Hostname: page-component-7bb8b95d7b-lvwk9 Total loading time: 0 Render date: 2024-09-26T08:54:55.258Z Has data issue: false hasContentIssue false

Maternal dietary practices during pregnancy and obesity of neonates: a machine learning approach towards hierarchical and nested relationships in a Tibet Plateau cohort study

Published online by Cambridge University Press:  26 September 2024

Xiao Tang
Affiliation:
Nutrition and Health Promotion Center, Department of Public Health, Medical College, Qinghai University, Xining 810008, People’s Republic of China
Bin Zhang
Affiliation:
School of Mathematics and Statistics, Qinghai Minzu University, Xining 810007, People’s Republic of China
Mengzi Sun
Affiliation:
Global Health Institute, School of Public Health, Xi’an Jiaotong University, Xi’an 710061, People’s Republic of China
Hong Xue
Affiliation:
Department of Health Administration and Policy, College of Public Health, George Mason University, Fairfax, VA, USA
Ruihua Xu
Affiliation:
Nutrition and Health Promotion Center, Department of Public Health, Medical College, Qinghai University, Xining 810008, People’s Republic of China
Wenxiu Jian
Affiliation:
Nutrition and Health Promotion Center, Department of Public Health, Medical College, Qinghai University, Xining 810008, People’s Republic of China
Xiaomin Sun
Affiliation:
Global Health Institute, School of Public Health, Xi’an Jiaotong University, Xi’an 710061, People’s Republic of China
Pinhua Wang
Affiliation:
Department of Obstetrics, Qinghai Red Cross Hospital, Xining 810099, People’s Republic of China
Jiangcuo Zhaxi
Affiliation:
Nangqian People’s Hospital, Yushu 815299, People’s Republic of China
Xuejun Wang
Affiliation:
Department of Anesthesiology, Qinghai Red Cross Hospital, Xining 810099, People’s Republic of China
Liehong Wang
Affiliation:
Department of Obstetrics, Qinghai Red Cross Hospital, Xining 810099, People’s Republic of China
Xinguang Chen
Affiliation:
Global Health Institute, School of Public Health, Xi’an Jiaotong University, Xi’an 710061, People’s Republic of China
Yankai Xia
Affiliation:
State Key Laboratory of Reproductive Medicine, Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing 211166, People’s Republic of China
Youfa Wang*
Affiliation:
Global Health Institute, School of Public Health, Xi’an Jiaotong University, Xi’an 710061, People’s Republic of China
Wen Peng*
Affiliation:
Nutrition and Health Promotion Center, Department of Public Health, Medical College, Qinghai University, Xining 810008, People’s Republic of China Qinghai Provincial Key Laboratory of Prevention and Control of Glucolipid Metabolic Diseases with Traditional Chinese Medicine, Xining, People’s Republic of China
*
*Corresponding authors: Dr Wen Peng, email wen.peng2014@foxmail.com; Youfa Wang, email youfawang@gmail.com
*Corresponding authors: Dr Wen Peng, email wen.peng2014@foxmail.com; Youfa Wang, email youfawang@gmail.com
Rights & Permissions [Opens in a new window]

Abstract

Studies on obesity and risk factors from a life-course perspective among residents in the Tibet Plateau with recent economic growth and increasing obesity are important and urgently needed. The birth cohort in this area provides a unique opportunity to examine the association between maternal dietary practice and neonatal obesity. The study aims to detect the prevalence of obesity among neonates, associated with maternal diet and other factors, supporting life-course strategies for obesity control. A cohort of pregnant women was enrolled in Tibet Plateau and followed till childbirth. Dietary practice during pregnancy was assessed using the Chinese FFQ – Tibet Plateau version, food items and other variables were associated with the risk for obesity of neonates followed by logistic regression, classification and regression trees (CART) and random forest. Of the total 1226 mother–neonate pairs, 40·5 % were Tibetan and 5·4 % of neonates with obesity. Consuming fruits as a protective factor for obesity of neonates with OR (95 % CI) = 0·61 (0·43, 0·87) from logistic regression; as well as OR = 0·20 (0·12, 0·35) for consuming fruits (≥ weekly) from CART. Removing fruit consumption to avoid overshadowing effects of other factors, the following were influential from CART: maternal education (more than middle school, OR = 0·22 (0·13, 0·37)) and consumption of Tibetan food (daily, OR = 3·44 (2·08, 5·69). Obesity among neonates is prevalent in the study population. Promoting healthy diets during pregnancy and strengthening maternal education should be part of the life-course strategies for obesity control.

Type
Research Article
Copyright
© The Author(s), 2024. Published by Cambridge University Press on behalf of The Nutrition Society

The long history of the agricultural economy has fostered a social norm in China that it is desirable for mothers to have large and heavy babies. Birthweights are even used to name a newborn if the weight is high. For example, ‘Ba Jin’, a traditional Chinese weight unit equivalent to 4000 grams, has been a common first name for many Chinese. This traditional culture is now challenged in China because of the growing obesity epidemic. Along with a four-decade-long economic growth, obesity has become a new public health challenge(Reference Gao, Bhurtyal and Wei1,Reference Pan, Wang and Pan2) The obesity of neonates has long been recognised as a risk factor for subsequent obesity and related health consequences (such as metabolic syndromes, CVD and cancer) during adolescence and adulthood(Reference Barker, Godfrey and Osmond3Reference Rasmussen and Johansson5). Research indicates that higher neonatal adiposity correlates with elevated BMI and an increased likelihood of overweight or obesity during early childhood(Reference Moore, Harrall and Sauder6).

Maternal diets during pregnancy can affect the birth weight of neonates through fetal programming or epigenetic mechanisms(Reference Kensara, Wootton and Phillips7). The ponderal index (PI) provides the best measure of the adiposity of neonates(Reference Polin, Fox and Abman8). From literature research, we found that maternal and infant health studies focus on low birth weight for women with low socio-economic status(Reference Chia, de Seymour and Colega9,Reference Yang, Chang and Tian10) , and few studies if any examined the dietary factors associated with neonates with obesity (PI > 90 percentile). One cohort study with 570 mother–infant dyads from Dublin, Ireland reported a positive association between nutrition intake during pregnancy and neonatal birthweight, but the risk of obesity was not examined(Reference Geraghty, O’Brien and Alberdi11). A recent cohort study of 937 mother–child dyads from Shenyang, an industrial city in northeast China observed a negative relationship between diet with more fruits and vegetables during pregnancy and infants’ BMI(Reference Chen, Aris and Bernard12). However, the study’s participants were mainly Han Chinese, resulting in a homogeneous diet due to the population’s geographical and ethnic uniformity(Reference Chen, Aris and Bernard12). While some studies have explored outcomes related to babies with large gestational age or high birth weight, which may serve as indicators of neonatal obesity to some extent, their relationship with maternal diet remains elusive. For instance, a cohort study identified a positive association between a high intake of milk, vegetables and sweets during pregnancy with large gestational age births(Reference Barchitta, Magnano San Lio and La Rosa13). Conversely, research conducted in Iran revealed that high consumption of sugar, fruit juice, candy and desserts was positively correlated with low-birth-weight infants(Reference Hajianfar, Esmaillzadeh and Feizi14). Additionally, studies have investigated the impact of maternal carbohydrate intake on total gestational weight gain and neonatal birth weight(Reference Pathirathna, Sekijima and Sadakata15). However, the results appear to be contradictory, as higher carbohydrate intake in early pregnancy has been linked to lower birth weight(Reference Godfrey, Robinson and Barker16).

After decades of overall economic growth in China, the remote Tibet Plateau area experienced rapid economic growth recently(Reference Fu17). Along with increases in food supply and improvements in education, many mothers may have altered their dietary practices when they become pregnant. For example, some women may start adding fruits and protein-rich foods to their table; while others may still stick to the traditional Tibetan food, a typical example is samba, a traditional Tibetan food of a mixture of roasted barley, butter and sugar, featuring high calories and fat(Reference De Franco, Lampugnani and Gelmetti18Reference Peng, Liu and Malowany20). Furthermore, it is noteworthy that Tibetan religious and cultural practices discourage fish consumption, but with the urbanisation of Tibetan areas, Han Chinese dietary influences are permeating and enriching traditional Tibetan diets, particularly among the younger generation(Reference Wang, Dang and Yan21,Reference Zhou, Li and Liu22) . The recent economic growth and improved infrastructure in the Tibet Plateau area have led to the diversification and transition in diets among pregnant women, offering a unique opportunity to study dietary practices during pregnancy and factors associated with neonatal obesity. The Tibetan region’s distinct geography and culture lead to a unique diet and lifestyle compared with other regions. Additionally, health challenges brought by the high-altitude environment and remoteness contributed to the inferior health status in Tibet areas. Evidence suggests that high-altitude hypoxia may contribute to lower birth weight and length, thereby leading to an increased PI in newborns. There is currently no evidence supporting the notion that obesity in newborns in high-altitude areas offers protective effects on future health outcomes(Reference Soria, Julian and Vargas23,Reference Bigham, Julian and Wilson24) . Thus, studies on the association between diets and birth outcomes have important public health implications.

In this study, we focused on the relationship between maternal dietary practice during pregnancy and the risk of obesity among newborns with a large cohort of mother–newborn dyads in the Tibet Plateau area. Our goal is to detect the prevalence of obesity in neonates and related factors and to provide evidence supporting the development of life-course strategies to control the growing obesity epidemic in China(Reference Peng, Chen and Chen25).

Materials and methods

Study design and participants

This cohort study targeted maternal–neonate dyads from the Tibet Plateau area in Qinghai Province where Tibetan and Han Chinese dominate. Pregnant women were recruited from two typical maternity hospitals serving all women in the region. Of the two hospitals, one provides care mainly for urban areas and another for rural areas. We completed participant recruitment during 2019–2020 when pregnant women visited the hospital for routine pre-delivery exams; we then followed them up till child delivery. The following inclusion criteria were used for enrollment: (1) legal local residence; (2) determined ethnicity of Tibetan or Han; (3) singleton pregnancy; (4) live birth without obvious congenital diseases and (5) agreed to participate by signing the informed consent. The following criteria were used to exclude unqualified participants: (1) mothers who were non-local residents, (2) undetermined ethnicity, (3) stillbirth and (4) neonates with congenital diseases such as Down syndrome. Of 1593 eligible women approached, 1518 met the criteria and were enrolled by signing the informed consent.

After enrollment, trained investigators interviewed the participants face to face to collect baseline survey data on demographic factors, socio-economic status and data on dietary practice. After the baseline assessment, all participants were followed until childbirth. After child delivery in the hospital, neonatal data were retrieved from the medical records, including gestation age, sex, birth status, Apgar scoring, congenital diseases, birth weight and length. After completion of data collection, 292 participants were excluded, including congenital diseases (7), stillbirths (10), no birthweight (56), no birth length (10), incomplete medical record (11), incomplete survey (120) and incomplete food frequency (78). Further analysis indicated that the incompleteness and missingness were related to difficulties in transportation and follow-up assessments despite tedious efforts by the study team. Online Fig. S1 summarises the recruitment and follow-up assessment using a flowchart.

This study was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving human subjects were approved by the Ethics Committee of the Medical College at Qinghai University, Qinghai Province, China (Approval No: 2018–36). Written informed consent was obtained from all subjects.

The study focuses on neonatal obesity as the primary outcome of interest. This variable was assessed based on the PI for newborns(Reference Gozal, Ndombo and Ze Minkande26Reference Andreasyan, Ponsonby and Dwyer28). The PI was calculated as: PI = birth weight (kg)/(birth length (m))3. A neonate was scored 1 (with obesity) if his/her PI > the 90th percentile, or 0 (with no obesity). This classification was made following the gender and gestational age-specific PI percentiles developed for Chinese newborns(Reference Zong, Li and Zhang29). Of various weight status measures for neonates, we elected to use PI because of the greater validity of this measure than others such as BMI in measuring adiposity(Reference Polin, Fox and Abman8,Reference Roje, Banovic and Tadin30,Reference Zaniqueli, Oliosa and Neves31) .

Maternal dietary practice during pregnancy

The Chinese FFQ – Tibet Plateau version (CFFQ-TP) was used to assess maternal dietary practices during the third trimester of pregnancy. With difficulties in locating a measurement tool for assessing the dietary practice of the study population, we developed the CFFQ-TP following the Chinese Dietary Guideline in four steps. Step 1, obtaining the food items common for Chinese by a careful review of the Chinese Dietary Guideline. Step 2, obtaining food items specifically for the study population and verifying which food items for Chinese in general were also common in the study population. This was achieved through intensive focused-group studies with the residents in local mountain villages and towns. Step 3, forming a draft CFFQ-TP by including both Chinese food and Tibetan food that were common in the study area for pilot testing. Step 4, generating the final version for use after revising based on the result from pilot tests. This instrument has adequate reliability and validity in predicting outcome variables(Reference Zhao, Wang and Liu32).

The CFFQ-TP contained fourteen items (including refined carbohydrates, multigrain and roots, samba and butter, vegetables, fruits, red meats, poultry, fish and sea food, eggs, dairy products, beans and related products, pickles and other processed foods, soda and sugar beverages and snacks), reflecting the local dietary practice, including the consumption of samba, traditional high calories and high fat Tibetan food (roasted Tibetan barley, mixed with butter and sugar). We administered the CFFQ-TP in the hospital setting when the enrolled mothers were waiting for care, the average gestational age was 38 weeks, with a minimum of 28 weeks and a maximum of 43 weeks. Following the pilot-tested protocol, our trained investigators asked the mothers to rate the frequency of consuming individual foods during the past month. We assessed the reported frequencies using a four-point scale with 0 (less than monthly), 1 (monthly), 2 (weekly) and 3 (daily) for statistical analysis. The Cronbach alpha of CFFQ-TP was 0·704 in our study.

Covariates

Demographic factors for mothers were age (in years), education (< 9 years, 9–12 years v. more than 12 years), pre-pregnancy BMI and residential status (rural v. urban). Demographic factors for neonates were sex (male, female), ethnicity (Tibetan or Han) and birth order (if first-born).

Statistical analysis

Descriptive statistics were used to obtain estimates of the study sample. We constructed logistic regression models to assess the relationship between food items and obesity risk for all influential factors using two models. Model 1 contained all fourteen food frequency measures. To adjust for demographic and SES, seven additional covariates had been adjusted. Three maternal covariates were residence (rural v. urban), age at enrollment and education (< 9 years, 9–12 years v. more than 12 years); and four neonatal covariates were first birth (yes/no), race (Tibetan v. Han) and sex (male v. female). We used stepwise logistic regression to perform feature selection. As an alternative, model 2 was constructed by removing the most influential variable ‘fruit consumption’ in model 1 to avoid overshadowing the effects of other factors.

In addition to conventional methods, classification and regression trees (CART) was used as a classification tool to examine the potential hierarchal and nested relationships among the variables in our study(Reference Chen, Mo and Yu33). CART is a popular classification tool widely used in the field of machine learning(Reference Chen, Mo and Yu33). To begin the CART analysis, simple random sampling without replacement was used to split the sample into 80 % sized train samples and 20 % validation samples. Using CART, we were able to partition our data sequentially by selecting splitting variables (nodes) based on the Gini index which measures the degree of purity of class distribution at a given node. The CART algorithm searches for the splitting variable with the lowest Gini impurity at each step and keeps splitting the subsets until it cannot reduce impurity. The tree-like structure produced by CART enabled us to investigate the hierarchical and nested relationships among the variables, advancing regression analysis. However, the CART algorithm has its disadvantages, such as susceptibility to overfitting, particularly when dealing with complex datasets. To address this and potential collinearity issues, we utilised the Random Forest SHapley Additive Explanation (SHAP) decomposition for result validation. Sensitivity and specificity are employed to evaluate and compare the predictive performance of both logistic regression and CART.

All statistical analyses were completed using software R version 4·1·3. The R functions glm() was used for logistic regression, rpart() was used for CART and randomForest() was used for random forest analysis.

Results

Demographic and lifestyle characteristics

As shown in Table 1, most mothers were aged 25–34 years with a mean (sd) of 28·8(5·0) years. Of the sample, 682 (56·3 %) were from rural areas and 530 (43·7 %) were from urban areas and 794 (66·7 %) with a middle (9-year) or higher levels of education. Table 1 also presents the characteristics of the offspring. Of these newborns, 496 (40·5 %) were Tibetan and 730 (59·5 %) were Han, 621 (50·7 %) were males and 604 (49·3 %) were females with a mean birthweight of 3151·2 (sd 525·8) g. Of the total neonates, 66 (5·4 % with 95 % CI of 4·2–6·8 %) were classified as having obesity.

Table 1. Characteristics of the study participants, including the mothers and neonates (n 1226)

PI,ponderal index.

* Means these variables contain missing data. Methods: Pearson’s χ 2 tests or students’ t-test.

Food frequencies

Table 2 presents the frequencies of all fourteen foods consumed during pregnancy, overall and stratified by maternal ethnicity. The results suggest a general healthy dietary practice, such as high frequencies of consuming vegetables (92·3 % daily), fruits (77·1 % daily), dairy products (56·9 % daily) and low frequencies of consuming prepared foods such as pickles. Additionally, the reported food frequencies reflected the traditional cultures and the impact of economic growth. For example, 77·1 % of the mothers reported consuming fruits on a daily basis; 52·9 % reported consuming red meats (such as beef) on a daily basis and significantly more Tibetan mothers than Han mothers (44·2 % v. 12·2 %) consumed Samba daily.

Table 2. Maternal dietary practice during pregnancy as measured using the food frequency*, overall and by ethnic group (n 1226)

* Means the food frequency was measured using the Chinese FFQ – Tibet Plateau version (CFFQ-TP).

Methods: Pearson’s χ 2 test or Fisher’s exact test.

Results from logistic regression

In model 1 with all twenty-one variables analysed using logistic regression to control for both maternal and neonatal covariates, results indicate that of the fourteen food items, only consuming fruits was associated with reduced risk of obesity with OR (95 % CI) = 0·61 (0·43, 0·87). With stepwise logistic regression, only one variable was associated with reduced risk of obesity, consuming fruits (OR (95 % CI) = 0·61 (0·44, 0·84)). Likewise, in model 2 with logistic regression after removing of the variable fruit consumption (determined by the CART in model 1), only one of the remaining thirteen food items was associated with obesity, consuming eggs (OR (95 % CI) = 0·76 (0·58, 0·99)) (Table 3). Additionally, with stepwise logistic regression, consuming eggs (OR = 0·72 (0·57, 0·92)) was significantly associated with a reduced risk of obesity. Furthermore, interaction analyses revealed a significant interaction between ethnic groups and pre-pregnancy BMI (p interaction value is 0·037 in model 1 and 0·046 in model 2) (online Supplement Fig. 2).

Table 3. Multivariable logistic regression of maternal dietary practice and neonatal obesity (PI > 90 %)

* Means model 1 contained twenty-one variables, including fourteen food frequency measures and seven covariates. Four maternal covariates were residence (rural v. urban), age at enrollment and education (< 9 years, 9–12 years v. more than 12 years) and pre-pregnancy BMI; and three neonatal covariates were first birth (yes/no), race (Tibetan v. Han) and sex (male v. female). Model 2 was built based on model 1 with the removal of ‘fruit consumption’, a most influential variable in model 1.

Means food frequency measures: 0 = less than monthly, 1 = monthly, 2 = weekly and 3 = daily.

Means significant predictors from stepwise logistic regression (not shown in the table): model 1: fruits with OR (95 % CI) = 0.61 (0.44, 0.84) and years of maternal education with OR = 0.88 (0.79, 0.98); model 2: eggs with OR = 0.72 (0.57, 0.92) and years of maternal education with OR = 0.86 (0.77, 0.97).

We also detect the association between PI and fourteen food items, as presented in the online Supplement Table 1. In model 1, consuming fruit (β = –0·43 (–0·77, –1·27)) was negatively associated with PI, and consuming samba (β = 0·21 (0·01, 0·63)) was positively associated with PI. Likewise, in model 2 only consuming samba (β = 0·26 (0·06,0·77)) was positively associated with PI.

Result from classification and regression trees

In model 1 with all twenty-one variables with CART, the resulting OR (95 % CI) indicates the following two food items were associated with reduced odds for obesity, including consuming fruit weekly or more frequently (0·20 (0·12, 0·35), consuming eggs monthly or more frequently (0·22 (0·06, 0·65), respectively (Fig. 1). However, the mother’s age and pre-pregnancy BMI were not associated with the risk of obesity.

Fig. 1. Machine learning method CART determined hierarchical and nested relationship of dietary and other factors with neonatal obesity: (a) Decision tree of model 1 for neonatal obesity with 21 independent variables. Model 1 contained fourteen food frequency measures (less than monthly, monthly, weekly and daily) and seven covariates. Four maternal covariates were: residence (rural v. urban), age at enrollment, education (< 9 years, 9–12 years v. more than 12 years) and pre-pregnancy BMI; and three neonatal covariates were first birth (yes/no), race (Tibetan v. Han) and sex (male v. female); (b) decision tree of model 2 with fruits removed from model 1. Model 2 was built based on model 1 with the removal of ‘fruit consumption’, a most influential variable in model 1. P means the proportion of neonatal obesity. CART, classification and regression trees.

In model 2 with the most influential diet of fruit consumption was removed, the following factors were significantly associated with the risk of obesity (Fig. 2(b)). Receiving more than middle school years of education by mothers was associated with reduced risk (OR (95 % CI) = 0·22 (0·13, 0·37)), and consuming samba daily (OR = 2·58 (1·09, 7·10)) was associated with increased risk. The CART demonstrates superior sensitivity (0·818 v. 0·617) and specificity (0·953 v. 0·738) when compared with traditional logistic models, providing it with a notable advantage in terms of prediction accuracy.

Fig. 2. Random forest method determined the relationship of dietary and other factors with neonatal obesity: (a) Explainability and interpretability of the SHAP framework for twenty-one independent variables. (b) The SHAP framework for individual predictions. The model contained fourteen food frequency measures (less than monthly, monthly, weekly and daily) and seven covariates. Four maternal covariates were residence (rural v. urban), age at enrollment, education (< 9 years, 9–12 years v. more than 12 years) and pre-pregnancy BMI; and three neonatal covariates were first birth (yes/no), race (Tibetan v. Han) and sex (male v. female). SHAP, Random Forest SHapley Additive Explanation.

Result from random forest

Figure 2 presents a SHAP summary plot that succinctly displays the importance of all 21 variables, the magnitude of their impact (i.e., the effect size) and the direction of a specific feature’s association with neonatal obesity. As shown in Fig. 2(a), the SHAP value and the contribution of all 21 variables are represented in the beeswarm figure. Variables are ordered based on their importance. The higher positive SHAP value of a variable indicated more likelihood to the occurrence of neonatal obesity. The red colour dots signify higher predictor values, and the blue colour dots signify lower predictor values. Fruit is the most important variable and was associated with reduced odds of obesity. The education level of mothers was associated with reduced odds of obesity. Samba and butter (Tibetan food) was associated with increased odds of obesity. Figure 2(b) shows the SHAP framework for individual predictions. The red colour bar represents the positive effect on neonatal obesity, while the blue colour bar represents the opposite. For example, consuming fruit less than a month (SHAP value = 0·12) and mother with no education (SHAP value = 0·06) are positively associated with neonatal obesity; however, consuming fruit daily (SHAP value = –0·03) and mother with primary education (SHAP value = –0·03) are negatively associated with neonatal obesity.

Discussion

In this large cohort study of mother–neonate dyads, we are the first to detect the high prevalence of obesity among neonates in the Tibet Plateau area, and its associated maternal dietary and other influential factors during pregnancy. We are also the first to innovatively employ CART and random forest, a machine learning method to gain insights into the complex hierarchical nested relationship among all predictor variables, thus offering a new approach to enhance statistical causal inference. Findings from this study are promising and provide timely data much needed for the development of life-course interventions for obesity control by starting actions during pregnancy.

High prevalence of obesity in neonates as a health threat

In this study, we first detected that 5·4 % (95 % CI: 4·2–6·8 %) of neonates have obesity at birth. The prevalence of macrosomia in China was 7·35 % in 2013, which was higher than that reported in Mexico(Reference Avendaño-Alvarez, Monterrubio-Flores and Omaña-Guzmán34,Reference Shen, Wang and Duan35) . This finding is of significant concern, particularly when considering the long-term health implications for these infants. A cross-sectional survey conducted in China from 2015 to 2018 reported a prevalence of large gestational age at 9·9 %, which is comparable to the prevalence reported in the USA, a high-income country, in 2011(Reference Jones-Smith, Dow and Oddo36,Reference Zhang, Li and Zong37) . Although there is a lack of prevalence data identified by PI in China and other countries in the world for comparison, the observed obesity prevalence from our study underscores the urgency for further research in other areas of China. Tibet Plateau areas are the least developed area that only experienced rapid growth in recent years. We believe that the obesity rate of neonates could be much higher in other areas, presenting a great health threat to China(Reference Bao, Zhou and Jiang38,Reference Tu, Wang and Tan39) . Population statistics indicated a total of 10·6 million newborns per year in China(40). Applying the prevalence rate of 5·4 % as a conservative estimate, there would be at least 572 400 (ranging from 445 200 to 1 088 000) new babies who will have obesity at birth.

Following the life-course perspective, we recommend that effective control of the obesity epidemic must start from the fetus(Reference Pérez-Escamilla and Kac41,Reference Yacamán-Méndez, Trolle-Lagerros and Zhou42) . Development of obesity during pregnancy has long been linked to obesity and a series of health consequences in adolescence and adulthood, including metabolic syndrome and CVD(Reference Barker, Godfrey and Osmond3Reference Rasmussen and Johansson5). There is a rapid increase in overweight and obesity among youth and adults in China(Reference Gao, Bhurtyal and Wei1,Reference Pan, Wang and Pan2) . One reason for the increase could be in part attributable to the high obesity rate among neonates. This impact will continue if no action is taken.

Dietary factors and the risk of obesity in neonates

First, our results from bivariate, multivariable logistic regression, CART and random forest all indicated that fruit consumption during pregnancy was associated with a substantial reduction in the obesity risk for neonates. Further, this protective effect persisted after controlling for a group of key covariates, including maternal education. For example, according to model 1 with CART, consuming fruits at least once a week was associated with a 4·4 times reduction (OR = 0·202) in the obesity risk in neonates. Studies supporting our research include one cohort study among Chinese in northeast China that reported a negative association between healthy diets of mothers and BMI in infants(Reference Chen, Aris and Bernard12); another cohort study among Koreans reported a protective relationship between fruit consumption and fetal growth but did not examine its relationship with risk of obesity(Reference Jang, Kim and Lee43).

Second, results from CART indicated that consuming more eggs were associated with a reduced risk of obesity. Poor nutrition with low birth weight has been well documented(Reference Bi, Nuyt and Weiler44Reference Ramakrishnan47). Our study detected the impact of good nutrition in reducing the risk of obesity in neonates, this is consistent with reported studies in Tas-mania, Australia(Reference Andreasyan, Ponsonby and Dwyer48).

Third, this study revealed that some traditional Tibetan dietary products, although practiced only by a few women, were associated with an increased risk of obesity in neonates. For example, if a less educated mother (< 9 years of education) consumed samba on a weekly basis or more, her newborns would be 2·58 more times likely to be obese. The high energy provided by the large amount of added butter and sugar in samba due to recent economic growth may explain the association. Although there might be reductions in consuming traditional Tibetan food in the Tibet Plateau region, the impact of traditional food on the obesity risk cannot be ignored.

Fruits, dairy products and eggs were once consumed often only by mothers in a few high-income families in the Tibet Plateau area because of the poor economic status and the difficulties in accessibility. Recently, supplies of these products have been increased greatly along with economic growth. To reduce obesity risk in neonates, intervention programs should encourage pregnant women to consume these obesity-reduction foods for healthy babies.

Maternal education as a protective factor for obesity in neonates

Another important finding of this study is the negative association between maternal education and risk of obesity in neonates. Mothers with middle school or more education were associated with a 4·5 times decrease in the risk. This finding suggests the importance of enhancing maternal education in the Tibet Plateau area for obesity control in neonates and maternal health. Low levels of maternal education are reported to be associated with low birth weight and high infant mortality(Reference Assari49,Reference Gage, Fang and O’Neill50) . Our study is the first to detect that low maternal education is a risk factor for obesity in neonates.

The relationship between maternal education and obesity in neonates remains unclear, and a lot of research studies are needed. An Australian study found no association between maternal education level and birth outcomes, whereas pre-pregnancy BMI did exhibit an influence(Reference Ashwin, Gibson and Hagemann51). This contradicts our findings, possibly due to the unique characteristics of our study population. In our research, we noted an impact of maternal education on neonatal obesity, potentially influenced by significant disparities in education levels between Han and Tibetan populations (Tibetan: 57·1 % with less than 9 years of education, compared with Han: 17·1 %). Additionally, there exists an interaction between pre-pregnancy BMI and ethnicity, which to some extent influenced our analysis outcomes. Moreover, our population generally exhibits lower pre-pregnancy BMI (mean: 21·0). Most prior studies have predominantly focused on maternal obesity leading to neonatal obesity, which may not apply to our population(Reference Sun, Shen and Zhan52). Therefore, it is imperative to conduct further research to explore whether mothers with more education may not adhere to the norm of having a ‘large baby’, less likely to consume traditional foods, such as samba, and pay more attention to a healthy diet. Additional studies are needed to examine this important factor and potential mechanisms underlying the relationship between maternal education and obesity risk in neonates. Despite many unknowns, room to improve maternal education is enormous in the Tibet Plateau area where more than 57 % of Tibetan mothers have received education less than 9 years even today. In addition to the quality of life, enhancing maternal education will be an intervention to reduce neonatal obesity in a short term and population obesity in the long term for residents in Tibet Plateau areas.

Limitations

Several limitations need to be addressed. First, we conducted the study in the Tibet Plateau areas with rather limited technologies and resources despite recent growth in economy. Although we devoted much effort to combatting a number of challenges and barriers in completing the planned research, still a small number of participants were lost to follow-up. Of those who completed the follow-up, a small portion did not provide complete data. Second, we assessed dietary practice during pregnancy through self-recall. Despite wide use of the method in research, we have to admit that recall bias cannot be ruled out. Also, most mothers were recruited close to term. Dietary patterns across gestation may have changed close to term, which may not be captured in the current study. Lastly, although CART is a powerful tool to detect hierarchical nested relationships, but this machine learning method is data driving in nature, thus can best be used as a complementary approach to many conventional statistical methods such as logistic regression and Poisson regression.

Conclusions

In conclusion, obesity in neonates is prevalent in the study population. Promoting a healthy diet during pregnancy including increasing the intake of fruits and reducing the intake of traditional Tibetan food and strengthening maternal education could be part of the life-course strategies for obesity control in this area.

Acknowledgements

We would like to express our sincere gratitude to the Professor Chen Xinguang. It is with great sadness that we acknowledge Professor Chen’s passing away. His significant contributions to this paper, unwavering pursuit of academic excellence and strong commitment to nurturing young scholars will continue to profoundly influence us. We are deeply grateful for his invaluable contributions to this work and his lasting impact on the academic community. We thank Guolian Qi, Min He, Jinxue Wang and Runhua Li from Qinghai University and all of the medical care personnel in the obstetrics department of Qinghai Red Cross Hospital and Nangqian People’s Hospital for their help and support of this study.

The study was funded by the National Science Foundation of China (grant number 81860579) and Natural Science Foundation in Qinghai (grant number 2019-ZJ-932Q). This work was also partly supported by the Danone Nutrition Center (grant number DIC 2018–08) and the Medical College of Qinghai University (foundation grant number 2019-kyt-02).

W. P., X. C. and Y. W.: designed the research. W. P., J. Z., X. W. and L. W.: investigation and resources. X. T., X. C., B. Z., M. Z. S. and W. P.: writing – original draft preparation. B. Z. and X. T.: formal analysis. X. T., R. X. and W. J.: literature search. X. T., B. Z., H. X., B. Z., X. S., Y. X., Y. W. and W. P.: writing – review and editing. All authors have read and agreed to the published version of the manuscript.

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Ethics approval was granted by the Ethics Committee of the Medical College at Qinghai University, Qinghai Province, China (Approval No: 2018–36). Informed consent was obtained from all subjects involved in the study.

The data used in this study can be obtained by contacting the corresponding author.

Supplementary material

For supplementary material/s referred to in this article, please visit https://doi.org/10.1017/S0007114524002009

Footnotes

These authors contributed equally to this work.

References

Gao, L, Bhurtyal, A, Wei, J, et al. (2020) Double burden of malnutrition and nutrition transition in Asia: a case study of 4 selected countries with different socioeconomic development. Adv Nutr 11, 16631670.CrossRefGoogle Scholar
Pan, XF, Wang, L & Pan, A (2021) Epidemiology and determinants of obesity in China. Lancet Diabetes Endocrinol 9, 373392.CrossRefGoogle ScholarPubMed
Barker, DJ, Godfrey, KM, Osmond, C, et al. (1992) The relation of fetal length, ponderal index and head circumference to blood pressure and the risk of hypertension in adult life. Paediatr Perinat Epidemiol 6, 3554.CrossRefGoogle ScholarPubMed
Howe, LD, Tilling, K, Benfield, L, et al. (2010) Changes in ponderal index and body mass index across childhood and their associations with fat mass and cardiovascular risk factors at age 15. PLoS One 5, e15186.CrossRefGoogle ScholarPubMed
Rasmussen, F & Johansson, M (1998) The relation of weight, length and ponderal index at birth to body mass index and overweight among 18-year-old males in Sweden. Eur J Epidemiol 14, 373380.CrossRefGoogle ScholarPubMed
Moore, BF, Harrall, KK, Sauder, KA, et al. (2020) Neonatal adiposity and childhood obesity. Pediatr 146, e20200737.CrossRefGoogle ScholarPubMed
Kensara, OA, Wootton, SA, Phillips, DI, et al. (2005) Fetal programming of body composition: relation between birth weight and body composition measured with dual-energy X-ray absorptiometry and anthropometric methods in older Englishmen. Am J Clin Nutr 82, 980987.CrossRefGoogle ScholarPubMed
Polin, RF, Fox, WW & Abman, SH (2011) Fetal and Neonatal Physiology, vol. 1, 4th ed. Amsterdam: Elsevier.Google Scholar
Chia, AR, de Seymour, JV, Colega, M, et al. (2016) A vegetable, fruit, and white rice dietary pattern during pregnancy is associated with a lower risk of preterm birth and larger birth size in a multiethnic Asian cohort: the growing up in Singapore towards healthy outcomes (GUSTO) cohort study. Am J Clin Nutr 104, 14161423.CrossRefGoogle Scholar
Yang, J, Chang, Q, Tian, X, et al. (2022) Dietary protein intake during pregnancy and birth weight among Chinese pregnant women with low intake of protein. Nutr Metab 19, 43.CrossRefGoogle ScholarPubMed
Geraghty, AA, O’Brien, EC, Alberdi, G, et al. (2018) Maternal protein intake during pregnancy is associated with child growth up to 5 years of age, but not through insulin-like growth factor-1: findings from the ROLO study. Br J Nutr 120, 12521261.CrossRefGoogle Scholar
Chen, LW, Aris, IM, Bernard, JY, et al. (2016) Associations of maternal dietary patterns during pregnancy with offspring adiposity from birth until 54 months of age. Nutrients 9, 2.CrossRefGoogle ScholarPubMed
Barchitta, M, Magnano San Lio, R, La Rosa, MC, et al. (2023) The effect of maternal dietary patterns on birth weight for gestational age: findings from the MAMI-MED cohort. Nutrients 15, 1922.CrossRefGoogle ScholarPubMed
Hajianfar, H, Esmaillzadeh, A, Feizi, A, et al. (2018) Major maternal dietary patterns during early pregnancy and their association with neonatal anthropometric measurement. Biomed Res Int 2018, 4692193.CrossRefGoogle ScholarPubMed
Pathirathna, ML, Sekijima, K, Sadakata, M, et al. (2017) Impact of second trimester maternal dietary intake on gestational weight gain and neonatal birth weight. Nutrients 9, 627.CrossRefGoogle ScholarPubMed
Godfrey, K, Robinson, S, Barker, DJ, et al. (1996) Maternal nutrition in early and late pregnancy in relation to placental and fetal growth. Bmj 312, 410414.CrossRefGoogle ScholarPubMed
Fu, B (2021) Socio-Economic Data Set of Qinghai-Tibet Plateau (1982–2018). Beijing: National Tibetan Plateau Data Center.Google Scholar
De Franco, S, Lampugnani, R, Gelmetti, M, et al. (1978) Intra-operative findings and immediate results of 3 methods of termino-lateral portacaval anastomosis in the rat. Chirurgia e Patologia Sperimentale 26, 1132.Google ScholarPubMed
Jones, JR, Smibert, JG, McCullough, CJ, et al. (1987) Tendon implantation into bone: an experimental study. J Hand Surg 12, 306312.CrossRefGoogle ScholarPubMed
Peng, W, Liu, Y, Malowany, M, et al. (2021) Metabolic syndrome and its relation to dietary patterns among a selected urbanised and semi-urbanised Tibetan population in transition from nomadic to settled living environment. Public Health Nutr 24, 984992.CrossRefGoogle ScholarPubMed
Wang, Z, Dang, S & Yan, H (2010) Nutrient intakes of rural Tibetan mothers: a cross-sectional survey. BMC Public Health 10, 801.CrossRefGoogle ScholarPubMed
Zhou, C, Li, M, Liu, L, et al. (2021) Food consumption and dietary patterns of local adults living on the Tibetan Plateau: results from 14 countries along the Yarlung Tsangpo river. Nutrients 13, 2444.CrossRefGoogle ScholarPubMed
Soria, R, Julian, CG, Vargas, E, et al. (2013) Graduated effects of high-altitude hypoxia and highland ancestry on birth size. Pediatr Res 74, 633638.CrossRefGoogle ScholarPubMed
Bigham, AW, Julian, CG, Wilson, MJ, et al. (2014) Maternal PRKAA1 and EDNRA genotypes are associated with birth weight, and PRKAA1 with uterine artery diameter and metabolic homeostasis at high altitude. Physiol Genomics 46, 687697.CrossRefGoogle ScholarPubMed
Peng, W, Chen, S, Chen, X, et al. (2024) Trends in major non-communicable diseases and related risk factors in China 2002–2019: an analysis of nationally representative survey data. Lancet Reg Health West Pac 43, 100809.Google Scholar
Gozal, D, Ndombo, PK, Ze Minkande, J, et al. (1991) Anthropometric measurements in a newborn population in west Africa: a reliable and simple tool for the identification of infants at risk for early postnatal morbidity. J Pediatr 118, 800805.CrossRefGoogle Scholar
Persson, M, Pasupathy, D, Hanson, U, et al. (2012) Disproportionate body composition and perinatal outcome in large-for-gestational-age infants to mothers with type 1 diabetes. BJOG: Int J Gynecol 119, 565572.CrossRefGoogle ScholarPubMed
Andreasyan, K, Ponsonby, AL, Dwyer, T, et al. (2007) Higher maternal dietary protein intake in late pregnancy is associated with a lower infant ponderal index at birth. Eur J Clin Nutr 61, 498508.CrossRefGoogle ScholarPubMed
Zong, XN, Li, H, Zhang, YQ, et al. (2021) Reference values and growth curves of weight/length, body mass index, and ponderal index of Chinese newborns of different gestational ages. Chin J Pediatr 59, 181188.Google ScholarPubMed
Roje, D, Banovic, I, Tadin, I, et al. (2004) Gestational age--the most important factor of neonatal ponderal index. Yonsei Med J 45, 273280.CrossRefGoogle ScholarPubMed
Zaniqueli, D, Oliosa, PR, Neves, FS, et al. (2019) Ponderal index classifies obesity in children and adolescents more accurately than body mass index z-scores. Pediatr Res 86, 128133.CrossRefGoogle ScholarPubMed
Zhao, L, Wang, S, Liu, M, et al. (2023) Maternal urinary metal(loid)s and risk of preterm birth: a cohort study in the Tibetan Plateau. Environ Pollut 333, 122085.CrossRefGoogle ScholarPubMed
Chen, X, Mo, Q, Yu, B, et al. (2022) Hierarchical and nested associations of suicide with marriage, social support, quality of life, and depression among the elderly in rural China: machine learning of psychological autopsy data. Front Psychiatry 13, 1000026.CrossRefGoogle ScholarPubMed
Avendaño-Alvarez, F, Monterrubio-Flores, E, Omaña-Guzmán, I, et al. (2022) Incidence of macrosomia in Mexico: national and subnational estimations. PLoS One 17, e0276518.CrossRefGoogle ScholarPubMed
Shen, L, Wang, J, Duan, Y, et al. (2021) Prevalence of low birth weight and macrosomia estimates based on heaping adjustment method in China. Sci Rep 11, 15016.CrossRefGoogle ScholarPubMed
Jones-Smith, JC, Dow, WH & Oddo, VM (2017) Association between Native American-owned casinos and the prevalence of large-for-gestational-age births. Int J Epidemiol 46, 12021210.CrossRefGoogle ScholarPubMed
Zhang, YQ, Li, H, Zong, XN, et al. (2023) Comparison of updated birth weight, length and head circumference charts by gestational age in China with the INTERGROWTH-21st NCSS charts: a population-based study. World J Pediatr 19, 96105.CrossRefGoogle Scholar
Bao, C, Zhou, Y, Jiang, L, et al. (2011) Reasons for the increasing incidence of macrosomia in Harbin, China. BJOG: Int J Gynecol 118, 9398.CrossRefGoogle ScholarPubMed
Tu, S, Wang, AL, Tan, MZ, et al. (2019) Family socioeconomic position and abnormal birth weight: evidence from a Chinese birth cohort. World J Pediatr 15, 483491.CrossRefGoogle ScholarPubMed
National Burean of Statistical of China (2021) Statistical Communiqué of the People’s Republic of China on the 2021 National Economic and Social Development. Beijing: China Statistics Press.Google Scholar
Pérez-Escamilla, R & Kac, G (2013) Childhood obesity prevention: a life-course framework. Int J Obes Suppl 3, S3S5.CrossRefGoogle ScholarPubMed
Yacamán-Méndez, D, Trolle-Lagerros, Y, Zhou, M, et al. (2021) Life-course trajectories of weight and their impact on the incidence of type 2 diabetes. Sci Rep 11, 12494.CrossRefGoogle ScholarPubMed
Jang, W, Kim, H, Lee, BE, et al. (2018) Maternal fruit and vegetable or vitamin C consumption during pregnancy is associated with fetal growth and infant growth up to 6 months: results from the Korean mothers and children’s environmental health (MOCEH) cohort study. Nutr J 17, 105.CrossRefGoogle ScholarPubMed
Bi, WG, Nuyt, AM, Weiler, H, et al. (2018) Association between vitamin D supplementation during pregnancy and offspring growth, morbidity, and mortality: a systematic review and meta-analysis. JAMA Pediatr 172, 635645.CrossRefGoogle ScholarPubMed
Brahams, D (1988) Lessons from an anaesthetic accident. Lancet 1, 14081409.CrossRefGoogle ScholarPubMed
Da Silva Lopes, K, Ota, E, Shakya, P, et al. (2017) Effects of nutrition interventions during pregnancy on low birth weight: an overview of systematic reviews. BMJ Glob Health 2, e000389.CrossRefGoogle ScholarPubMed
Ramakrishnan, U (2004) Nutrition and low birth weight: from research to practice. Am J Clin Nutr 79, 1721.CrossRefGoogle ScholarPubMed
Andreasyan, K, Ponsonby, AL, Dwyer, T, et al. (2007) Higher maternal dietary protein intake in late pregnancy is associated with a lower infant ponderal index at birth. Eur J Clin Nutr 61, 498508.CrossRefGoogle ScholarPubMed
Assari, S (2020) Protective effects of maternal education against low birth weight deliveries: blacks’ diminished returns. Res Health Sci 5, 117.CrossRefGoogle ScholarPubMed
Gage, TB, Fang, F, O’Neill, E, et al. (2013) Maternal education, birth weight, and infant mortality in the United States. Demography 50, 615635.CrossRefGoogle ScholarPubMed
Ashwin, D, Gibson, L, Hagemann, E, et al. (2022) The impact a Mediterranean diet in the third trimester of pregnancy has on neonatal body fat percentage. J Dev Origins Health Dis 13, 500507.CrossRefGoogle ScholarPubMed
Sun, Y, Shen, Z, Zhan, Y, et al. (2020) Effects of pre-pregnancy body mass index and gestational weight gain on maternal and infant complications. BMC Pregnancy Childb 20, 390.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Characteristics of the study participants, including the mothers and neonates (n 1226)

Figure 1

Table 2. Maternal dietary practice during pregnancy as measured using the food frequency*, overall and by ethnic group (n 1226)

Figure 2

Table 3. Multivariable logistic regression‡ of maternal dietary practice and neonatal obesity (PI > 90 %)

Figure 3

Fig. 1. Machine learning method CART determined hierarchical and nested relationship of dietary and other factors with neonatal obesity: (a) Decision tree of model 1 for neonatal obesity with 21 independent variables. Model 1 contained fourteen food frequency measures (less than monthly, monthly, weekly and daily) and seven covariates. Four maternal covariates were: residence (rural v. urban), age at enrollment, education (< 9 years, 9–12 years v. more than 12 years) and pre-pregnancy BMI; and three neonatal covariates were first birth (yes/no), race (Tibetan v. Han) and sex (male v. female); (b) decision tree of model 2 with fruits removed from model 1. Model 2 was built based on model 1 with the removal of ‘fruit consumption’, a most influential variable in model 1. P means the proportion of neonatal obesity. CART, classification and regression trees.

Figure 4

Fig. 2. Random forest method determined the relationship of dietary and other factors with neonatal obesity: (a) Explainability and interpretability of the SHAP framework for twenty-one independent variables. (b) The SHAP framework for individual predictions. The model contained fourteen food frequency measures (less than monthly, monthly, weekly and daily) and seven covariates. Four maternal covariates were residence (rural v. urban), age at enrollment, education (< 9 years, 9–12 years v. more than 12 years) and pre-pregnancy BMI; and three neonatal covariates were first birth (yes/no), race (Tibetan v. Han) and sex (male v. female). SHAP, Random Forest SHapley Additive Explanation.

Supplementary material: File

Tang et al. supplementary material 1

Tang et al. supplementary material
Download Tang et al. supplementary material 1(File)
File 21.8 KB
Supplementary material: File

Tang et al. supplementary material 2

Tang et al. supplementary material
Download Tang et al. supplementary material 2(File)
File 70.6 KB
Supplementary material: File

Tang et al. supplementary material 3

Tang et al. supplementary material
Download Tang et al. supplementary material 3(File)
File 144.2 KB