Hostname: page-component-586b7cd67f-vdxz6 Total loading time: 0 Render date: 2024-11-25T04:06:14.610Z Has data issue: false hasContentIssue false

Association between pre-pregnancy weight status and dietary patterns during pregnancy: results from the Japan Environment and Children’s Study

Published online by Cambridge University Press:  02 May 2023

Kazue Ishitsuka*
Affiliation:
Medical Support Center of JECS Study, National Center for Child Health and Development, Tokyo 1578535, Japan
Kiwako Yamamoto-Hanada
Affiliation:
Medical Support Center of JECS Study, National Center for Child Health and Development, Tokyo 1578535, Japan
Hidetoshi Mezawa
Affiliation:
Medical Support Center of JECS Study, National Center for Child Health and Development, Tokyo 1578535, Japan
Mayako Saito-Abe
Affiliation:
Medical Support Center of JECS Study, National Center for Child Health and Development, Tokyo 1578535, Japan
Hatoko Sasaki
Affiliation:
Medical Support Center of JECS Study, National Center for Child Health and Development, Tokyo 1578535, Japan
Minaho Nishizato
Affiliation:
Medical Support Center of JECS Study, National Center for Child Health and Development, Tokyo 1578535, Japan
Miori Sato
Affiliation:
Medical Support Center of JECS Study, National Center for Child Health and Development, Tokyo 1578535, Japan
Yukihiro Ohya
Affiliation:
Medical Support Center of JECS Study, National Center for Child Health and Development, Tokyo 1578535, Japan
Japan Environment and Children’s Study Group
Affiliation:
Medical Support Center of JECS Study, National Center for Child Health and Development, Tokyo 1578535, Japan
*
*Corresponding author: Email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Objective:

Pre-pregnancy weight status is related to offspring health and may influence dietary patterns during pregnancy. We aimed to evaluate the link between pre-pregnancy weight status and dietary patterns during pregnancy.

Design:

Dietary data were collected using a FFQ during middle or late pregnancy. Dietary patterns were identified using principal component analysis. Anthropometric data were extracted from medical charts. Multiple linear regression was used to assess associations between pre-pregnancy weight status (severely or moderately underweight, mildly underweight, normal weight, overweight and obese) and dietary patterns during pregnancy after adjusting for socio-demographic characteristics.

Setting:

Nationwide Japan.

Participants:

Pregnant Japanese women enrolled in the Japan Environment and Children’s Study, a prospective birth cohort study (n 90 765).

Results:

We identified three dietary patterns. Compared with women with pre-pregnancy normal weight, those with pre-pregnancy obesity were less likely to habitually consume ‘fruits and vegetables’ pattern (coefficient, –0·18; 95 % CI, –0·21, –0·14) and ‘confectionery’ pattern (coefficient, –0·18; 95 % CI, –0·21, –0·14) and more likely to consume ‘white rice and soy products’ pattern (coefficient, 0·08; 95 % CI, 0·04, 0·11), and those with severely or moderately pre-pregnancy underweight were more likely to consume ‘confectionery’ pattern (coefficient, 0·06; 95 % CI, 0·03, 0·09) during pregnancy, after adjusting for confounders.

Conclusion:

We found that moderately and severely pre-pregnancy underweight women and those with obesity had unhealthy dietary patterns compared to those with pre-pregnancy normal weight. Our findings suggest that prenatal dietary advice is important and should be based on the pre-pregnancy weight status.

Type
Research Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2023. Published by Cambridge University Press on behalf of The Nutrition Society

Preconception care is crucial for maternal and child health. Accumulating evidence indicates that a woman’s pre-pregnancy weight status is related to women’s and child health(Reference Girsen, Mayo and Carmichael1Reference Stothard, Tennant and Bell4). Pre-pregnancy overweight or obese women have an increased risk of macrosomia, neural tube defects and cardiovascular anomalies(Reference Poston, Caleyachetty and Cnattingius3,Reference Stothard, Tennant and Bell4) . Dietary intake may mediate the associations between pre-pregnancy weight status and child outcomes(Reference Laraia, Bodnar and Siega-Riz5Reference Barker10). Some studies have shown that pregnant women with obesity are less likely to adhere to a health-conscious dietary pattern, which can result in unfavourable child outcomes(Reference Laraia, Bodnar and Siega-Riz5Reference De-Regil, Peña-Rosas and Fernández-Gaxiola8).

Pre-pregnancy underweight pregnant women have an increased risk of fetal growth failure and preterm delivery(Reference Girsen, Mayo and Carmichael1,Reference Salihu, Mbah and Alio2) . The growth failure of the fetus in underweight pregnant women may be due to inadequate macro- and micro-nutrients, which may also lead to CVD in later life(Reference Abu-Saad and Fraser9,Reference Barker10) .

Thinness is considered an ideal beauty standard for women of reproductive age(Reference Owen and Seller11,Reference Swami, Frederick and Aavik12) . The desire for thinness, which leads to inappropriate attempts to lose weight in an unhealthy way, sometimes results in women being underweight(Reference Choi, Cho and Kang13). A European study showed that underweight women were more likely to skip meals than normal-weight women, resulting in inadequate nutrient intake(Reference Wronka, Suliga and Pawlinska-Chmara14). In addition, women who attempt to lose weight may avoid foods that they believe might make them fat. Therefore, understanding dietary patterns in underweight women can help establish strategies for nutritional recommendations. Furthermore, the traditional single-nutrient approach in some studies overlooks collinearity among nutrients(Reference Hu15,Reference Newby, Muller and Hallfrisch16) . Thus, examining dietary patterns instead can better indicate a person’s overall diet and may help elucidate the interactive and synergistic effects of nutrients(Reference Hu15).

Notably, Japan has a high prevalence of underweight women of reproductive age, and many women desire to be thin(Reference Otsuka, Tabata and Someya17). However, to the best of our knowledge, no study has investigated the dietary patterns in pregnant women according to the pre-pregnancy weight status in Japan. A large Japanese cohort study has obtained information on dietary intake at the second and third trimesters.

This study aimed to investigate the association of pre-pregnancy weight status with dietary patterns during pregnancy using data from a nationwide Japanese birth cohort study. We hypothesised that both pre-pregnancy underweight and overweight pregnant women follow nutrient-poor dietary patterns than women with normal pre-pregnancy weight.

Materials and methods

Study participants

This study was a secondary analysis based on data gathered from the Japan Environment and Children’s Study (JECS), a nationwide birth cohort study. The design of the JECS has been described in detail previously(Reference Kawamoto, Nitta and Murata18,Reference Michikawa, Nitta and Nakayama19) . Briefly, the main objective of the JECS was to investigate the influence of environmental chemical exposures on child health and development. Women were recruited throughout pregnancy (mean gestational age at recruitment: 13·2 weeks, sd 8·4 weeks). Dietary intake during pregnancy was assessed using a FFQ, which was administered during middle or late pregnancy (mean gestational age: 27·9 weeks, sd 6·5 weeks).

Pregnant women were recruited at the clinic during prenatal checkups or at local government offices, where they were requested to register their pregnancy after learning about their conception, in regional centres located in urban and rural areas across Japan. The eligibility criteria were pregnant women who lived in the study area, and whose expected delivery date was between 2011 and 2014. The number of eligible women in each study area ranged from 130 000 to 600 000. Pregnant women were continuously recruited until the number of total study participants in all areas reached over 100 000. Women who could not use the Japanese language to complete the self-administered questionnaires were excluded from the JECS. A total of 103 070 pregnancies were registered in JECS (Fig. 1). Of these, 100 796 answered the baseline questionnaire for JECS. For this analysis, we included women who answered the FFQ to assess their dietary intake during pregnancy. We excluded women without pre-pregnancy data for height and weight. Furthermore, we excluded women with excessively low (< 4500 kJ) or high (≥ 20 000 kJ) daily energy intake(Reference Meltzer, Brantsæter and Ydersbond20).

Fig. 1 Flow diagram of study participants. Abbreviation: FFQ, food frequency questionnaire; JECS, the Japan Environment and Children’s study

Measurements

Food and nutrient intake information during pregnancy were assessed using an FFQ validated for the Japanese population(Reference Yokoyama, Takachi and Ishihara21,Reference Tsugane, Kobayashi and Sasaki22) . Detailed information on the FFQ has been provided elsewhere(Reference Ishitsuka, Sasaki and Yamamoto-Hanada23). Briefly, pregnant women were administered a paper-based 172-items self-reported FFQ to assess dietary intake after pregnancy awareness. Women were asked to indicate how often they typically consumed specific foods, with nine options ranging from ‘never’ to ‘at least six times per day.’ The women chose the portion size for individual items by selecting small (50 % smaller than the standard portion size), medium (the same as the standard portion size) or large (50 % larger than the standard portion size). Food and nutrient intakes were calculated using an ad hoc computer algorithm based on the Standard Tables of Food Composition in Japan(24) and then adjusted using the energy density method(Reference Willett, Howe and Kushi25). The correlation coefficients between FFQ and 12-day weighted dietary records ranged from 0·25 (seasonings) to 0·75 (fruits)(Reference Yokoyama, Takachi and Ishihara21).

Information regarding folic acid supplementation was obtained through interviews. Dietary supplement intake was not included in the nutrient calculation because a reliable database for dietary supplements does not exist in Japan.

Dietary patterns

We conducted a principal component analysis based on thirty food groups to identify specific dietary patterns. The foods were grouped according to categories listed in the Food Composition Table (5th) in Japan, and items with similar nutrient profiles or culinary applications were combined(24) (online Supplementary Table 1).

Correlated food items were grouped as dietary patterns using principal component analysis. The principal component analysis can capture the population’s variation in the combination of food intake and is the most widely used method for deriving dietary patterns(Reference Zhao, Li and Gao26). Dietary patterns were named based on the values of factor loadings, which indicated how much each food group correlated with each dietary pattern. Three dietary patterns were selected based on the scree plot for determining the breaking point of eigenvalues and interpretability(Reference Hu15). Varimax rotation was used to maximise the sum of eigenvalues (the variance of the loading factors). Each woman’s score for each dietary pattern was calculated by summing the intake of food groups weighted by their factor loadings after energy-adjusted by the density method and standardisation. Food intake was log-transformed when the intake of food groups showed a skewed distribution.

Table 2 shows the results of the factor loading matrix for each dietary pattern. Furthermore, we conducted principal component analysis on two random halves of the data to confirm reproducibility(Reference Northstone, Emmett and Rogers27). The results of the factor loadings and component scores aligned well with our initial findings.

Weight status

We obtained pre-pregnancy heights and weights from medical charts during prenatal visits to determine their BMI: < 17·0 kg/m2, severely or moderately underweight; 17·0–18·4 kg/m2, mildly underweight; 18·5–24·9 kg/m2, normal weight; 25·0–29·9 kg/m2, overweight and ≥ 30 kg/m2, obese(28). Anthropometric data in medical charts were extracted by physicians, midwives, nurses and research coordinators in a standardised manner for JECS.

Covariates

Covariates were chosen based on previous literature(Reference Northstone, Emmett and Rogers27,Reference Arkkola, Uusitalo and Kronberg-Kippilä29) . All covariates were obtained through the self-reported questionnaires. A woman’s age was categorised as < 25, 25–29, 30–34 or ≥ 35 years; parity as primiparous or multiparous; marital status as married or unmarried; annual household income as < 2 000 000, 2 000 000–3 999 999, 4 000 000–5 999 999 or ≥ 6 000 000 Japanese yen; the educational level as ≤ 12, 13–15 or ≥ 16 years and smoking status as ‘never,’ ‘stopped smoking before becoming aware of the pregnancy,’ ‘stopped smoking after becoming aware of the pregnancy’ or ‘continued smoking during pregnancy.’

Statistical analyses

Food intake was energy-adjusted by density method. We calculated the mean and sd for the energy-adjusted intake of food groups across the quintile scores of three dietary patterns. Spearman’s correlation coefficients were also calculated to determine the correlations between dietary patterns and energy-adjusted nutrient intake.

Multivariate regression analysis was performed using the outcomes of dietary pattern scores. Pre-pregnancy BMI was considered an explanatory variable and adjusted for women’s age, parity, educational level, smoking status and trimester (the second or the third trimester)(Reference Arkkola, Uusitalo and Kronberg-Kippilä29). The models were mutually adjusted for the three dietary patterns. Because this study was a secondary analysis of data, we calculated the power of the analysis. A sample of 90 765 pregnant women would be sufficient to detect a 0·01 difference with more than 99·9 % power and an alpha of 0·05. All statistical analyses were performed using SAS version 9.4 (SAS Institute Inc.).

Results

A total of 90 765 pregnant women were included in this study. The numbers (percentages) of women that were severely or moderately underweight, mildly underweight, normal weight, overweight and obese were 2463 (2·7 %), 12 105 (13·3 %), 66 640 (73·4 %), 7316 (8·1 %) and 2241 (2·5 %), respectively. Table 1 shows the characteristics of the women, grouped by pre-pregnancy weight status. Compared with normal-weight women, severely or moderately underweight women were younger, whereas those with obesity were older. Women with obesity and those who were severely or moderately underweight had lower income and lower education and continued to smoke during pregnancy compared with normal-weight women.

Table 1 Characteristics of women according to pre-pregnancy weight status

Three dietary patterns were identified using principal component analysis. Table 2 lists the factor loading matrices. The patterns were named according to the food groups with high loadings. For example, the first dietary pattern was named ‘vegetable and fruit,’ which had high loadings for green and white vegetables, potatoes, mushrooms, seaweed, fruits, fish, fat and oil and seasoning, but low white rice. The second dietary pattern was named ‘white rice and soy product’, which had high loadings for white rice, soya products and seasonings but low loadings for bread. The third dietary pattern was named ‘confectionery’, which had high loadings for confectionery and savory snack foods but low loadings for fresh and processed meat. These three principal components explained 18·9 % of the variance.

Table 2 Factor-loading matrix for three dietary patterns

Definitions for the food groupings are provided in Supplementary Table 1.

Supplementary Table 2 shows the mean consumption according to each food group across the three dietary patterns. The ‘vegetable and fruit’ pattern was characterised by a high intake of green and white vegetables, potatoes, mushrooms, seaweed, fruits, fat and oil and seasoning but a low intake of white rice. The ‘white rice and soy product’ pattern was characterised by a high intake of white rice, soya products and seasonings but a low intake of bread. The ‘confectionery’ pattern had a high intake of confectionery and savory snack foods but a low intake of fresh and processed meat.

Supplementary Table 3 shows the correlation between women’s dietary patterns and nutrient intake. Specifically, the ‘vegetables and fruits’ pattern was correlated positively with the intake of fibre and most vitamins and minerals. The ‘white rice and soya products’ pattern was correlated positively with the intake of carbohydrates and negatively with the intake of saturated fat, Ca, vitamin B2 and vitamin E. The ‘confectionery’ pattern was correlated negatively with the intake of Ca, Zn and pantothenic acid.

Table 3 shows associations between women’s pre-pregnancy BMI and their dietary patterns. Women with obesity before pregnancy were significantly less likely to adhere to the ‘fruits and vegetables’ pattern (coefficient, –0·18; 95 % CI, –0·21, –0·14) and the ‘confectionery’ pattern (coefficient, –0·18; 95 % CI, –0·21, –0·14) and more likely to adhere to the ‘white rice and soy products’ pattern (coefficient, 0·08; 95 % CI, 0·04, 0·11) during pregnancy than normal pre-pregnancy weight. Women who were severely or moderately underweight were more likely to adhere to the ‘confectionery’ pattern (coefficient, 0·06; 95 % CI, 0·03, 0·09) than women with normal pre-pregnancy weight.

Table 3 Associations between women’ dietary patterns during pregnancy and BMI before pregnancy

Ref, reference.

Multiple regression analysis was performed after adjustment for age, parity, educational level, smoking status and trimester. All dietary pattern scores were mutually adjusted.

Discussion

We found that obesity before pregnancy was associated with reduced adherence to ‘fruits and vegetables’ and ‘confectionery’ dietary patterns and increased adherence to ‘white rice and soy products’ and ‘confectionery’ dietary patterns during pregnancy. Additionally, a severely or moderately underweight status before pregnancy was associated with higher adherence to ‘confectionery’ dietary patterns during pregnancy.

Several studies have reported that women with obesity often consume fewer fruits and vegetables than their lean counterparts in non-pregnant women in Western and Asian countries(Reference Newby, Muller and Hallfrisch16,Reference He, Hu and Colditz30Reference Okubo, Sasaki and Murakami32) . However, few studies have investigated the relationship between pre-pregnancy weight status and food intake in pregnant women. A study in New Zealand showed that a health-conscious dietary pattern characterised by fruits, vegetables and whole grains was associated with a lower pre-pregnancy BMI(Reference Wall, Gammon and Bandara33). In the present study, obesity before pregnancy was associated with lower adherence to the fruits and vegetable pattern during pregnancy; this finding is consistent with the aforementioned findings in pregnant and non-pregnant women(Reference He, Hu and Colditz30Reference Okubo, Sasaki and Murakami32). Pregnant women with obesity are at risk of a low intake of fruits and vegetables. Therefore, dieticians and other health care professionals should inquire with obese pregnant women about the adequacy of intake of fruits and vegetables. They can then give dietary advice on how to ensure sufficient vitamin and mineral intake.

Our analyses also revealed that women with pre-pregnancy obesity adhered to a traditional Japanese diet characterised by high amounts of white rice and soya products and low quantities of bread and oils. Similarly, tangential investigations have demonstrated that high consumption of white rice and soya products elevates the risk of high BMI in young Japanese women(Reference Okubo, Sasaki and Murakami32) and that eating white rice is linked to obesity across various Asian populations(Reference Kim, Jo and Joung34,Reference Sartorius, Sartorius and Madiba35) . These findings from the earlier and present studies may be explained by the fact that white rice has a high glycaemic index and load, which stimulates insulin secretion and promotes weight gain, thereby resulting in obesity(Reference Blaak, Antoine and Benton36).

Interestingly, our findings also demonstrated that underweight women were more likely to follow a ‘confectionery’ dietary pattern during pregnancy. A Japanese study showed that, compared to normal-weight women, underweight young women with a desire for thinness had sweet foods, composed of a higher percentage of their energy intake(Reference Mori, Asakura and Sasaki37). Another study indicated that women with anorexia nervosa, characterised by overestimation of weight and shape as well as self-starvation, preferred sweets taste and frequently consumed artificially sweetened foods(Reference Schebendach, Klein and Mayer38,Reference Klein, Boudreau and Devlin39) . These results may suggest that starvation physiologically enhances one’s desire for sweets and that underweight women strive to eat highly palatable food during pregnancy(Reference Brown and Keel40). Another possible reason might be that pregnant underweight women may try to gain weight during pregnancy by the intake of palatable and less expensive food, such as confectionery. In contrast, overweight and obese women are less likely to follow a ‘confectionery’ dietary pattern during pregnancy. This may be because they are trying to avoid excessive weight gain during pregnancy.

The strengths of this study were the large sample size and the generalisability of the results to Japanese women. However, this study has several limitations. First, the dietary assessment was self-reported, which might have resulted in misreporting(Reference Livingstone and Black41,Reference McGowan and Mcauliffe42) . Overweight women might be likely to under-report their dietary intake, whereas underweight women might over-report their dietary intake(Reference Murakami, Sasaki and Okubo43). This might have led to an underestimation of the differences in dietary patterns. Second, data on BMI before pregnancy were reported by women, which might have underestimated or overestimated their weight. However, categorising self-reported pre-pregnancy weight status has been proven to be valid(Reference Shin, Chung and Weatherspoon44). Furthermore, the prevalence of women who were underweight in this study was not markedly different from that of the Japanese women of reproductive age in other Japanese studies(Reference Enomoto, Aoki and Toma45). Lastly, the FFQ has been validated for the Japanese population, but not specifically for pregnant women(Reference Yokoyama, Takachi and Ishihara21,Reference Tsugane, Kobayashi and Sasaki22) .

Nutrient requirements increase during pregnancy. Our findings suggest that dietary advice should be according to weight status. In the present study, underweight women were more likely to have confectionery patterns, suggesting a high preference for sweets or palatable foods. Thus, dietary advice for underweight women should consider both food preferences and nutrient requirements. For overweight or obese women, dieticians and other healthcare professionals should ensure adequate intake of fruits and vegetables and advise against excessive consumption of white rice.

In conclusion, we found that maternal dietary patterns differed according to the pre-pregnancy weight status. Women with obesity or those who were severely or moderately underweight were more likely to consume the ‘confectionery’ pattern than normal weight women. These findings suggest that prenatal dietary advice is needed for pregnant women according to pre-pregnancy weight status.

Acknowledgements

Acknowledgements: Members of the JECS Group as of 2021: Michihiro Kamijima (principal investigator, Nagoya City University, Nagoya, Japan), Shin Yamazaki (National Institute for Environmental Studies, Tsukuba, Japan), Yukihiro Ohya (National Center for Child Health and Development, Tokyo, Japan), Reiko Kishi (Hokkaido University, Sapporo, Japan), Nobuo Yaegashi (Tohoku University, Sendai, Japan), Koichi Hashimoto (Fukushima Medical University, Fukushima, Japan), Chisato Mori (Chiba University, Chiba, Japan), Shuichi Ito (Yokohama City University, Yokohama, Japan), Zentaro Yamagata (University of Yamanashi, Chuo, Japan), Hidekuni Inadera (University of Toyama, Toyama, Japan), Takeo Nakayama (Kyoto University, Kyoto, Japan), Hiroyasu Iso (Osaka University, Suita, Japan), Masayuki Shima (Hyogo College of Medicine, Nishinomiya, Japan), Hiroshige Nakamura (Tottori University, Yonago, Japan), Narufumi Suganuma (Kochi University, Nankoku, Japan), Koichi Kusuhara (University of Occupational and Environmental Health, Kitakyushu, Japan) and Takahiko Katoh (Kumamoto University, Kumamoto, Japan). Analyses in this study were conducted using data from the data file named ‘jecs-ag-20160424.’ Authorship: K.I. analysed the data and drafted the manuscript; K.I., K.Y., H.M. and Y.O. designed the study, K.Y., H.M., H.S., M.N. and M.S. carried out the study; K.Y., H.M., H.S., M.N., M.S. and Y.O. interpreted and critically reviewed the results and revised the manuscript. Ethics of human subject participation: The JECS was conducted in accordance with the guidelines set forth by the Declaration of Helsinki. The protocol was reviewed and approved by the Ministry of the Environment’s Institutional Review Board on Epidemiological Studies and the ethics committees of the participating institutions. Written informed consent was obtained from all the participants.

Financial support:

This work was funded by the Ministry of the Environment, Japan. The findings and conclusions of this study are solely the responsibility of the authors and do not represent the official views of the above governmental department.

Conflict of interest:

None of the authors have any conflicts of interest to declare.

Supplementary material

For supplementary material/s referred to in this article, please visit https://doi.org/10.1017/S1368980023000770

References

Girsen, AI, Mayo, JA, Carmichael, SL et al. (2016) Women’s prepregnancy underweight as a risk factor for preterm birth: a retrospective study. BJOG 123, 20012007.CrossRefGoogle ScholarPubMed
Salihu, HM, Mbah, AK, Alio, AP et al. (2009) Low pre-pregnancy body mass index and risk of medically indicated v. spontaneous preterm singleton birth. Eur J Obstet Gynecol Reprod Biol 144, 119123.CrossRefGoogle Scholar
Poston, L, Caleyachetty, R, Cnattingius, S et al. (2016) Preconceptional and maternal obesity: epidemiology and health consequences. Lancet Diabetes Endocrinol 4, 10251036.CrossRefGoogle ScholarPubMed
Stothard, KJ, Tennant, PWG, Bell, R et al. (2009) Maternal overweight and obesity and the risk of congenital anomalies: a systematic review and meta-analysis. JAMA 301, 636650.CrossRefGoogle ScholarPubMed
Laraia, BA, Bodnar, LM & Siega-Riz, AM (2007) Pregravid body mass index is negatively associated with diet quality during pregnancy. Public Health Nutr 10, 920926.CrossRefGoogle ScholarPubMed
Shin, D, Lee, KW & Song, WO (2016) Pre-pregnancy weight status is associated with diet quality and nutritional biomarkers during pregnancy. Nutrients 8, 112.CrossRefGoogle ScholarPubMed
Mojtabai, R (2004) Body mass index and serum folate in childbearing age women. Eur J Epidemiol 19, 10291036.CrossRefGoogle ScholarPubMed
De-Regil, LM, Peña-Rosas, JP, Fernández-Gaxiola, AC et al. (2015) Effects and safety of periconceptional oral folate supplementation for preventing birth defects. Cochrane Database Syst Rev 14, CD007950.Google Scholar
Abu-Saad, K & Fraser, D (2010) Maternal nutrition and birth outcomes. Epidemiol Rev 32, 525.CrossRefGoogle ScholarPubMed
Barker, DJ (1997) Maternal nutrition, fetal nutrition, and disease in later life. Nutrition 13, 807813.CrossRefGoogle ScholarPubMed
Owen, RP & Seller, EL (2000) Weight and shape ideals: thin is dangerously in. J Appl Soc Psychol 30, 979990.CrossRefGoogle Scholar
Swami, V, Frederick, DA, Aavik, T et al. (2010) The attractive female body weight and female body dissatisfaction in 26 countries across 10 world regions: results of the international body project I. Pers Soc Psychol Bull 36, 309325.CrossRefGoogle ScholarPubMed
Choi, OJE, Cho, YG, Kang, JH et al. (2013) Weight control attempts in underweight Korean adults: Korea national health and nutrition examination survey, 2007–2010. Korean J Fam Med 34, 393402.CrossRefGoogle ScholarPubMed
Wronka, I, Suliga, E & Pawlinska-Chmara, R (2013) Evaluation of lifestyle of underweight, normal weight and overweight young women. Coll Antropol 37, 359365.Google ScholarPubMed
Hu, FB (2002) Dietary pattern analysis: a new direction in nutritional epidemiology. Curr Opin Lipidol 13, 39.CrossRefGoogle ScholarPubMed
Newby, PK, Muller, D, Hallfrisch, J et al. (2003) Dietary patterns and changes in body mass index and waist circumference in adults. Am J Clin Nutr 77, 14171425.CrossRefGoogle ScholarPubMed
Otsuka, H, Tabata, H, Someya, Y et al. (2021) Trends in the prevalence of underweight in women across generations in Japan. J Bone Miner Metab 39, 719720.CrossRefGoogle ScholarPubMed
Kawamoto, T, Nitta, H, Murata, K et al. (2014) Rationale and study design of the Japan Environment and Children’s Study (JECS). BMC Public Health 14, 25.CrossRefGoogle ScholarPubMed
Michikawa, T, Nitta, H, Nakayama, SF et al. (2018) Baseline profile of participants in the Japan Environment and Children’s Study (JECS). J Epidemiol 28, 99104.CrossRefGoogle ScholarPubMed
Meltzer, HM, Brantsæter, AL, Ydersbond, TA et al. (2008) Methodological challenges when monitoring the diet of pregnant women in a large study: experiences from the Norwegian Mother and Child Cohort Study (MoBa). Matern Child Nutr 4, 1427.CrossRefGoogle Scholar
Yokoyama, Y, Takachi, R, Ishihara, J et al. (2016) Validity of short and long self-administered food frequency questionnaires in ranking dietary intake in middle-aged and elderly Japanese in the Japan Public Health Center-Based Prospective Study for the Next Generation (JPHC-NEXT) protocol area. J Epidemiol 26, 420432.CrossRefGoogle Scholar
Tsugane, S, Kobayashi, M, Sasaki, S; JPHC (2003) Validity of the self-administered food frequency questionnaire used in the 5-year follow-up survey of the JPHC Study Cohort I: comparison with dietary records for main nutrients. J Epidemiol 13, S51S56.CrossRefGoogle ScholarPubMed
Ishitsuka, K, Sasaki, S, Yamamoto-Hanada, K et al. (2020) Changes in dietary intake in pregnant women from periconception to pregnancy in the Japan Environment and Children’s Study: a nationwide Japanese birth cohort study. Matern Child Health J 24, 389400.CrossRefGoogle ScholarPubMed
Science and Technology Agency (2015) Standard Tables of Food Composition in Japan, 7th revised. Tokyo: Printing Bureau of the Ministry of Finance.Google Scholar
Willett, WC, Howe, GR & Kushi, LH (1997) Adjustment for total energy intake in epidemiologic studies. Am J Clin Nutr 65, 1220S1228S; discussion 1229S–1231S.CrossRefGoogle ScholarPubMed
Zhao, J, Li, Z, Gao, Q, et al. (2021) A review of statistical methods for dietary pattern analysis. Nutr J 19, 37.CrossRefGoogle Scholar
Northstone, K, Emmett, P & Rogers, I (2008) Dietary patterns in pregnancy and associations with socio-demographic and lifestyle factors. Eur J Clin Nutr 62, 471479.CrossRefGoogle ScholarPubMed
Arkkola, T, Uusitalo, U, Kronberg-Kippilä, C et al. (2008) Seven distinct dietary patterns identified among pregnant Finnish women – associations with nutrient intake and sociodemographic factors. Public Health Nutr 11, 176182.CrossRefGoogle ScholarPubMed
He, K, Hu, FB, Colditz, GA et al. (2004) Changes in intake of fruits and vegetables in relation to risk of obesity and weight gain among middle-aged women. Int J Obes Relat Metab Disord 28, 15691574.CrossRefGoogle ScholarPubMed
Togo, P, Osler, M, Sørensen, TIA et al. (2001) Food intake patterns and body mass index in observational studies. Int J Obes Relat Metab Disord 25, 17411751.CrossRefGoogle ScholarPubMed
Okubo, H, Sasaki, S, Murakami, K et al. (2008) Three major dietary patterns are all independently related to the risk of obesity among 3760 Japanese women aged 18–20 years. Int J Obes 32, 541549.CrossRefGoogle Scholar
Wall, CR, Gammon, CS, Bandara, DK et al. (2016) Dietary patterns in pregnancy in New Zealand-influence of maternal socio-demographic, health and lifestyle factors. Nutrients 8, 300.CrossRefGoogle ScholarPubMed
Kim, J, Jo, I & Joung, H (2012) A rice-based traditional dietary pattern is associated with obesity in Korean adults. J Acad Nutr Diet 112, 246253.CrossRefGoogle ScholarPubMed
Sartorius, K, Sartorius, B, Madiba, TE et al. (2018) Does high-carbohydrate intake lead to increased risk of obesity? A systematic review and meta-analysis. BMJ Open 8, e018449.CrossRefGoogle ScholarPubMed
Blaak, EE, Antoine, JM, Benton, D et al. (2012) Impact of postprandial glycaemia on health and prevention of disease. Obes Rev 13, 923984.CrossRefGoogle ScholarPubMed
Mori, N, Asakura, K & Sasaki, S (2016) Differential dietary habits among 570 young underweight Japanese women with and without a desire for thinness: a comparison with normal weight counterparts. Asia Pac J Clin Nutr 25, 97107.Google ScholarPubMed
Schebendach, J, Klein, DA, Mayer, LES et al. (2017) Assessment of the motivation to use artificial sweetener among individuals with an eating disorder. Appetite 109, 131136.CrossRefGoogle ScholarPubMed
Klein, DA, Boudreau, GS, Devlin, MJ et al. (2006) Artificial sweetener use among individuals with eating disorders. Int J Eat Disord 39, 341345.CrossRefGoogle ScholarPubMed
Brown, TA & Keel, PK (2013) What contributes to excessive diet soda intake in eating disorders: appetitive drive, weight concerns, or both? Eat Disord 21, 265274.CrossRefGoogle ScholarPubMed
Livingstone, MBE & Black, AE (2003) Markers of the validity of reported energy intake. J Nutr 133, 895S920S.CrossRefGoogle ScholarPubMed
McGowan, C & Mcauliffe, F (2012) Maternal nutrient intakes and levels of energy underreporting during early pregnancy. Eur J Clin Nutr 66, 906913.CrossRefGoogle ScholarPubMed
Murakami, K, Sasaki, S, Okubo, H et al. (2012) Characteristics of under- and over-reporters of energy intake among young Japanese women. J Nutr Sci Vitaminol 58, 253262.CrossRefGoogle ScholarPubMed
Shin, D, Chung, H, Weatherspoon, L et al. (2013) Validity of prepregnancy weight status estimated from self-reported height and weight. Matern Child Health J 18, 16671674.CrossRefGoogle Scholar
Enomoto, K, Aoki, S, Toma, R et al. (2016) Pregnancy outcomes based on pre-pregnancy body mass index in Japanese women. PLoS One 11, e0157081.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1 Flow diagram of study participants. Abbreviation: FFQ, food frequency questionnaire; JECS, the Japan Environment and Children’s study

Figure 1

Table 1 Characteristics of women according to pre-pregnancy weight status

Figure 2

Table 2 Factor-loading matrix for three dietary patterns

Figure 3

Table 3 Associations between women’ dietary patterns during pregnancy and BMI before pregnancy

Supplementary material: File

Ishitsuka et al. supplementary material

Tables S1-S2

Download Ishitsuka et al. supplementary material(File)
File 268.7 KB