Skip to main content
Frontiers in Public Health logoLink to Frontiers in Public Health
. 2025 Dec 15;13:1729509. doi: 10.3389/fpubh.2025.1729509

Prevalence and associated factors of multi-ethnic adolescent idiopathic scoliosis in Longlin, Southwestern China: a school-based cross-sectional study

Chengxiang Hu 1, Baocheng Lin 1, Fengtao Li 2, Zhixing Li 1, Xiaozhuan Chen 1,*
PMCID: PMC12745271  PMID: 41473732

Abstract

Objective

To determine the prevalence of adolescent idiopathic scoliosis (AIS) and its associated factors among multi-ethnic schoolchildren in Southwestern China.

Methods

A cross-sectional school-based study was conducted involving 22,814 students aged 10–18 years. Screening comprised the Adams forward bend test; positives underwent radiographic confirmation (Cobb angle ≥10°). Demographic and behavioral data were collected via questionnaires. Multivariate logistic regression identified independent associated factors.

Results

The screening positive rate was 3.83%, and the confirmed AIS prevalence rate was 1.37%. While no significant ethnic difference existed in screening positive rates (p = 0.078), the confirmed prevalence rates differed (p = 0.029), being relatively higher in Yi (1.52%) and GeLao (1.54%) adolescents. Girls showed a significantly higher screening positive rate than boys (4.64% vs. 3.12%, p < 0.001), but no statistically significant gender difference was found in the confirmed prevalence rates (p = 0.157). Notably, the positive predictive value was higher in boys (40.90%) than girls (31.72%). Multivariate analysis revealed several factors independently associated with AIS, including abnormal BMI, lack of desk/chair adjustment, poor sleep posture, physical inactivity, improper reading/writing posture, excessive electronic device use, insufficient outdoor activity, inadequate sleep, and frequent sweet consumption.

Conclusion

The AIS prevalence in this multi-ethnic region aligns with global figures. School screening coupled with health interventions targeting modifiable associated factors is essential for AIS prevention and control. Comprehensive health promotion and early intervention targeting the identified significant factors should be an important future direction for AIS prevention.

Keywords: adolescent idiopathic scoliosis, prevalence, associated factors, cross-sectional study, multi-ethnic region

1. Introduction

Scoliosis is a disease characterized by three-dimensional torsion and deformity of the spine, manifesting in the coronal plane as a lateral curvature with one or more segments deviating from the body's midline; it is typically diagnosed based on a Cobb angle of ≥10° (1, 2). Adolescent Idiopathic Scoliosis (AIS) is the predominant type of scoliosis, accounting for approximately 80% of all cases and predominantly affecting adolescents aged 10–18 years (35). AIS not only affects the patient's appearance but can also lead to low back pain, psychological distress, and in severe cases, restricted respiratory function and mobility impairment, imposing a significant burden on families and society (1, 2). Furthermore, the perceived association between poor posture in adolescents and AIS often raises widespread concern and anxiety among patients and their parents (68). Therefore, implementing early screening is crucial for the timely detection of AIS, enabling effective intervention and delaying disease progression.

The period from 9 to 13 years old typically represents the peak height velocity (PHV) stage in adolescents, during which the progression of scoliosis is most pronounced (9). Compared to the complex conditions of adult scoliosis, children and adolescent populations are more suitable for screening, and consequently, most domestic and international screening efforts focus on this age group. The global prevalence of AIS is approximately 1.34%, ranging from 0.4% to 2.5% in Asia (6), and about 1% to 3% among individuals aged 10–16 years in the United States (10, 11). Studies in China indicate that the peak prevalence of AIS in individuals aged 4–20 years is concentrated between 13 and 15 years (12).

Numerous studies have indicated a gender difference in AIS prevalence, with rates generally higher in females than in males, at a ratio ranging from 1.5 to 2.5 (1218). For instance, a screening study covering individuals aged 4–20 years in China reported prevalence rates of 0.87% in males and 1.22% in females, a statistically significant difference (12). However, some studies report contrasting trends, such as one in the Jammu region of India where the prevalence was lower in females (0.31%) than in males (0.88%) (19), suggesting that the clinical presentation of AIS may be influenced by various factors, e.g., genetics, height, body mass index (BMI), and ethnicity (20, 21). A screening study conducted in Tianzhu Tibetan Autonomous County, which is a high-altitude, multi-ethnic region with relatively underdeveloped resources, revealed ethnic disparities in scoliosis prevalence and the angle of trunk rotation, with Han adolescents exhibiting a higher prevalence than their Tibetan minority counterparts. This work addresses a critical epidemiological gap in Western China and elucidates the collective influence of geographic, ethnic, and socioeconomic factors on spinal development, underscoring the value of this unique setting for such research (22). These findings suggest that ethnic background may be one of the factors associated with AIS risk, likely interacting with diverse genetic predispositions, nutritional status, and physical activity patterns.

Studies have shown that for skeletally immature adolescents, especially those with milder curves, non-surgical interventions such as bracing and scoliosis-specific exercises can effectively slow curve progression and reduce the need for surgery (23, 24). Schools, being settings with high concentrations of adolescents, offer convenient venues for large-scale screening, which is why most scoliosis screening programs, both internationally and domestically, are school-based (2528). Management Measures for Health Examinations of Primary and Secondary School Students (2021 Edition, China) explicitly mandates annual health check-ups in primary and secondary schools, providing an institutional foundation for centralized AIS screening. Therefore, utilizing schools as the screening venue facilitates the early diagnosis of AIS and can reduce the need for surgical intervention. However, school screening also faces challenges such as inefficient referral mechanisms (29). It is recommended to incorporate professional collaboration with hospitals during the screening process, establishing a “school organization—hospital support” cooperative model. This ensures the professionalism of screening while facilitating subsequent follow-up and management for those with abnormal screening results.

Based on this, our study targets in-school students at the critical PHV stage, aiming to investigate the prevalence and influencing factors of AIS among adolescents in a multi-ethnic region of Southwestern China, thereby providing a scientific basis for formulating student physical fitness monitoring and health intervention strategies in this region.

2. Objects and methods

2.1. Study design and participants

This study employed a cross-sectional design and was conducted between March and November 2022 in the Longlin Various Nationalities Autonomous County in Southwestern China. To balance sample representativeness and practical feasibility, this study adopted a stratified cluster sampling approach. Initially, all 39 schools in the county were stratified according to educational stage (primary, junior high, and senior high schools) and geographical location (county/town, village). Following this, schools were randomly selected from each stratum (Supplementary Table S1). Subsequently, all eligible students from grade 4 (primary school) to grade 12 (high school), aged 10 to 18 years, from 16 selected primary and secondary schools in the county were recruited as study participants. During the screening phase, 0.42% (n = 96) of the initially eligible participants were excluded. Exclusions were based on the following criteria: lack of parental informed consent; diagnosis of non-idiopathic scoliosis or other organic pathologies, such as congenital malformations, osteochondrodystrophy, or metabolic disorders, as confirmed by three senior spine surgeons; or the presence of communication barriers that could compromise examination validity (Figure 1). Missing data were evaluated using Little's MCAR test (p = 0.32), which indicated that values were missing completely at random. Given the low proportion of missing observations and the absence of systematic bias, a complete case analysis was employed, resulting in the exclusion of incomplete records. The final analytical sample included 22,814 students.

Figure 1.

Flowchart depicting scoliosis screening process in schools. Initially, 67,846 students from 39 schools underwent stratified cluster sampling. From 22,908 students across 16 schools, 96 were excluded due to various barriers. The screening and questionnaire involved 22,870 students, with 874 testing positive. Of these, 312 had confirmed prevalence, and 562 had non-confirmed prevalence, while 21,996 were non-positive.

Flow diagram of AIS screening process and sample selection.

2.2. Scoliosis screening workflow

A dedicated screening team, comprising 20 examiners (all certified orthopedic surgeons or rehabilitation therapists with over 3 years of clinical experience), conducted the examinations. Scoliosis screening was integrated with the school's annual health check-up. The procedure strictly adhered to the Guideline for adolescent scoliosis screening in China (version 2024) and the national standard Screening of spinal curvature abnormality of children and adolescents (GB/T 16133-2014, China) (30). Participants were assessed by examiners of the same gender. To ensure diagnostic consistency, each child was independently evaluated by two examiners according to a standardized protocol. Any discrepancies between their assessments were adjudicated by a senior spine surgeon to establish the final diagnosis. Screening was conducted at schools by a uniformly trained screening team and included collection of basic information and anthropometric measurements, physical examination, and measurement of the angle of trunk rotation (ATR). Basic information such as age, gender, and ethnicity was collected. Height and weight were measured by trained personnel using calibrated instruments (each measured three times with the average taken, height accurate to 0.1 cm, weight accurate to 0.1 kg). BMI was subsequently calculated and categorized into underweight (BMI < 18.5), normal (18.5 ≤ BMI < 24), overweight (24 ≤ BMI < 28), and obese (BMI ≥ 28) according to the National student physical health standard (2014 revision, China).

To manage the large cohort efficiently, students were scheduled in batches. The average daily screening capacity was approximately 150–200 students. Participants progressed through a standardized sequence of assessments, beginning with registration and basic anthropometric measurement, followed by the Adams Forward Bend Test, visual and instrumental pelvic assessment, and spinal motion assessment. An ATR measurement was performed when clinically indicated, prior to final on-site data recording and verification.

2.3. Scoliosis examination procedure

The screening protocol comprised a sequential physical examination followed by radiographic confirmation for positive cases. The physical examination began with visual inspection of the standing posture for truncal asymmetry, followed by the Adams Forward Bend Test. In this test, participants stood with feet shoulder-width apart, knees fully extended, and bent forward slowly at the hips until the trunk was approximately parallel to the floor, with arms hanging relaxed and palms opposed. This maneuver facilitates the observation of a fixed rib hump or lumbar para-spinal prominence, serving to differentiate structural scoliosis, where asymmetry persists, from non-structural causes, where it may diminish with postural change. For those with a positive Adams forward bend test, a scoliometer was used to measure the ATR at the point of most significant back asymmetry, and the maximum value was recorded (31).

Pelvic alignment was assessed in the standing position via visual inspection of the iliac crests and quantified with a pelvic inclinometer on the posterior superior iliac spines, recording an asymmetry greater than 5°. Active spinal motions (forward bending, lateral bending, axial rotation) were also observed to assess flexibility and dynamic asymmetry.

A positive screening result was defined as meeting any one of the following criteria: positive visual inspection, positive Adams forward bend test, or ATR ≥5° (10). Subsequently, all screening positives were referred to the collaborating hospital for full-spine posteroanterior and lateral radiographs. Cobb angle in the coronal plane was measured by radiologists, and individuals with a Cobb angle ≥10° were ultimately diagnosed with scoliosis.

2.4. Questionnaire survey

To explore relevant influencing factors, a structured questionnaire was designed based on a review of domestic and international literature (3234) and was pre-tested for clarity and comprehension in a pilot study. The questionnaire content covered demographic characteristics (e.g., age, gender, ethnicity, height, weight, BMI), family history (family history of scoliosis, frequency of posture reminders from guardians), learning-related factors [weekly physical education class frequency, backpack type, daily exercise types, reading/writing posture, desk/chair height adjustment (refers to adjustable classroom furniture)], and lifestyle habits (daily electronic device usage time, weekly outdoor activity time, daily sleep duration, sleep posture, engagement in physical labor, frequency of sweet food consumption). All variables were defined by well-defined, unambiguous survey questions to facilitate clear determination. For instance, the variable “desk/chair height adjustment” was assessed by a direct student self-report question: “Can the height of the desk and chair you use at school be adjusted to suit your height?”, with binary (Yes/No) response options. All questionnaire items were designed to be specific and closed-ended to minimize subjective interpretation. To mitigate recall bias and improve accuracy, the questionnaires were administered in a controlled classroom setting under the supervision of trained staff, who provided standardized instructions and were available to clarify questions. Students completed the questionnaires concurrently with the spinal screening to contextualize the questions within the health assessment framework.

2.5. Quality control

Strict quality control measures were implemented to ensure the reliability and accuracy of the research data, and to minimize inter-rater variability among all the examiners across the extensive screening period. Firstly, a screening team consisting of professional doctors and therapists from the Rehabilitation Medicine Department of Longlin Traditional Chinese Medicine Hospital was established. All staff involved in physical examinations and questionnaire administration received uniform standardized training and assessment to ensure consistency in the screening process and judgment criteria. This included theoretical review of the screening protocol, practical demonstrations, and hands-on practice sessions on examiners to standardize assessment techniques and interpretation of findings.

During screening, individuals with positive screening results required re-examination by a second physician; a case was only considered suspected if both deemed it positive, thereby reducing subjective error. Besides, senior research team members periodically observed and supervised screening sessions across different schools and time points to ensure ongoing adherence to the protocol. Brief re-calibration sessions were conducted monthly to address any procedural drift.

For data management, questionnaire data were double-entered by dedicated personnel, with a random sample of 5% of all completed screening forms was selected daily for cross-verification by a different examiner on-site for accuracy to maximize data entry correctness.

2.6. Ethical considerations

Parents, students, and teachers were informed about the purpose of the study and the details of the examination. Informed consent was obtained from all participating students and their parents, with signed consent forms. Given the multi-ethnic composition of the population (including Zhuang, Yi, and GeLao groups) and potential language barriers, the informed consent process was carefully adapted. Consent forms and participant information sheets were professionally translated and provided in both Mandarin Chinese and the predominant local minority languages. Bilingual research staff were present during consent sessions at each school to explain the study's purpose, procedures, risks, and benefits, and to answer any questions in the parent's preferred language, ensuring comprehensive understanding prior to signing. The study protocol has been granted administrative approval by the Longlin County Health Bureau (Approval No. 2021-2) and has been approved by the Longlin County Traditional Chinese Medicine Hospital Ethics Committee (Approval No. K2019-090-02). The guidelines, regulations, and principles of the Declaration of Helsinki were strictly followed.

2.7. Statistical analysis

Data organization was performed using Microsoft Office Excel 2007, and data analysis was conducted using SPSS 22.0 statistical software. Categorical data were described using frequencies (n) and percentages (%), and group comparisons were made using the χ2 test. To identify factors independently associated with scoliosis, we adopted a comprehensive modeling strategy. First, univariate analyses were performed on all 16 candidate variables. Variables showing statistical significance (p < 0.05) in the univariate analysis, along with a priori confounders (gender, age, and family history of scoliosis) deemed clinically relevant. To account for the potential clustering of students within schools, we estimated robust standard errors, clustering at the school level. Multicollinearity among the independent variables was assessed using the variance inflation factor (VIF), with a mean VIF of 1.85 indicating no substantial multicollinearity (all VIFs < 3.0; see Supplementary Table S2). The results are presented as adjusted odds ratios (aOR) with 95% confidence intervals (CI). A p-value < 0.05 was considered statistically significant for all analyses.

3. Results

3.1. AIS screening and severity distribution

A total of 22,814 adolescents aged 10 to 18 years were screened in this study, including 12,149 boys and 10,665 girls. There were 874 screening positives, resulting in an overall positive rate of 3.83%. Following radiographic confirmation, 312 AIS cases were diagnosed, yielding a total prevalence of 1.37%. The positive predictive value of the screening was 35.70% (Supplementary Table S3).

3.1.1. Gender, ethnicity, and age screening

Screening results showed significant variations across gender, ethnicity, and age groups (Supplementary Table S3). The screening positive rate was significantly higher in girls than in boys (4.64% vs. 3.12%, χ2 = 50.67, p < 0.001). However, the difference in the confirmed prevalence rates between genders was not statistically significant (1.47% in girls vs. 1.28% in boys, χ2 = 1.42, p = 0.233). Notably, the positive predictive value (PPV) (i.e., confirmed prevalence-to-screening positive ratio) was substantially higher among screening positive boys (40.90%) than girls (31.72%).

While no statistically significant difference was observed in the screening positive rate among students of different ethnicities (χ2 = 12.79, p = 0.078), the confirmed prevalence rate varied significantly across ethnic groups by the statistical test (χ2 = 15.62, p = 0.029). It should be noted, however, that the numerical prevalence was relatively higher in Yi (1.52%) and GeLao (1.54%) adolescents than in Han (1.33%) and Yao (1.27%) adolescents (Supplementary Table S3). In terms of screening accuracy, the Yi ethnic group demonstrated a PPV of 39.13%, while the GeLao and Yao ethnic groups both reached a PPV of 40.00% (Figure 2). However, it is important to note that the small number of cases in these and other minority groups (e.g., BuYi, Yao) results in wide confidence intervals that include values comparable to the overall prevalence, limiting firm conclusions about ethnic-specific differences at this stage (Supplementary Table S3).

Figure 2.

Bar chart comparing screening and diagnosis rates across ethnicities (Han, Miao, Zhuang, BuYi, GeLao, Yi, Yao, Others). Orange bars represent screening positive rates, green bars show confirmed prevalence rates, and a blue line with dots indicates positive predictive values. Screening rates are generally higher than confirmed prevalence, with predictive values varying across groups.

Trends in screening positive rates and confirmed AIS prevalence rates across different ethnic groups.

Both the screening positive rate and the confirmed prevalence rate across age groups demonstrated a trend of initial increase followed by a decrease, peaking in the 13-year-old group (screening positive rate: 6.38%; confirmed prevalence rate: 2.92%) and reaching the lowest point in the 10-year-old group (screening positive rate: 1.52%; confirmed prevalence rate: 0.21%) (Figure 3). The PPV showed considerable variation across age groups, ranging from 13.64% in the 10-year-old group to 45.69% in the 13-year-old group, indicating substantially higher screening accuracy in the latter group.

Figure 3.

Bar and line graph showing screening positive rate, confirmed prevalence rate, and positive predictive value across ages ten to eighteen. Orange bars represent screening positive rate, green bars represent confirmed prevalence rate, and a blue dashed line represents the positive predictive value. The screening positive rate peaks at age thirteen, while the confirmed prevalence rate is relatively low. Positive predictive value fluctuates, with a high at ages twelve to fourteen, then stabilizes. Percentages are on the left and right axes for rate and predictive value, respectively.

Trends in screening positive rates and confirmed AIS prevalence rates across different age groups.

3.1.2. Cobb angle severity of gender and ethnicity

Among the 312 confirmed patients, the numbers of male and female patients were roughly equivalent (155 males, 49.68%; 157 females, 50.32%). Analysis of Cobb angle severity showed that male patients were predominantly in the mild scoliosis category (10°- < 20°) (89.68%), while 80.89% of female patients had mild scoliosis, with proportions of moderate and severe cases slightly higher than in males. However, Fisher's exact test indicated that the distribution of Cobb angle severity among patients of different genders was not statistically significant (p = 0.071) (Table 1).

Table 1.

Distribution of Cobb angle severity [n (%)] among scoliosis patients by gender and ethnicity.

Variable Confirmed cases (n) Cobb angle
Mild 10°<20° Moderate 20°<30° Severe30°
Gender
Boy 155 139 (89.68%) 14 (9.03%) 2 (1.29%)
Girl 157 127 (80.89%) 28 (17.83%) 2 (1.27%)
Ethnicity
Han 75 66 (88.00%) 8 (10.67%) 1 (1.33%)
Miao 64 57 (89.06%) 6 (9.38%) 1 (1.56%)
Zhuang 150 123 (82.00%) 25 (16.67%) 2 (1.33%)
BuYi 1 1 (100.00%) 0 (0.00%) 0 (0.00%)
GeLao 7 7 (100.00%) 0 (0.00%) 0 (0.00%)
Yi 13 12 (92.31%) 1 (7.69%) 0 (0.00%)
Yao 2 2 (100.00%) 0 (0.00%) 0 (0.00%)
Total 312 266 (85.26%) 42 (13.46%) 4 (1.28%)

Regarding ethnic composition, the Zhuang ethnicity had the highest number of confirmed cases (150 cases, 48.08%), followed by the Han (75 cases, 24.04%) and Miao (64 cases, 20.51%) ethnicities. The Cobb angle distribution for patients across all ethnic groups was predominantly mild. All confirmed cases from the BuYi, GeLao, and Yao ethnic groups were mild. The distribution of Cobb angle severity among confirmed patients of different ethnicities showed no statistically significant difference (p = 0.829). Overall, among the AIS patients confirmed in this study, 85.26% (266/312) were mild, 13.46% (42/312) were moderate, and only 1.28% (4/312) were severe (Table 1).

3.2. Analysis of influencing factors of scoliosis

3.2.1. Univariate analysis

Univariate analysis of the 16 potential associated factors revealed that nine factors were significantly associated with the occurrence of scoliosis (all p < 0.05). These included BMI, desk/chair height adjustment, nighttime sleep posture, frequent sweet consumption, weekly physical education (PE) class frequency, maintaining correct reading/writing posture, total daily electronic device usage time, weekly outdoor activity time, and daily sleep duration. The remaining seven factors (gender, age, family history of scoliosis, backpack type, daily exercise type, engagement in physical labor) showed no significant influence (all p > 0.05) (Table 2).

Table 2.

Univariate analysis of associated factors for scoliosis.

Variable Category Total (n) Scoliosis cases (n) Prevalence χ2 value p-value
Gender Boy 12,149 155 1.28% 1.42 0.233
Girl 10,665 157 1.47%
Age (years) ≤ 14 10,591 154 1.45% 1.17 0.28
>14 12,223 158 1.29%
BMI Underweight 613 43 7.01% 158.6 < 0.001
Normal 22,004 264 1.20%
Overweight 51 2 3.92%
Obese 146 3 2.05%
Family history of scoliosis Yes 419 5 1.19% 0.11 0.738
No 22,395 307 1.37%
Backpack type Single-shoulder 1,056 15 1.42% 0.05 0.82
Backpack 21,758 297 1.37%
Daily exercise type Unilateral sports 350 6 1.71% 0.31 0.581
Bilateral sports 22,464 306 1.36%
Desk/chair height adjustment No 450 27 6.00% 72.8 < 0.001
Yes 22,364 285 1.27%
Nighttime sleep posture Supine 5,000 35 0.70% 24.6 < 0.001
Lateral 9,000 157 1.74%
Variable 8,814 120 1.36%
Engagement in physical labor No 17,856 245 1.37% 0.04 0.838
Yes 4,958 67 1.35%
Frequent sweet consumption Yes 11,932 185 1.55% 6.19 0.013
No 10,882 127 1.17%
Weekly PE class frequency 0 times 500 22 4.40% 40.9 < 0.001
1 time 8,952 96 1.07%
2 times 13,362 194 1.45%
Maintaining correct reading/writing posture No 986 35 3.55% 105.5 < 0.001
Occasionally 1,975 66 3.34%
Always 19,853 211 1.06%
Total daily electronic device time (h) < 1 h 9,973 50 0.50% 45.2 < 0.001
1–2 h 7,965 158 1.98%
>2 h 4,876 94 1.93%
Weekly outdoor activity time (h) < 1 h 4,982 82 1.65% 20.1 < 0.001
1–3 h 9,976 160 1.60%
>3 h 7,856 70 0.89%
Daily sleep time (h) < 6 h 4,968 61 1.23% 17 < 0.001
6–8 h 7,893 142 1.80%
>8 h 9,953 109 1.09%

Specifically, adolescents who were underweight had the highest prevalence rate (7.01%), significantly higher than those in the normal weight, overweight, and obese groups (χ2 = 158.6, p < 0.001). The prevalence rate among those without adjusted desk/chair height (6.00%) was significantly higher than in the adjusted group (1.27%) (χ2 = 72.8, p < 0.001). Regarding sleep posture, those who slept in a lateral position had a higher prevalence rate (1.74%) than those who slept supine (0.70%) or changed positions (1.36%) (χ2 = 24.6, p < 0.001). Furthermore, lack of physical exercise (prevalence 4.40% in the group with 0 weekly PE classes), poor reading/writing posture (prevalence 3.55% in the group not maintaining correct posture), daily electronic device use exceeding 1 h, insufficient weekly outdoor activity, and daily sleep duration of 6–8 h were all associated with higher risk (Table 2).

3.2.2. Multivariate logistic regression analysis

To further identify independent risk factors, the nine variables that were significant in the univariate analysis were included in a multivariate logistic regression model. The results showed that abnormal BMI (especially underweight and overweight), lack of desk/chair height adjustment, poor sleep posture (lateral and variable positions), lack of physical exercise (0 weekly PE classes), poor reading/writing habits, daily electronic device use time >1 h, insufficient outdoor activity, abnormal sleep duration (6–8 h), and frequent sweet consumption were all independently associated with adolescent scoliosis (all p < 0.05) (Tables 3 and Supplementary Table S4).

Table 3.

Multivariate logistic regression analysis of associated factors for scoliosis.

Independent variable Variable category β value SE Wald χ2 value P-value aOR 95% CI
BMI Normal 1 1.0
Underweight 1.609 0.227 50 < 0.001 5 3.197.81
Overweight 0.96 0.45 4.57 0.032 2.61 1.08–6.30
Obese 0.511 0.362 2 0.157 1.67 0.80–3.48
Nighttime sleep posture Supine 1 1.0
Lateral 0.788 0.159 24.6 0.011 2.2 1.61–3.00
Variable 0.405 0.16 6.4 < 0.001 1.5 1.09–2.07
Desk/chair height adjustment Yes 1 1.0
No 1.386 0.164 72.8 < 0.001 4 2.90–5.51
Frequent sweet consumption No 1 1.0
Yes 0.262 0.105 6.19 0.013 1.3 1.06–1.59
Weekly PE class frequency 2 times 1 1.0
1 time −0.223 0.158 2 0.157 0.8 0.59–1.09
0 times 1.029 0.161 40.9 < 0.001 2.8 2.04–3.84
Maintaining correct reading/writing posture Always 1 1.0
Occasionally 0.916 0.167 30 < 0.001 2.5 1.80–3.46
No 1.098 0.107 105.5 < 0.001 3 2.43–3.69
Total daily electronic device time (h) < 1 h 1 1.0
1–2 h 1.253 0.186 45.2 < 0.001 3.5 2.43–5.05
>2 h 1.098 0.199 30 < 0.001 3 2.03–4.43
Weekly outdoor activity time (h) >3 h 1 1.0
1–3 h 0.531 0.137 15 0.001 1.7 1.30–2.23
< 1 h 0.587 0.131 20.1 < 0.001 1.8 1.39–2.33
Daily sleep time (h) >8 h 1 1.0
6–8 h 0.47 0.114 17 0.001 1.6 1.28–2.00
< 6 h 0.095 0.134 0.5 0.48 1.1 0.85–1.43

Specifically, compared to those with normal BMI, the association of developing scoliosis increased to 5.00 times (95% CI: 3.19–7.81) for underweight adolescents and 2.61 times (95% CI: 1.08–6.30) for overweight adolescents. The association for those without desk/chair height adjustment was 4.0 times (95% CI: 2.90–5.51) that of those with adjustment. Regarding sleep posture, the association for those sleeping in a lateral position and those with variable positions was 2.2 times (95% CI: 1.61–3.00) and 1.5 times (95% CI: 1.09–2.07) that of those sleeping supine, respectively. Adolescents with no weekly PE classes had a 2.8 times higher association (95% CI: 2.04–3.84) compared to those with 2 classes per week. Concerning reading/writing posture, the risk for those who did not maintain and those who occasionally maintained correct posture was 3.0 times (95% CI: 2.43–3.69) and 2.50 times (95% CI: 1.80–3.46) that of those who always maintained correct posture, respectively. Furthermore, the association for the groups using electronic devices for 1–2 h and >2 h daily was 3.5 times and 3.0 times that of the group using them for < 1 h, respectively (Table 3).

4. Discussion

This study represents a large-scale screening for AIS among adolescents aged 10–18 years in a multi-ethnic region in Southwestern China, systematically analyzing its prevalence, demographic characteristics, and key data from the school screening process. Our multivariate analysis identified a cluster of modifiable lifestyle and behavioral factors as independent predictors for AIS. The results not only provide valuable first-hand data on the spinal health status of adolescents in this region but also offer new insights and directions for thought regarding the epidemiological characteristics of AIS, screening strategies, and potential etiological mechanisms.

4.1. Overall prevalence analysis

This study found the overall prevalence of AIS in this region to be 1.37%, a result largely consistent with reported prevalence ranges globally and in Asia. For instance, a systematic review reported a global AIS prevalence of 1.34%, while studies in Asia report figures between 0.4% and 2.5% (6), and the prevalence among 10- to 16-year-olds in the United States is approximately 1%−3% (10). Our data align with these macro-level figures, indicating that despite regional and ethnic variations, AIS, as a common skeletal development issue in adolescents, exhibits a certain universality in its incidence.

Furthermore, this study observed that the AIS prevalence peaked at 13–14 years of age, highly correlating with the adolescent PHV period (9). During PHV, both the biomechanical load on the spine and its growth rate reach their peak, which is considered a critical window for the onset and progression of AIS. A previous large-scale study of individuals aged 4–20 years in China also showed that the peak incidence of AIS was concentrated between 13 and 15 years (12). The findings of this study further corroborate the scientific basis and necessity of focusing school screening efforts on adolescents aged 10–15, particularly those aged 13–14.

4.2. The impact of ethnic differences on AIS

This study identified differences in AIS screening outcomes among students of different ethnicities. It is noteworthy that these disparities were primarily observed at the confirmation stage rather than during screening. Specific data revealed that students of Yi (1.52%) and GeLao (1.54%) ethnicity demonstrated relatively higher AIS confirmation rates, while Han (1.33%) and Yao (1.27%) students showed comparatively lower rates. While our study reveals intriguing ethnic variations, the relatively small sample sizes for some minority groups (e.g., BuYi, Yi) necessitate cautious interpretation and call for validation in larger, multi-center studies. This observation aligns with trends noted in previous research (19, 20, 22, 3538), suggesting that the epidemiological characteristics of AIS may vary among different ethnic populations. However, these differences likely reflect the complex interplay of multiple factors rather than being determined solely by ethnicity.

The observed ethnic variations suggest the potential involvement of a complex interplay of factors. While genetic predisposition is postulated to play a role in AIS based on the existing literature (3941), our study was not designed to identify specific genetic determinants. The differences we observed may be more directly attributable to, or confounded by, varying environmental conditions, nutritional status, and lifestyle behaviors across ethnic groups (4244). Factors such as the intake of specific micronutrients, vitamin D levels, and participation in particular types of physical activity may indirectly affect the occurrence and progression of AIS by influencing bone development and biomechanical balance (45).

Therefore, future research in similar multi-ethnic regions should employ more representative samples and refined study designs to systematically evaluate the complex relationships between genetic, environmental, and lifestyle factors. This approach will enable a more comprehensive understanding of the etiological characteristics of AIS and provide scientific evidence for developing targeted prevention strategies.

4.3. Atypical manifestation of gender differences

Although numerous literatures report a significantly higher prevalence of AIS in females than in males (12, 17, 18, 46, 47), this study found no statistical difference in the confirmed prevalence between girls (1.47%) and boys (1.28%). However, during the screening process, the screening positive rate was significantly higher in girls (4.64%) than in boys (3.12%), while PPV was much higher in boys (40.90%) than in girls (31.72%). This phenomenon reveals that gender may influence the AIS screening and diagnosis process in more complex ways.

The higher screening positive rate coupled with lower PPV in girls invites several non-mutually exclusive hypotheses. Firstly, biological factors specific to female adolescence may contribute. It has been postulated that hormonal fluctuations, particularly in estrogen levels, could temporarily affect spinal tissue compliance and postural control during the peripubertal growth spurt (48, 49). This might lead to observable asymmetries in the forward bend test that do not yet correspond to a fixed structural curvature meeting the Cobb angle criterion (50, 51). Secondly, gender differences in body composition, with girls typically having a higher fat-to-muscle ratio, might influence the biomechanical presentation and the sensitivity of the Adams test (52, 53). Furthermore, we explored other potential contributing factors. The age distribution of our cohort was similar between genders, making this an unlikely sole explanation. However, the screening criteria themselves, which are highly sensitive, might interact differently with the female physiology described above. Sociocultural factors, such as heightened body awareness leading to earlier care-seeking or more cautious examiner assessment, could also contribute to the initial higher positive rate, though this study was not designed to test this specifically.

Conversely, the higher PPV in boys suggests that when a positive screen occurs, it is more likely to represent true AIS. This could be explained if stronger para-spinal muscles in males conceal milder curves, meaning that screening tends to detect only the more pronounced deformities in boys. The biological mechanism behind this phenomenon remains unclear, but it reminds us that when interpreting screening results and formulating referral strategies, gender specificity should be fully considered to avoid neglecting attention to boys due to the inherent notion of “higher girl incidence.”

4.4. Significant associated factors for adolescent scoliosis

The results of this study indicate that abnormal BMI, poor postural habits, lack of exercise, excessive electronic device use, and irregular routines are the main associated factors for the development of scoliosis in adolescents, while cultivating healthy lifestyle habits and exercise patterns may help reduce the risk. This finding aligns with several international studies, emphasizing the important role of multi-dimensional lifestyle factors in AIS onset. Firstly, the association between abnormal BMI (especially low BMI) and AIS has been confirmed in previous research (54, 55). Low BMI may reflect poor nutritional status or weak bone and muscle development, thereby reducing spinal stability and increasing the risk of curvature (56). Low body weight (often indicated by a low BMI) may predispose adolescents to spinal curvature due to diminished para-spinal muscular mass and lower bone mineral density. Conversely, it is also plausible that progressive scoliosis contributes to weight loss or a failure to gain weight appropriately (57). Secondly, poor postural habits (such as incorrect reading/writing posture, sitting with crossed legs, inappropriate desk height) have been associated with spinal deformity through asymmetric biomechanical loading (58, 59). For instance, maintaining a forward-leaning standing posture or consistently sleeping on one side may exacerbate asymmetric stress distribution on the spine (59). Thirdly, the association between lack of exercise and AIS may stem from insufficient core muscle strength, unable to provide adequate support for the spine (60). It is noteworthy that the type of exercise is also crucial; certain high-risk sports (like ballet) may increase the risk due to repetitive asymmetric movements (44, 54), while regular moderate-intensity exercise has a protective effect (60). Fourthly, excessive electronic device use (daily screen time >2 h) not only directly prolongs the duration of maintaining static poor postures but may also displace physical activity time, creating a vicious cycle (58, 61). Finally, irregular routines (such as insufficient sleep in this study) may be related to impaired muscle fatigue recovery and hormonal secretion disorders (e.g., abnormal rhythms of growth hormone and melatonin), indirectly affecting spinal health (56, 62). Moreover, sleep insufficiency (6–8 h) was associated with higher odds of AIS compared to the recommended duration (>8 h). Although typical guidelines recommend 8–10 h, empirical data from our study indicate that a substantial majority of adolescents, likely due to academic pressures and substantial homework loads, consistently achieve less than 8 h of sleep (63). In summary, AIS prevention requires comprehensive strategies, including nutritional intervention [e.g., increasing dairy intake (58)], postural correction education, exercise guidance (emphasizing symmetric exercises and core muscle training), and screen time management. Future research should focus on the interactions among these modifiable factors to provide a basis for developing precise public health intervention measures. However, as a cross-sectional study, the associations observed here do not imply causation, and the temporal sequence between these factors and AIS onset cannot be determined.

4.5. Consideration of reverse causality and unmeasured confounding

It is crucial to consider alternative explanations for the observed associations, particularly reverse causality. For instance, adolescents with subclinical or undiagnosed spinal deformity might avoid physical activities due to discomfort or self-consciousness, leading to physical inactivity and potentially lower BMI, rather than these factors causing the scoliosis. Similarly, excessive screen time could be a consequence of social withdrawal related to postural concerns. While we adjusted for key demographic and clinical variables, the potential for residual confounding by unmeasured factors, such as socioeconomic status, parental education, and precise pubertal stage, remains. These factors could influence both lifestyle habits (e.g., nutrition, access to sports) and spinal health. Therefore, our findings should be interpreted as identifying important and modifiable correlates of AIS, which merit further investigation in longitudinal studies to elucidate their potential causal roles.

4.6. Optimization and challenges of school screening strategy

The total screening positive rate of 3.83% and the positive predictive value of 35.70% in this study highlight the significant value of school screening as the first line of defense for the early detection of AIS. Simultaneously, to optimize screening strategies, establishing an efficient “school-hospital” collaborative referral mechanism is crucial. This model helps ensure the quality of screening and the continuity of subsequent management. However, international experience shows that even with established screening programs, low referral compliance and loss to follow-up remain common challenges (64, 65). Therefore, a successful cooperation model requires not only a clear referral process but also health education for students and parents, psychological support, and a convenient follow-up appointment system to improve referral rates and treatment compliance (66). Especially in multi-ethnic, relatively remote areas like those involved in this study, establishing a tiered diagnosis and treatment network involving telemedicine consultations and primary healthcare institutions could be an effective way to overcome geographical and cultural barriers. Additionally, this study observed a certain proportion of false-positive results in the screening. Future efforts could explore a multi-stage screening process or incorporate more discriminative auxiliary tools (such as surface topography) to enhance screening specificity, while strengthening regular follow-up for high-risk groups to reduce the risk of false negatives.

4.7. Study limitations and future directions

This study reveals the prevalence characteristics of AIS in a multi-ethnic region of Southwestern China, providing new perspectives, particularly regarding ethnic and gender differences. These findings not only enrich our understanding of AIS epidemiology but also provide a solid scientific basis for optimizing regional school screening programs and formulating precise public health intervention strategies. Although this study has yielded some important findings, it still has certain limitations. Firstly, the sample sizes for some minority ethnic groups (such as BuYi, Yi) were relatively small, and the calculated prevalence rates might have some random error, requiring validation in larger populations. Secondly, the cross-sectional design precludes causal inference and necessitates caution in interpreting the direction of the observed associations, as reverse causality (e.g., AIS leading to reduced activity) is plausible. Furthermore, although we adjusted for several confounders, residual confounding by unmeasured variables such as socioeconomic status, parental education, and precise pubertal staging cannot be ruled out. For example, we cannot determine whether girls who were initially screen-positive but not confirmed will develop AIS in the future. Thirdly, we acknowledge that engagement could be influenced by variations in health literacy and communication channels among parents. To address this, future studies will implement more tailored, community-based strategies to strengthen inclusivity and ensure equitable representation across all groups.

Based on the findings and limitations of this study, future research could be developed in the following directions. First, a long-term adolescent cohort should be established, with particular emphasis on regularly following up students who screened positive initially but were not diagnosed. Specifically, as a key component of comprehensive school screening strategies, these individuals should undergo periodic clinical monitoring until skeletal maturity. This approach would help track the progression of spinal morphology and further investigate the roles of hormonal levels, biomechanical parameters, and lifestyle in the onset and development of AIS. Second, prospective studies conducted in identified high-risk groups would be valuable to assess the effectiveness of early non-surgical interventions, including scoliosis-specific exercises and postural correction guidance, in preventing the onset or slowing the progression of AIS. Third, future studies should explore the integration of advanced screening and assessment tools, such as 3D ultrasound and deep learning technologies (67, 68). These innovative approaches show promise in enhancing the objectivity, efficiency, and accessibility of screening, while providing more accurate quantification of spinal three-dimensional morphology and progression risk. Fourth, the measurement of lifestyle factors relied on self-reported questionnaires, which are susceptible to recall and misclassification biases. Students might inaccurately recall certain behaviors (e.g., exact screen time) or provide socially desirable answers. Although we implemented measures such as questionnaire pre-testing and standardized administration to enhance data quality, the potential for non-differential misclassification remains. Such misclassification would typically bias the observed associations toward the null, suggesting that the true strengths of the associations we identified might be even stronger than reported.

5. Conclusion

This large-scale study establishes a 1.37% prevalence of AIS among multi-ethnic adolescents in Southwestern China, which is consistent with global figures. It reveals notable variations in prevalence across ethnic groups and a distinct gender-specific pattern in screening accuracy, with girls showing a higher false-positive rate. Importantly, we observed several modifiable factors associated with AIS, including abnormal BMI, poor postural habits, physical inactivity, prolonged electronic device use, and inadequate sleep. These findings underscore the necessity of implementing tailored school-screening programs and integrating multifaceted public health interventions targeting these associated factors to mitigate the burden of AIS in this and similar populations.

Acknowledgments

We are grateful to all the school health care staff participating in this study

Funding Statement

The author(s) declared that financial support was received for this work and/or its publication. This work was supported by the Shenzhen Outstanding Doctors, Outstanding Hospitals and Outstanding Clinics Project (SZSM201812066).

Footnotes

Edited by: Marios Tryfonidis, European University Cyprus, Cyprus

Reviewed by: Ruike Zhang, Fifth Affiliated Hospital of Guangzhou Medical University, China

Eleni Theodorou, University of Nicosia, Cyprus

Data availability statement

The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author.

Ethics statement

The studies involving humans were approved by the Ethics Committee of Longlin Traditional Chinese Medicine Hospital. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants' legal guardians/next of kin.

Author contributions

CH: Investigation, Methodology, Software, Validation, Writing – original draft, Writing – review & editing. BL: Data curation, Writing – original draft, Writing – review & editing. FL: Resources, Software, Validation, Writing – original draft, Writing – review & editing. ZL: Investigation, Software, Validation, Writing – original draft, Writing – review & editing. XC: Funding acquisition, Supervision, Writing – original draft, Writing – review & editing.

Conflict of interest

The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declared that generative AI was not used in the creation of this manuscript.

Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpubh.2025.1729509/full#supplementary-material

Supplementary_file_1.docx (34.2KB, docx)

References

  • 1.Weinstein SL, Dolan LA, Cheng JC, Danielsson A, Morcuende JA. Adolescent idiopathic scoliosis. Lancet. (2008) 371:1527–37. doi: 10.1016/S0140-6736(08)60658-3 [DOI] [PubMed] [Google Scholar]
  • 2.Altaf F, Gibson A, Dannawi Z, Noordeen H. Adolescent idiopathic scoliosis. BMJ. (2013) 346:f2508. doi: 10.1136/bmj.f2508 [DOI] [PubMed] [Google Scholar]
  • 3.Hu M, Zhang Z, Zhou X, Gao R, Wang C, Ma J, et al. Prevalence and determinants of adolescent idiopathic scoliosis from school screening in Huangpu district, Shanghai, China. Am J Transl Res. (2022) 14:4132–8. [PMC free article] [PubMed] [Google Scholar]
  • 4.Fong DY, Lee CF, Cheung KM, Cheng JC, Ng BK, Lam TP, et al. A meta-analysis of the clinical effectiveness of school scoliosis screening. Spine (Phila Pa 1976). (2010) 35:1061–71. doi: 10.1097/BRS.0b013e3181bcc835 [DOI] [PubMed] [Google Scholar]
  • 5.Luk KD, Lee CF, Cheung KM, Cheng JC, Ng BK, Lam TP, et al. Clinical effectiveness of school screening for adolescent idiopathic scoliosis: a large population-based retrospective cohort study. Spine (Phila Pa 1976). (2010) 35:1607–14. doi: 10.1097/BRS.0b013e3181c7cb8c [DOI] [PubMed] [Google Scholar]
  • 6.Cheng JC, Castelein RM, Chu WC, Danielsson AJ, Dobbs MB, Grivas TB, et al. Adolescent idiopathic scoliosis. Nat Rev Dis Primers. (2015) 1:15030. doi: 10.1038/nrdp.2015.30 [DOI] [PubMed] [Google Scholar]
  • 7.Chen X, Ye Y, Zhu Z, Zhang R, Wang W, Wu M, et al. Association between incorrect postures and curve magnitude of adolescent idiopathic scoliosis in china. J Orthop Surg Res. (2024) 19:300. doi: 10.1186/s13018-024-04767-z [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Yan B, Lu X, Qiu Q, Nie G, Huang Y. Association Between Incorrect Posture and Adolescent Idiopathic Scoliosis Among Chinese Adolescents: findings from a large-scale population-based study. Front Pediatr. (2020) 8:548. doi: 10.3389/fped.2020.00548 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Stokes OM, Luk KD. The current status of bracing for patients with adolescent idiopathic scoliosis. Bone Joint J. (2013) 95-b:1308–16. doi: 10.1302/0301-620X.95B10.31474 [DOI] [PubMed] [Google Scholar]
  • 10.Grossman DC, Curry SJ, Owens DK, Barry MJ, Davidson KW, Doubeni CA, et al. Screening for adolescent idiopathic scoliosis: US preventive services task force recommendation statement. JAMA. (2018) 319:165–72. doi: 10.1001/jama.2017.19342 [DOI] [PubMed] [Google Scholar]
  • 11.Dunn J, Henrikson NB, Morrison CC, Blasi PR, Nguyen M, Lin JS. Screening for adolescent idiopathic scoliosis: evidence report and systematic review for the US preventive services task force. JAMA. (2018) 319:173–87. doi: 10.1001/jama.2017.11669 [DOI] [PubMed] [Google Scholar]
  • 12.Zhang H, Guo C, Tang M, Liu S, Li J, Guo Q, et al. Prevalence of scoliosis among primary and middle school students in Mainland China: a systematic review and meta-analysis. Spine (Phila Pa 1976). (2015) 40:41–9. doi: 10.1097/BRS.0000000000000664 [DOI] [PubMed] [Google Scholar]
  • 13.Ueno M, Takaso M, Nakazawa T, Imura T, Saito W, Shintani R, et al. 5-year epidemiological study on the prevalence rate of idiopathic scoliosis in Tokyo: school screening of more than 250,000 children. J Orthop Sci. (2011) 16:1–6. doi: 10.1007/s00776-010-0009-z [DOI] [PubMed] [Google Scholar]
  • 14.Wong HK, Hui JH, Rajan U, Chia HP. Idiopathic scoliosis in Singapore schoolchildren: a prevalence study 15 years into the screening program. Spine (Phila Pa 1976). (2005) 30:1188–96. doi: 10.1097/01.brs.0000162280.95076.bb [DOI] [PubMed] [Google Scholar]
  • 15.Ugras AA, Yilmaz M, Sungur I, Kaya I, Koyuncu Y, Cetinus ME. Prevalence of scoliosis and cost-effectiveness of screening in schools in Turkey. J Back Musculoskelet Rehabil. (2010) 23:45–8. doi: 10.3233/BMR-2010-0247 [DOI] [PubMed] [Google Scholar]
  • 16.Tu Q, Xu W, Feng Y, Zhang Z, Zhuang W. Prevalence and determinants of adolescent idiopathic scoliosis from school screening in Xiaoshan District, Hangzhou, China. Front Public Health. (2025) 13:1595793. doi: 10.3389/fpubh.2025.1595793 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Qian G, Zhang L, Zhao Z, Wang Y, Lu J, Bi N, et al. Prevalence of scoliosis and congenital heart disease based on school screening in Jinghong City, Yunnan Province. Front Public Health. (2025) 13:1517542. doi: 10.3389/fpubh.2025.1517542 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Fu X, Meng S, Huang X, Li W, Ye B, Chen S. The prevalence of scoliosis among adolescents in China: a systematic review and meta-analysis. J Orthop Surg Res. (2024) 19:585. doi: 10.1186/s13018-024-05077-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Singh H, Shipra, Sharma V, Sharma I, Sharma A, Modeel S, et al. The first study of epidemiology of adolescent idiopathic scoliosis shows lower prevalence in females of Jammu and Kashmir, India. Am J Transl Res. (2022) 14:1100–6. [PMC free article] [PubMed] [Google Scholar]
  • 20.Zhou J, Wang Y, Xie J, Zhao Z, Shi Z, Li T, et al. Scoliosis school screening of 139,922 multi-ethnic children in Dali, southwestern China: a large epidemiological study. iScience. (2023) 26:108305. doi: 10.1016/j.isci.2023.108305 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Zou Y, Lin Y, Meng J, Li J, Gu F, Zhang R. The prevalence of scoliosis screening positive and its influencing factors: a school-based cross-sectional study in Zhejiang Province, China [Original Research]. Front Public Health. (2022) 10:773594. doi: 10.3389/fpubh.2022.773594 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Guo H, Chen N, Yang Y, Zhou X, Li X, Jiang Y, et al. Ethnic disparity in the incidence of scoliosis among adolescents in Tianzhu Tibetan Autonomous County, China [Original Research]. Front Public Health. (2022) 10:791550. doi: 10.3389/fpubh.2022.791550 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Uno H, Wei LJ, Hughes M. Effects of bracing in adolescents with idiopathic scoliosis. N Engl J Med. (2014) 370:680. doi: 10.1056/NEJMc1314229 [DOI] [PubMed] [Google Scholar]
  • 24.Du Q, Zhou X, Negrini S, Chen N, Yang X, Liang J, et al. Scoliosis epidemiology is not similar all over the world: a study from a scoliosis school screening on Chongming Island (China). BMC Musculoskelet Disord. (2016) 17:303. doi: 10.1186/s12891-016-1140-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Kuroki H, Nagai T, Chosa E, Tajima N. School scoliosis screening by Moiré topography - overview for 33 years in Miyazaki Japan. J Orthop Sci. (2018) 23:609–13. doi: 10.1016/j.jos.2018.03.005 [DOI] [PubMed] [Google Scholar]
  • 26.Cho NI, Hwang CJ, Kim HY, Baik JM, Joo YS, Lee CS, et al. Referral patterns and patient characteristics at the first visit to a scoliosis center: a 2-year experience in South Korea without a school scoliosis-screening program. J Neurosurg Pediatr. (2018) 21:414–20. doi: 10.3171/2017.10.PEDS17348 [DOI] [PubMed] [Google Scholar]
  • 27.Moalej S, Asadabadi M, Hashemi R, Khedmat L, Tavacolizadeh R, Vahabi Z, et al. Screening of scoliosis in school children in Tehran: the prevalence rate of idiopathic scoliosis. J Back Musculoskelet Rehabil. (2018) 31:767–74. doi: 10.3233/BMR-171078 [DOI] [PubMed] [Google Scholar]
  • 28.Zheng Y, Dang Y, Wu X, Yang Y, Reinhardt JD, He C, et al. Epidemiological study of adolescent idiopathic scoliosis in Eastern China. J Rehabil Med. (2017) 49:512–9. doi: 10.2340/16501977-2240 [DOI] [PubMed] [Google Scholar]
  • 29.Kadhim M, Lucak T, Schexnayder S, King A, Terhoeve C, Song B, et al. Current status of scoliosis school screening: targeted screening of underserved populations may be the solution. Public Health. (2020) 178:72–7. doi: 10.1016/j.puhe.2019.08.020 [DOI] [PubMed] [Google Scholar]
  • 30.Zhao Y, Zhao Y, Lu S, Yang Q, Chen L, Ma X, et al. Guideline for adolescent scoliosis screening in China (public version 2024). J Orthop Transl. (2025) 50:364–72. doi: 10.1016/j.jot.2024.09.006 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Li Y, Xiang Y, Wang Y, Zhang X, Xin Y, Xue H, et al. Detection rate and risk factors of abnormal spinal curvature among children and adolescents - Jiangsu Province, China, 2021-2023. China CDC Wkly. (2025) 7:208–16. doi: 10.46234/ccdcw2025.033 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Malaquias LC, da Silva MCM, Menezes DYA, Magalhães MO. Measurement properties of the Spinal Appearance Questionnaire in adolescents with idiopathic scoliosis: a systematic review. BMC Musculoskelet Disord. (2023) 24:587. doi: 10.1186/s12891-023-06708-z [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Leone E, Chockalingam N, Needham R, Healy A, Eddison N, Jevtic N, et al. Development and preliminary testing of the staffordshire questionnaire for adolescent idiopathic scoliosis (SQ-AIS): content and face validity. Health Sci Rep. (2024) 7:e70213. doi: 10.1002/hsr2.70213 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Paradkar R, Paradkar R, Singh M, Knebel A, Balmaceno-Criss M, Kim J, et al. The impact of the social determinants of health on adolescent idiopathic scoliosis: a systematic review. Spine Deformity. (2025) 13:997–1006. doi: 10.1007/s43390-025-01065-4 [DOI] [PubMed] [Google Scholar]
  • 35.Daruwalla JS, Balasubramaniam P, Chay SO, Rajan U, Lee HP. Idiopathic scoliosis. Prevalence and ethnic distribution in Singapore schoolchildren. J Bone Joint Surg Br. (1985) 67:182–4. doi: 10.1302/0301-620X.67B2.3980521 [DOI] [PubMed] [Google Scholar]
  • 36.Fisher S, Chihuri S, Guglielminotti J, Li G, Eisler L. Racial and ethnic differences in transfusion rates in adolescent scoliosis surgery: preoperative anemia as a mediator of disparity. Transfusion. (2024) 64:2124–32. doi: 10.1111/trf.18023 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Huang J, Zhang H, Wen J, Liu L, Xu S, Wang X, et al. Evaluation of the prevalence of adolescent scoliosis and its associated factors in Gansu Province, China: a cross-sectional study. Front Public Health. (2024) 12:1381773. doi: 10.3389/fpubh.2024.1381773 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Shohat M, Shohat T, Nitzan M, Mimouni M, Kedem R, Danon YL. Growth and ethnicity in scoliosis. Acta Orthop Scand. (1988) 59:310–3. doi: 10.3109/17453678809149370 [DOI] [PubMed] [Google Scholar]
  • 39.Gorman KF, Julien C, Moreau A. The genetic epidemiology of idiopathic scoliosis. Eur Spine J. (2012) 21:1905–19. doi: 10.1007/s00586-012-2389-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Fadzan M, Bettany-Saltikov J. Etiological theories of adolescent idiopathic scoliosis: past and present. Open Orthop J. (2017) 11:1466–89. doi: 10.2174/1874325001711011466 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Gao W, Peng Y, Liang G, Liang A, Ye W, Zhang L, et al. Association between common variants near LBX1 and adolescent idiopathic scoliosis replicated in the Chinese Han population. PLoS ONE. (2013) 8:e53234. doi: 10.1371/journal.pone.0053234 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Li M, Nie Q, Liu J, Jiang Z. Prevalence of scoliosis in children and adolescents: a systematic review and meta-analysis [Systematic Review]. Front Pediatr. (2024) 12:1399049. doi: 10.3389/fped.2024.1399049 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Zhang C, Wang Y, Yu J, Jin F, Zhang Y, Zhao Y, et al. Analysis of sagittal curvature and its influencing factors in adolescent idiopathic scoliosis. Medicine (Baltimore). (2021) 100:e26274. doi: 10.1097/MD.0000000000026274 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Scaturro D, Costantino C, Terrana P, Vitagliani F, Falco V, Cuntrera D, et al. Risk factors, lifestyle and prevention among adolescents with idiopathic juvenile scoliosis: a cross sectional study in eleven first-grade secondary schools of Palermo Province, Italy. Int J Env Res Pub He. (2021) 18:12335. doi: 10.3390/ijerph182312335 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Ghanbari F, Otomo N, Gamache I, Iwami T, Koike Y, Khanshour AM, et al. Interrogating causal effects of body composition and puberty-related risk factors on adolescent idiopathic scoliosis: a two-sample mendelian randomization study. JBMR Plus. (2023) 7:e10830. doi: 10.1002/jbm4.10830 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Shakil H, Iqbal ZA, Al-Ghadir AH. Scoliosis: review of types of curves, etiological theories and conservative treatment. J Back Musculoskelet Rehabil. (2014) 27:111–5. doi: 10.3233/BMR-130438 [DOI] [PubMed] [Google Scholar]
  • 47.Peng Z, Li Y, Yang H, Jiang Y, Li Y, Gao M, et al. Positive rate and influencing factors of adolescent idiopathic scoliosis among school children aged 9 to 18 years in Xiamen, China. BMC Pediatr. (2025) 25:216. doi: 10.1186/s12887-025-05566-z [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 48.Kulis A, Gozdzialska A, Drag J, Jaśkiewicz J, Knapik-Czajka M, Lipik E, et al. Participation of sex hormones in multifactorial pathogenesis of adolescent idiopathic scoliosis. Int Orthop. (2015) 39:1227–36. doi: 10.1007/s00264-015-2742-6 [DOI] [PubMed] [Google Scholar]
  • 49.Kruse LM, Buchan JG, Gurnett CA, Dobbs MB. Polygenic threshold model with sex dimorphism in adolescent idiopathic scoliosis: the Carter effect. J Bone Joint Surg Am. (2012) 94:1485–91. doi: 10.2106/JBJS.K.01450 [DOI] [PubMed] [Google Scholar]
  • 50.Addai D, Zarkos J, Bowey AJ. Current concepts in the diagnosis and management of adolescent idiopathic scoliosis. Childs Nerv Syst. (2020) 36:1111–9. doi: 10.1007/s00381-020-04608-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Takahashi Y, Matsumoto M, Karasugi T, Watanabe K, Chiba K, Kawakami N, et al. Replication study of the association between adolescent idiopathic scoliosis and two estrogen receptor genes. J Orthop Res. (2011) 29:834–7. doi: 10.1002/jor.21322 [DOI] [PubMed] [Google Scholar]
  • 52.Grivas TB, Vasiliadis E, Mazioti C, Mamzeri A, Papagianni D, Katzouraki G, et al. To screen or not to screen: “False Positive” cases-can they be treated as definitely false? Properly selecting the screening age-range groups in scoliosis screening programs. Healthcare (Basel). (2025) 13:600. doi: 10.3390/healthcare13060600 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Grivas TB, Vasiliadis E, Mouzakis V, Mihas C, Koufopoulos G. Association between adolescent idiopathic scoliosis prevalence and age at menarche in different geographic latitudes. Scoliosis. (2006) 1:9. doi: 10.1186/1748-7161-1-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Watanabe K, Michikawa T, Yonezawa I, Takaso M, Minami S, Soshi S, et al. Physical activities and lifestyle factors related to adolescent idiopathic scoliosis. J Bone Joint Surg Am. (2017) 99:284–94. doi: 10.2106/JBJS.16.00459 [DOI] [PubMed] [Google Scholar]
  • 55.Ng PTT, Tucker K, Zahir SF, Izatt MT, Straker L, Claus A. Comparison of physiological and behavioral nutrition-related factors in people with and without adolescent idiopathic scoliosis, from cohort data at 8 to 20 years. JBMR Plus. (2024) 8:ziad013. doi: 10.1093/jbmrpl/ziad013 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Cai Z, Wu R, Zheng S, Qiu Z, Wu K. Morphology and epidemiological study of idiopathic scoliosis among primary school students in Chaozhou, China. Environ Health Prev Med. (2021) 26:71. doi: 10.1186/s12199-021-00989-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Gibson D, Stein A, Khatri V, Wesselink D, Sitko S, Mehler PS. Associations between low body weight, weight loss, and medical instability in adults with eating disorders. Int J Eat Disord. (2024) 57:869–78. doi: 10.1002/eat.24129 [DOI] [PubMed] [Google Scholar]
  • 58.Dou Q, Zhu Z, Zhu L, Wang W, Guo L, Ru S, et al. Academic-related factors and daily lifestyle habits associated with adolescent idiopathic scoliosis: a case-control study. Environ Health Prev Med. (2023) 28:23–23. doi: 10.1265/ehpm.22-00243 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Yang J, Huang S, Cheng M, Tan W, Yang J. Postural habits and lifestyle factors associated with adolescent idiopathic scoliosis (AIS) in China: results from a big case–control study. J Orthop Surg Res. (2022) 17:472. doi: 10.1186/s13018-022-03366-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.de Assis SJC, Sanchis GJB, de Souza CG, Roncalli AG. Influence of physical activity and postural habits in schoolchildren with scoliosis. Arch Public Health. (2021) 79:63. doi: 10.1186/s13690-021-00584-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Cheung MC, Lai JSK, Yip J, Cheung JPY. Increased computer use is associated with trunk asymmetry that negatively impacts health-related quality of life in early adolescents. Patient Prefer Adherence. (2021) 15:2289–302. doi: 10.2147/PPA.S329635 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Sedrez JA, Da Rosa MIZ, Noll M. Medeiros FdS, Candotti CT. Fatores de risco associados a alterações posturais estruturais da coluna vertebral em crianças e adolescents. Rev Paulista Pediatria. (2015) 33:72–81. doi: 10.1016/j.rpped.2014.11.012 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Li T, Liu X, Cao C, Yang F, Ding P, Xu S, et al. Association between screen time, homework and reading duration, sleep duration, social jetlag and mental health among Chinese children and adolescents. BMC Psychiatry. (2024) 24:781. doi: 10.1186/s12888-024-06233-w [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Guo Y, Jiang Q, Tanimoto T, Kami M, Luo C, Leppold C, et al. Low hospital referral rates of school scoliosis screening positives in an urban district of mainland China. Medicine (Baltimore). (2017) 96:e6481. doi: 10.1097/MD.0000000000006481 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Beauséjour M, Goulet L, Ehrmann Feldman D, Da Silva RB, Pineault R, Rossignol M, et al. Scoliosis referral project m. Pathways of healthcare utilisation in patients with suspected adolescent idiopathic scoliosis: a cross-sectional study. BMC Health Serv Res. (2015) 15:500. doi: 10.1186/s12913-015-1152-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Grivas TB, Hresko MT, Labelle H, Price N, Kotwicki T, Maruyama T. The pendulum swings back to scoliosis screening: screening policies for early detection and treatment of idiopathic scoliosis - current concepts and recommendations. Scoliosis. (2013) 8:16. doi: 10.1186/1748-7161-8-16 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Zhang C, Zheng Y, McAviney J, Ling SH. SSAT-Swin: deep learning-based spinal ultrasound feature segmentation for scoliosis using self-supervised swin transformer. Ultrasound Med Biol. (2025) 51:999–1007. doi: 10.1016/j.ultrasmedbio.2025.02.013 [DOI] [PubMed] [Google Scholar]
  • 68.Wang H, Zhu Y, Bao Q, Lu Y, Yan F, Du L, et al. novel portable and radiation-free method for assessing scoliosis: an accurate and reproducible study. BMC Musculoskelet Disord. (2025) 26:200. doi: 10.1186/s12891-025-08415-3 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary_file_1.docx (34.2KB, docx)

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author.


Articles from Frontiers in Public Health are provided here courtesy of Frontiers Media SA

RESOURCES