Critical Threshold of Average Weekly Weight Gain in Overweight Pregnant Women During the Second and Third Trimesters: A Strategy to Prevent Macrosomia

Introduction

The American College of Obstetricians and Gynecologists (2016) defines fetal macrosomia as a birth weight beyond a specific weight (4000 g).1 Although many scientists hope to control the incidence of macrosomia by studying the risk factors of macrosomia, the current study shows that the incidence of macrosomia is still high. A retrospective cohort study of US natality data files from 1971 to 2017 reported that the overall incidence of fetal macrosomia was 9.6%.2 From 1994 to 2005, the prevalence of macrosomia in southeast China showed an increasing trend, from 6.0% in 1994 to 8.5% in 2000, which then stabilized to 7.8% in 2005.3 A study of 15 hospitals in Beijing, China in 2013 showed that the overall prevalence of macrosomia was 7.7%. The lowest prevalence was 5.4% (89/1659), and the highest prevalence was 8.8%.4 The incidence of macrosomia in Beijing increased from 6.6% in 1996 to 9.5% in 2000 and decreased to 7.0% in 2010.5

Fetal macrosomia is closely associated with maternal and neonatal complications. Maternal complications include emergency cesarean section due to fetal distress or slow or stalled labor, postpartum hemorrhage, and anal sphincter injury. Neonatal complications include shoulder dystocia and related sequelae such as brachial plexus injury, clavicle or humerus fracture, and birth asphyxia.6 Macrosomia also increases the risk of childhood obesity.7 Macrosomia is an important global public health concern. It is therefore crucial to elucidate the risk factors of macrosomia and to develop effective intervention approaches to promote maternal health. Macrosomia results from basic conditions such as overweight and presence of diabetes before pregnancy and complications and weight management during pregnancy.8 Excessive weight gain during pregnancy is a critical factor that affects macrosomia.9 Previous studies have shown that the increased incidence of macrosomia is related to pregnancy weight gain, maternal age, maternal height, and maternal education level.10,11 Different studies have, however, yielded inconsistent results, and their findings do not accurately represent the status of Chinese pregnant women. Moreover, most cohort studies lack adequate guidelines regarding weight gain management during pregnancy.

Previously, some scholars have conducted studies on the optimal gestational weight gain under different pre-pregnancy BMI categories. In general, women with higher pre-pregnancy BMI categories should gain less weight during pregnancy.12 However, although the study included a large sample size of 196,670 women, multiple adverse pregnancy outcomes were selected and many factors affected them. It is less targeted to a certain disease. Hence, in the present study, retrospective birth data collected from Peking Union Medical College Hospital (PUMCH) covering a two-year period (July 2020 to June 2022) were used to determine the relationships among pre-pregnancy body mass index (BMI), gestational weight gain (GWG), and macrosomia. We also attempted to introduce a new index of GWG, which might become a popular concept in future clinical practice. Pre-pregnancy BMI and GWG were classified according to the group standard of “Monitoring and Evaluation of Gestational Weight in Chinese Women” [(T/CNSS-009-2021)],13 which is more representative of the status of Chinese pregnant women.

MethodsData Sources

This study received ethical approval from PUMCH (JS-2763). The modular collection of case information was implemented using the medical records of the Obstetrics Center of PUMCH. This study is a retrospective analysis, only involving the clinical information of the patients, and there is no additional sample collection and testing, so the process of signing informed consent is exempted in this study. However, we ensured that the personal information of all our patients was kept confidential, that all data were used only for scientific research, and that the final disclosure did not disclose private information. All procedures were performed in accordance with the Declaration of Helsinki. We recruited all pregnant women who gave birth in the hospital in the corresponding years. The use of an electronic system for all data collection avoided selection bias due to manual collection. A total of 5409 maternal and neonatal cases from July 2020 to June 2022 were enrolled, and the data regarding basic maternal information, pregnancy complications, and neonatal conditions were obtained. Inclusion criteria: (1) singleton pregnancy; (2) maternal age ≥18 years old; (3) the hospital was established and the prenatal examination was performed on time during the whole pregnancy; (4) Complete clinical data (This means that all measures needed for the study should be properly recorded and maintained, and very few women referred for critical conditions will be excluded because of a lack of information about previous prenatal care). Exclusion criteria: (1) abortion; (2) preterm birth (gestational age <37 weeks); (3) There were obvious abnormalities in electronic data (such as neonatal length 3500 cm, weight 52 g, etc). Finally, according to the inclusion criteria, 4856 pregnant women and their newborns were included in the analysis. The data exclusion rate was 10.22% (553/5409). Figure 1 shows the flowchart of the enrollment and exclusion process for the study population.

Figure 1 Flowchart of the selection process for the study population. The absence of weight data may be caused by the failure to obtain early electronic data as pregnant women missed early birth examination due to referral from other hospitals. Outliers usually refer to values that are inconsistent with clinical experience (eg, 3520 cm in length and 51 g in weight), which may be related to a recording error and should be excluded.

Method of Grouping

According to the birth weight, the neonates were assigned to two groups: macrosomia group (≥4000 g) and non-macrosomia group (<4000 g). Based on the pre-pregnancy BMI, the parturients were assigned to four groups: low weight group, <18.5 kg/m2; normal weight group, 18.5 to <24 kg/m2; overweight group, 24 to <28 kg/m2; and obese group, ≥28.0 kg/m2. In accordance with the latest group standard of “Monitoring and Evaluation of Gestational Weight during Pregnancy in China” the total GWG (the difference between before delivery weight and pre-pregnancy weight) was further divided into three groups according to different pre-pregnancy BMI groups as follows: excessive weight gain (>16.0 kg in the underweight group, >14.0 kg in the normal weight group, >11.0 kg in the overweight group, and >9.0 kg in the obese group); appropriate weight gain (11.0–16.0 kg in the underweight group, 8.0–14.0 kg in the normal weight group, 7.0–11.0 kg in the overweight group, and 5.0–9.0 kg in the obese group); and inadequate weight gain (<11.0 kg in the underweight group, <8.0 kg in the normal weight group, <7.0 kg in the overweight group, and <5.0 kg in the obese group).

Indicators of Observation

The following observation indicators were used: (1) general information: age, pre-pregnancy weight, pre-pregnancy BMI, gravidity, parity, physical labor level, and education level and (2) delivery data: weight before delivery, gestational age at delivery, and neonatal birth weight (g). All obstetric examinations and procedures were performed by trained professionals. Age was calculated based on the information provided in the identity documents. Height and weight were measured in the hospital. Pre-pregnancy BMI was calculated using the formula of pre-pregnancy weight (kg) divided by square of height (m2). General information, pre-pregnancy weight, and medical history were self-reported by the pregnant women at the first visit. Pregnancy-related complications were obtained from obstetric case information, and all diagnoses met the community criteria. Neonatal weight was measured at birth by using a medical neonatal weight scale. “v” represents the mean weekly weight gain during the second and third trimesters and was calculated by subtracting the weight measured at 24 weeks of gestation from the weight before delivery divided by the corresponding number of weeks (Unit, kg). GWG is the difference between the weight measured at delivery and the weight before pregnancy. The incidence of macrosomia was determined as the number of macrosomia cases divided by the total number of newborns. Logistic regression analysis and heat map were used to analyze the associations of pre-pregnancy BMI and GWG with macrosomia.

Statistical Analysis

Python 3.8 and Statsmodels 0.12.2 were used for statistical analysis of the data. Count data were expressed as examples (%), and Chi-square test or Fisher’s exact probability method was used for comparison between the groups. Measurement data showing normal distribution were represented by “”. Independent sample t-test was used for comparison between the groups. Multi-variable binary logistic regression was used to analyze the related factors of macrosomia. Incidence heatmaps and line plots were used to explain associations between variables. All statistical tests of significance were two-sided. P < 0.05 was considered statistically significant.

ResultsCharacteristics of the Study Population

Table 1 shows the descriptive statistics of this study. The macrosomia and non-macrosomia groups included 189 and 4667 pregnant women, respectively, and the incidence of macrosomia was approximately 3.89%. The macrosomia group showed significantly higher pre-pregnancy BMI, total weight gain during pregnancy, average weekly weight gain during the second and third trimesters of pregnancy, proportion of women with junior college or below education level, gestational age at delivery, proportion of overweight/obese women in the pre-pregnancy period, and proportion of pregnant women with excessive weight gain during pregnancy than the non-macrosomia group (all P < 0.05). The incidence of macrosomia was higher with lower education level, older gestational age at delivery, higher pre-pregnancy BMI grade, excessive weight gain during pregnancy, and excessive weight gain per week during the second and third trimesters of pregnancy. The two groups showed no significant differences in maternal age, physical labor intensity, multiparity, primiparity, gestational diabetes mellitus (GDM), gestational hypertension, polycystic ovary syndrome, smoking history, drinking history, and family disease history.

Table 1 Summary of Patient Characteristics of the Macrosomia and Non-Macrosomia Groups

Subgroup Analysis with Pre-Pregnancy BMI and GWG

Based on the group standard of “Monitoring and Evaluation of Gestational Weight of Chinese Women during Pregnancy” (T/CNSS-009-2021), the GWG of pregnant women with different pre-pregnancy BMI grades was classified and analyzed (Table 2). It was observed that excessive GWG increased the incidence of macrosomia in pregnant women with different pre-pregnancy BMI grades, and the incidence of macrosomia increased with the increase in pre-pregnancy BMI grade. The incidence of macrosomia was 1.6% and 3.0% in the pre-pregnancy underweight group and the excessive GWG group, respectively. Furthermore, the incidence of macrosomia was 2.9% and 7.0% in the normal pre-pregnancy weight group and the excessive weight gain group, respectively. The pre-pregnancy overweight group and the excessive GWG group showed macrosomia incidence of 5.8% and 11.0%, respectively. Furthermore, macrosomia incidence was 9.3% and 17.0% in the pre-pregnancy obese group and the excessive GWG group, respectively. The average newborn weight also increased with the increase in the maternal pre-pregnancy BMI grade. The average weights of newborns born to women who were underweight, normal weight, overweight, and obese before pregnancy were 3180.05 (375.64) g, 3294.78 (368.67) g, 3372.61 (405.39) g, and 3416.17 (455.91) g, respectively; the mean birth weight of newborns was significantly different among the different groups (P < 0.001).

Table 2 Weight Gain in Different Pre-Pregnancy Body Mass Index Subgroups

Logistic Regression Analysis

Figure 2a shows the result of the logistic regression model based on pre-pregnancy BMI and weight gain during pregnancy as target variables. Excessive weight gain (OR: 2.47, 95% CI: 1.74–3.51), overweight (OR: 2.16, 95% CI: 1.57–2.97), and obesity (OR: 4.08, 95% CI: 2.66–6.14) were associated with macrosomia, and the risk of delivery of the fetus with macrosomia was also significantly increased under the corresponding conditions. To further validate the findings, adjustment was made for the risk values of GWG and pre-pregnancy BMI by incorporating basic maternal information and other relevant confounding factors (Figure 2b). Compared to the initial model, the risk direction of the corrected model showed no significant change. In the combined corrected model, excessive weight gain (OR: 2.39, 95% CI: 1.67–3.43), overweight (OR: 2.24, 95% CI: 1.62–3.10), and obesity (OR: 4.56, 95% CI: 2.93–6.98) remained the risk factors for macrosomia, with a little change in the risk degree. This indicates that the basic characteristics of pregnant women and the occurrence of pregnancy-related complications do not act as confounding factors. The results of the present study showed that gestational age of 39–41 weeks at childbirth (OR: 3.83, 95% CI: 2.56–5.95), gestational age of more than 41 weeks at childbirth (OR: 7.88, 95% CI: 4.37–14.19), and the education level of junior college or below (OR: 1.95, 95% CI: 1.19–3.09; OR: 1.62, 95% CI: 1.09–2.42) were also the risk factors for macrosomia. To provide more timely and detailed information on GWG, we introduced the concept of average weekly weight gain (v, kg) in the second and third trimesters. By keeping the adjustment variables unchanged, the OR value of the rate of weight gain in the second and third trimesters of pregnancy was again calculated by logistic regression, and the results are shown in Figure 2c. The risk of macrosomia increased 2.6-fold (95% CI: 1.37–4.89, P = 0.003) when the average weekly weight gain was relatively high in the second and third trimesters. In the same situation, based on stratification by pre-pregnancy BMI grade, the overweight pregnant women OR for macrosomia was 4.57 (95% CI: 2.27–9.10, P < 0.001); obese pregnant women OR for macrosomia was 11.33 (95% CI: 4.95–25.18, P < 0.001).

Figure 2 Logistic regression analysis based on pre-pregnancy BMI and weight gain during pregnancy as target variables for macrosomia. (a) and (b). The red line represents the baseline of OR = 1, the black square represents the point estimate of the OR value, and the line segment interval represents the 95% confidence interval. (c). Logistic regression analysis of the weight gain rate in the second and third trimesters in the different BMI groups. v represents the average weekly weight gain (v, kg) in the second and third trimesters. BMI class-x: v represents the corresponding risk of macrosomia in different pre-pregnancy BMI groups when the average weekly weight gain was excessive in the second and third trimesters. P values represent differences between groups; P < 0.05 was considered statistically significant.

Critical Threshold of Weight Gain in the Overweight Population

Because of the unbalanced number of subgroups, we did not discuss the comparison results of v separately under the pre-pregnancy BMI groups. To show the relationship between pre-pregnancy BMI, v, and macrosomia more intuitively, we used the incidence of macrosomia to construct a heatmap (Figure 3a). The color depth in the heatmap indicates the incidence of macrosomia in the corresponding population. Squares with a darker color indicated that a higher pre-pregnancy BMI or a larger v was associated with a higher incidence of macrosomia. The incidence of macrosomia in Figure 3b refers to the cumulative incidence of macrosomia, that is, the incidence of macrosomia in all pregnant women included in the upper limit of a certain v value. The overall incidence of macrosomia in the normal weight pre-pregnancy BMI group was 3.00%, which is the desired threshold for controlling the incidence of macrosomia. We observed that the incidence of macrosomia in the entire study population crossed the standard line at the levels of v<0.01 kg and v=0.32 kg, respectively, and showed a steady increasing trend after v = 0.32 kg.

Figure 3 Heatmap of macrosomia incidence, pre-pregnancy BMI, and v. (a). The abscissa represents the pre-pregnancy BMI value, the ordinate represents v, and the scale on the right represents the incidence of macrosomia in the population under the corresponding conditions. The darker the blue color, the higher is the incidence of macrosomia in the corresponding population. (b). Line plots of macrosomia incidence in different pre-pregnancy BMI populations. The horizontal axis v represents the mean weekly weight gain during the second and third trimesters (kg), and the vertical axis represents the incidence of macrosomia in all women with a v value as the upper limit. The lower right corner is the distinguishing mark; blue represents the entire study population, green represents the normal weight pre-pregnancy BMI group, and red represents the overweight pre-pregnancy BMI overweight group. The green dotted line represents the average incidence in the normal population.

Discussion

A previous study conducted in 2013 revealed that the overall prevalence of macrosomia in Beijing was 7.7%.4 In the present study, we retrospectively analyzed birth records of PUMCH from July 2020 to June 2022 for maternity and childbirth-related information to determine the incidence and risk factors for macrosomia. The results showed that the incidence of macrosomia was 3. 9% among the 4856 single-term newborns included in the analysis. The incidence of macrosomia in this study was lower than that reported in previous studies. On the one hand, the pregnant women in PUMCH have higher education level and pay more attention to weight change. Reasonable control of weight gain during pregnancy is beneficial to reduce the incidence of macrosomia. On the other hand, the Obstetrics Center of PUMCH provided systematic diet and exercise knowledge for pregnant women through the pregnant women’s school. Another study by our team also confirmed that prenatal health education for pregnant women can improve the incidence of adverse pregnancy outcomes to a certain extent.14 Both BMI and GWG showed significant differences in the descriptive statistics presented in Table 2. The results suggest that women who are overweight or obese before pregnancy have a higher propensity to gain more weight during pregnancy. Furthermore, an increasing trend was observed in the proportion of women with excessive GWG in the pre-pregnancy underweight group (10. 6%), pre-pregnancy normal weight group (184%), pre-pregnancy overweight group (20.4%) and pre-pregnancy obese group (18.5%). This implies that although pre-pregnancy BMI and GWG are independent risk factors for macrosomia, a certain correlation exists between them. This might be related to the long-term unhealthy lifestyle and dietary habits of pregnant women. Hence, lifestyle intervention should be included in the comprehensive management of pregnant women.

The regression model showed that the inclusion of maternal characteristics and comorbidities during pregnancy did not significantly alter the direction and risk values of pre-pregnancy BMI and GWG. The gestational age of delivery can also be interpreted as the intrauterine growth time of the fetus. In our study group, the delivery at 39–41 weeks had already increased the risk of macrosomia in the fetus; this finding suggests that in addition to the ultrasound-based determination of fetal weight exceeding 4000 g, the gestational age of delivery should also considered a risk factor of macrosomia. Particularly, if the pregnant woman also has other large infant risk factors, the appropriate adjustment of childbirth intervention time after comprehensive assessment could be beneficial to the pregnancy outcome. Low education level leads to an increased risk of macrosomia delivery, which may be associated with the living and dietary habits of pregnant women.15 The pregnancy outcome can be improved by educating pregnant women about pregnancy health, enhancing their health literacy, and adjusting their lifestyle. A retrospective cohort study analyzed women who delivered three consecutive births at the same medical center (1994–2013) and included only nondiabetic women who delivered at full term (≥37 weeks) in all three births. The results showed that the mean birth weight percentages of the first, second, and third births were 47.2% ± 26.3%, 58.3% ± 25.8%, and 61.5% ± 24.7% (P < 0.001). A total of 45.9% of the women had the highest fetal birth weight at the third delivery (P < 0.001). That is, women who have repeated full-term births show an increase in fetal birth weight at the third birth as compared to that in the first two births.16 Previous studies have also shown that women who underwent an emergency cesarean section to induce labor and delivery, particularly those having abnormal delivery, are more likely to give birth to infants with macrosomia.17 In recent years, few studies have investigated the influence of multipara on pregnancy outcomes, and most of these investigations were cohort studies that lacked mechanistic exploration. In addition, in the present study, although the results of the chi-square test suggested differences in the incidence of macrosomia for the three occupational intensity groups, it was difficult to conduct accurate assessment due to the large differences in the number of subgroups, differences between physical activity and standardized exercise during pregnancy, high heterogeneity, and certain deviations in self-reporting; hence, a specific analysis could not be performed. However, in future studies, it is essential to specifically investigate the role of occupational intensity on pregnancy outcomes, which requires to clearly delineate the degree of physical labor and correlate it with physical activity (sports) outside of daily work.

Presently, the recommended ranges of GWG for pregnant women have been clearly defined. However, many pregnant women show excessive GWG or insufficient GWG at different stages of pregnancy and finally meet the overall requirements. Considering that large fluctuations in body weight within a short period of time could harm the growth and development of the fetus and affect the stable hormone levels of pregnant women, and because the majority of pregnant women do not have a stable body weight in the first trimester due to nausea and vomiting, we introduced the concept of average weekly weight gain (v) in the second and third trimesters in this study. This will help pregnant women to assess for themselves whether their daily weight gain is stable and appropriate. In the present study, the average weekly weight gain in the second and third trimesters of pregnancy in the macrosomia and non-macrosomia groups was 0.53 ± 0.22 and 0.48 ± 0.23 kg, respectively, with a significant difference between the two groups (P = 0.008). As shown in Figure 3a, the overall trend in the incidence of macrosomia revealed that if the pre-pregnancy BMI reaches a high value, the incidence of macrosomia will remain high even if the weight gain during pregnancy is controlled at zero or negative levels. Similarly, if the weight gain during pregnancy is not properly controlled, even if the pre-pregnancy BMI is good, the incidence of macrosomia will still be significantly increased. The heatmap (Figure 3a) of macrosomia incidence represents the incidence of macrosomia in the study population under the corresponding conditions. As shown in the figure, pre-pregnancy BMI = 21.4 and v = −0.2 are taken as examples. Although few cases met this condition, the occurrence of macrosomia will be regarded as special cases; this is, however, not within the scope of the discussion of the overall trend. Hence, we conclude that pre-pregnancy BMI and v are independent influencing factors for macrosomia. Pre-pregnancy BMI and v should be considered important evaluation factors for appropriate weight management during pregnancy. Strengthening targeted management could reduce the incidence of macrosomia and improve delivery outcomes to a certain extent.

This study also analyzed the average weekly weight gain in the second and third trimesters of pregnancy that was more likely to be beneficial for reducing the incidence of macrosomia in overweight women (BMI ≥ 24 kg/m2). As shown in Figure 3b, the increase in macrosomia incidence in the entire study population after v = 0.32 can be considered to be contributed by overweight women, after controlling for other confounding variables. The figure illustrates that the incidence of macrosomia in the overweight group converges with the standard line at v = −0.15, reaches the first peak at v = 0.01, and then begins to decline; thus, the incidence of macrosomia is controlled below 0.05, within the range of v = 0.16–0.32. Limiting the incidence of macrosomia to that in women with normal pre-pregnancy weight would require an average weekly weight gain of 0.15 kg in overweight women during the second and third trimesters; this is, however, not consistent with clinical practice. Hence, we consider v = 0.32 as the recommended upper limit of average weekly weight gain for overweight pregnant women in the second and third trimesters to allow these women to gain the maximum allowable weight during pregnancy while reducing the incidence of macrosomia. These results are applicable to overweight pregnant women who wish to reduce the risk of macrosomia and to assist them to monitor and evaluate their weight gain during the second and third trimesters. There is a synergistic effect between pre-pregnancy overweight or obesity and gestational weight gain, and their co-existence will increase the risk of many diseases in pregnant women.18 Therefore, weight management for this population is particularly important.

Currently, the proportion of adults who are overweight or obese is increasing worldwide.19 Overweight and obesity in women have a remarkable effect on reproductive health, particularly pregnancy.20,21 Obese women have a higher risk of GDM, preeclampsia, complicated surgical delivery, fetal macrosomia, and neonatal morbidity.22 Although we analyzed and studied only macrosomia in the present study, several studies have confirmed that excessive weight gain during pregnancy is associated with various pregnancy-related complications. Platner et al studied 515,148 birth records in New York and found that weight gain of more than 9 kg during pregnancy was associated with a 20% increase in severe maternal morbidity as compared to women who gained the recommended weight during pregnancy (the upper limit was 25 kg).23

Macrosomia also increases the risk of childhood obesity. An association between macrosomia and an increased risk of obesity was noted in children under 3 years of age in western China. For example, in one study, 714 of 1767 infants had macrosomia. The risk of childhood obesity in macrosomia defined according to the height-weight ratio was 1.9-fold (95% CI: 1.04–3.49) that of the normal birth weight.7 Studies on the pathogenetic factors of macrosomia have shown that the expression levels of five miRNAs in the miR-17-92 cluster are significantly increased in the placenta of macrosomia births; these miRNAs can promote macrosomia development by targeting regulators in the cell cycle pathway.24 Brian T Joyce et al also confirmed that the MEST and IGF2 genes play a potential regulatory role in fetal growth and development.25 There is even a 60-year follow-up study investigating the association of overweight before pregnancy, weight gain during pregnancy, and colorectal cancer in adulthood, proving that in utero events are important colorectal cancer risk factors.26 This implies that obesity could become a vicious cycle of genetic, epigenetic, and metabolic factors that are transmitted from the mother to the child.

Effective weight management during pregnancy will critically affect maternal and infant health outcomes. However, many pregnant women have very limited understanding of excessive weight gain during pregnancy.27 Pregnant women have a lower level of health knowledge, show passive involvement in interactions with doctors, and rely on family advice and cultural practices to adopt health behaviors suitable for pregnancy. A small number of pregnant women with high health literacy actively seek health information but have difficulty in finding reliable resources. Therefore, the effectiveness of lifestyle interventions during pregnancy should be emphasized in clinical practice,28 and patient attention and education level of the related practitioners should be improved to consider overweight and obesity as important risk factors of macrosomia. Strict control of GWG is simultaneously required to improve pregnancy outcomes.

The present study has certain strengths and limitations. In terms of strengths, first, we used the electronic medical records from the hospital to collect all the prenatal examination data; this reduced the manual work time and the possible errors during manual data entry, thus facilitating error correction and review of the accuracy of medical records. Second, this study provides new evidence for the importance of weight management during pregnancy; the study further indicates that it is even more critical for women with poor pre-pregnancy health conditions to maintain a healthy lifestyle during pregnancy. Finally, this study introduced a new index of GWG, ie, the average weekly weight gain in the second and third trimesters; this index could guide healthcare providers and pregnant women and their families to evaluate the appropriate weight gain in each trimester. Regarding limitations, the present study was a single-center study, the pregnant women had higher education levels than those in other regions, and the population representation was poor. The results from the study may not be entirely generalizable and this was an observational study and thus causality cannot be inferred. The relevance of our research results and the significance of the new indicator of weight gain should be verified in larger samples and multicenter populations. Moreover, our sample size did not allow us to determine the appropriate average weekly weight gain in the second and third trimesters in more specific subgroups; this aspect should be the focus of future research studies.

Conclusion

This study found that pre-pregnancy BMI and gestational weight gain had a certain effect on the macrosomia, and there was an interaction between them. Pregnant women who are overweight before pregnancy should keep their body weight gain to less than 0.32kg/week during the second and third trimesters to reduce the incidence of macrosomia. This finding highlights the importance of healthy pre-pregnancy preparation and weight management during pregnancy to reduce adverse pregnancy outcomes. Although the results of our study have some limitations, they also provide some evidence for research in this field. Further discussion on the differentiation of weight management under different BMI category refinement is needed in the future, which is essential for improving maternal and child health.

Data Sharing Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Ethics Approval and Informed Consent

This study was reviewed by the Ethics Committee of Peking Union Medical College Hospital (JS-2763). All experimental protocols were approved by a named institutional and licensing committee. All the steps/ methods were performed in accordance with the relevant guidelines and regulations.

Consent for Publication

All the authors approved the publication of the manuscript.

Acknowledgment

We would like to thank TopEdit (www.topeditsci.com) for its linguistic assistance during the preparation of this manuscript.

Author Contributions

All authors made a significant contribution to the work reported, whether that is in the conception, study design, execution, acquisition of data, analysis and interpretation, or in all these areas; took part in drafting, revising or critically reviewing the article; gave final approval of the version to be published; have agreed on the journal to which the article has been submitted; and agree to be accountable for all aspects of the work.

Funding

This study was funded by The National Key Research and Development Program of China (Grant number: 2022YFC2703304); Medical and Health Technology Innovation Project of Chinese Academy of Medical Sciences (Grant number. 2020-I2M-2-009, 2021-I2M-1-023, 2021-I2M-1-056); Recommendations for weight gain in women with gestational diabetes mellitus (Grant number. 20191901); Clinical and Translational Medicine Research Fund of the Central Public welfare Research Institutes of the Chinese Academy of Medical Sciences (Grant number. 2019XK320007).

Disclosure

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

References

1. American College of Obstetricians and Gynecologists’ Committee on Practice Bulletins—Obstetrics. Practice bulletin no. 173: fetal macrosomia. Obstet Gynecol. 2016;128(5):e195–e209. doi:10.1097/AOG.0000000000001767

2. Salihu HM, Dongarwar D, King LM, Yusuf KK, Ibrahimi S, Salinas-Miranda AA. Trends in the incidence of fetal macrosomia and its phenotypes in the United States, 1971-2017. Arch Gynecol Obstet. 2020;301(2):415–426. doi:10.1007/s00404-019-05400-9

3. Lu Y, Zhang J, Lu X, Xi W, Li Z. Secular trends of macrosomia in southeast China, 1994-2005. BMC Public Health. 2011;11(1):818. doi:10.1186/1471-2458-11-818

4. Ren JH, Wang C, Wei YM, Yang HX. Incidence of singleton macrosomia in Beijing and its risk factors. Zhonghua Fu Chan Ke Za Zhi. 2016;51(6):410–414. doi:10.3760/cma.j.issn.0529-567X.2016.06.002

5. Shan X, Chen F, Wang W, et al. Secular trends of low birthweight and macrosomia and related maternal factors in Beijing, China: a longitudinal trend analysis. BMC Pregnancy Childbirth. 2014;14(1):105. doi:10.1186/1471-2393-14-105

6. Wang D, Hong Y, Zhu L, et al. Risk factors and outcomes of macrosomia in China: a multicentric survey based on birth data. J Matern Fetal Neonatal Med. 2017;30(5):623–627. doi:10.1080/14767058.2016.1252746

7. Pan XF, Tang L, Lee AH, et al. Association between fetal macrosomia and risk of obesity in children under 3 years in Western China: a cohort study. World J Pediatr. 2019;15(2):153–160. doi:10.1007/s12519-018-0218-7

8. Vats H, Saxena R, Sachdeva MP, Walia GK, Gupta V. Impact of maternal pre-pregnancy body mass index on maternal, fetal and neonatal adverse outcomes in the worldwide populations: a systematic review and meta-analysis. Obes Res Clin Pract. 2021;15(6):536–545. doi:10.1016/j.orcp.2021.10.005

9. Li M, Zhang CY, Yue CY. Effects of pre-pregnancy BMI and gestational weight gain on adverse pregnancy outcomes and complications of GDM. J Obstet Gynaecol. 2022;42(4):630–635. doi:10.1080/01443615.2021.1945009

10. Aji AS, Lipoeto NI, Yusrawati Y, et al. Association between pre-pregnancy body mass index and gestational weight gain on pregnancy outcomes: a cohort study in Indonesian pregnant women. BMC Pregnancy Childbirth. 2022;22(1):492. doi:10.1186/s12884-022-04815-8

11. Ke JF, Liu S, Ge RL, Ma L, Li MF. Associations of maternal pre-pregnancy BMI and gestational weight gain with the risks of adverse pregnancy outcomes in Chinese women with gestational diabetes mellitus. BMC Pregnancy Childbirth. 2023;23(1):414. doi:10.1186/s12884-023-05657-8

12. Voerman E, Santos S, Inskip H, et al.; LifeCycle Project-Maternal Obesity and Childhood Outcomes Study Group. Association of gestational weight gain with adverse maternal and infant outcomes. JAMA. 2019;321(17):1702–1715. doi:10.1001/jama.2019.3820

13. Chinese Nutrition Association. T/ CNSS-009 ‐2021. Monitoring and evaluation of Body Weight During Pregnancy in Chinese Women [S]. Beijing: Working Committee of Regulations and Standards of Chinese Nutrition Association; 2021.

14. Hao J, Yang L, Wang Y, et al. Mobile prenatal education and its impact on reducing adverse pregnancy outcomes: retrospective real-world study. JMIR mHealth UHealth. 2023;11:e46910. doi:10.2196/46910

15. Horan MK, McGowan CA, Doyle O, McAuliffe FM. Well-being in pregnancy: an examination of the effect of socioeconomic, dietary and lifestyle factors including impact of a low glycaemic index dietary intervention. Eur J Clin Nutr. 2014;68(1):19–24. doi:10.1038/ejcn.2013.212

16. Hiersch L, Shinar S, Melamed N, et al. Birthweight and large for gestational age trends in non-diabetic women with three consecutive term deliveries. Arch Gynecol Obstet. 2018;298(4):725–730. doi:10.1007/s00404-018-4872-8

17. Vinturache AE, Chaput KH, Tough SC. Pre-pregnancy body mass index (BMI) and macrosomia in a Canadian birth cohort. J Matern Fetal Neonatal Med. 2017;30(1):109–116. doi:10.3109/14767058.2016.1163679

18. Sridhar SB, Darbinian J, Ehrlich SF, et al. Maternal gestational weight gain and offspring risk for childhood overweight or obesity. Am J Obstet Gynecol. 2014;211(3):259.e1–259.e2598. doi:10.1016/j.ajog.2014.02.030

19. Ahmed B, Konje JC. The epidemiology of obesity in reproduction. Best Pract Res Clin Obstet Gynaecol. 2023;89:102342. doi:10.1016/j.bpobgyn.2023.102342

20. Akinyemi OA, Tanna R, Adetokunbo S, et al. Increasing pre-pregnancy body mass index and pregnancy outcomes in the United States. Cureus. 2022;14(9):e28695. doi:10.7759/cureus.28695

21. Kondracki AJ, Valente MJ, Ibrahimou B, Bursac Z. Risk of large for gestational age births at early, full and late term in relation to pre-pregnancy body mass index: mediation by gestational diabetes status. Paediatr Perinat Epidemiol. 2021;1–11. doi:10.1111/ppe.12809

22. Rockhill K, Dorfman H, Srinath M, Hogue C. The effects of prepregnancy body mass index and gestational weight gain on fetal macrosomia among American Indian/Alaska native women. Matern Child Health J. 2015;19(11):2480–2491. doi:10.1007/s10995-015-1769-z

23. Leonard SA, Carmichael SL, Abrams B. Gestational weight gain and severe maternal morbidity at delivery hospitalization. Obstet Gynecol. 2019;134(2):420. doi:10.1097/AOG.0000000000003389

24. Li J, Chen L, Tang Q, et al. The role, mechanism and potentially novel biomarker of microRNA-17-92 cluster in macrosomia. Sci Rep. 2015;5(1):17212. doi:10.1038/srep17212

25. Joyce BT, Liu H, Wang L, et al. Novel epigenetic link between gestational diabetes mellitus and macrosomia. Epigenomics. 2021;13(15):1221–1230. doi:10.2217/epi-2021-0096

26. Murphy CC, Cirillo PM, Krigbaum NY, et al. Maternal obesity, pregnancy weight gain, and birth weight and risk of colorectal cancer. Gut. 2022;71(7):1332–1339. doi:10.1136/gutjnl-2021-325001

27. Di Stefano A, Godard S, Bellaire J. Excessive gestational weight gain: assessing patients’ and providers’ perceptions. Can Fam Physician. 2021;67(7):e188–e196. doi:10.46747/cfp.6707e188

28. Ferrara A, Hedderson MM, Brown SD, et al. A telehealth lifestyle intervention to reduce excess gestational weight gain in pregnant women with overweight or obesity (GLOW): a randomised, parallel-group, controlled trial 2020;8(6):490-500. Lancet Diabetes Endocrinol. 2023;11(4):e6. doi:10.1016/S2213-8587(23)00055-4

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