysis study. J Hum Lact 2018;34:768-88.
Kenneth LJ Smith’s Recognizable Patterns of Human Malformation. 6th ed. Philadelphia: WB Saunders Co; 2006. p. 9.
Proffit WR, Fields HW, Larson B, Sarver DM Contemporary Orthodontics-E-Book. Philadelphia: Elsevier Health Sciences; 2018. p. 30-60.
Cobourne MT, DiBiase AT Handbook of Orthodontics E-Book. United Kingdom: Elsevier Health Sciences; 2015. p. 16.
Shkarin VV, Ivanov SY, Dmitrienko SV, Domenyuk DA, Lepilin AV, Domenyuk SD Morphological specifics of craniofacial complex in people with various types of facial skeleton growth in case of transversal occlusion anomalie. Archiv EuroMedica 2019;9:5-16.
Franchi L, Baccetti T Transverse maxillary deficiency in class II and class III malocclusions: A cephalometric and morphometric study on postero-anterior films. Orthod Craniofac Res 2005;8:21-8.
Rubenstein AJ, Langlois JH, Roggman LA What makes a face attractive and why: The role of averageness in defining facial beauty. In: American Psychological Association, editor. Facial Attractiveness: Evolutionary, Cognitive, and Social Perspectives. Washington, USA: Ablex Publishing; 2002. p. 1-33.
Prokopakis EP, Vlastos IM, Picavet VA, Nolst Trenite G, Thomas R, Cingi C, et al
. The golden ratio in facial symmetry. Rhinology 2013;51:18-21.
Hoss RA, Langlois JH Infants Prefer Attractive Faces. The Development of Face Processing in Infancy and Early Childhood: Current Perspectives. Washington, USA: Nova Science Publishers; 2003. p. 27-38.
Farkas LG, Kolar JC, Munro IR Craniofacial disproportions in Apert’s syndrome: An anthropometric study. Cleft Palate J 1985;22:253-65.
Allanson JE Objective techniques for craniofacial assessment: What are the choices? Am J Med Genet 1997;70:1-5.
Jayaratne YS, Zwahlen RA, Lo J, Tam SC, Cheung LK Computer-aided maxillofacial surgery: An update. Surg Innov 2010;17: 217-25.
Mohamed DA, Alatroshi AM Effectiveness of an educational program on nurses’ knowledge regarding neonatal sepsis: A quasi-experimental study. Med J Babylon 2022;19:185.
Bravi F, Wiens F, Decarli A, Dal Pont A, Agostoni C, Ferraroni M Impact of maternal nutrition on breast-milk composition: A systematic review. Am J Clin Nutr 2016;104:646-62.
Alnemer KA, Pani SC, Althubaiti AM, Bawazeer M Impact of birth characteristics, breast feeding and vital statistics on the eruption of primary teeth among healthy infants in Saudi Arabia: An observational study. BMJ Open 2017;7:e018621.
Aly E, Darwish AA, Lopez-Nicolas R, Frontela-Saseta C, Ros-Berruezo G Bioactive components of human milk: Similarities and differences between human milk and infant formula. Selected Topics in Breastfeeding; 2018. p. 11.
Ballard O, Morrow AL Human milk composition: Nutrients and bioactive factors. Pediatr Clin 2013;60:49-74.
Spence JE Deciduous Tooth Emergence, Maternal and Infant Condition, and Infant Feeding Practices in the Brazilian Amazon (Doctoral Dissertation). The Ohio State University; 2017. Available from: https://rave.ohiolink.edu/etdc/view?acc_num=osu151211453566353
. [Last accessed on January 2022].
Dean JA, editor. McDonald and Avery’s Dentistry for the Child and Adolescent-E-book. USA: Elsevier Health Sciences; 2021. p. 526.
Wise GE, Frazier-Bowers S, D’souza RN Cellular, molecular, and genetic determinants of tooth eruption. Crit Rev Oral Biol Med 2002;13:323-35.
Ahmed HS, Al-Dahan ZA Time of emergence of permanent teeth and impact of nutritional status among 4–15 years old children and teenagers in Basrah City, Iraq. J Baghdad Coll Dent 2016;325:1-7.
Kiran K, Swati T, Kamala BK, Jaiswal D Prevalence of systemic and local disturbances in infants during primary teeth eruption: A clinical study. Eur J Paediatr Dent 2011;12:249-52.
Hall JG, Froster-Iskenius UG, Allanson JE Craniofacies. Handbook of Normal Physical Measurements. Oxford: Oxford University Press; 1989. p. 138-9.
Ghoddousi H, Edler R, Haers P, Wertheim D, Greenhill D Comparison of three methods of facial measurement. Int J Oral Maxillofac Surg 2007;36:250-8.
Deutsch CK, Shell AR, Francis RW, Bird BD The Farkas system of craniofacial anthropometry: methodology and normative databases. In: Handbook of Anthropometry. New York, NY: Springer; 2012 .p. 561-73
Farkas LG, Munro IR Anthropometric examination in patients with congenital anomalies of the head and anthropometric facial proportions in medicine. North-Holland, New York: Elsevier. 1987. p. 79.
Kohli MV, Patil GB, Kulkarni NB, Bagalkot K, Purohit Z, Dave N, et al
. A changing trend in eruption age and pattern of first deciduous tooth: Correlation to feeding pattern. J Clin Diagn Res 2014;8:199.
Sherwood WB, Kothalawala DM, Kadalayil L, Ewart S, Zhang H, Karmaus W, et al
. Epigenome-wide association study reveals duration of breastfeeding is associated with epigenetic differences in children. Int J Environ Res Public Health 2020;17:3569.
Ling HTB, Sum FHKMH, Zhang L, Yeung CPW, Li KY, Wong HM, et al
. The association between nutritive, non-nutritive sucking habits and primary dental occlusion. BMC Oral Health 2018;18:1-10.
Folayan MO, Oziegbe EO, Esan AO Breastfeeding, timing and number of erupted teeth in first twelve months of life in Nigerian children. Eur Arch Paediatr Dent 2010;11:279-82.
Al-Ansari R, Farrag N The effect of breast feeding on eruption of first primary tooth in a group of 6–12 month Saudi children. Br J Med Med Res 2016;16:1-6.
Nsaif AK, Al-Joborae SFF Medical and social analysis of preschool children under the age of six years at secondary and tertiary care after home accidents in Hilla City. Med J Babylon 2022:19:169.
Radzi Z, Yahya NA Relationship between breast-feeding & bottle-feeding to craniofacial & dental development. Ann Dent Univ Malaya 2005;12:9-17.
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6]