Abstract
This study examined the factors related to eating disorders (ED) and the relationship between ED and subjective health or subjective oral health in adolescents. The 46,146 adolescents (age 12–18 years) who participated in the Korea Youth Risk Behavior Web-based Survey were selected, including those who had attempted to lose weight within the past 30 days during the survey period. The variables included were eating behavior, BMI, body image subjective health, and subjective oral health. The weight-loss method was divided into two groups (regular exercise, RE, and eating disorder, ED). The data were analyzed using the Rao-Scott χ2 test and logistic regression analysis. The adolescents with an obese body image had a lower risk of ED (OR = 0.75, 95% CI 0.38–1.49) than adolescents with a very thin body image. Adolescents with ED had a higher risk of a poor subjective health assessment (OR = 2.32, 95% CI 1.85–2.91). On the other hand, they had a lower risk of a poor subjective oral health assessment (OR = 0.89, 95% CI 0.71–1.12). ED is closely associated with eating behavior, BMI, body image, oral health behavior, subjective health, and subjective oral health in Korean adolescents.
Keywords: adolescent, eating disorder, eating behavior, oral health, body mass index
1. Introduction
Eating disorders (EDs) are psychogenic disorders associated with several serious psychological and physical complications and are among the nine most serious problems affecting adolescents [1]. According to the World Health Organization (WHO) International Classification of Diseases, EDs are classified into three types: Anorexia, Bulimia, and Binge eating disorders, which feature abnormal eating habits and pain or extreme anxiety about weight control, body shape and weight [2,3].
EDs are common in women, usually starting during puberty [4]. Adolescent EDs typically last for more than five years, indicating that EDs persist throughout adolescence and the transitional period to early adulthood. As such, prolonged eating disorders can have a significant impact on the growth and development of adolescence [5,6]. Although the incidence and severity of EDs may vary over time and between individuals, early diagnosis and treatment can significantly increase the chances of disease recovery [7]. On the other hand, few seek treatment because most ED patients tend to deny or hide their disease and avoid professional help [8]. Therefore, identifying the symptoms and factors associated with the onset of EDs in adolescence, an important period of biopsychosocial development in an individual’s life, is important for effective prevention and early intervention strategies.
People with EDs are at increased risk for mental health problems and additional health problems, including diabetes, loss of menses in females, heart failure, metabolic disorders, and cardiovascular and endocrine disorders [9]. In addition to these systemic problems, EDs are closely related to oral diseases, such as dental erosion, dental caries, dry mouth, salivary gland edema, and periodontal disease. [10]. Of these, the most obvious and well-explained oral complication is gastric acid-induced dental erosion during self-induced vomiting [11]. A recent review reported that individuals with EDs were five times more likely to have dental erosion than healthy individuals. Moreover, those with self-induced vomiting had a seven times higher risk [12]. Dry mouth was reported to be related to behaviors caused by anorexia nervosa [13], but there is a difference of opinion in the literature regarding the effects of EDs on the major oral diseases, gingivitis, and periodontal disease [14,15]. Although there are some related prior studies [16,17], studies evaluating the oral symptoms occurring in EDs are insufficient. Because oral symptoms differ according to the specific behaviors associated with various types of eating disorders, it will be necessary to identify the symptoms and factors to reduce oral and medical complications associated with eating disorder behaviors.
Therefore, this study examined the relationship between eating EDs and subjective health and oral health in adolescence to provide primary data for establishing a system to combat EDs.
2. Materials and Methods
2.1. Research Design and Research Tool
This cross-sectional study is a secondary analysis of descriptive research using the 15th Korea Youth Risk Behavior Web-based Survey (KYRBS, 2019) to find the factors that can affect EDs and to investigate the relationship between EDs and subjective health or oral health among Korean adolescents. The KYRBS was approved by the Korea Disease Control and Prevention Agency before the investigation (Approval No. 117058). The study was conducted according to the relevant guidelines and regulations. The present study received approval (Approval No. P01-202108-21-004) from the Public Institutional Review Board Designated by the Ministry of Health and Welfare. In this paper, an evaluation was done of the quality of reporting for cross-sectional studies using the STROBE guideline.
2.2. Description of Variables
The 15th KYRBS had 15 parts and 105 questions in an anonymous, self-reported format. In this study, the questions related to the subject’s demographic characteristics (five items), eating behavior (six items), obesity and weight control (five items), oral health behaviors and symptoms (10 items), subjective health (one item), and subjective oral health (one item) were extracted. Subsequently, each variable was reclassified according to the purpose of this study.
2.3. General Characteristics
Gender, age, subjective body type recognition, body mass index (BMI), academic grades, and economic status and residential type were selected as the analytical variables. Gender was divided into “male” and “female”. The age ranged from 12 to 18 years old. For classifications according to subjective academic performance and domestic economic status over the most recent 12 months, “top”, “mid-upper”, “mid”, “middle-low” and “low” were reclassified into “high”, “middle” and “low”.
2.4. Eating Behavior
The variables related to the eating behavior included six items as follows; fruit consumption more than once a day, milk consumption more than once a day, soft drinks more than three times a week, caffeinated beverage consumption more than three times a week, water intake more than 600 mL a day, and educational experience concerning eating habits and nutrition in the past year.
2.5. Obesity and Losing Weight Attempts
Before analysis, the BMI was calculated as the weight (kg)/height (cm) using the data collected from adolescents. The calculated BMI was divided into five levels according to the Korean Society for the study of obesity. Subjective body type recognition was divided into very thin, slightly thin, normal, slightly overweight, and obese. In KYRBS, subjects had to select how to control their weight if they had tried to lose weight in the last 30 days. Thus, the weight control attempts and weight loss methods (regular exercise, vomiting after eating) were included as variables. Among the weight loss methods, subjects who tried to lose weight with regular exercise were defined as RE, and those who tried to lose weight by vomiting after eating were defined as eating disorder (ED).
2.6. Oral Health Behavior and Oral Disease Symptom
There are 10 items regarding oral health behavior and oral disease symptoms. Oral behavior consisted of the number of times of brushing per day, experience of dental visits and oral health education in the past year, and whether or not brushing occurred before bedtime. Oral diseases consisting of broken teeth, pain during chewing, tingling and throbbing, bleeding gingiva, pain in the tongue or inside the cheek, and symptoms of bad breath were included as variables.
2.7. Subjective Health and Subjective Oral Health
Subjective health and subjective oral health variables were selected. The values were divided into five levels originally and these were divided into three levels, “healthy”, “normal”, and “unhealthy” for analysis.
2.8. Statistical Analysis
Following the KYRBS data analysis guidelines, complex sample data analysis was conducted using the corrections for strata, cluster, weight, and a finite population. All analyses included the use of weighted variables. A Rao-Scott χ2 test was conducted to examine the relationship between variables. To identify the characteristics of factors affecting eating disorders in adolescents and to evaluate the effects of eating disorders on subjective health and oral health, variables with p-values < 0.05 in univariate analysis were selected as independent variables by correcting for sex, age, and BMI. As a result, multiple logistic regression was performed. Differences with p-values <0.05 were considered significant. All data were analyzed by IBM SPSS Statistics program version 21.0 (SPSS, Chicago, IL, USA).
3. Results
3.1. General Characteristics
As a result of the general characteristics of the participant, a total of 46,146 adolescents were included, of which 22,672 (49.1%) were male, and 23,474 (50.9%) were female (Table 1). Significant differences in gender, age, subjective academic performance, and home economy were observed in the participants who responded that they had tried to lose weight within the last one month or had not (p < 0.001). Among the 19,167 participants who had tried to lose weight, the response rate of female students was approximately 1.5 times higher than that of male students. On the other hand, the current residence type of the target group was mostly living with a family (approximately 94.9%), and there was no difference in characteristics according to the type of residence (p = 0.114).
Table 1.
General characteristics according to losing weight effort within the last one Month.
| Variables | Categories | Tried to Lose Weight | χ2 | p | |
|---|---|---|---|---|---|
| No (n = 26,979) |
Yes (n = 19,167) |
||||
| Sex | Male | 15,120 (56.0) | 7552 (39.4) | 260.259 | 0.000 |
| Female | 11,859 (44.0) | 11,615 (60.6) | |||
| Age (Years) |
12 | 2109 (7.8) | 1613 (8.4) | 70.843 | 0.000 |
| 13 | 4359 (16.2) | 3172 (16.6) | |||
| 14 | 4520 (16.8) | 3355 (17.6) | |||
| 15 | 4521 (16.8) | 3285 (17.2) | |||
| 16 | 4338 (16.1) | 3183 (16.7) | |||
| 17 | 4689 (17.4) | 3056 (16.0) | |||
| 18 | 2350 (8.7) | 1439 (7.5) | |||
| Subjective body type recognition | Very thin | 1432 (5.3) | 118 (0.6) | 825.243 | 0.000 |
| A little thin | 7569 (28.1) | 1113 (5.8) | |||
| Normal | 10305 (37.9) | 6279 (32.8) | |||
| A little overweight | 6367 (23.9) | 9508 (49.9) | |||
| Obesity | 1306 (4.8) | 387 (10.9) | |||
| BMI | Underweight | 7425 (28.4) | 1459 (8.0) | 2436.327 | 0.000 |
| Normal | 13,153 (51.1) | 8820 (49.3) | |||
| Overweight | 2428 (9.6) | 3229 (18.1) | |||
| Obesity | 2365 (9.2) | 3821 (21.2) | |||
| High obesity | 422 (1.7) | 627 (3.5) | |||
| Subjective academic performance | High | 10,839 (40.2) | 6610 (34.5) | 37.073 | 0.000 |
| Middle | 7979 (29.6) | 5973 (31.2) | |||
| Low | 8161 (30.2) | 6584 (34.4) | |||
| Household economic status | High | 10,358 (38.4) | 7416 (38.7) | 36.132 | 0.000 |
| Middle | 13,321 (49.4) | 9060 (47.3) | |||
| Low | 330 (12.2) | 2691 (14.0) | |||
| Residential type | Family | 25,594 (94.9) | 18,185 (94.9) | 1.951 | 0.114 |
| Relative | 129 (0.5) | 116 (0.6) | |||
| Live alone | 132 (0.5) | 136 (0.7) | |||
| Dormitory | 1022 (3.8) | 662 (3.5) | |||
| Child care facilities | 102 (0.4) | 68 (0.4) | |||
The values are presented as unweighted number (weighted %). The total numbers of some variables are different due to missing values. Calculated using the general linear model for continuous variables or by Rao-Scott χ2 test for each variable.
3.2. Eating Behavior According to Weight Loss Methods
Table 2 lists the difference between the participants’ eating behavior and whether they had tried to lose weight, such as ‘Regular exercise’ or ‘Vomiting after eating’. In all eating behavior variables, there was a significant difference according to the effort to lose weight, such as ‘Regular exercise’ or ‘Vomiting after eating’ (p < 0.05). In the RE or ED group, 21.7% and 21.2%, respectively, responded that they ate fruit more than once a day, while the proportion of participants who responded that they consumed milk more than once a day was 26.4% and 23.0%, respectively. In addition, the proportion of participants who responded that they consumed carbonated beverages four or more times a week was 34.9% and 47.1%, respectively, and for consumed caffeinated beverages four or more times a week 11.9% and 24.4%, respectively. As a result of the analysis of the eating behaviors and nutritional education over the past year, 52.7% of the participants currently were performing ‘Regular exercise’, and 43.9% of the participants who tried to lose weight through ‘Vomiting after eating’ had some educational experience.
Table 2.
Eating behavior according to the weight-loss methods.
| Variables | Categories | Regular Exercise | Vomiting after Eating | ||||||
|---|---|---|---|---|---|---|---|---|---|
| Yes (n = 22,029) |
No (n = 8295) |
χ2 | p | Yes (n = 717) |
No (n = 26,979) |
χ2 | p | ||
| Fruit consumption (more than one time/day) |
No | 17,241 (37.0) |
6871 (15.1) |
86.111 | 0.000 | 565 (1.2) |
23,547 (51.0) |
8.640 | 0.027 |
| Yes | 4788 (41.0) |
1424 (12.5) |
152 (1.4) |
6060 (52.2) |
|||||
| Milk consumption (more than one time/day) |
No | 16,204 (36.5) |
6688 (15.3) |
183.837 | 0.000 | 552 (1.2) |
22,340 (50.5) |
34.648 | 0.000 |
| Yes | 5825 (42.5) |
1607 (12.1) |
165 (1.2) |
7267 (53.4) |
|||||
| Soft drinks consumption (less than three times/week) |
No | 7690 (35.9) |
3093 (14.7) |
58.115 | 0.000 | 338 (1.6) |
10,445 (49.0) |
89.733 | 0.000 |
| Yes | 14,339 (39.0) |
5202 (14.5) |
379 (1.0) |
19,162 (52.5) |
|||||
| Caffeine drinks consumption (less than three times/week) |
No | 2619 (38.0) |
1058 (15.7) |
10.312 | 0.022 | 175 (2.5) |
3502 (51.2) |
108.637 | 0.000 |
| Yes | 19,410 (37.8) |
7237 (14.4) |
542 (1.0) |
26,105 (51.2) |
|||||
| Water intake (more than 600 mL/day) |
No | 3757 (27.2) |
2422 (18.1) |
870.599 | 0.000 | 169 (1.2) |
6010 (44.1) |
366.441 | 0.000 |
| Yes | 18,272 (41.2) |
5872 (13.5) |
548 (1.2) |
23,596 (53.4) |
|||||
| Nutrition and eating behaviors education (during one year) |
No | 10,424 (35.1) |
4478 (15.4) |
80.685 | 0000 | 402 (1.3) |
14,500 (49.3) |
95.537 | 0.000 |
| Yes | 11,605 (40.8) |
3817 (13.6) |
315 (1.1) |
15,107 (53.3) |
|||||
The values are presented as unweighted numbers (weighted %). The total numbers of some variables are different due to missing values. Calculated using the general linear model for continuous variables or by Rao-Scott χ2 test for each variable.
3.3. Subjective Health and Subjective Oral Health According to Weight Loss Methods
Table 3 lists the difference between the participants’ subjective health and subjective oral health and whether they had tried to lose weight, such as ‘Regular exercise’ or ‘Vomiting after eating’. In subjective health, in adolescents who had tried to lose weight through regular exercise, the proportion of those who perceived that they were healthy was high, whereas approximately 53.4% of adolescents who had tried to lose weight by vomiting after eating recognized that they were currently unhealthy. In the case of subjective oral health, approximately 40.1% and 3.1% of adolescents who had tried to lose weight through regular exercise or ‘Vomiting after eating’ perceived that they were healthy, respectively (p < 0.001).
Table 3.
Subjective health and subjective oral health according to the weight loss method.
| Variables | Categories | Regular Exercise | Vomiting after Eating | ||||||
|---|---|---|---|---|---|---|---|---|---|
| Yes (n = 22,029) |
No (n = 8295) |
χ2 | p | Yes (n = 717) |
No (n = 26,979) |
χ2 | p | ||
| Subjective health | healthy | 16,348 (40.1) |
5120 (12.8) |
511.136 | 0.000 | 134 (3.1) |
21,085 (51.9) |
186.365 | 0.000 |
| Normal | 4409 (33.6) |
2318 (18.2) |
200 (1.5) |
6527 (50.4) |
|||||
| Unhealthy | 1272 (29.5) |
857 (20.4) |
383 (0.9) |
1995 (46.8) |
|||||
| Subjective oral health | healthy | 7795 (41.7) |
2308 (12.8) |
220.861 | 0.000 | 207 (1.1) |
9896 (53.4) |
78.660 | 0.000 |
| Normal | 10,617 (36.8) |
4219 (14.9) |
320 (1.1) |
14,516 (50.6) |
|||||
| Unhealthy | 3617 (34.1) |
1768 (16.7) |
190 (1.1) |
5195 (49.1) |
|||||
The values are presented as unweighted numbers (weighted %). The total numbers of some variables are different due to missing values. Calculated using the general linear model for continuous variables or by Rao-Scott χ2 test for each variable.
3.4. Oral Health Behavior and Oral Disease Symptoms According to Weight Loss Method
Table 4 lists the difference between the participants’ oral health behavior and symptoms and whether they had tried to lose weight, such as ‘Regular exercise’ or ‘Vomiting after eating’. All oral health behavior and symptoms variables showed significant differences in whether weight loss was attempted, such as ‘Regular exercise’ or ‘Vomiting after eating’ (p < 0.001). In the RE group, the frequency of toothbrushing at least three times a day (54.9%), visiting the dental clinic for oral examination at least once in the past year (67.7%), and toothbrushing before sleep (87.3%), showed a high rate. In addition, the ED group who had a frequency of brushing at least three times a day (58.7%), visiting the dental clinic for oral examination at least once in the past year (66.5%), and toothbrushing before sleep (79.2%) showed a higher rate than participants who tried other methods. The RE group had experienced more ‘tooth fractures’ during the past year.
Table 4.
Oral health behavior and oral disease symptoms according to weight loss method.
| Variables | Categories | Regular Exercise | Vomiting after Eating | |||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Yes (n = 22,029) |
No (n = 8295) |
χ2 | p | Yes (n = 717) |
No (n = 26,979) |
χ2 | p | |||
| Oral health behavior | Frequency tooth-brushing(more than three time/day) | No | 9333 (35.2) |
4149 (14.9) |
169.960 | 0.000 | 312 (1.1) |
13,770 (49.0) |
119.553 | 0.000 |
| Yes | 12,096 (40.4) |
4146 (14.2) |
405 (1.3) |
15,837 (53.3) |
||||||
| Oral examination in dental clinic (more than one time/year) | No | 7105 (36.3) |
2841 (14.8) |
31.084 | 0.000 | 240 (1.2) |
9706 (49.8) |
21.193 | 0.000 | |
| Yes | 14,924 (38.6) |
14.5 (0.2) |
477 (1.2) |
19,901 (51.9) |
||||||
| Tooth-brushing before sleep | No | 2634 (32.4) |
1303 (16.8) |
122.522 | 0.000 | 112 (1.4) |
3825 (48.1) |
169.763 | 0.000 | |
| Yes | 19,229 (38.7) |
6899 (14.2) |
568 (1.1) |
25,560 (51.7) |
||||||
| Experience of oral health education (during one year) |
No | 14,775 (36.0) |
6113 (15.2) |
228.220 | 0.000 | 516 (1.2) |
20,372 (50.0) |
140.982 | 0.000 | |
| Yes | 7254 (42.7) |
2182 (12.8) |
201 (1.2) |
9235 (54.4) |
||||||
| Tooth fracture (during one year) |
No | 19,763 (37.5) |
7478 (14.5) |
42.539 | 0.000 | 590 (1.1) |
26,651 (50.9) |
95.183 | 0.000 | |
| Yes | 2266 (41.5) |
817 (15.0) |
127 (2.4) |
2956 (0.8) |
||||||
| Pain during chewing (during one year) |
No | 14,463 (38.6) |
5085 (13.9) |
46.129 | 0.000 | 382 (1.0) |
19,166 (51.5) |
37.731 | 0.000 | |
| Yes | 7566 (36.5) |
3210 (15.8) |
335 (1.6) |
10,441 (50.7) |
||||||
| Tingling & throbbing (during one year) |
No | 17,394 (38.3) |
6185 (13.9) |
67.035 | 0.000 | 446 (1.0) |
23,133 (51.2) |
104.377 | 0.000 | |
| Yes | 4635 (36.3) |
2110 (16.8) |
171 (2.1) |
6474 (5.,0) |
||||||
| Gingiva pain & bleeding (during one year) |
No | 18,021 (37.8) |
6598 (14.2) |
33.655 | 0.000 | 480 (1.0) |
24,139 (51.0) |
112.390 | 0.000 | |
| Yes | 4008 (37.9) |
1687 (16.3) |
237 (2.2) |
5469 (52.0) |
||||||
| Pain of tongue & intraoral side (during one year) |
No | 19,734 (38.2) |
7199 (14.2) |
47.980 | 0.000 | 537 (1.0) |
26,396 (51.4) |
134.950 | 0.000 | |
| Yes | 2295 (35.2) |
1096 (17.1) |
180 (2.7) |
3211 (49.6) |
||||||
| Bad breath (during one year) |
No | 17,635 (38.5) |
6407 (14.3) |
41.826 | 0.000 | 505 (1.1) |
23,537 (51.6) |
38.910 | 0.000 | |
| Yes | 4394 (35.5) |
1888 (15.8) |
212 (1.2) |
6070 (49.6) |
||||||
The values are presented as unweighted numbers (weighted %). The total numbers of some variables are different due to missing values. Calculated using the general linear model for continuous variables or by Rao-Scott χ2 test for each variable.
3.5. Factors Related to Weight Loss Attempts
Table 5 lists the influences of body type recognition, eating behavior, and oral health behavior and symptoms on the groups that attempted to lose weight by regular exercise or vomiting after eating according to the participant’s gender, age, and adjusted BMI.
Table 5.
Factors related to the association between body type recognition, eating behavior, oral health behavior and symptoms, and weight loss attempts.
| Variables | Categories | Regular Exercise | Vomiting after Eating | ||||
|---|---|---|---|---|---|---|---|
| OR | 95% CI | p | OR | 95% CI | p | ||
| Sex | Male | Ref | Ref | ||||
| Female | 0.59 | (0.55–0.63) | 0.000 | 1.62 | (1.32–1.99) | 0.000 | |
| Age | 0.94 | (0.93–0.96) | 0.000 | 1.75 | (1.42–2.17) | 0.001 | |
| BMI | Normal | Ref | Ref | ||||
| Underweight | 0.75 | (0.69–0.81) | 0.000 | 0.66 | (0.47–0.92) | 0.000 | |
| Overweight | 1.16 | (1.06–1.26) | 0.000 | 0.81 | (0.62–1.05) | 0.000 | |
| Obesity | 1.21 | (1.09–1.33) | 0.000 | 0.97 | (0.74–1.28) | 0.000 | |
| High obesity | 1.29 | (1.06–1.57) | 0.000 | 1.04 | (0.57–1.89) | 0.000 | |
| Subjective body type recognition | Very thin | Ref | |||||
| A little thin | 1.43 | (1.24–1.65) | 0.000 | 0.82 | (0.48–1.37) | 0.000 | |
| Normal | 1.75 | (1.51–2.03) | 0.000 | 0.71 | (0.40–1.24) | 0.000 | |
| A little overweight | 1.60 | (1.36–1.88) | 0.000 | 0.86 | (0.48–1.55) | 0.000 | |
| Obesity | 1.36 | (1.11–1.66) | 0.000 | 0.75 | (0.38–1.49) | 0.000 | |
| Fruit consumption (more than one time/day) |
Yes | Ref | Ref | ||||
| No | 0.81 | (0.75~0.87) | 0.000 | 0.93 | (0.76~1.14) | 0.485 | |
| Milk consumption (more than one time/day) |
Yes | Ref | Ref | ||||
| No | 0.80 | (0.75~0.86) | 0.000 | 1.00 | (0.82~1.21) | 0.968 | |
| Soft drinks consumption (less than three times/week) |
Yes | Ref | Ref | ||||
| No | 0.86 | (0.81–0.91) | 0.000 | 1.52 | (1.27–1.81) | 0.000 | |
| Caffeine drinks consumption (less than three times/week) |
Yes | Ref | Ref | ||||
| No | 0.98 | (0.89–1.07) | 0.603 | 1.72 | (1.42–2.09) | 0.000 | |
| Water intake (more than 600 mL/day) |
Yes | Ref | Ref | ||||
| No | 0.89 | (0.84–0.95) | 0.000 | 0.93 | (0.75–1.15) | 0.507 | |
| Experience of nutrition and eating behaviors education |
Yes | Ref | Ref | ||||
| No | 0.89 | (0.84–0.95) | 0.000 | 1.14 | (0.96–1.36) | 0.141 | |
| Frequency tooth-brushing (more than three times/day) |
Yes | Ref | Ref | ||||
| No | 0.82 | (0.78–0.87) | 0.000 | 0.89 | (0.74–1.06) | 0.187 | |
| oral examination in a dental clinic (more than one time/year) | Yes | Ref | Ref | ||||
| No | 0.95 | (0.89–1.00) | 0.068 | 1.18 | (0.98–1.42) | 0.090 | |
| Tooth-brushing before sleep | Yes | Ref | Ref | ||||
| No | 0.78 | (0.72–0.84) | 0.000 | 1.08 | (0.86–1.36) | 0.514 | |
| Tooth fracture (during one year) |
No | Ref | Ref | ||||
| Yes | 1.15 | (1.04–1.26) | 0.006 | 1.35 | (1.08–1.68) | 0.008 | |
| Pain during chewing (during one year) |
No | Ref | Ref | ||||
| Yes | 0.96 | (0.90–1.02) | 0.156 | 1.13 | (0.94–1.36) | 0.206 | |
| Tingling & throbbing (during one year) |
No | Ref | Ref | ||||
| Yes | 0.95 | (0.88–1.03) | 0.221 | 1.37 | (1.12–1.68) | 0.002 | |
| Gingiva pain & bleeding (during one year) |
No | Ref | Ref | ||||
| Yes | 1.04 | (0.96–1.12) | 0.379 | 1.32 | (1.09–1.60) | 0.005 | |
| Pain of tongue & intraoral side (during one year) |
No | Ref | Ref | ||||
| Yes | 0.87 | (0.80–0.94) | 0.001 | 1.68 | (1.33–2.12) | 0.000 | |
| Bad breath (during one year) |
No | Ref | Ref | ||||
| Yes | 0.91 | (0.84–0.97) | 0.007 | 1.18 | (0.97–1.44) | 0.097 | |
| Experience of oral health education (during one year) |
Yes | Ref | Ref | ||||
| No | 0.81 | (0.76–0.86) | 0.000 | 1.01 | (0.84–1.23) | 0.886 | |
OR = Odds ratio; CI = Confidential intervals. Multiple logistic regression analysis.
As a result of body type recognition, those who perceived themselves as slightly overweight or obese were 1.60 and 1.36 times more likely to try to lose weight through regular exercise, respectively. On the other hand, the group using vomiting after eating had a 0.86 times and 0.75 times lower score, respectively (p < 0.001) than those who did not.
As a result of the eating behavior, adolescents who did not consume carbonated drinks or caffeinated beverages more than three times a week were 0.86 times and 0.98 times less likely to try to lose weight with regular exercise, respectively, but the possibility of trying to lose weight by vomiting after eating was 1.52 times lower and 1.72 times higher (p < 0.001).
An analysis of the relationship between oral health behaviors and symptoms showed that weight loss was attempted with regular exercise 0.82 times and 0.78 times less in those who brushed their teeth three times a day and those who did not brush their teeth before sleep, respectively (p < 0.001). Adolescents who had experienced symptoms of tooth fracture during the past year were 1.15 times and 1.35 times more likely to try to lose weight through regular exercise or vomiting after eating, respectively (p < 0.01). Adolescents who complained of tingling & throbbing, gingiva pain & bleeding, pain of the tongue & intraoral side were significantly more likely to attempt weight control by vomiting after eating (p < 0.01).
3.6. Factors Related to Subjective Health and Subjective Oral Health
Table 6 lists the influence of body type recognition, eating behavior, oral health behavior and symptoms, and ED on subjective health and oral health according to the participants’ gender, age, and BMI adjusted.
Table 6.
Factors related to the association between body type recognition, eating behavior, oral health behavior and symptoms, eating disorder, and subjective health and oral health.
| Variables | Categories | Health | Oral Health | ||||
|---|---|---|---|---|---|---|---|
| OR | 95% CI | p | OR | 95% CI | p | ||
| Sex | Male | Ref | Ref | ||||
| Female | 1.67 | (1.53–1.82) | 0.000 | 1.62 | (1.32–1.99) | 0.403 | |
| Age | 1.15 | (1.13–1.18) | 1.07 | (1.05–1.08) | 0.000 | ||
| BMI | Normal | Ref | Ref | ||||
| Underweight | 0.97 | (0.85–1.09) | 0.000 | 1.07 | 0.99–1.15 | 0.000 | |
| Overweight | 0.95 | (0.84–1.07) | 0.000 | 0.87 | 0.80–0.94 | 0.000 | |
| Obesity | 0.99 | (0.86–1.12) | 0.000 | 0.71 | 0.65–0.77 | 0.000 | |
| High obesity | 1.50 | (1.21–1.87) | 0.000 | 0.67 | 0.55–0.81 | 0.000 | |
| Subjective body type recognition | Very thin | Ref | |||||
| A little thin | 0.45 | 0.39–0.53 | 0.000 | 0.67 | 0.60–0.75 | 0.000 | |
| Normal | 0.31 | 0.23–0.37 | 0.000 | 0.63 | 0.56–0.72 | 0.000 | |
| A little overweight | 0.47 | 0.39–0.57 | 0.000 | 0.88 | 0.77–1.00 | 0.000 | |
| Obesity | 1.16 | 0.92–1.48 | 0.000 | 1.49 | 1.25–1.76 | 0.000 | |
| Fruit consumption (more than one time/day) |
Yes | Ref | Ref | ||||
| No | 1.22 | 1.11–1.34 | 0.000 | 1.14 | 1.08–1.21 | 0.000 | |
| Milk consumption (more than one time/day) |
Yes | Ref | Ref | ||||
| No | 1.17 | 1.06–1.29 | 0.001 | 1.05 | 0.99–1.11 | 0.090 | |
| Soft drinks consumption (less than three times/week) |
Yes | Ref | Ref | ||||
| No | 1.06 | 0.99–1.14 | 0.077 | 1.23 | 1.17–1.30 | 0.000 | |
| Caffeine drinks consumption (less than three times/week) |
Yes | Ref | Ref | ||||
| No | 1.36 | 1.24–1.48 | 0.000 | 1.10 | 1.03–1.19 | 0.006 | |
| Water intake (more than 600 mL/day) |
Yes | Ref | Ref | ||||
| No | 1.20 | 1.11–1.29 | 0.000 | 1.16 | 1.09–1.22 | 0.000 | |
| Experience of nutrition and eating behaviors education |
Yes | Ref | Ref | ||||
| No | 1.18 | 1.09–0.27 | 0.000 | 1.03 | 0.98–1.09 | 0.203 | |
| Frequency tooth-brushing(more than three times/day) | Yes | Ref | Ref | ||||
| No | 1.03 | 0.95–1.11 | 0.524 | 1.39 | 1.32–1.46 | 0.000 | |
| oral examination in a dental clinic (more than one time/year) | Yes | Ref | Ref | ||||
| No | 1.13 | 1.05–1.22 | 0.001 | 1.02 | 0.97–1.08 | 0.373 | |
| Tooth-brushing before sleep | Yes | Ref | Ref | ||||
| No | 1.31 | 1.19–1.43 | 0.000 | 1.41 | 1.32–1.51 | 0.000 | |
| Tooth fracture (during 1 year) |
No | Ref | Ref | ||||
| Yes | 0.95 | 0.84–1.08 | 0.440 | 1.75 | 1.62–1.89 | 0.000 | |
| Pain during chewing (during one year) |
No | Ref | Ref | ||||
| Yes | 1.40 | 1.30–1.51 | 0.000 | 1.61 | 1.53–1.70 | 0.000 | |
| Tingling & throbbing (during one year) |
No | Ref | Ref | ||||
| Yes | 1.24 | 1.14–1.35 | 0.000 | 2.18 | 2.06–2.31 | 0.000 | |
| Gingiva pain & bleeding (during one year) |
No | Ref | Ref | ||||
| Yes | 1.35 | 1.25–1.47 | 0.000 | 1.45 | 1.36–1.54 | 0.000 | |
| Pain of tongue & intraoral side (during one year) |
No | Ref | Ref | ||||
| Yes | 1.51 | 1.38–1.66 | 0.000 | 0.91 | 0.84–0.98 | 0.013 | |
| Bad breath (during one year) |
No | Ref | Ref | ||||
| Yes | 1.54 | 1.42–1.67 | 0.000 | 2.06 | 1.95–2.18 | 0.000 | |
| Experience of oral health education (during one year) |
Yes | Ref | Ref | ||||
| No | 1.09 | 0.99–1.20 | 0.068 | 0.95 | 0.90–1.01 | 0.104 | |
| Regular exercise | No | Ref | Ref | ||||
| Yes | 0.66 | 0.58–0.74 | 0.000 | 0.89 | 0.83–0.95 | 0.001 | |
| Vomiting after eating | No | Ref | Ref | ||||
| Yes | 2.32 | 1.85–2.91 | 0.000 | 0.89 | 0.71–1.12 | 0.046 | |
OR = Odds ratio; CI = Confidential intervals. Multiple logistic regression analysis.
As a result of body type recognition, the risk of recognizing that subjective health was poor was 1.16 times higher when obesity was perceived than when very thin was perceived. The probability of recognizing that subjective oral health was poor was 1.49 times higher (p < 0.001). As a result of eating behavior, in the case of consuming carbonated beverages three or more times a week, the risk ratio that subjective health was poor was 1.06 times higher, and the risk ratio that subjective oral health was poor was 1.23 times higher (p < 0.001).
An analysis of the effect of oral health behavior and symptoms on subjective health and subjective oral health showed that the risk of affecting subjective health and subjective oral health was 1.03 times and 1.39 times higher, respectively, when brushing was not performed more than three times a day (p < 0.001). In the case of not tooth brushing before sleep, the subjects were 1.13 times and 1.41 times more likely to respond that their subjective health and subjective oral health were not good (p < 0.001), respectively. In the case of subjective oral symptoms, an experience of tooth fracture, pain during chewing, tingling and throbbing, gingiva pain and bleeding, or bad breath in the past year, the probability of recognizing that subjective oral health was bad was significantly high. Among these, tingling and throbbing had the strongest influence at 2.18 times (p < 0.01).
An analysis of the effect of ED on subjective health showed that the risk of recognizing that subjective health and subjective oral health were bad was low when weight loss was attempted with regular exercise. By contrast, the risk of weight loss attempt by vomiting after eating was 2.32 times higher (p < 0.001) (p < 0.001). In subjective oral health, when participants tried to lose weight with regular exercise and vomiting after eating, the risk of recognizing that subjective oral health was poor was low (p < 0.05).
4. Discussion
Adolescence is a term that refers to the period between childhood and youth, and adolescents undergo various physical and mental changes [18]. It is a period in which the importance of appearance is recognized as a social factor in developing the values, attitudes, and skills necessary for social participation [19]. Recently, a social environment that emphasizes appearance has developed in Korea. As a result, the interest in and pressure on appearance in adolescence is increasing. Accordingly, many adolescents try to lose weight to manage their appearance [20]. Although there are many ways to lose weight, ED in adolescents is becoming a serious problem. Therefore, this study analyzed various factors that could affect ED as a problem in Korean adolescents.
As a result, 46,146 (80.5%) of the adolescents who participated in the study had attempted to lose weight, of which 39.4% were male students and 60.6% female students (Table 1, p < 0.001). The results confirmed that female students were more interested in losing weight. This suggests that women have higher expectations of a thin appearance, which is ideally required in modern society [19,21]. In other words, the social and psychological pressure towards skinny bodies may have led to weight loss attempts. As a basis for this, it can be compared with the BMI results investigated in this study. The BMI was calculated based on the weight and height information, and each value was divided into five stages. As a result, 10,279 subjects (approximately 53.6%) had attempted to lose weight, even though they were underweight or of normal weight. (Table 1, p < 0.001). The cause of this is presumed to be the influence of cognitive distortion regarding their weight, which is a problem in adolescents [22,23]. As a result of checking whether or not to lose weight according to subjective body type recognition, approximately 60.8% of adolescents who answered ‘I appear to have gained weight’ were not gaining weight compared to 42.8% of students who were ‘overweight’ or ‘obese’ based on the BMI. However, many students subjectively perceived that they had gained weight and attempted to lose weight. Hence, cognitive distortions about weight are becoming a global problem. There are also reports of cases where the incorrect recognition of body shape leads to extreme weight control, leading to death [24,25]. Because the BMI index reflects only height and weight, there are limitations in that it does not perfectly reflect the individual’s actual body shape. On the other hand, efforts are needed to narrow the gap between objective body status and subjective cognition. Therefore, forming a healthy body image to solve eating disorders and other health-related problems in adolescents is required.
One of the greatest problems among adolescents is limiting nutritional intake by vomiting after eating to lose weight [26]. Therefore, this study attempted to identify the dietary habits of adolescents suspected of ED by trying to lose weight through vomiting after eating. As a result, there were significant differences between the subjects’ eating behavior and whether they attempted to lose weight. The eating behavior patterns of adolescents who tried to lose weight through regular exercise and those who lost weight by vomiting after eating were similar (Table 2). On the other hand, in the case of girls, the probability of trying to lose weight by vomiting after eating was 1.62 times higher than for boys. Furthermore, the possibility of trying to lose weight by regular exercise was 0.59 times less than boys. Considering this result, ED problems in girls need to be considered more carefully. The risk of ED was higher in girls, who were 0.59 times less likely than men to try to lose weight through regular exercise (Table 5, p < 0.001). ED appear to have become more common among younger females during the period when icons of beauty (e.g., contestants at beauty contests) have become thinner, and women’s magazines publish significantly more articles on weight loss methods [21]. As mentioned above, erroneous values and social perceptions of body image can harm the physical development of adolescents. Nevertheless, it is positive that the eating behavior patterns of the RE and ED groups were similar (Table 2). Therefore, this problem will likely be improved if a plan is prepared to help people realize that healthy weight control is possible through proper nutrition and regular exercise.
The eating behavior of the target group attempting to lose weight was analyzed in detail. To the question ‘Do you drink soft drinks more than three times a week?’, approximately 34.9% of the RE group answered ‘yes’, whereas 47.1% of the ED group answered ‘yes’ (Table 2). Thus, the rate of intake of soft drinks was higher in the ED group. Compared to the results of more than 50% of adolescents consuming soft drinks four or more times a week in a previous study, this is a relatively positive result [27]. Nevertheless, soft drinks were consumed relatively frequently in the ED group. Adolescents who consumed soft drinks three or more times a week were 1.52 times more likely to have ED (Table 5, p < 0.001). In the case of soft drinks, the possibility of tooth erosion has already been reported in several studies. In general, tooth erosion due to frequent vomiting in ED patients has also been reported [28,29]. Therefore, it is necessary to consider the effects of soft drinks intake in adolescents on ED and on dental health. On the other hand, as for the intake of caffeinated beverages, 11.9% and 24.4% of both groups consumed these four or more times a week, respectively (Table 2). Although the consumption rate of caffeinated beverages was relatively low, the likelihood of complaining of ED was increased by 1.72 times when caffeine was consumed three or more times a week (Table 5, p < 0.001). The side effects caused by caffeine may be considered the cause of these results. Caffeine stimulates the central nervous system and peripheral nervous system, so when consumed in an appropriate amount it has positive effects, such as stimulating nerve activity and reducing fatigue. On the other hand, when taken in high doses, it can cause nervousness, excitement, and insomnia, and can adversely affect patients with digestive, endocrine, and heart diseases or gastric ulcers [30,31]. In other words, although it is limited in identifying the direct cause, it will be necessary to consider the effects of caffeine on eating disorders. In particular, adolescents are quite sensitive to caffeine, which can cause neurological disorders and heart disorders. Therefore, caution is required regarding caffeine intake in adolescents [32,33].
In dietary and nutrition educational experience, among the RE group and ED group, 52.7% and 56.1% of the subjects who received education, respectively, showed no significant difference in the ratio between the group (Table 2). On the other hand, in an analysis of whether education affected weight loss methods, the rate of weight loss through regular exercise was 0.81 times lower in subjects who did not receive dietary education (Table 5, p < 0.001). By contrast, education did not affect the subjects who tried to lose weight by vomiting after eating (Table 5, p = 0.141). Currently, textbooks on eating habits for adolescents officially published by the Korean government include the importance of forming correct eating habits in adolescence, how to eat healthily, and education on food safety and nutrition. Although it contains various contents for consuming healthy nutrition in adolescence, it appears that education did not have a positive effect on correct eating and nutritional intake in adolescents. Adolescents are greatly influenced by the media and peers [34]. Therefore, it will be necessary to develop an appropriate medium to deliver the correct values regarding body shape and to promote changes in social perception.
In relation to subjective health, approximately 74.2% of adolescents who had attempted to lose weight through regular exercise answered that they thought they were healthy, whereas approximately 53.4% of adolescents with ED answered that they were not healthy (Table 3). In the case of the RE group, the probability of responding to ‘subjective health is not good’ was reduced by 0.66 times, whereas the result was increased 2.32 fold in subjects who complained of ED problems. Hence, weight loss method can affect the subjective health of the subject (Table 6, p < 0.001). On the other hand, in the RE and ED groups trying to lose weight, 35.4% and 28.9% of the subjects responded that their oral health was healthy, respectively. The RE and ED subjects who answered ‘not good oral health’ were 16.4% and 26.5%, respectively; the proportion of subjects who answered ‘not good oral health’ among adolescents with ED was relatively high (Table 3). The effect of the weight-loss method on the oral health of the subjects was low, and the difference between the RE group and the ED group could not be confirmed (Table 6, p < 0.05). Overall, adolescents had less consideration for oral health than for their general health. In particular, oral health is sufficiently closely related to be used as an indicator to detect ED in subjects for the first time. Therefore, it is necessary to confirm the effect of ED on oral health in detail in this study [35,36].
The ‘number of brushing per day’, ‘frequency of brushing before bedtime’, and ‘the rate of visiting the dentist at least once in the past year’ were high in the RE and ED groups (Table 4). Nevertheless, their effect on ED could not be confirmed (Table 5, p > 0.05). In the case of oral health symptoms, the possibility of ED increased when adolescents had symptoms, such as broken teeth (1.75 times), pain when eating food (1.61 times), throbbing teeth (2.18 times), and gingival bleeding (1.45 times) (Table 6, p < 0.01). Many studies have reported that oral problems, such as tooth erosion, decreased salivation, and dental caries, occur in patients with eating disorders. Therefore, it is essential to consider oral health in subjects trying to lose weight by vomiting after eating [12,35]. Nevertheless, the fact that adolescents suffering from EDs do not consider oral health is an area that needs to be improved through accurate identification of the causes and systematic oral health education. In addition, as EDs in adolescence are mentioned as a serious problem, it is urgent to develop and disseminate educational content that comprehensively considers their overall health and oral health. For this, convergence research among various occupational groups, such as dental medical personnel, medical personnel, and nutritionists, should be attempted.
This study is meaningful in that it identifies the factors that can affect EDs, which are emerging as serious problems in adolescents, and the effects of EDs on the subjective health and oral health of adolescents. In addition, it suggests alternatives. Nevertheless, this study was a cross-sectional study using the results of the KYRBS, and there was a limitation in inferring a causal relationship between each variable. These limitations can be overcome by conducting a well-organized follow-up study based on the results confirmed in this study.
5. Conclusions
Eating disorders in adolescents are affected by eating habits and oral health behaviors that may influence subjective general health and oral health status. Therefore, various media and systematic institutional measures are needed to improve the factors that can affect eating disorders in adolescents. Considering these study results, increased care about eating disorders could improve adolescents’ general and oral health.
Author Contributions
Conceptualization, M.-K.J. and E.-H.J.; methodology, E.-H.J. and M.-K.J.; software, M.-K.J.; validation, E.-H.J.; formal analysis, E.-H.J.; investigation, M.-K.J.; data curation, E.-H.J. and M.-K.J.; writing—original draft preparation, E.-H.J. and M.-K.J.; writing—review and editing, M.-K.J. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Not applicable.
Conflicts of Interest
The authors deny any conflicts of interest related to this study.
Funding Statement
This research received no external funding.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Snyder L. Health-care needs of the Adolescent. Ann. Intern. Med. 1989;110:930–935. doi: 10.7326/0003-4819-110-11-930. [DOI] [PubMed] [Google Scholar]
- 2.World Health Organization . The ICD-10 Classification of Mental and Behavioural Disorders: Clinical Descriptions and Diagnostic Guidelines. World Health Organization; Geneva, Switzerland: 1992. [Google Scholar]
- 3.Fairburn C.G., Cooper Z., Shafran R. Cognitive behaviour therapy for eating disorders: A “transdiagnostic” theory and treatment. Behav. Res. Ther. 2003;41:509–528. doi: 10.1016/S0005-7967(02)00088-8. [DOI] [PubMed] [Google Scholar]
- 4.Micali N., Hagberg K.W., Petersen I., Treasure J.L. The incidence of eating disorders in the UK in 2000–2009: Findings from the General Practice Research Database. BMJ Open. 2013;3:e002646. doi: 10.1136/bmjopen-2013-002646. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Vos T., Mathers C., Herrman H., Harvey C., Gureje O., Bui D., Watson N., Begg S. The burden of mental disorders in Victoria, 1996. Soc. Psychiatry Psychiatr. Epidemiol. 2001;36:53–62. doi: 10.1007/s001270050290. [DOI] [PubMed] [Google Scholar]
- 6.Slane J.D., Klump K.L., McGue M., Iacono W.G. Developmental trajectories of disordered eating from early adolescence to young adulthood: A longitudinal study. Int. J. Eat. Disord. 2014;47:793–801. doi: 10.1002/eat.22329. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Hazelton L.R., Faine M.P. Diagnosis and dental management of eating disorder patients. Int. J. Prosthodont. 1996;9:65–73. [PubMed] [Google Scholar]
- 8.Cavanaugh C.J., Lemberg R. Eating Disorders: A Reference Sourcebook: A Reference Sourcebook. Volume 107 Oryx Press; Phoenix, AZ, USA: 1998. What we know about eating disorders: Facts and statistics. [Google Scholar]
- 9.Hicks T.M., Lee J.Y., Nguyen T., La Via M., Roberts M.W. Knowledge and practice of eating disorders among a group of adolescent dental patients. J. Clin. Pediatric Dent. 2013;38:39–43. doi: 10.17796/jcpd.38.1.p764642162107355. [DOI] [PubMed] [Google Scholar]
- 10.Romanos G.E., Javed F., Romanos E.B., Williams R.C. Oro-facial manifestations in patients with eating disorders. Appetite. 2012;59:499–504. doi: 10.1016/j.appet.2012.06.016. [DOI] [PubMed] [Google Scholar]
- 11.Uhlen M.-M., Tveit A.B., Stenhagen K.R., Mulic A. Self-induced vomiting and dental erosion–a clinical study. BMC Oral Health. 2014;14:1–7. doi: 10.1186/1472-6831-14-92. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Kisely S., Baghaie H., Lalloo R., Johnson N.W. Association between poor oral health and eating disorders: Systematic review and meta-analysis. Br. J. Psychiatry. 2015;207:299–305. doi: 10.1192/bjp.bp.114.156323. [DOI] [PubMed] [Google Scholar]
- 13.Little J.W. Eating disorders: Dental implications. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endodontol. 2002;93:138–143. doi: 10.1067/moe.2002.116598. [DOI] [PubMed] [Google Scholar]
- 14.De Moor R. Eating disorder-induced dental complications: A case report. J. Oral Rehabil. 2004;31:725–732. doi: 10.1111/j.1365-2842.2004.01282.x. [DOI] [PubMed] [Google Scholar]
- 15.Milosevic A., Slade P. The orodental status of anorexics and bulimics. Br. Dent. J. 1989;167:66–70. doi: 10.1038/sj.bdj.4806915. [DOI] [PubMed] [Google Scholar]
- 16.Johansson A.K., Norring C., Unell L., Johansson A. Eating disorders and oral health: A matched case—Control study. Eur. J. Oral Sci. 2012;120:61–68. doi: 10.1111/j.1600-0722.2011.00922.x. [DOI] [PubMed] [Google Scholar]
- 17.Panico R., Piemonte E., Lazos J., Gilligan G., Zampini A., Lanfranchi H. Oral mucosal lesions in anorexia nervosa, bulimia nervosa and EDNOS. J. Psychiatr. Res. 2018;96:178–182. doi: 10.1016/j.jpsychires.2017.09.022. [DOI] [PubMed] [Google Scholar]
- 18.Garrote García J. Estudio del Nivel de Actividad Física y su Vinculación con el Rendimiento Académico y el Desplazamiento Activo al Centro Educativo en Alumnos de Secundaria. [(accessed on 6 May 2022)]. Available online: https://buleria.unileon.es/bitstream/handle/10612/9095/2016_Jorge_Garrote_Garcia_01709777-1.pdf?sequence=1&isAllowed=y.
- 19.Sinton M.M., Birch L.L. Individual and sociocultural influences on pre-adolescent girls’ appearance schemas and body dissatisfaction. J. Youth Adolesc. 2006;35:157–167. doi: 10.1007/s10964-005-9007-4. [DOI] [Google Scholar]
- 20.McCabe M., Ricciardelli L. Parent, peer and media influences on body image and strategies to both increase and decrease body size among adolescent boys and girls. Adolescence. 2001;36:225–240. [PubMed] [Google Scholar]
- 21.Sharan P., Sundar A.S. Eating disorders in women. Indian J. Psychiatry. 2015;57:S286. doi: 10.4103/0019-5545.161493. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Helfert S., Warschburger P. A prospective study on the impact of peer and parental pressure on body dissatisfaction in adolescent girls and boys. Body Image. 2011;8:101–109. doi: 10.1016/j.bodyim.2011.01.004. [DOI] [PubMed] [Google Scholar]
- 23.Voelker D.K., Reel J.J., Greenleaf C. Weight status and body image perceptions in adolescents: Current perspectives. Adolesc. Health Med. Ther. 2015;6:149–158. doi: 10.2147/AHMT.S68344. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Dakanalis A., Favagrossa L., Clerici M., Prunas A., Colmegna F., Zanetti M.A., Riva G. Body dissatisfaction and eating disorder symptomatology: A latent structural equation modeling analysis of moderating variables in 18-to-28-year-old males. J. Psychol. 2015;149:85–112. doi: 10.1080/00223980.2013.842141. [DOI] [PubMed] [Google Scholar]
- 25.Tylka T.L. The Relation Between Body Dissatisfaction and Eating Disorder Symptomatology: An Analysis of Moderating Variables. J. Couns. Psychol. 2004;51:178. doi: 10.1037/0022-0167.51.2.178. [DOI] [Google Scholar]
- 26.Johnson J.G., Cohen P., Gould M.S., Kasen S., Brown J., Brook J.S. Childhood adversities, interpersonal difficulties, and risk for suicide attempts during late adolescence and early adulthood. Arch. Gen. Psychiatry. 2002;59:741–749. doi: 10.1001/archpsyc.59.8.741. [DOI] [PubMed] [Google Scholar]
- 27.Kim A., Kim J., Kye S. Sugar-sweetened beverage consumption and influencing factors in Korean adolescents: Based on the 2017 Korea Youth Risk Behavior Web-based Survey. J. Nutr. Health. 2018;51:465–479. doi: 10.4163/jnh.2018.51.5.465. [DOI] [Google Scholar]
- 28.Algarello M., Visconti G., Barone-Adesi L. Interlocking circumareolar suture with undyed polyamide thread: A personal experience. Aesthetic Plast. Surg. 2013;37:1061–1062. doi: 10.1007/s00266-013-0186-1. [DOI] [PubMed] [Google Scholar]
- 29.Hermont A.P., Oliveira P.A., Martins C.C., Paiva S.M., Pordeus I.A., Auad S.M. Tooth erosion and eating disorders: A systematic review and meta-analysis. PLoS ONE. 2014;9:e111123. doi: 10.1371/journal.pone.0111123. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Cornelis M.C., El-Sohemy A. Coffee, caffeine, and coronary heart disease. Curr. Opin. Lipidol. 2007;18:13–19. doi: 10.1097/MOL.0b013e3280127b04. [DOI] [PubMed] [Google Scholar]
- 31.Chou T. Wake up and smell the coffee. Caffeine, coffee, and the medical consequences. West. J. Med. 1992;157:544. [PMC free article] [PubMed] [Google Scholar]
- 32.Wikoff D., Welsh B.T., Henderson R., Brorby G.P., Britt J., Myers E., Goldberger J., Lieberman H.R., O’Brien C., Peck J. Systematic review of the potential adverse effects of caffeine consumption in healthy adults, pregnant women, adolescents, and children. Food Chem. Toxicol. 2017;109:585–648. doi: 10.1016/j.fct.2017.04.002. [DOI] [PubMed] [Google Scholar]
- 33.Hering-Hanit R., Gadoth N. Caffeine-induced headache in children and adolescents. Cephalalgia. 2003;23:332–335. doi: 10.1046/j.1468-2982.2003.00576.x. [DOI] [PubMed] [Google Scholar]
- 34.Littleton H.L., Ollendick T. Negative Body Image and Disordered Eating Behavior in Children and Adolescents: What Places Youth at Risk and How Can These Problems be Prevented? Clin. Child Fam. Psychol. Rev. 2003;6:51–66. doi: 10.1023/A:1022266017046. [DOI] [PubMed] [Google Scholar]
- 35.Frydrych A., Davies G., McDermott B. Eating disorders and oral health: A review of the literature. Aust. Dent. J. 2005;50:6–15. doi: 10.1111/j.1834-7819.2005.tb00079.x. [DOI] [PubMed] [Google Scholar]
- 36.Johansson A.K., Norring C., Unell L., Johansson A. Diet and behavioral habits related to oral health in eating disorder patients: A matched case-control study. J. Eat. Disord. 2020;8:7. doi: 10.1186/s40337-020-0281-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
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