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Article

Correlation between BMI and Oral Health Status (DMFT, PI, mSBI, and Salivary 1,5-AG) among the Pediatric Population in Saudi Arabia: A Clinico-Biochemical Study

by
Sara Ayid Alghamdi
1,*,
Aziza Aljohar
2,
Basim Almulhim
1,
Abdullah Alassaf
1,
Smita Singh Bhardwaj
1,
Julie Toby Thomas
1,
Abdullah Almalki
1,
Areej Owaid Aljuaid
3 and
Sreekanth Kumar Mallineni
1,4,*
1
Department of Preventive Dental Sciences, College of Dentistry, Majmaah University, Al Majmaah 11952, Saudi Arabia
2
Department of Pediatric Dentistry, King Faisal Hospital and Research Center, Riyadh 11564, Saudi Arabia
3
Border Guard Medical Center, Riyadh 11135, Saudi Arabia
4
Center for Transdisciplinary Research (CFTR), Saveetha Institute of Medical and Technical Sciences, Saveetha Dental College, Saveetha University, Chennai 600077, India
*
Authors to whom correspondence should be addressed.
Children 2022, 9(7), 1017; https://doi.org/10.3390/children9071017
Submission received: 6 June 2022 / Revised: 1 July 2022 / Accepted: 5 July 2022 / Published: 8 July 2022
(This article belongs to the Special Issue Advance Research in Pediatric Dental Disease)

Abstract

:
The study aimed to investigate the association of varying body mass index (BMI) with oral health status among children aged 5–14 years and correlate the concentration of salivary levels of 1,5-AG with varying BMI, dental caries, and periodontal disease. This cross-sectional study was conducted on subjects aged 5 to 14 years. The children were recruited from the Pediatric Dental Clinic, College of Dentistry, Majmaah University, by convenient sampling method. Sociodemographic details and clinical parameters, including body mass index (BMI), DMFT/def (deciduous decayed tooth (d), deciduous extracted tooth (e), deciduous filled tooth (f), permanent tooth decayed (D), permanent missing tooth (M), and permanent filled tooth (F)), plaque index (PI), and modified sulcular bleeding index (mSBI), were evaluated. Salivary 1,5-anhydroglucitol (1,5-AG) was analyzed using an enzyme-linked immunosorbent assay (ELISA) for all the subjects. Statistical analyses performed using SPSS v. 27 (IBM Statistics, Chicago, IL, USA) and the Kruskal–Wallis and chi-square tests were used for comparisons. The Spearman rank correlation coefficient was used to examine the association between the study subjects’ independent variables, BMI, and caries activity. The mean def score, PI, and mSBI scores were higher in obese children. PI score, mSBI score, and salivary concentrations of 1,5-AG between the BMI categories were statistically significant (p < 0.001). The study emphasizes promoting preventive oral health regimes, health awareness campaigns, and nutritional educational programs among the pediatric population.

1. Introduction

Good oral health reflects an individual’s positive well-being and ability to adjust to all the physiological and psychological changes throughout his or her lifetime. Dental practice often sets up an ideal environment for motivating children and young adults to carry out independent self-care dental hygiene procedures, maintain a healthy diet, and initiate the preventive process [1]. The current COVID-19 pandemic has increased the prevalence of chronic oral diseases, such as dental caries and gingivitis, despite being highly preventable among the pediatric population around the globe. This surge could be related to the fact that pediatric dentists focused primarily on emergency interventions, and specific dental protocols were followed to control the spread of viral transmission [2]. Children are deprived of a healthy diet and access to oral health care facilities, further getting accustomed to electronic gadgets, mental stress, and social isolation [3].
Dental caries manifests as demineralization of the complex tooth structure, resulting in deep cavitation and toothache if allowed to progress. The increased prevalence of dental caries among the Saudi Arabian pediatric population is more associated with poor brushing habits, snacking between meals, low consumption of fruits, and frequent consumption of soft drinks and flavored milk, irrespective of socioeconomic factors, as seen in low-income and middle-income countries [4]. This could reflect on the child’s overall well-being and behavioral pattern, negatively impacting school performance and exacerbating social inequalities. From a dental practitioner’s perspective, it makes solid sense to initiate an oral health improvement program and monitor the effective implementation of oral disease prevention measures [5].
Over the past decade, the increasing burden of overweight and obesity among Saudi children and adolescents has profoundly impacted their physical health and social and emotional well-being [6]. WHO reports state that childhood obesity is linked to various comorbidities, including metabolic, cardiovascular, orthopedic, neurological, hepatic, pulmonary, renal, and periodontal disease [7,8]. Globally, periodontal disease is considered the 11th most prevalent condition [9]. A cross-sectional study conducted among Saudi Arabian high school children demonstrated a prevalence of gingivitis at 65%, with the primary etiology being attributed to poor oral hygiene practices [10]. Obesity, dental caries, and periodontal disease share common risk factors, such as increased sugar consumption, dental biofilm, socioeconomic factors, and behavioral and genetic predisposing factors [11]. Despite conflicting reports, Al-Ansari et al. [12] demonstrated that obese children are 2.21 times more likely to have been affected by dental caries than children with a low caries experience.
A longitudinal southern Chinese study revealed that poor dental health care among overweight/obese individuals with a higher body mass index in the teenage years of 15 was associated with periodontal inflammation at the age of 18, building the need for public health to prioritize improving knowledge on oral hygiene practices and healthy eating habits among secondary school students [13]. Reduced salivary flow rate, higher visual plaque index (VPI), and bleeding on probing (BOP) were observed among obese 14-year-old patients with dental caries [14]. Oral health education and reinforcement of oral health practices in children are quite challenging for dental clinicians [15]. Noninvasive techniques are becoming popular in the present era, and clinicians and researchers are preferring to use saliva samples over blood samples [16]. Saliva has added advantages over blood as it hardly coagulates, is simple to collect, and is easy to transport and store for further analysis [17].
1,5-Anhydroglucitol (1,5-AG), a naturally occurring monosaccharide, is derived from diet and absorbed in the gut. Patients with standard glycemic control maintain constant plasma and salivary concentrations of 1,5-AG. It has been considered as an emerging marker for glycemic control. It has been found to have an inverse association with blood sugar concentration [18]. Its levels vary depending on the type and proportion of the consumed carbohydrates [19]. Studies have found a significant difference in the levels of salivary 1,5-AG among high-caries-risk and caries-free children [18,19]. Syed et al. [20] demonstrated a strong negative correlation between salivary levels of AG and the high-caries-risk group. This could serve as an early indicator of caries status in children prior to tactile detection. There is still limited substantive literature on salivary diagnostics in the early identification of oral disease among children. Public health-care sectors should prioritize screening for early diagnosis and oral monitoring conditions, further implementing preventive practices by educating the parents on the importance of a healthy diet regimen and lifestyle pattern for better oral health. Henceforth, the objective of this study was to investigate the association of varying body mass index (BMI) with oral health status among children aged 5–14 years and to correlate the concentration of salivary levels of 1,5-AG with BMI dental caries and periodontal disease.

2. Materials and Methods

Ethical approval for this study was granted by the Institutional Review Board of Majmaah University (Ethics Number: MUREC- August.25/COM-2021 I 2-1), following the principles stated in the Declaration of Helsinki (25/08/2021). Written consent was obtained from the parents/guardians of all the subjects, along with verbal consent from all the study subjects. A convenient sample of children attending the Pediatric Dental Clinic, College of Dentistry, Majmaah University, was collected between 1 September 2022 and 20 September 2021. A minimum sample size of 95 children was included in the study, considering the statistical power of 80% from the study reported by Al-Ansari et al. [12]. Healthy children aged 5–14 years from the regular patients’ pool were included in the study. Children who were attending an emergency treatment, were undergoing orthodontic treatment, were medically compromised, were using any medications for the past 6 months, and had arrested carious lesions were excluded from the study. The participation of the children in the interview session and clinical examinations was conducted as per the COVID-19 protocol standards set by the World Health Organization (WHO). The parents of the children were requested to respond to the interview session conducted by a single examiner, who recorded the sociodemographic details digitally, including age, gender, education levels, previous dental and medical history, diet histories such as number of meals and consumption of sugar-containing snack or beverages per day, and oral hygiene practices.
Body height and body weight were measured for all the subjects by one trained and calibrated examiner following the standardized protocol recommended by Lohman et al. using a physician’s scale and stadiometer [21]. Body mass index (BMI) was evaluated by dividing the weight (kg) by the square of the height (m2). All the subjects were categorized based on the BMI score, which included underweight (<18 kg average), normal weight (18.5–24.9 kg/m2), overweight (25–29.9 kg/m2), and obese (≥30 kg/m2) [22].
Two calibrated examiners performed clinical assessments using a dental mirror, community periodontal index (CPI) probe, dental explorer, gauze, artificial light source, and plaque disclosing agent. Intra- and interinvestigator reliabilities were evaluated to be 0.89 and 0.83 using the kappa coefficient. Dental caries and periodontal health were assessed using the decayed, missing, and filled teeth index for permanent (DMFT) and deciduous teeth (dmf/def index), modification of Quigley–Hein plaque index, and modified sulcular bleeding index (mSBI) [23,24,25]. The periodontal pocket depth and clinical attachment loss were used to assess periodontal health [26].
The plaque index (PI) was evaluated using a two-tone disclosing agent with a microbrush on the tooth surfaces. The tooth surfaces were rinsed after 2 min for 30 s with the help of water spray and high-volume suction. The color-stained plaque was assigned a score in the range of 1–5 based on these criteria: 0 = no plaque, 1 = separate flecks of plaque at the cervical margin of the tooth, 2 = a thin continuous band of plaque (up to 1 mm) at the cervical margin of the tooth, 3 = a band of plaque wider than 1 mm but covering less than one-third of the crown of the tooth, 4 = plaque covering at least one-third but less than two-thirds of the crown of the tooth, and 5 = plaque covering two-thirds or more of the crown of the tooth.
mSBI and periodontal pocket depth (PPD) were evaluated using a sterile CPI periodontal probe [27]. An mSBI score ranging from 0 to 3 was assigned to each facial and lingual nonrestored surface of all the teeth according to the following criteria: 0 = no bleeding when the periodontal probe is passed along the gingival margin, 1 = isolated bleeding spots visible, 2 = blood forms a confluent red line on the gingival margin, and 3 = heavy or profuse bleeding. The average score for all the teeth was taken for data analysis. A 5 mL of saliva was collected 2 h after breakfast by the spitting method from all the children in the study sample [28]. The children were instructed to spit into sterile graduated 5 mL polypropylene vials after 30 s. The principal investigator labeled the samples blinded to the subjects’ sociodemographic and clinical assessment records. All the samples were stored at −80 °C until further analysis.

2.1. Quantitative Estimation of Salivary 1,5-AG Using Enzyme-Linked Immunosorbent Assay (ELISA)

An ELISA kit for 1,5-AG (CEB046Ge, Cloud-Clone Corp., Katy, TX, USA) was used with minor modifications of the protocol provided by the manufacturer. The stored saliva was thawed and centrifuged (Kenley, London, UK, rotor radius: 7 cm) at 3500 rpm for 10 min to remove proteins; the clear supernatant was collected to estimate 1,5-AG levels. To make the calculation more accessible, the OD value of the standard (X-axis) was plotted against the standard’s concentration (Y-axis) log. The best-fit straight line was drawn through the standard points, as determined by regression analysis, using the plotting software CurveExpert version 2.6.4. The concentration of 1,5-AG in the saliva samples was determined from this curve.

2.2. Statistical Analysis

All the data obtained were entered into MS Excel (Microsoft 2019, Redmond, WA, USA) for further statistical analysis with SPSS v. 27 (IBM Statistics, Chicago, IL, USA). The Kolmogorov–Smirnov test showed that the data distribution of 1,5-AG violates the normality assumption, and we opted for nonparametric statistical methods to analyze the collected data on study variables. The Kruskal–Wallis and chi-square tests were applied to compare all the study subjects’ BMI scores and clinical parameters. The Spearman rank correlation coefficient was used to examine the association between the study subjects’ independent variables, BMI, and caries activity. Descriptive statistics, such as frequency distributions, percentages, means, and standard deviations, were used to summarize the data collected. A calculated p-value less than 0.05 is considered statistically significant.

3. Results

The mean age of the children that participated in the study sample was 8.5 (2.0) years. The mean BMI of the subjects was 18.8 (7.08). The mean def score was 3.0 (3.4). This was found to be higher when compared with the mean DMFT score of 2.9 (2.7). The mean number of decayed teeth ‘d’ scores of the participants was 5.7 (2.4), while the number of permanent decayed ‘D’ scores was 2.5 (2.2). The mean PI and mSBI scores were 2.1 (1.2) and 0.6 (0.6). The mean biochemical salivary levels of 1,5-AG was 1.9 (1.6) μg/mL (Table 1). The majority of the participants reported an average eating speed (50.0%), while 20.4% reported eating fast. The majority of the subjects (86%) had no family history of periodontal disease or diabetes mellitus. About 95% of the participants used a brush, and 80.6% reported brushing once daily. Most of the subjects (67.3%) visited the dentist once a year (Table 2). Most of the subjects did not have any physical activity as part of their daily routine. Figure 1 shows the distribution of the participants based on four categories of BMI, and Figure 2 shows the frequency of food and sugar intake among the subjects. The majority of the children (91.8%) reported having food between main meals. About 89.8% reported having sweetened drinks between their main meals, and 67.3% of the subject’s sugar consumption was limited to the main meals.
The relationship between BMI and clinical parameters among the study subjects is shown in Table 3). The mean def score was higher among the participants belonging to the obese BMI category. The mean DMF score was higher among the participants belonging to the normal BMI category. However, these differences were not found to be statistically significant. The PI and mSBI scores were high among the normal and overweight BMI categories. The salivary 1,5-AG levels were highest among the obese participants. The difference in the PI score, mSBI score, and salivary concentrations of 1,5-AG between the BMI categories was statistically significant (p < 0.001).
The association between the independent variables, BMI, and caries activity of these children is shown in Table 4. The BMI score was positively correlated with PI, mSBI, and salivary 1,5-AG levels. This indicates that as BMI scores increased, the PI, mSBI, and salivary 1,5-AG levels were also increased (p-value = 0.003, 0.001, and 0.001, respectively). The mean DMF scores were positively correlated with the PI scores (p-value = 0.007). The PI scores were positively correlated with mSBI, and the results were statistically significant (p < 0.001). The association between sociodemographic characteristics and BMI in shown in Table 5. There was a significant association between sugar intake between main meals and obesity (p-value = 0.02). The majority of the participants who reported eating at an average speed (52.8%) belonged to the nonobese category.

4. Discussion

The study population comprised 95 pediatric patients aged 5–14 years. Based on the BMI score, about 60% belonged to the underweight category, 9.2% were found to be obese, and 6% were overweight subjects. The study’s findings were in accordance with the observations of Hijji et al. [29], who reported an increasing prevalence of underweight status among the adolescent group in Saudi Arabia. Studies have also reported that the overall growing prevalences of childhood overweight and obesity in Riyadh were about 13.4 and 18.2 [5]. The emergence of the global pandemic was thought to have hardly affected the childhood population, despite indirectly creating a drastic change in behavioral lifestyle patterns among the pediatric population. Various studies have demonstrated the unprecedented consequences of childhood home confinement; certain studies have stated that deprivation of oral health care facilities, unhealthy diet patterns, sedentary lifestyle, and decreased physical activity resulted in childhood obesity in high-income and developed countries. In contrast, other studies reported underweight and malnutrition among the population belonging to low-income countries. This dual burden of overweight and underweight among the pediatric population could negatively influence their overall health status [30]. The salivary biomarker 1,5-AG has been used as a noninvasive marker for screening at-risk diabetic patients. Juraschek et al. [19] concluded that reducing the type and amount of dietary carbohydrates reduced 1,5-AG concentrations in a population without diabetes. In the present study, concentrations of salivary 1,5-AG were found to be increased in the obese category (p < 0.05). Yeong et al. [31] demonstrated that overweight/obese subjects had greater 1,5-AG levels and lower glycated hemoglobin levels (HbA1c) than the diabetes group.
Caries estimation in this study population was performed by evaluating the def and DMF index scores [24]. Summarizing the results from descriptive statistics of the study, it was found that the def score was found to be greater than the mean DMF score, indicating that deciduous dentition was more affected compared with permanent dentition. The mean deciduous decay score (d) of 5.67 (2.37) was comparatively higher than the mean permanent decay score (D) of 2.53 (2.19). The findings in the study are consistent with those in a study by Farooqi et al. [32], where the mean dmft value was 3.66 (3.13) and the mean DMFT value was 1.94 (2.0). Data reports stated a dramatic rise in the prevalence of dental caries of about 60–85% among the pediatric population with a mean def score of 1.4 and a DMFT score of 1.72–2.66 [33]. There is a necessity to alert public health workers to concentrate more on educating and creating awareness among parents of the importance of regularizing the need for dental hygiene after feeding and promoting preventive measures to arrest the progression of dental caries [34,35].
The sociodemographic characteristics observed in this study’s caries activity were related to inadequate oral hygiene practices, infrequent dental visits, increased sugar content, and unhealthy dietary pattern. These findings are consistent with those of an investigation conducted among high school students by Fagerberg et al. [36]. The authors reported a conclusive remark on the association between the objectively measured eating rate with students’ weight status. They found that students with fast eating rates consumed more food during school lunch compared with students with a slow eating rate.
Investigative research has been focusing on specific salivary biomarkers that could serve as a potential tool for early diagnosis and preventing the progression of dental caries. A weak negative correlation between caries index and salivary 1,5-AG was observed in this study. In contrast, an Arabian recent survey [20] demonstrated a strong negative correlation between salivary 1,5-AG and the caries active group and the authors concluded that salivary 1,5-AG can act as an indicator of caries status in children. AG, a metabolically inert monosaccharide, inhibits the growth of cariogenic bacteria, thus decreasing the caries activity in the oral environment. Nonetheless, the development of cariogenic bacteria favors increased fermentation of the saccharide substrate for cellular metabolism, thus reducing the salivary 1,5-AG levels [19].
Gingivitis rarely progresses to periodontitis in children. Therefore, none of the study subjects demonstrated clinical loss of attachment. In the present study, the mean scores of PI and mSBI were 2.11 (1.21) and 0.65 (0.65). A cross-sectional study of high school children observed a high prevalence of gingivitis mainly due to poor oral hygiene practices [9]. So far, no studies have reported the periodontal health status among children aged 5–14 years. On analyzing the degree of association of chronic oral diseases with BMI scores, it was found that obese children demonstrated a higher def score. Still, the findings were not found to be statistically significant. This could be probably due to an inadequate sample size in different BMI categories. The result was consistent with other observational studies in the Saudi Arabian population, where the caries index and obesity relationship did not infer any statistically significant impact [37]. A cross-sectional study [11] observed that obese participants had a higher mean DMFT score than nonobese participants. This infers the need to create awareness among the child population to modify their lifestyle and behavioral patterns concerning intake of healthy balanced nutrition, indulging more in physical activity, and practicing regular oral health care.
Analysis by the Kruskal–Wallis test demonstrated a statistically significant (p < 0.05) positive correlation between the PI, mSBI, and higher BMI scores. These findings were in accordance with a recent Arabian study [38] that concluded that obese subjects are more prone to gingival diseases than nonobese subjects. Oral bacteria could contribute to increased metabolic deficiency, leading to unwanted weight gain irrespective of calorie consumption, diet, or exercise. An increase in bleeding observed in obese children could probably be due to an increased level of C-reactive protein and fibrinogen produced by the liver to initiate the chronic subclinical systemic inflammatory response. Furthermore, the prevalence of periodontal disease decreased with increased physical activity and was directly proportional to the frequency of activity. Oral bacteria could increase appetite following weight gain, alter tissue resistance to insulin by increasing the levels of proinflammatory cytokines, and reduce adiponectin levels, disrupting its modulatory role in periodontal health [39]. Saliva, being a natural reservoir, can harbor various biochemical molecules, which can mitigate triggering inflammation and cause deterioration of the tooth-supporting tissue [40,41]. Goodson et al. [42] identified multiple metabolites in saliva at different levels of obesity and gingivitis. 1,5-AG, being a diet-derived monosaccharide, excess in calorie consumption is positively associated with obesity. Statistical analysis of the study data demonstrated a significant positive correlation between the BMI scores and PI, mSBI, and salivary concentrations of 1,5-AG. Statistically effective results were observed for chronic oral diseases, such as dental caries (p < 0.007) and gingivitis (p < 0.001), with PI. Further longitudinal studies are warranted to detect the role of 1,5-AG in dental caries and gingivitis in correlation with various dietary patterns. The association of 1,5-AG with dental caries and gingivitis was not statistically evident in this study. This could be due to the premises of the cross-sectional study design and the insufficient expression of the biomarker in saliva. To accomplish sustainable improvements in children’s health, the nation must emphasize the need to create awareness among the pediatric population of the predisposing factors affecting health and develop effective strategies for early diagnosis, monitoring, and maintenance of global oral health.

5. Conclusions

Within the study’s limitations, the mean def, PI, and mSBI scores were higher in obese children. The PI score, mSBI score, and salivary concentrations of 1,5-AG between the BMI categories were statistically significant. The study suggests that salivary 1,5-AG levels could be used as a noninvasive indicator to assess the obesity status of children.

Author Contributions

Conceptualization, S.A.A. and J.T.T.; methodology, S.A.A.; software, A.A. (Aziza Aljohar); validation, B.A., A.A. (Abdullah Almalki) and A.O.A.; formal analysis, S.S.B.; investigation, S.A.A., J.T.T. and S.S.B.; resources, S.A.A., S.K.M. and A.A. (Aziza Aljohar); data curation, J.T.T.; writing—original draft preparation, S.A.A., S.S.B. and S.K.M.; writing—review and editing, S.K.M.; visualization, S.S.B.; supervision, A.A. (Aziza Aljohar), B.A. and A.O.A.; project administration, S.A.A. and A.O.A.; funding acquisition, S.A.A., B.A., A.A. (Aziza Aljohar), A.O.A. and A.A. (Abdullah Alassaf). All authors have read and agreed to the published version of the manuscript.

Funding

The authors would like to thank the Scientific Research at Majmaah University for supporting this work under R2022-XX.

Institutional Review Board Statement

The ethical approval for this study was granted by the Institutional Review Board of Majmaah University (Ethics Number: MUREC-August.25/COM-2021 I 2-1) in accordance with the principles stated in the Declaration of Helsinki.

Informed Consent Statement

Informed consent was obtained from all the subjects involved in the study.

Data Availability Statement

The data will be available upon request to the correspondence author.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Peres, M.A.; Macpherson, L.M.D.; Weyant, R.J.; Daly, B.; Venturelli, R.; Mathur, M.R.; Listl, S.; Celeste, R.K.; Guarnizo-Herreño, C.C.; Kearns, C.; et al. Oral diseases: A global public health challenge. Lancet 2019, 394, 249–260. [Google Scholar] [CrossRef]
  2. Mallineni, S.K.; Nuvvula, S.; Bhumireddy, J.C.; Ismail, A.F.; Verma, P.; Sajja, R.; Alassaf, A.; Almulhim, B.; Alghamdi, S.; Saha, A.; et al. Knowledge and Perceptions Regarding Coronavirus (COVID-19) among Pediatric Dentists during Lockdown Period. Int. J. Environ. Res. Public Health 2022, 19, 209. [Google Scholar] [CrossRef] [PubMed]
  3. Luzzi, V.; Ierardo, G.; Bossù, M.; Polimeni, A. Pediatric Oral Health during and after the COVID-19 Pandemic. Int. J. Paediatr. Dent. 2021, 31, 20–26. [Google Scholar] [CrossRef] [PubMed]
  4. Alhabdan, Y.A.; Albeshr, A.G.; Yenugadhati, N.; Jradi, H. Prevalence of dental caries and associated factors among primary school children: A population-based cross-sectional study in Riyadh, Saudi Arabia. Environ. Health Prev. Med. 2018, 23, 60. [Google Scholar] [CrossRef] [Green Version]
  5. Carounanidy, U.; Sathyanarayanan, R. Dental caries—A complete changeover (Part I). J. Conserv. Dent. 2009, 12, 46–54. [Google Scholar] [CrossRef] [Green Version]
  6. Al-Hussaini, A.; Bashir, M.S.; Khormi, M.; AlTuraiki, M.; Alkhamis, W.; Alrajhi, M.; Halal, T. Overweight and obesity among Saudi children and adolescents: Where do we stand today? Saudi J. Gastroenterol. Off. J. Saudi Gastroenterol. Assoc. 2019, 25, 229. [Google Scholar] [CrossRef]
  7. Sahoo, K.; Sahoo, B.; Choudhury, A.K.; Sofi, N.Y.; Kumar, R.; Bhadoria, A.S. Childhood obesity: Causes and consequences. J. Fam. Med. Prim. Care 2015, 4, 187–192. [Google Scholar] [CrossRef]
  8. Martinez-Herrera, M.; Silvestre-Rangil, J.; Silvestre, F.J. Association between obesity and periodontal disease. A systematic review of epidemiological studies and controlled clinical trials. Med. Oral. Patol. Oral. Cir. Bucal. 2017, 22, e708–e715. [Google Scholar] [CrossRef]
  9. Nazir, M.; Al-Ansari, A.; Al-Khalifa, K.; Alhareky, M.; Gaffar, B.; Almas, K. Global Prevalence of Periodontal Disease and Lack of Its Surveillance. Sci. World J. 2020, 2020, 2146160. [Google Scholar] [CrossRef]
  10. Alghamdi, A.S.; Almarghlani, A.A.; AlYafi, R.A.; Kayal, R.A.; Al-Zahrani, M.S. Gingival health and oral hygiene practices among high school children in Saudi Arabia. Ann. Saudi Med. 2020, 40, 126–135. [Google Scholar] [CrossRef]
  11. Chapple, I.L.; Bouchard, P.; Cagetti, M.G.; Campus, G.; Carra, M.C.; Cocco, F.; Nibali, L.; Hujoel, P.; Laine, M.L.; Lingstrom, P.; et al. Interaction of lifestyle, behaviour or systemic diseases with dental caries and periodontal diseases: Consensus report of group 2 of the joint EFP/ORCA workshop on the boundaries between caries and periodontal diseases. J. Clin. Periodontol. 2017, 44, S39–S51. [Google Scholar] [CrossRef] [Green Version]
  12. Al-Ansari, A.; Nazir, M. Relationship between Obesity and Dental Caries in Saudi Male Adolescents. Int. J. Dent. 2020, 7, 8811974. [Google Scholar] [CrossRef]
  13. Li, L.-W.; Wong, H.M.; McGrath, C.P. Longitudinal association between obesity and periodontal diseases among secondary school students in Hong Kong: A prospective cohort study. BMC Oral Health 2018, 18, 189. [Google Scholar] [CrossRef]
  14. Modeer, T.; Blomberg, C.C.; Wondimu, B.; Julihn, A.; Marcus, C. Association between obesity, flow rate of whole saliva, and dental caries in adolescents. Obesity 2010, 18, 2367–2373. [Google Scholar] [CrossRef]
  15. Farronato, M.; Tadakamadla, S.K.; Ali Quadri, M.F.; Acharya, S.; Tadakamadla, J.; Love, R.M.; Jamal, M.; Mulder, R.; Maspero, C.; Farronato, D.; et al. A Call for Action to Safely Deliver Oral Health Care during and Post COVID-19 Pandemic. Int. J. Environ. Res. Public Health 2020, 17, 6704. [Google Scholar] [CrossRef]
  16. Anthonappa, R.P.; King, N.M.; Rabie, A.B. Evaluation of the long-term storage stability of saliva as a source of human DNA. Clin. Oral Investig. 2013, 17, 1719–1725. [Google Scholar] [CrossRef]
  17. Ying, L.; Jian, C.; Ma, X.; Ge, K.; Zhu, W.; Wang, Y.; Zhao, A.; Zhou, J.; Jia, W.; Bao, Y. Saliva 1,5-anhydroglucitol is associated with early-phase insulin secretion in Chinese patients with type 2 diabetes. BMJ Open Diabetes Res. Care 2021, 9, e002199. [Google Scholar] [CrossRef]
  18. Halama, A.; Kulinski, M.; Kader, S.A.; Satheesh, N.J.; Abou-Samra, A.B.; Suhre, K.; Mohammad, R.M. Measurement of 1,5-anhydroglucitol in blood and saliva: From non-targeted metabolomics to biochemical assay. J. Transl. Med. 2016, 14, 140. [Google Scholar] [CrossRef] [Green Version]
  19. Juraschek, S.P.; Miller, E.R., 3rd; Appel, L.J.; Christenson, R.H.; Sacks, F.M.; Selvin, E. Effects of dietary carbohydrate on 1, 5-anhydroglucitol in a population without diabetes: Results from the OmniCarb trial. Diabet. Med. 2017, 34, 1407–1413. [Google Scholar] [CrossRef] [Green Version]
  20. Syed, S.; Yassin, S.M.; Dawasaz, A.A.; Amanullah, M.; Alshahrani, I.; Togoo, R.A. Salivary 1,5-Anhydroglucitol and Vitamin Levels in Relation to Caries Risk in Children. BioMed Res. Int. 2019, 2019, 4503450. [Google Scholar] [CrossRef]
  21. Lohman, T.G.; Ring, K.; Pfeiffer, K.; Camhi, S.; Arredondo, E.; Pratt, C.; Pate, R.; Webber, L.S. Relationships among fitness, body composition, and physical activity. Med. Sci. Sports Exerc. 2008, 40, 1163–1170. [Google Scholar] [CrossRef] [Green Version]
  22. World Health Organization. Summary Report of the Update of Systematic Reviews of the Evidence to Inform the WHO Guidelines on Physical Activity, Sedentary Behaviour and Sleep in Children under 5 Years of Age; World Health Organization: Geneva, Switzerland, 2018.
  23. World Health Organization. Oral Health Survey 1997: Basic Methods, 4th ed.; World Health Organization: Geneva, Swizerland, 1997.
  24. Greenstein, G. The role of bleeding upon probing in the diagnosis of periodontal disease. A literature review. J. Periodontol. 1984, 55, 684–688. [Google Scholar] [CrossRef] [PubMed]
  25. Newbrun, E. Indices to measure gingival bleeding. J. Periodontol. 1996, 67, 555–561. [Google Scholar] [CrossRef]
  26. American Academy of Pediatric Dentistry. Classification of Periodontal Diseases in Infants, Children, Adolescents, and Individuals with Special Health Care Needs. The Reference Manual of Pediatric Dentistry; American Academy of Pediatric Dentistry: Chicago, IL, USA, 2020; pp. 418–432. [Google Scholar]
  27. Wei, S.H.; Lang, K.P. Periodontal epidemiological indices for children and adolescents: I. Gingival and periodontal health assessments. Pediatr. Dent. 1981, 3, 353–360. [Google Scholar]
  28. Lee, J.M.; Garon, E.; Wong, D.T. Salivary diagnostics. Orthod. Craniofac. Res. 2009, 12, 206–211. [Google Scholar] [CrossRef]
  29. Hijji, T.M.; Saleheen, H.; AlBuhairan, F.S. Underweight, body image, and weight loss measures among adolescents in Saudi Arabia: Is it a fad or is there more going on? Int. J. Pediatr. Adolesc. Med. 2021, 8, 18–24. [Google Scholar] [CrossRef]
  30. Pietrobelli, A.; Pecoraro, L.; Ferruzzi, A.; Heo, M.; Faith, M.; Zoller, T.; Antoniazzi, F.; Piacentini, G.; Fearnbach, S.N.; Heymsfield, S.B. Effects of COVID-19 Lockdown on Lifestyle Behaviors in Children with Obesity Living in Verona, Italy: A Longitudinal Study. Obesity 2020, 28, 1382–1385. [Google Scholar] [CrossRef]
  31. Yoo, H.Y.; Kwak, B.O.; Son, J.S.; Kim, K.S.; Chung, S. Value of serum 1, 5-anhydroglucitol measurements in childhood obesity in the continuum of diabetes. Ann. Pediatr. Endocrinol. Metab. 2015, 20, 192–197. [Google Scholar] [CrossRef] [Green Version]
  32. Farooqi, F.A.; Khabeer, A.; Moheet, I.; Khan, S.Q.; Farooq, I.; Ar Rejaie, A.S. Prevalence of dental caries in primary and permanent teeth and its relation with tooth brushing habits among school children in Eastern Saudi Arabia. Saudi Med. J. 2015, 36, 737–742. [Google Scholar] [CrossRef]
  33. Al-Rafee, M.A.; AlShammery, A.R.; AlRumikan, A.S.; Pani, S.C. A Comparison of Dental Caries in Urban and Rural Children of the Riyadh Region of Saudi Arabia. Front. Public Health 2019, 7, 195. [Google Scholar] [CrossRef] [Green Version]
  34. Kotha, S.B.; Terkawi, S.A.; Mubaraki, S.A.; Saffan, A.D.A.; Kotha, S.L.; Mallineni, S.K. Association between Body Mass Index (BMI) and Dental Caries among 6–12-Year-Old School Children. Children 2022, 9, 608. [Google Scholar] [CrossRef] [PubMed]
  35. AlBlehed, A.K.; AlThumairy, A.F.; AlTurayri, W.S.; Alassaf, A.; Almulhim, B.; Alghamdi, S.; Almalki, A.; Mallineni, S.K. Assessment of Knowledge, Attitude and Practices Regarding Oral Hygiene among the Parents of Pre-School Children: A Cross-Sectional Study: A Cross-Sectional Study. Ann. Med. Health Sci. Res. 2021, 11, 82–86. [Google Scholar]
  36. Fagerberg, P.; Charmandari, E.; Diou, C.; Heimeier, R.; Karavidopoulou, Y.; Kassari, P.; Koukoula, E.; Lekka, I.; Maglaveras, N.; Maramis, C.; et al. Fast Eating Is Associated with Increased BMI among High-School Students. Nutrients 2021, 13, 880. [Google Scholar] [CrossRef] [PubMed]
  37. Farsi, D.J.; Elkhodary, H.M. The prevalence of overweight/obesity in high school adolescents in Jeddah and the association of obesity association with dental caries. Ann Saudi Med. 2017, 37, 114–121. [Google Scholar] [CrossRef] [Green Version]
  38. Thomas, J.T.; Thomas, T.; Ahmed, M.; Kannan, S.K.; Abdullah, Z.; Alghamdi, S.A.; Joseph, B. Prevalence of Periodontal Disease among Obese Young Adult Population in Saudi Arabia—A Cross-Sectional Study. Medicina 2020, 56, 197. [Google Scholar] [CrossRef] [Green Version]
  39. Ferreira, R.; Corrêa, M.G.; Magno, M.; Almeida, A.P.; Fagundes, N.C.; Rosing, C.; Maia, L.C.; Lima, R.R. Physical activity reduces the prevalence of periodontal disease: Systematic review and meta-analysis. Front. Physiol. 2019, 10, 234. [Google Scholar] [CrossRef]
  40. Khurshid, Z.; Zohaib, S.; Najeeb, S.; Zafar, M.S.; Slowey, P.D.; Almas, K. Human Saliva Collection Devices for Proteomics: An Update. Int. J. Mol. Sci. 2016, 17, 846. [Google Scholar] [CrossRef] [Green Version]
  41. Warsi, I.; Khurshid, Z.; Shazam, H.; Umer, M.F.; Imran, E.; Khan, M.O.; Slowey, P.D.; Goodson, J.M. Saliva Exhibits High Sensitivity and Specificity for the Detection of SARS-CoV-2. Diseases 2021, 9, 38. [Google Scholar] [CrossRef]
  42. Goodson, J.M. Disease reciprocity between gingivitis and obesity. J. Periodontol. 2020, 91 (Suppl. 1), S26–S34. [Google Scholar] [CrossRef]
Figure 1. Distribution of participants according to four categories of BMI.
Figure 1. Distribution of participants according to four categories of BMI.
Children 09 01017 g001
Figure 2. Frequency of food and sugar intake among the study participants.
Figure 2. Frequency of food and sugar intake among the study participants.
Children 09 01017 g002
Table 1. Details of the study sample.
Table 1. Details of the study sample.
VariablesMean ± S.D.
Age8.59 ± 2.06
Height127.0 ± 16.20
Weight30.75 ± 13.78
Body mass index (BMI)18.86 ± 7.08
Deciduous decayed tooth (d)5.67 ± 2.37
Deciduous extracted tooth (e)1.50 ± 0.57
Deciduous filled tooth (f)1.78 ± 0.97
def score3.00 ± 3.35
Permanent tooth decayed (D)2.53 ± 2.19
Permanent missing tooth (M)0.93 ± 0.73
Permanent filled tooth (F)1.68 ± 1.35
DMF score2.90 ± 2.46
Plaque index (PI)2.11 ± 1.21
Modified sulcular bleeding index (mSBI)0.65 ± 0.65
Salivary 1,5-AG level in μg/mL1.88 ± 1.56
DMF = Decayed missing, and filled teeth.
Table 2. Characteristics of the sample.
Table 2. Characteristics of the sample.
Characteristics of the Study SubjectsFrequency (n = 95)Percentage (%)
Eating speedVery slow77.1
Slow1919.4
Ordinary4950.0
Fast2020.4
Very fast33.1
Family history of periodontal diseaseYes1313.3
No8586.7
Family history of diabetes mellitusYes1313.3
No8586.7
Use of brush in routine Daily oral hygieneYes9495.1
No44.9
Brushing frequencyNo22.0
Occasional11.0
Once7980.6
Twice1616.3
Frequency of dental visitNever 99.2
Occasionally2222.4
Once a year6667.3
More than once a year 11.0
Physical exercise in their daily routineNo activity99.2
Sometimes8788.8
Regular22.0
Table 3. Relationship between BMI and clinical parameters among the study participants.
Table 3. Relationship between BMI and clinical parameters among the study participants.
VariablesBMIMeanStd. DeviationStd. Errorp-Value
DefUnderweight3.183.650.480.748
Normal weight2.723.060.61
Overweight 1.501.970.80
Obese3.552.870.95
Total3.003.350.33
DMFUnderweight2.842.530.330.066
Normal weight3.642.410.48
Overweight 1.002.000.81
Obese2.551.870.62
Total2.902.460.24
PIUnderweight1.741.030.130.003 *
Normal weight2.841.370.27
Overweight 2.331.030.42
Obese2.331.110.37
Total2.111.210.12
mSBIUnderweight0.390.610.080.001 *
Normal weight0.960.610.12
Overweight 1.330.510.21
Obese1.000.000.00
Total0.650.650.06
Salivary 1,5-AG levels
(μg/mL)
Underweight1.411.230.160.001 *
Normal weight2.071.100.22
Overweight 1.701.400.57
Obese4.522.140.71
Total1.881.560.15
Body mass index (BMI), deciduous decayed tooth (d), deciduous extracted tooth (e), deciduous filled tooth (f), permanent tooth decayed (D), permanent missing tooth (M), permanent filled tooth (F), plaque index (PI), modified sulcular bleeding index (mSBI), Kruskal–Wallis test, * p-value < 0.05 statistically significant.
Table 4. Association between independent variables, BMI, and caries activity.
Table 4. Association between independent variables, BMI, and caries activity.
VariablesDefDMFPImSBISalivary 1,5-AG
BMICorrelation coefficient−0.0890.1220.2220.4410.402
Sig. (2-tailed)0.3830.2320.028 *0.001 *0.001 *
n9898989898
defCorrelation coefficient −0.468−0.0750.107−0.048
Sig. (2-tailed) 0.001 *0.4600.2950.637
n 98989898
DMFCorrelation coefficient 0.2690.095−0.081
Sig. (2-tailed) 0.007 *0.3500.426
n 989898
PICorrelation coefficient 0.5480.159
Sig. (2-tailed) 0.001 *0.119
n 9898
mSBICorrelation coefficient 0.128
Sig. (2-tailed) 0.209
n 98
Body mass index (BMI), deciduous decayed tooth (d), deciduous extracted tooth (e), deciduous filled tooth (f), permanent tooth decayed (D), permanent missing tooth (M), permanent filled tooth (F), plaque index (PI), modified sulcular bleeding index (mSBI), Spearman correlation. * Correlation is significant at the 0.05 level.
Table 5. Association between sociodemographic characteristics and BMI.
Table 5. Association between sociodemographic characteristics and BMI.
Socio Demographic Charters TicsOptions BMIOverall p-Value
Not Obese Obese
Eating speedVery slow7 (7.9)0 (0)7 (7.1)0.001 *
Slow18 (20.2)1 (11.1)19 (19.4)
Ordinary47 (52.8)2 (22.2)49 (50)
Fast17 (19.1)3 (33.3)20 (20.4)
Very fast0 (0)3 (33.3)3 (3.1)
Food intake between main mealsYes81 (91)9 (100)90 (91.8)0.348
No8 (9)0 (0)8 (8.2)
Intake of sweetened drinks between mealsYes81 (91)7 (77.8)88 (89.8)0.211
No8 (9)2 (22.2)10 (10.2)
Sugar intake limited to main mealsYes32 (36)0 (0)32 (32.7)0.028 *
No57 (64)9 (100)66 (67.3)
Family history of periodontal diseaseYes12 (13.5)1 (11.1)13 (13.3)0.842
No77 (86.5)8 (88.9)85 (86.7)
Family history of diabetes mellitusYes12 (13.5)1 (11.1)13 (13.3)0.84
No77 (86.5)8 (88.9)85 (86.7)
Brush usageNo4 (4.5)0 (0)4 94.1)0.516
Yes 85 (95.5)9 (100)94 (95.9)
Brushing frequencyNo2 (2.2)0 (0)2 (2)0.497
Sometimes1 (1.1) 0 (0)1(1)
Once70 (78.7)9 (100)79 (80.6)
Twice16 (18)0 (0)16 (16.3)
Previous dental visitRarely8 (9)1 (11.1)9 (9.2)0.384
Less often18 (20.2)4 (44.4)22 (22.4)
Once a year62 (69.7)4 (44.4)66 (67.3)
More than once1 (1.1)0 (0)1 (1)
Chi-square test; * p-value < 0.05 is considered statistically significant.
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Alghamdi, S.A.; Aljohar, A.; Almulhim, B.; Alassaf, A.; Bhardwaj, S.S.; Thomas, J.T.; Almalki, A.; Aljuaid, A.O.; Mallineni, S.K. Correlation between BMI and Oral Health Status (DMFT, PI, mSBI, and Salivary 1,5-AG) among the Pediatric Population in Saudi Arabia: A Clinico-Biochemical Study. Children 2022, 9, 1017. https://doi.org/10.3390/children9071017

AMA Style

Alghamdi SA, Aljohar A, Almulhim B, Alassaf A, Bhardwaj SS, Thomas JT, Almalki A, Aljuaid AO, Mallineni SK. Correlation between BMI and Oral Health Status (DMFT, PI, mSBI, and Salivary 1,5-AG) among the Pediatric Population in Saudi Arabia: A Clinico-Biochemical Study. Children. 2022; 9(7):1017. https://doi.org/10.3390/children9071017

Chicago/Turabian Style

Alghamdi, Sara Ayid, Aziza Aljohar, Basim Almulhim, Abdullah Alassaf, Smita Singh Bhardwaj, Julie Toby Thomas, Abdullah Almalki, Areej Owaid Aljuaid, and Sreekanth Kumar Mallineni. 2022. "Correlation between BMI and Oral Health Status (DMFT, PI, mSBI, and Salivary 1,5-AG) among the Pediatric Population in Saudi Arabia: A Clinico-Biochemical Study" Children 9, no. 7: 1017. https://doi.org/10.3390/children9071017

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