Associations of maternal, perinatal and postnatal factors with the eruption timing of the first primary tooth

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ABSTRACT We recruited 1296 mothers in their first trimester from the Affiliated Obstetrics and Gynecology Hospital of Nanjing Medical University between May 2014 and September 2015 to


investigate the associations of maternal, perinatal and postnatal factors with the eruption timing of the first primary tooth (ETFPT) in a Chinese population. We collected maternal


demographic information and clinical data during the perinatal and postnatal period, and oral examinations of the infants were performed by a doctor at 6, 9 and 12 months of age. Multiple


regression analysis was used to identify significant explanatory variables for ETFPT. The mean age at eruption of the first primary tooth for all the infants was 6.82 ± 1.90 months. After


adjustment for confounders, higher maternal childbearing age (β = 0.57; 95%CI = 0.13–1.02), female sex (β = 0.26; 95%CI = 0.07–0.52), and low birth weight (β = 0.98; 95%CI = 0.20–1.76) were


significantly associated with delayed eruption of the first primary tooth, while macrosomia (β = −0.79; 95%CI = −1.30–−0.28) was significantly associated with earlier eruption of the first


primary tooth. Maternal childbearing age, infant sex and infant birth weight were significant determinants of ETFPT. SIMILAR CONTENT BEING VIEWED BY OTHERS PREVALENCE OF MOLAR-INCISOR


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CROSS-SECTIONAL SURVEYS Article Open access 08 April 2024 INTRODUCTION The formation and development of human primary teeth begins at the end of the fifth week of gestation1. Teeth are


formed in the upper and lower jaw through mutual, subtle and sophisticated interactions between the dental epithelium and oral ectomesenchyme involving the expression of several


tooth-related genes1. Primary tooth eruption is a complex and highly regulated process in which teeth enter the mouth and become visible during a certain time period. In most infants, the


first primary tooth to erupt is the central mandibular incisor, which erupts between 2 and 15 months of age2. The complete primary dentition erupts from 10 to 33 months depending on the


position and type of tooth3. Variations in the eruption timing of the first primary tooth (ETFPT) are considered multifactorial. Eruption is under strong genetic control, and the estimates


of narrow-sense heritability are over 70%4. Furthermore, genome-wide association studies (GWAS) have identified some candidate genes associated with tooth development, such as _KCNJ2_,


_EDA_, _HOXB2_, _RAD51L1_, _IGF2BP1_, _HMGA2_ and _MSRB3_5. There are ethnicity- and sex-related differences in the timing of primary tooth eruption6. However, external environmental factors


also make significant contributions to the timing of the primary tooth eruption. Maternal exposure to tobacco during pregnancy7,8, infant birth weight9,10, birth length11, nutritional state


at birth and at postnatal timepoints12, gestational age13, method of infant feeding8,14 and socioeconomic situation15 have been reported to be significant determinants of the eruption of


primary teeth. Delayed tooth eruption has been reported in premature infants13,16 with small gestational age and low birth weight and in those with systemic disorders, such as


hypothyroidism17, while accelerated tooth eruption has been observed in children whose mothers smoked during pregnancy7,8 as well as in those with childhood obesity18 and diabetes


mellitus19. Although several studies have examined the factors influencing tooth eruption, their results are inconsistent8,14,20,21,22. Most of the studies focused only on factors within a


defined period of time and based their findings on evidence from small cohorts, while some studies focused on the whole pregnancy. A prospective cohort study in Turkey23 found that growth


parameters and feeding patterns may be determinants of the timing of tooth eruption. The GUSTO cohort study in Singapore24 found that infant weight gain from birth to 3 months, ethnicity and


maternal childbearing age were associated with the timing of the eruption of the first tooth. A study from the Southampton Women’s Survey25 found that maternal smoking and socioeconomic


status were associated with tooth eruption. Taken together, these cohort studies23,24,25 were based on relatively large populations and focused on comprehensive data, including maternal,


perinatal and postnatal data; in contrast, their results are not entirely consistent. There is definite evidence that children in different geographic regions have different eruption timing


of the primary teeth26,27. Importantly, other factors, including socioeconomic factors, nutritional status, maternal educational levels and overall maternal health vary from country to


country14,28. In the United States, primary tooth eruption timing differs among American Indian, Black and White children29. The GUSTO cohort study in Singapore24 found that compared to


Chinese children, Malay and Indian children experienced significantly delayed tooth eruption. Meanwhile, primary tooth eruption timing differs between Indian children in Singapore24 and in


India30,31. However, there is a lack of population data for residents in Nanjing of China. Therefore, our study aimed to evaluate the relationships between maternal, perinatal and postnatal


factors and ETFPT of infants in a large cohort of Chinese mothers in Nanjing, China. RESULTS SUBJECT CHARACTERISTICS The demographic and clinical characteristics of 1109 mother-child pairs


are shown in Table 1. The maternal childbearing age ranged from 20 to 41 years. Among the mothers, 84 (7.57%) were over 35 years of age, and 50 (4.51%) gave birth at a gestational age of


less than 37 weeks. Among the infants, 524 (47.20%) were females, 26 (2.34%) were classified as low birth weight (<2500 g) and 58 (5.23%) had macrosomia (>4000 g). ETFPT The mean ETFPT


of all the infants was 6.82 ± 1.90 months. As shown in Table 1, ETFPT was significantly delayed in infants born to mothers older than 35 years, infants with a low gestational age and


infants with low birth weight, while the ETFPT was earlier in male infants and those with macrosomia (all _p_ < 0.05). Interestingly, the first eruption peak for both females and males


was 6 months, and the second peak was 8 months (Fig. 1). Within the first 7 months of life, 68.55% of the males had erupted their first primary tooth, compared with only 60.88% of the


females (_p_ = 0.008) (Fig. 2). POTENTIAL DETERMINANTS OF ETFPT Several factors showed significant associations with ETFPT in the univariate analysis, including maternal factors, such as


increased maternal childbearing age and low gestational age, and perinatal and postnatal factors, such as female sex, low birth weight and macrosomia (all _p_ < 0.05, Table 2). No


significant associations with ETFPT were observed for other maternal, perinatal and postnatal factors, including exposure to secondhand smoke during pregnancy, prepregnancy body mass index


(BMI), feeding model or breast feeding duration. The multivariate analysis indicated that the significant determinants of ETFPT were maternal childbearing age and infant sex and birth


weight. Mothers of higher maternal childbearing age (β = 0.57, 95%CI = 0.13–1.02, _p_ = 0.010), female infants (β = 0.26, 95%CI = 0.07–0.52, _p_ = 0.022), and low infant birth weight (β = 


0.98, 95%CI = 0.20–1.76, _p_ = 0.010) were significantly associated with delayed ETFPT, while macrosomia (β = −0.79, 95%CI = −1.30–−0.28, _p_ = 0.000) was significantly associated with


earlier ETFPT (Table 2). DISCUSSION In this prospective study, we systematically analyzed the association of maternal, perinatal and postnatal factors with the ETFPT. We observed that the


first eruption peak for all infants was in the 6th month, and the second peak was in the 8th month. However, the ETFPT was earlier in male infants than in females. Subsequently, we found


that higher maternal childbearing age and low birth weight were significantly associated with delayed ETFPT, while macrosomia was significantly associated with earlier ETFPT. Comparing our


study with the GUSTO study24 revealed some differences in results. First, we found substantial differences (_p_ < 0.001) in the ETFPT between Chinese children in Nanjing, China, and


Singapore. The mean ETFPT of all the infants in our study was 6.82 ± 1.90 months, while in the GUSTO study in Singapore, the mean ETFPT of the Chinese children was 7.80 ± 2.20 months.


Similarly, the mean ETFPT of Indian children was 8.15 ± 1.69 months in a major city in North India30 and 9.50 ± 2.70 months in Singapore24. Meanwhile, another study in India reported that


the mean ETFPT of Indian children in Bhopal was 11.40 ± 3.43 months31. Although differences in tooth eruption timing between shared ancestry populations in different countries/communities do


exist, the reasons may include nutrition, socioeconomic status, climate, and environmental factors, such as the fluoride content in drinking water30. Common environmental toxins can also


affect tooth development in human embryos32. However, for any one factor, the results are inconsistent and inconclusive. The tooth eruption timing reported in this study differs from those


reported in longitudinal studies in other countries33,34, suggesting that population-level differences in the ETFPT may exist. The ETFPT is ethnicity and community dependent. Since the


current standards of primary teeth eruption timing are based mainly on Western populations, our data can be used as a reference for future clinical studies in Nanjing of China. Furthermore,


our study showed that maternal childbearing age as a continuous variable have no statistics significance, however as a ordinal variable that increasing maternal childbearing age is


associated with delayed ETFPT in infants. This finding disagrees with the results of the GUSTO study in Singapore24, which previously uncovered an association between higher maternal


childbearing age and earlier ETFPT in infants. Previous work has demonstrated a similar relationship between maternal childbearing age and child growth parameters in which increased maternal


childbearing age was associated with taller stature in children - on average, children of mothers who were older than 30 years at childbirth were 1.5 cm taller than those of mothers who


were younger than 30 years35. The mechanisms underlying these differences are unclear but may include ethnic or population history differences and environmental and/or genetic factors.


Additionally, the literature suggests that factors such as ethnicity or population history may influence tooth formation and eruption36. The GUSTO study in Singapore24 did not find a


sex-related difference; however, in the present study, we found a sex difference in the ETFPT, which was earlier in males. Our results align with previous studies that found that the primary


teeth erupt earlier in males than in females37,38,39,40. The reason for the differences in the timing of tooth eruption between males and females is poorly understood. We hypothesize that


the earlier onset of the primary dentition is related to differences in sexual maturity and may be partially attributed to environmental and/or genetic influences on growth41. Previous


studies have also suggested that the timing of primary tooth eruption is significantly related to general somatic growth and nutritional status42. Birth weight has been used as a marker of


intrauterine nutritional environment, with low birth weight indicating poor fetal nutrition. Additionally, children who have experienced nutritional deficiencies show delayed primary teeth


eruption43. Interestingly, we found that the first primary tooth eruption occurred earlier in infants with macrosomia, while it was delayed in infants with low birth weight; these findings


are consistent with studies that focused on other populations44,45. Even when chronological age was adjusted for prematurity, infants with low birth weight have been shown to have greater


likelihood of delayed ETFPT46. According to previous research, there was an association between the earlier eruption of permanent teeth and childhood obesity18. Similarly, the GUSTO study in


Singapore24 reported that earlier tooth eruption was associated with infant weight gain from birth to 3 months. Additionally, our study demonstrated that macrosomia is associated with


earlier eruption of the primary teeth. Because birth weight is related to pregnancy and perinatal nutritional status and conditions, the findings of this study also suggest that primary


tooth eruption may be an indicator of the nutritional status of the mother during pregnancy. As a result, we proposed that adequate nutrition during pregnancy and early life may prevent


delayed ETFPT in infants. Previous studies have also found that children born to mothers who smoked during pregnancy had an earlier ETFPT7. Reports indicate that only 2.4% of the women in


China are tobacco smokers47, and most women who do smoke quit after they became pregnant48. Few mothers in China actively smoke during pregnancy, but secondhand smoke exposure still exists.


However, we did not find an association between ETFPT and the mother’s exposure to secondhand smoke during pregnancy. Additionally, some previous studies have noted an association between


breast feeding and the timing of the eruption of primary teeth, finding that children who were not breast fed had delayed tooth eruption49. The effect of breast feeding was also examined in


this study, but we found that neither the breast feeding model nor the duration of breast feeding were significantly related to the ETFPT, which agreed with another report50. Our study has a


number of strengths. First, our participants were drawn from a systematic screening of pregnant women in a population-based, large study performed in Nanjing, China. Moreover, the


relatively large sample size in this study provided good statistical power. There are also several limitations to this study. First, it used information from a cohort based on only one


hospital in one city. The annual delivery rate of Nanjing babies in this hospital was about 20%. Therefore, the results should be considered with caution. Second, some reported risk factors


for ETFPT, such as sociodemographic and socioeconomic characteristics, were not considered for adjustment in this study due to the high percentage of missing data. Third, the data on the


timing of tooth eruption were reported by the mothers and are thus subject to error. To further explore the link between primary tooth eruption and other postnatal factors, further studies


are ongoing. In particular, future studies will explore the association between the eruption timing of primary teeth and the development of subsequent dental caries, which has received


little attention in the literature. CONCLUSIONS Based on this study’s findings, the following conclusions can be drawn: * 1. Higher maternal childbearing age, female sex in infants and low


infant birth weight were significantly associated with delayed ETFPT, while macrosomia was significantly associated with earlier ETFPT. * 2. Considering the limitations of this study, no


associations were observed between other maternal, perinatal or postnatal factors and ETFPT. * 3. The ETFPT differs depending on infants’ ethnicity and community, likely in response to


variation in environmental, developmental and genetic factors. METHODS STUDY DESIGN This study was conducted according to the guidelines in the Declaration of Helsinki, and all procedures


involving human subjects were approved by the Institutional Review Board of Nanjing Maternity and Child Health Care Institute. A total of 1296 singleton pregnant women in their first


trimester were recruited between May 2014 and September 2015. The inclusion criteria included women who intended to give birth at the Affiliated Obstetrics and Gynecology Hospital of Nanjing


Medical University and planned to reside in Nanjing, China, for the 5 years after being recruited into this study. The exclusion criteria included women who had chronic diseases requiring


medication (e.g., prediagnosed diabetes) and those who abused alcohol or substances. All participants signed written free informed consent forms for themselves and their children. MATERNAL


QUESTIONNAIRES AND CLINICAL DATA Maternal general demographic information regarding childbearing age, prepregnancy BMI, pregnancy tobacco exposure, parity, personal health and family history


of disease were collected from a detailed questionnaire. The clinical data of the women during pregnancy, including gestational age and delivery method, were extracted from hospital


laboratory records. The maternal childbearing age of the participants was divided into three groups: <25 years, 25–35 years, >35 years. BMI was calculated as weight (kg)/height (m)2.


The World Health Organization (WHO) criteria were used to classify the women’s BMIs into four groups: underweight (<18.5 kg/m2), normal (18.5–23.9 kg/m2), overweight (24–27.9 kg/m2), and


obese (>28.0 kg/m2). The infants’ gestational age at birth was divided into two groups: low gestational age, which was less than 37 weeks, and normal gestational age, which was at least


37 weeks. Perinatal details, such as infant sex and birth weight, were also obtained. Infant birth weight was divided into three groups: low birth weight (<2500 g), normal birth weight


(2500–4000 g), and macrosomia (>4000 g). CHILD QUESTIONNAIRES AND ORAL EXAMINATIONS Questionnaires regarding child factors, including feeding mode (breast feeding, artificial feeding or


mixed feeding) and duration of breast feeding were collected at subsequent return visits. All oral examinations of the infants were performed at 6, 9, and 12 months of age by one experienced


senior dentist. Meanwhile, a licensed dental assistant checked and recorded the data for each child. Training and calibration sessions were done before the oral examinations. Kappa was used


to assess the intra-examiner reliability and the inter-examiner reliability. To this end, test-retest was done in first 20 samples for the observers and in 50 cases selected randomly, oral


examinations were completed by the two examiners. The agreement between test and retest was 100% and the agreement between the dentist and the dental assistant was also excellent (Kappa = 


1). The examinations were performed under natural light in a dental chair. At each visit, the mothers were asked the age or date at which the child’s first primary tooth erupted. The aim of


the oral examinations was to ascertain the eruption of the child’s first primary tooth and its eruption mode. The eruption of a tooth was defined as the appearance of any part of the tooth


piercing the gum by using Federation Dentaire Internationale (FDI) standards51. Of the total 1296 singleton pregnant women, 45 were excluded because of prediagnosed diabetes, alcohol or


substance abuse, and 1251 live-born infants were delivered. During the 6-, 9-, and 12-month return visits, 40, 53 and 49 patients dropped out because of loss to follow-up, personal reasons,


inconvenience and other factors. After 12 months of oral examinations, sufficient information was available for 1109 mother-child pairs to perform further analysis (Fig. 3). STATISTICAL


ANALYSIS Maternal, perinatal and postnatal information was collected to identify potential determinants of ETFPT (Table 3). Descriptive statistics, including means ± standard deviations,


minimums, maximums and frequencies (percentages) were calculated for all variables. For children with no tooth eruption at the age of one year, the maximum value was recorded as 13 months


because the 12-month visit occurred when the child between 11 to 13 months old. Student’s t-tests and Mann-Whitney U-tests were used to examine the difference in the ETFPT between groups.


Chi-squared and Fisher exact tests were used to examine differences between percentage of children and ETFPT group. Univariate and multivariate linear regression models were used to identify


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references ACKNOWLEDGEMENTS This study was financially supported by the Science and Technology Development Fund of Nanjing Medical University (2016NJMUZD064, 2016NJMUZD065). AUTHOR


INFORMATION AUTHORS AND AFFILIATIONS * Department of Polyclinics, The Affiliated Stomatological Hospital of Nanjing Medical University, Nanjing, 210029, China Huaying Wu, Qian Ma, Xiangqin


Xu & Yaming Chen * Department of Stomatology, The Affiliated Obstetrics and Gynecology Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing,


210004, China Huaying Wu & Xiangqin Xu * Nanjing Maternity and Child Health Care Institute, The Affiliated Obstetrics and Gynecology Hospital of Nanjing Medical University, Nanjing


Maternity and Child Health Care Hospital, Nanjing, 210004, China Ting Chen & Kaipeng Xie * Department of Women Health Care, The Affiliated Obstetrics and Gynecology Hospital of Nanjing


Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, 210004, China Kaipeng Xie * State key Laboratory of Reproductive Medicine, The Affiliated Obstetrics and


Gynecology Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, 210004, China Kaipeng Xie Authors * Huaying Wu View author publications You can


also search for this author inPubMed Google Scholar * Ting Chen View author publications You can also search for this author inPubMed Google Scholar * Qian Ma View author publications You


can also search for this author inPubMed Google Scholar * Xiangqin Xu View author publications You can also search for this author inPubMed Google Scholar * Kaipeng Xie View author


publications You can also search for this author inPubMed Google Scholar * Yaming Chen View author publications You can also search for this author inPubMed Google Scholar CONTRIBUTIONS


Huaying Wu, Ting Chen, Yaming Chen and Kaipeng Xie were involved in the study design. Huaying Wu, Xiangqin Xu and Qian Ma were involved the data collection. Huaying Wu, Ting Chen and Kaipeng


Xie performed the data analyses and drafted the manuscript. All the authors reviewed and revised the manuscript and approved the final manuscript as submitted. CORRESPONDING AUTHORS


Correspondence to Kaipeng Xie or Yaming Chen. ETHICS DECLARATIONS COMPETING INTERESTS The authors declare no competing interests. ADDITIONAL INFORMATION PUBLISHER’S NOTE: Springer Nature


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http://creativecommons.org/licenses/by/4.0/. Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Wu, H., Chen, T., Ma, Q. _et al._ Associations of maternal, perinatal and postnatal


factors with the eruption timing of the first primary tooth. _Sci Rep_ 9, 2645 (2019). https://doi.org/10.1038/s41598-019-39572-w Download citation * Received: 10 July 2018 * Accepted: 25


January 2019 * Published: 25 February 2019 * DOI: https://doi.org/10.1038/s41598-019-39572-w SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content:


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