Skip to main content
Revista de Saúde Pública logoLink to Revista de Saúde Pública
. 2019 Jun 25;53:52. doi: 10.11606/S1518-8787.2019053000909

Dietary patterns of pregnant women, maternal excessive body weight and gestational diabetes

Padrões alimentares de gestantes, excesso de peso materno e diabetes gestacional

Daniela Cristina Candelas Zuccolotto I, Lívia Castro Crivellenti I, Laércio Joel Franco II, Daniela Saes Sarotelli II
PMCID: PMC6629290  PMID: 31269091

ABSTRACT

OBJECTIVE

To investigate the relationship between the dietary patterns of pregnant women with maternal excessive body weight and gestational diabetes mellitus.

METHODS

A cross-sectional study conducted with a convenience sample of 785 adult pregnant women attended by the Unified Health System of Ribeirão Preto, state of São Paulo, between 2011 and 2012. Two 24-hour dietary recalls, corrected by the multiple source method, were employed . For the classification of the body mass index and the diagnosis of gestational diabetes mellitus, the criteria by Atalah and the World Health Organization were used, respectively. Dietary patterns were obtained by principal component analysis using the Varimax rotation method. The relationship between adherence to patterns, overweight and obesity was analyzed by multinomial logistic regression models and the relationship with gestational diabetes mellitus by adjusted unconditional logistic regression models.

RESULTS

We identified four dietary patterns: “traditional Brazilian”; “snacks”; “coffee” and “healthy”. Women with a higher adherence to the “Healthy” (OR = 0.52; 95%CI 0.33–0.83) and “Brazilian Traditional” patterns (OR = 0.61; 95%CI 0.38–0.96) presented a lower chance of obesity, when compared to women with lower adherence, regardless of confounding factors. After adjustment for maternal excessive body weight, there was no association between dietary patterns and gestational diabetes mellitus.

CONCLUSIONS

Among the pregnant women, greater adherence to “traditional Brazilian” and “healthy” patterns was inversely associated with obesity, but no relationship was identified with gestational diabetes mellitus after adjusting for excessive body weight. Prospective studies are recommended to investigate the relationship between dietary patterns, overweight and gestational diabetes mellitus, reducing the chance of reverse causality.

Keywords: Pregnant Women, Gestational Diabetes, Feeding Behavior, Risk Factors, Prenatal Nutrition

INTRODUCTION

Gestational diabetes mellitus (GDM), a hyperglycemia diagnosed for the first time during pregnancy, is the most common metabolic problem during pregnancy 1 . Its prevalence has been growing substantially 2 and projections suggest this increase will go on further given the expansion in the number of cases of excessive body weight among women of reproductive age 3 . The GDM can trigger the development of obstetric complications and losses to maternal and child health in the short and long term 4 , 5 . Thus, the identification of modifiable risk factors related to the genesis of the disease is extremely relevant.

Certain studies indicate that both nutrient and food intake alone and adherence to dietary patterns are directly related to the health of the mother-child binomial 3 , 6 . However, the approach of eating patterns is recognized as more comprehensive, considering the synergistic and inhibitory action of the simultaneous consumption of different foods and their relationship with health outcomes 7 , 8 .

In addition to being scarce, studies that evaluated the relationship between dietary patterns during gestation and GDM show inconsistent findings due to distinct characteristic of food cultures seen among the populations analyzed9–11. In a study conducted in China with 3063 pregnant women, higher adherence to the “sweet and seafood” pattern was directly associated with GDM 9 . On the other hand, Seymor et al. 10 , when analyzing the dietary pattern of 909 pregnant women in Singapore, identified that adherence to the diet pattern based on seafood and pasta was inversely associated with the disease 10 . The divergence in the results indicates that more studies should be conducted in order to elucidate the role of maternal diet in the occurrence of GDM, especially in regions with different eating behaviors.

In view of the implications of GDM on maternal-fetal health and the small number of investigations that relate the diet of pregnant women to the occurrence of the disease, the objective of this study was to evaluate the relationship between dietary patterns and GDM. Additionally, we analyzed the relationship between dietary patterns and excessive body weight, which is a convincing risk factor for GDM.

METHODS

Study Design and Population

A cross-sectional study was conducted with a convenience sample of 785 pregnant women users of the Unified Health System of Ribeirão Preto, state of São Paulo, between 2011 and 2012. The women were invited to participate in the study on the occasion of their oral glucose tolerance test in five laboratories that had an agreement with the Municipal Health Department, where there was higher demand for the examination. A follow-up scheme was established by trained nutritionists every day of the week. Women who met the inclusion criteria and agreed to participate in the study were interviewed. The study design was described in detail by Barbieiri et al. 12 .

The inclusion criteria of the study were: gestational age after the 24th week, age ≥ 20 years and pre-gestational body mass index (BMI) ≥ 20 kg/m 2 . Women with diabetes, those who reported usage of glucose-modifying drugs (such as glucocorticoids) and those with chronic renal failure, AIDS or cancer, were excluded.

Between the data collection period and the analysis of the results, there was a change in the diagnostic criteria 13 and in the estimated prevalence of GDM 14 , and therefore the sample size was calculated a posteriori . Considering a prevalence of 20% GDM among adult women 14 and an acceptable margin of error of 5%, the required sample size would be 512 women. A total of 1,446 pregnant women were contacted, of which 619 were excluded due to non-compliance with the study criteria, 19 did not agree to participate, 20 did not complete the examination and three presented incomplete data, totaling 785 women. Among them, 70% were interviewed between the 24th and 28th gestational weeks, and 30% between the 29th and 39th.

At the time of the interview, the pregnant women were subjected to anthropometric evaluation and answered to a structured questionnaire with socioeconomic data, obstetric and family history, lifestyle and food consumption.

Diagnosis of Gestational Diabetes Mellitus

Fasting blood samples, one and two hours after ingestion of a 75 g glucose overload, were obtained from all study participants. Determination of glycemia was performed using the glucose oxidase test. Diagnosis of GDM was based on World Health Organization criteria of 2014 13 , which takes into account pregnant women with at least one of their glycemia values altered at any stage of pregnancy: fasting glycemia between 92 and 125 mg/dl, glycemia one hour after glucose overload ≥ 180 mg/dl or glycemia two hours after glucose overload between 153 and 199 mg/dl. Pregnant women who had fasting glycemia ≥ 126 mg/dL or two hours after glucose overload ≥ 200 mg/dL were considered to have previous diabetes and were excluded from the study analyses.

Characteristics of Pregnant Women

With use of a structured questionnaire, we obtained data on age, schooling, smoking history, family history of type 2 diabetes (DM), previous GDM, and practice of physical activities. The physical activity questionnaire used was previously developed and validated for pregnant women 15 . However, given the difficulty of the women in responding, for this study we consider only data related to the practice of walking for locomotion or during leisure, as well as the practice of physical exercises (in minutes per week).

Gestational age was estimated based on the date of the last menstruation (DLM). DLM and pre-gestational weight data were obtained from the record on the pregnant woman’s card. At the time of the interview, measurements of weight (in kg) and height (in m) were acquired from a digital scale (TANITA model HS302) and a portable stadiometer (SANNY model ES2040), respectively. For the classification of BMI according to the gestational week, the criteria proposed by Atalah 16 were adopted.

Assessment of Food Consumption and Determination of Food Patterns

Dietary intake was assessed by two 24-hour dietary recalls (R24h) obtained by trained nutritionists using the three-steps multiple pass technique (participant reporting, detailing, and review). The first R24h was obtained at the time of the interview and the second by telephone contact after at least seven days, regardless of the day of the week or season, and before the woman receives the results of biochemical exams.

The Brazilian Table of Food Composition (TACO) 17 was used to estimate energy and nutrients. We analyzed the diets with the aid of the application software NutWin®18. In order to estimate the usual diet, we used the multiple source method 19 , a statistical modeling technique that considers the product between the probability of consumption and the usual intake 19 .

In total, 481 foods and preparations were reported in the R24h. Foods with less than 20% of consumers were excluded. Other foods and preparations were grouped into 23 groups of food (grams/day) based on the nutritional value or the logic of consumption: rice; beans; meat (red meat and chicken); fruits, vegetables; pasta; breads; butter and margarine; hard and soft cheese; cold meats (mortadella, turkey breast, ham, sausage, salami); milk and yogurt; chocolate milk and cappuccino; sugar; coffee and tea; candies ( paçoca, pavês, pé de moleque , popsicle, ice cream, pie, candy, beijinho, brigadeiro , chocolate , cocada, doce de leite , flan, blancmange, maria mole , milkshake , mousse , hazelnut cocoa spread, panettone, doughnut, sonho , buttery biscuit, cake); natural fruit juice; artificial juice and soda; snacks, pizzas and sandwiches (fried and baked snacks, chips, sandwich, hot dog, pizza, popcorn and instant noodles); tubers; eggs; fish; olive oil; and biscuits.

Food patterns were identified by means of principal component analysis, which allows food groups to be grouped based on the degree of correlation between them. Negative factor loadings indicate that the variable is inversely associated with the factor and positive charges, wherein the food group is directly associated with the factor. To identify the number of patterns to be retained, we use eigenvalues > 1.5. After orthogonal Varimax rotation, we kept the food groups with a factorial load ≥ 0.3. In total, 18 food groups were retained within the food patterns. The tubers, eggs, fish, olive oil and biscuits groups presented low commonality and were excluded.

Statistical Analysis

Descriptive and comparative analyses of the study variables according to dietary pattern were performed using the chi-square test for categorical variables, and ANOVA and Kruskal-Wallis for continuous variables.

Adjusted multinomial logistic regression models were used to evaluate the association between adherence to dietary patterns (in tertile) with overweight and obesity, adopting the eutrophic women as reference. For such analyses, 31 women with low weight for their gestational week were excluded. We considered the following adjustment variables for the models: age (years), gestational week at the time of interview, education (years of study), smoking (never smoked, interrupted during gestation or currently smokes), physical activity practice (minutes/week walking or exercise) and number of children.

Adjusted logistic regression models were used to assess the association between adherence to dietary patterns and GDM. GDM (yes or no) was considered a dependent variable, and dietary patterns (in tertile) were considered independent variables. Model 1 was adjusted for: age (years), gestational week at the time of the interview, previous GDM (yes; no), schooling (years of study), family history of DM (yes; no), smoking (never smoked, interrupted during gestation, or currently smokes), physical activity (minutes/week of walking or exercise) and number of children. In Model 2, in addition to the variables included in Model 1, further adjustment for maternal excessive body weight (yes or no) was considered.

The selection of adjustment variables for the models was based on the theoretical reference of food consumption influence on the occurrence of maternal excessive body weight, as well as on GDM. However, variables considered the causal pathway between exposure and outcomes, such as dietary energy, were not taken into account. A value of p < 0.05 was adopted as level of significance. The statistical analyses were performed with the aid of the application software IBM SPSS Statistics (version 24.0, SPSS Inc. Woking, Surrey, UK).

This study was approved by the Research Ethics Committee of the School and Health Center of the Ribeirão Preto Medical School, University of São Paulo (CEP/CSE-FMRP-USP-023/2015) and its execution authorized by the Municipal Secretary of Health of Ribeirão Preto (2030/10 GS).

RESULTS

Among the 785 pregnant women investigated, 139 (17.7%) had gestational diabetes, 261 (33.2%) were classified as overweight and 187 (23.8%) as obese.

Four dietary patterns were identified: “traditional Brazilian”, “snacks”, “coffee” and “healthy”, which together accounted for about 41% of the variance, and the observed KMO was 0.56. The “traditional Brazilian” pattern was characterized by consumption of rice; bean; meat; vegetables, and inversely associated with the consumption of hard and soft cheese; snacks, pizzas and sandwiches. The “snacks” patterns was characterized by the consumption of breads; butter and margarine; milk and yogurt; hard and soft cheese; sweets; chocolate milk and cappuccino . The “coffee” pattern was characterized by consumption of coffee; sugar, butter and margarine. The “healthy” pattern was characterized by the consumption of vegetables; fruit and natural fruit juice; and it was inversely associated with the consumption of soda and artificial juice ( Table 1 ).

Table 1. Factor loading of the dietary patterns of pregnant women obtained by principal component analysis. Ribeirão Preto, state of São Paulo, 2011–2012. (n = 785).

Food group (g/day) Feeding pattern

Traditional Brazilian Snacks Coffee Healthy
Rice 0.811 -0.014 0.015 0.015
Beans 0.738 -0.042 -0.024 0.125
Meats (red meat and chicken) 0.448 0.091 -0.047 -0.165
Snacks, pizzas and sandwiches -0.331 0.101 -0.232 -0.012
Pasta -0.291 0.155 0.118 -0.290
Breads 0.159 0.718 0.299 -0.049
Butter and margarine 0.222 0.547 0.321 -0.145
Cold meats 0.221 0.467 0.026 0.037
Milk and yogurt 0.134 0.448 -0.320 0.249
Hard and soft cheese -0.315 0.440 -0.168 0.221
Candies -0.141 0.330 -0.067 -0.180
Coffee and tea 0.051 0.067 0.787 -0.028
Sugar -0.009 0.134 0.651 0.114
Chocolate milk and cappuccino 0.101 0.467 -0.520 -0.080
Natural fruit juice -0.185 0.083 -0.070 0.616
Vegetables 0.383 0.048 -0.046 0.576
Soda and artificial juice 0.114 0.261 -0.208 -0.547
Fruits 0.021 0.022 0.074 0.544

Variance % 11.4 10.5 9.8 9.0
Cumulative variance % 11.4 22.0 31.8 40.8

a The foods whose factor loading is higher than 0.30 were kept in the matrix. Extraction method: principal component analysis. Rotation Method: Varimax with Kaiser normalization.

Factor loading values ≥ 0.3 or ≤ -0.3 are shown in bold.

Women with greater adherence to the “traditional Brazilian” pattern reported lower schooling, more time spent in physical activities, and lower pre-gestational BMI than women with greater adherence. There was also a difference in smoking frequency and family history of type 2 diabetes. The pregnant women with greater adherence to the “snacks” pattern were younger and reported more schooling and less time practicing physical activities than pregnant women with lower adherence. Those with higher adherence to the “coffee” pattern presented higher average age, a higher number of children and lower schooling than those with lower adherence. And women with greater adherence to the “healthy” pattern had a higher average age and reported more time spent on physical activities than women with lower adherence ( Table 2 ). However, some of these differences are not considered clinically relevant.

Table 2. Sociodemographic characteristics, anthropometric data and lifestyle according to dietary patterns during gestation. Ribeirão Preto, state of São Paulo, 2011–2012. (n = 785).

Mother characteristics All Pattern traditional Brazilian Pattern snack Pattern coffee Pattern healthy




1st tercile 3rd tercile 1st tercile 3rd tercile 1st tercile 3rd tercile 1st tercile 3rd tercile
With GDM/normoglycemic 139/646 58/203 40/222 48/213 43/219 43/218 48/214 45/216 50/212

  n (%)

Previous GDM 34 (4.3) 9 (3.4) 17 (6.5) 10 (3.8) 8 (3.1) 7 (2.7) 17 (6.5) 8 (3.1) 17 (6.5)
DM family history 205 (26.1) 67 (25.7) 82 (31.3)a 77 (29.5) 70 (26.7) 74 (28.4) 62 (23.7) 67 (25.7) 74 (28.2)
Smoking during pregnancy 71 (9.0) 16 (6.1) 33 (12.6) 26 (10.0) 24 (9.2) 20 (7.7) 29 (11.1) 26 (10.0) 18 (6.9)
BMI category according to gestational age                  
Low weight 27 (3.4) 6 (2.3) 12 (4.6) 11 (4.2) 10 (3.8) 11 (4.2) 6 (2.3) 12 (4.6) 10 (3.8)
Eutrophia 310 (39.5) 97 (37.2) 107 (40.8) 105 (40.2) 102 (38.9) 107 (41.0) 104 (39.7) 98 (37.5) 114 (43.5)
Overweight 261 (33.2) 84 (32.2) 92 (35.1) 74 (28.4) 94 (35.9) 88 (33.7) 84 (32.1) 79 (30.3) 87 (33.2)
Obesity 187 (23.8) 74 (28.4) 51 (19.5) 71 (27.2) 56 (21.4) 55 (21.1) 68 (26.0) 72 (27.6) 51 (19.5)

  Mean (SD)

Age (years) 27.6 (5.4) 28.1 (5.7) 27.0 (5.2) 28.5 (5.5) 26.8 (5.3)b 26.4 (4.8) 28.5 (5.8)b 26.7 (5.1) 28.6 (5.8)b
Schooling (years of study) 9.2 (2.7) 9.6 (2.6) 8.9 (2.7)b 8.7 (3.0) 9.6 (2.5)b 9.5 (2.3) 8.9 (2.9)b 9.0 (2.5) 9.3 (2.8)
Pre-gestational BMI (kg/m 2 ) 25.9 (5.0) 26.5 (5.2) 25.3 (4.6)b 26.4 (5.5) 25.5 (5.0) 25.5 (4.8) 26.0 (5.0) 26.1 (5.2) 25.3 (4.9)
Number of children 1.2 (1.2) 1.2 (1.2) 1.1 (1.2) 1.3 (1.3) 1.1 (1.2) 0.9 (1.1) 1.5 (1.4)b 1.2 (1.3) 1.2 (1.2)

  Median (P25; P75)

Physical activityd 40 (0; 140) 35 (0; 120) 60 (0; 150)c 50 (0; 150) 40 (0; 120)c 40 (0; 122) 50 (0; 140) 40 (0; 120) 60 (0; 150)c

GDM: gestational diabetes mellitus; DM: diabetes mellitus; BMI: body mass index

a p < 0.05, according to the X 2 test.

b p < 0.05, according to ANOVA.

c p < 0.05, according to the Kruskal-Wallis test.

d Physical activity (minutes per week of walking or exercise).

According to multinomial logistic regression models adjusted for age, gestational week at the time of the interview, schooling, smoking, number of children and physical activity, the pregnant women with greater adherence to the “traditional Brazilian” and “healthy” patterns showed less chance of obesity than those with lower adherence. Pregnant women classified as within the second tertile of adherence to the “snacks” pattern were more likely to be overweight than those in the first tertile, but this relationship was observed only at the intermediate level of adherence to the pattern ( Table 3 ).

Table 3. Association between dietary patterns during pregnancy with overweight and obesity. Ribeirão Preto, state of São Paulo, 2011–2012a. (n = 754).

Variable 1st tercile 2nd tercile 3rd tercile


OR 95%CI OR 95%CI
Traditional Brazilian pattern

Overweight          
Adjusted modelb 1.00 0.85 0.56–1.29 1.06 0.70–1.60
Obesity          
Adjusted modelb 1.00 0.70 0.45–1.08 0.61 0.38–0.96

Snacks pattern

Overweight          
Adjusted modelb 1.00 1.55 1.01–2.36 1.40 0.92–2.15
Obesity          
Adjusted modelb 1.00 0.88 0.56–1.38 0.86 0.55–1.35

Coffee pattern

Overweight          
Adjusted modelb 1.00 1.25 0.83–1.89 1.13 0.75–1.72
Obesity          
Adjusted modelb 1.00 1.27 0.81–2.00 1.12 0.71–1.76

Healthy pattern

Overweight          
Adjusted modelb 1.00 1.13 0.74–1.71 0.84 0.55–1.29
Obesity          
Adjusted modelb 1.00 0.89 0.57–1.38 0.52 0.33–0.83

a Multinomial logistic regression models, considering eutrophic models as reference.

b Multinomial logistic regression models adjusted for age, gestational week at the time of interview, schooling (years of study), smoking (never smoked, interrupted during gestation, and currently smokes), physical activity practice (minutes/week of walking for locomotion or physical exercise) and number of children.

In non-conditional logistic regression models adjusted for age, gestational week at the time of the interview, schooling, previous GDM, family history of DM, smoking, number of children and physical activity, it was found that women with higher adherence to the “traditional Brazilian” had a lower chance of GDM. However, this association was not independent of maternal excessive body weight ( Table 4 ).

Table 4. Relationship between dietary patterns during gestation and gestational diabetes mellitus. Ribeirão Preto, state of São Paulo, 2011–2012a. (n = 785).

Variable 1st tercile 2nd tercile 3rd tercile p trend


OR (95%CI) OR (95%CI)
Traditional Brazilian pattern        
Model 1b 1.00 0.64 (0.41–1.02) 0.62 (0.39–0.99) 0.04
Model 2c 1.00 0.66 (0.41–1.05) 0.64 (0.39–1.04) 0.06
Snacks pattern        
Model 1b 1.00 1.06 (0.67–1.69) 1.01 (0.63–1.63) 0.95
Model 2c 1.00 1.00 (0.63–1.61) 0.96 (0.59–1.55) 0.88
Coffee pattern        
Model 1b 1.00 1.01 (0.63–1.63) 0.97 (0.60–1.58) 0.91
Model 2c 1.00 1.00 (0.63–1.63) 0.97 (0.59–1.59) 0.92
Healthy pattern        
Model 1b 1.00 0.92 (0.57–1.48) 0.97 (0.61–1.56) 0.91
Model 2c 1.00 0.91 (0.57–1.47) 1.04 (0.64–1.68) 0.87

a Non-conditional logistic regression models, considering normoglycemic women as reference.

b Model 1 was adjusted for: age (years), gestational week at the time of the interview, previous GDM (yes/no), schooling (years of study), family history of DM (yes/no), smoking (never smoked, interrupted during gestation, or currently smokes), physical activity (minutes/week of walking or exercise) and number of children.

c Model 2: Additional adjustment for maternal excessive body weight (yes/no).

DISCUSSION

In this study, pregnant women with greater adherence to the “healthy” and “traditional Brazilian” patterns presented a lower chance of obesity. On the other hand, women classified in the intermediate level of adherence to the “snacks” pattern presented a greater chance of being overweight. Regarding GDM, the findings suggest that maternal excessive body weight portrays relevant causality with respect to the inverse association between the “traditional Brazilian” dietary pattern and GDM.

The prevalence of obesity has been increasing exponentially, which can be partially attributed to changes in the population’s eating behavior, where meal-based dietary patterns are replaced by those based on ready-to-eat industrialized products 20 . Our findings support this hypothesis, since women with greater adherence to the “traditional Brazilian” pattern, composed of typical food markers for meals, such as rice, beans, meats, vegetables, characterized by a lower consumption of snacks, pizzas and sandwiches, presented a lower chance of obesity.

The inverse association between adherence to the “healthy” pattern and obesity in pregnant women corroborates the scientific evidence of a possible protective effect of food intake with adequate nutrient intake and low caloric density in the energy balance. Fruits, vegetables are also high in fiber, which have the capacity to reduce gastric emptying time and promote satiety 21 . Moreover, the “healthy” pattern was inversely associated with the consumption of soda and artificial juices, which are considered relevant risk factors for obesity due to their high sugar content, high glycemic index and, consequently, low satiety capability. Sugary drinks are rapidly absorbed by the body and do not stimulate the signs of satiety in the same way as solid foods. Moreover, they are ineffective in stimulating insulin production, one of the physiological signals for energy balance 22 . In addition, women with greater adherence to “traditional Brazilian” and “healthy” patterns reported longer walking and exercise time, which could contribute to a greater energy expenditure and adequate weight maintenance 23 ; however, the associations were independent of physical activity practice.

The positive association found between the “snack” pattern and overweight is consistent with the literature 24 , 25 . However, in this study, this association was significant only for the second tertile, compared to the first. The “snacks” pattern consisted of breads, butter and margarine, cold meats, hard and soft cheese, and sweets, which suggests a pattern of food substitution from main meals to snacks. Frequent consumption of these foods with high energy density can lead to damage in the neuronal circuits involved with the regulation of appetite and satiety 26 .

Obesity is considered a significant risk factor for GDM. The accumulation of body fat, associated with physiological changes mediated by placental hormones in pregnancy, can increase insulin resistance and predisposition to GDM. It is known that DMG is due to both exacerbated insulin resistance and previous dysfunction of β-cells 27 . In this study, adjustment for maternal excessive body weight attenuated the association between the “traditional Brazilian” pattern and GDM.

Studies that investigated the relationship between dietary patterns during pregnancy and GDM are scarce and were conducted in regions with different eating habits to Brazilian culture, limiting the comparison of the findings 3 , 6 , 9 , 10 , 19 , 28 . A cohort study conducted in Singapore among 909 pregnant women showed that women with higher adherence to a pattern rich in vegetables, fruits, white rice, meats and fish with low consumption of potato chips, hamburgers and sugary drinks had a lower chance of GDM 10 . This pattern consists of some foods found in the “traditional Brazilian” and “healthy” standards of this study; however, these patterns were not related to the outcome.

Among the results of the study, a higher proportion of women with GDM were classified as within the highest tertile of the “healthy” pattern, which was not expected and cannot be explained in the literature. One of the hypotheses of the present study was an inverse association between adherence to the “healthy” pattern and GDM, which was not confirmed. According to the literature, the results are controversial 6 , 9 , 10 , 29 . It is suggested that dietary patterns rich in fruits and vegetables have a protective effect on the development of diseases such as GDM, given the low energy density, glycemic load and the high antioxidant and phytochemical content of these foods 21 . However, dietary habits are specific to each population, with different ethnicities and genetic predispositions, which could partially explain the disagreement between studies. Exposure to modifiable risk factors during the pre-gestational period, which was not considered in the present study, may also have influenced the results found.

A possible justification for the lack of association between the “healthy” and “snack” patterns and the outcomes analyzed is the fact that these food consumption patterns are more subject to social desirability bias. One study showed that individuals with higher social desirability tend to report higher consumption of fruits, vegetables, and lower food intake of breads and biscuits, thus attenuating associations 30 .

One cannot ignore the hypothesis that a voluntary change in food consumption may occur during pregnancy in order to promote the growth and development of the baby. However, the evidence regarding dietary changes in this life cycle is controversial 31 .

Evaluating dietary intake through analysis of dietary patterns is considered an adequate strategy, since it contemplates the diet as a whole, supplying the limitation of approaches that evaluate nutrients and food items alone 7 , 8 . Among the strengths of the study, we highlight the use of the multiple source method 19 for the estimation of the usual diet, and the use of the World Health Organization criteria from 2014 13 for the diagnosis of GDM, which were accepted by the International Federation of Gynecology and Obstetrics 32 . The main limitation of the study is its cross-sectional design, which made it impossible to identify a temporal relationship between dietary patterns and the outcomes investigated. Reverse causality may also have occurred, since 46% of the pregnant women evaluated had excessive body weight during the pre-gestational period. However, neither the pregnant women nor the interviewers knew the results of the diagnostic test for GDM at the time of the interview, which reduced the chance of information bias in the investigation of this outcome. Data on weight gain during the first trimester of pregnancy were not collected, which made it impossible to estimate the adequacy of weight gain; thus, the models were adjusted for excessive body weight according to gestational age as an indicator of both pre-gestational excessive body weight and excessive weight gain. Social desirability was not investigated in this study, making it impossible to confirm the hypothesis of reporting bias. Another limitation inherent to studies evaluating dietary data is a possible underreporting of dietary intake. In addition, the use of logistic regression in cross-sectional studies whose outcome is highly prevalent has been criticized by some authors. However, this measure of association was used because it is recommended for cross-sectional studies investigating the effect of an exploratory variable on the occurrence of a health outcome 33 . The data presented here suggest a lower chance of obesity among pregnant women with greater adherence to “traditional Brazilian” and “healthy” patterns. There was no association between dietary patterns and GDM regardless of maternal excessive body weight. Prospective studies are recommended to investigate the relationship between dietary patterns and excessive body weight and GDM, reducing the chance of reverse causality.

Footnotes

Funding: Research grant CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico, Process: 302498/2015-0 and 472221/2010-8), FAEPA (Fundação de Apoio ao Ensino, Pesquisa e Assistência do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo) and USP (Pró-Reitoria de Pesquisa da Universidade de São Paulo). Doctoral scholarship DCCZ and LCC CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior).

REFERENCES

  • 1.American Diabetes Association Standards of Medical Care in Diabetes 2017. Diabetes Care. 2017;40(Suppl 1):S11–S24. doi: 10.2337/dc17-0299. [DOI] [PubMed] [Google Scholar]
  • 2.Sociedade Brasileira de Diabetes . VI Diretrizes da Sociedade Brasileira de Diabetes 2015- 2016. São Paulo: SBD; 2016. [Google Scholar]
  • 3.Schoenaker DAJM, Mishra GD, Callaway LK, Soedamah-Muthu SS. The role of energy, nutrients, foods, and dietary patterns in the development of gestational diabetes mellitus: a systematic review of observational studies. Diabetes Care. 2016;39(1):16–23. doi: 10.2337/dc15-0540. [DOI] [PubMed] [Google Scholar]
  • 4.International Diabetes Federation . Diabetes atlas. 7. Brussels (BE): IDF; 2015. [Google Scholar]
  • 5.Scientific Advisory Committee on Nutrition . The influence of maternal, fetal and child nutrition on the development of chronic disease in later life. London: TSO; 2011. [cited 2018 Apr 14]. https://www.gov.uk/government/uploads/system/uploads/attachment_data/file/339325/SACN_Early_Life_Nutrition_Report.pdf. [Google Scholar]
  • 6.Chen X, Zhao D, Mao X, Xia Y, Baker PN, Zhang H. Maternal dietary patterns and pregnancy outcome. 351Nutrients. 2016;8(6) doi: 10.3390/nu8060351. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Cespedes EM, Hu FB. Dietary pattern: from nutritional epidemiologic analysis to national guidelines. Am J Clin Nutr. 2015;101(5):899–900. doi: 10.3945/ajcn.115.110213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Wirfält E, Drake I, Wallstrom P. What do review papers conclude about food and dietary pattern? Food Nutr Res. 2013;57 doi: 10.3402/fnr.v57i0.20523. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.He JR, Yuan MY, Chen NN, Lu JH, Hu CY, Mai WB, et al. Maternal dietary patterns and gestational diabetes mellitus: a large prospective cohort study in China. Br J Nutr. 2015;113(8):1292–1300. doi: 10.1017/S0007114515000707. [DOI] [PubMed] [Google Scholar]
  • 10.Seymour J, Chia A, Colega M, Jones B, McKenzie E, Shirong C, et al. Maternal dietary patterns and gestational diabetes mellitus in a multi-ethnic Asian cohort: The GUSTO study. Nutrients. 2016;8(9):E574. doi: 10.3390/nu8090574. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Shin D, Lee KW, Song WO. Dietary patterns during pregnancy are associated with risk of gestational diabetes mellitus. Nutrients. 2015;7(11):9369–9382. doi: 10.3390/nu7115472. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Barbieiri P, Nunes JC, Torres AG, Nishimura RY, Zuccolotto DC, Crivellenti LC, et al. Indices of dietary fat quality during midpregnancy is associated with gestational diabetes. Nutrition. 2016;32(6):656–661. doi: 10.1016/j.nut.2015.12.002. [DOI] [PubMed] [Google Scholar]
  • 13.World Health Organization Diagnostic criteria and classification of hyperglycemia first detected in pregnancy: a World Health Organization guideline. Diabetes Res Clin Pract. 2014;103(3):341–363. doi: 10.1016/j.diabres.2013.10.012. [DOI] [PubMed] [Google Scholar]
  • 14.Trujillo J, Vigo A, Reichelt A, Duncan BB, Schmidt MI. Fasting plasma glucose to avoid a full OGTT in the diagnosis of gestational diabetes. Diabetes Res Clin Pract. 2014;105(3):322–326. doi: 10.1016/j.diabres.2014.06.001. [DOI] [PubMed] [Google Scholar]
  • 15.Takito MY, Neri LCL, Benício MSA. Avaliação da reprodutibilidade e validade de questionário de atividade física para gestante. Rev Bras Med Esporte. 2008;14(2):132–138. doi: 10.1590/S1517-86922008000200010:132-8. [DOI] [Google Scholar]
  • 16.Atalah Samur E, Castillo-L C, Castro Santoro R, Aldea-P A. Propuesta de un nuevo estándar de evaluación nutricional en embarazadas. Rev Med Chile. 1997;125(12):1429–1436. [PubMed] [Google Scholar]
  • 17.Universidade Estadual de Campinas. Núcleo de Estudos e Pesquisas em Alimentação . Tabela brasileira de composição de alimentos – TACO. 2. Campinas: NEPA; 2006. http://www.crn1.org.br/wp-content/uploads/2015/04/taco.pdf?x53725. [Google Scholar]
  • 18.Anção MS, Cuppari L, Daibe AS, Sigulem D. Programa de Apoio à Nutrição – NutWin, versão 1.5. são Paulo: Departamento de Informática em saúde. UNIFESP/EPM; 2002. [Google Scholar]
  • 19.Harttig U, Haubrock J, Knüppel S, Boeing H, EFCOVAL Consortium The MSM program: web-based statistics package for estimating usual dietary intake using the Multiple Source Method. Eur J Clin Nutr. 2011;65(Suppl 1):S87–S91. doi: 10.1038/ejcn.2011.92. [DOI] [PubMed] [Google Scholar]
  • 20.Monteiro CA, Cannon G, Maubarac JC, Levy RB, Louzada MLC, Jaime PC. The UN Decade of Nutrition, the NOVA food classification and the trouble with ultra-processing. Public Health Nutr. 2017;21(1):5–17. doi: 10.1017/S1368980017000234. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Zhang C, Liu S, Solomon CG, Hu FB. Dietary fiber intake, dietary glycemic load, and the risk for gestational diabetes mellitus. Diabetes Care. 2006;29(10):2223–2230. doi: 10.2337/dc06-0266. [DOI] [PubMed] [Google Scholar]
  • 22.Woodward-Lopez G, Kao J, Ritchie L. To what extent have sweetened beverages contributed to the obesity epidemic? Public Health Nutr. 2010;14(3):499–509. doi: 10.1017/S1368980010002375. [DOI] [PubMed] [Google Scholar]
  • 23.Wall CR, Gammon CS, Bandara DK, Grant CC, Carr PEA, Morton SMB. Dietary patterns in pregnancy in New Zealand: influence of maternal socio-demographic, health and lifestyle factors. Nutrients. 2016;8(5):E300. doi: 10.3390/nu8050300. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Rohatgi KW, Tinius RA, Cade WT, Steele EM, Cahill AG, Parra DC. Relationships between consumption of ultra-processed foods, gestational weight gain and neonatal outcomes in a sample of US pregnant women. Peer J. 2017;5 doi: 10.7717/peerj.4091. e4091. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Uusitalo U, Arkkola T, Ovaskainen ML, Kronberg-Kippilä C, Kenward MG, Veijola R, et al. Unhealthy dietary patterns are associated with weight gain during pregnancy among Finnish women. Public Health Nutr. 2009;12(12):2392–2399. doi: 10.1017/S136898000900528X. [DOI] [PubMed] [Google Scholar]
  • 26.Lamyian M, Hosseinpour-Niazi S, Mirmiran P, Banaem LM, Goshtasebi A, Azizi F. Pre-pregnancy fast food consumption is associated with gestational diabetes mellitus among Tehranian women. Nutrients. 2017;9(3):E216. doi: 10.3390/nu9030216. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Ashwal E, Hod M. Gestational diabetes mellitus: where are we now? Clin Chim Acta. 2015;451(Pt A):14–20. doi: 10.1016/j.cca.2015.01.021. [DOI] [PubMed] [Google Scholar]
  • 28.Tryggvadotir EA, Medek H, Birgisdottir BE, Geirsson RT, Gunnarsdottir I. Association between healthy maternal dietary pattern and risk for gestational diabetes mellitus. Eur J Clin Nutr. 2016;70(2):237–242. doi: 10.1038/ejcn.2015.145. [DOI] [PubMed] [Google Scholar]
  • 29.Flynn AC, Seed PT, Patel N, Barr S, Bell R, Briley AL, et al. Dietary patterns in obese pregnant women; influence of behavioral intervention of diet and physical activity in the UPBEAT randomized controlled trial. 124Int J Behav Nutr Phys Act. 2016;13(1) doi: 10.1186/s12966-016-0450-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Barros R, Moreira P, Oliveira B. Influência da desejabilidade social na estimativa da ingestão alimentar obtida através de um questionário de frequência de consumo alimentar. Acta Med Port. 2005;18(4):241–247. [PubMed] [Google Scholar]
  • 31.Hillier SE, Olander EK. Women’s dietary changes before and during pregnancy: a systematic review. Midwifery. 2017;49:19–31. doi: 10.1016/j.midw.2017.01.014. [DOI] [PubMed] [Google Scholar]
  • 32.Hod M, Kapur A, Sacks DA, et al. The International Federation of Gynecology and Obstetrics (FIGO) Initiative on gestational diabetes mellitus: A pragmatic guide for diagnosis, management, and care. Int J Gynecol Obstet. 2015;131:173–272. doi: 10.1016/S0020-7292(15)30007-2. [DOI] [PubMed] [Google Scholar]
  • 33.Reichenheim ME, Coutinho ESF. Measures and models for causal inference in cross-sectional studies: arguments for the appropriateness of the prevalence odds ratio and related logistic regression. 66BMC Med Res Methodol. 2010;10 doi: 10.1186/1471-2288-10-66. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Revista de Saúde Pública are provided here courtesy of Universidade de São Paulo. Faculdade de Saúde Pública.

RESOURCES