Next Article in Journal
Association of Maternal Erythrocyte PUFA during Pregnancy with Offspring Allergy in the Chinese Population
Previous Article in Journal
Effects of a New Multicomponent Nutritional Supplement on Muscle Mass and Physical Performance in Adult and Old Patients Recovered from COVID-19: A Pilot Observational Case–Control Study
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Reproducibility and Relative Validity of a Food Frequency Questionnaire for Identifying Iron-Related Dietary Patterns in Pregnant Women

by
Mayra Lizeth Navarro-Padilla
1,
María Fernanda Bernal-Orozco
2,
Joan Fernández-Ballart
3,4,
Barbara Vizmanos
2,
Norma Patricia Rodríguez-Rocha
5 and
Gabriela Macedo-Ojeda
6,*
1
Health Sciences University Center, University of Guadalajara, Guadalajara 44340, Mexico
2
Institute of Translational Nutrigenetics and Nutrigenomics, Department of Clinics of Human and Health Reproduction, Growth and Child Development, Health Sciences University Center, University of Guadalajara, Guadalajara 44340, Mexico
3
Area of Preventive Medicine and Public Health, Faculty of Medicine and Health Sciences, Universitat Rovira i Virgili, IISPV, 43201 Reus, Spain
4
CIBERobn (CB06/03) Instituto de Salud Carlos III, 28029 Madrid, Spain
5
Department of Public Health, Regional Institute for Public Health Research, Health Sciences University Center, University of Guadalajara, Guadalajara 44340, Mexico
6
Department of Public Health, Institute of Research in Biomedical Sciences, Health Sciences University Center, University of Guadalajara, Guadalajara 44340, Mexico
*
Author to whom correspondence should be addressed.
Nutrients 2022, 14(11), 2313; https://doi.org/10.3390/nu14112313
Submission received: 15 April 2022 / Revised: 22 May 2022 / Accepted: 28 May 2022 / Published: 31 May 2022
(This article belongs to the Section Nutritional Epidemiology)

Abstract

:
Analyzing pregnant women’s iron intake using dietary patterns would provide information that considers dietary relationships with other nutrients and their sources. The objective of this study was to evaluate the reproducibility and relative validity of a Qualitative Food Frequency Questionnaire to identify iron-related dietary patterns (FeP-FFQ) among Mexican pregnant women. A convenience sample of pregnant women (n = 110) completed two FeP-FFQ (FeP-FFQ1 and FeP-FFQ2) and a 3-day diet record (3DDR). Foods appearing in the 3DDR were classified into the same food groupings as the FeP-FFQ, and most consumed foods were identified. Exploratory factor analysis was used to determine dietary patterns. Scores were compared (FeP-FFQ for reproducibility and FeP-FFQ1 vs. 3DDR for validity) through intraclass correlation coefficients (ICC), cross-classification, Bland–Altman analysis, and weighed Cohen kappa (κw), using dietary patterns scores tertiles. Two dietary patterns were identified: “healthy” and “processed foods and dairy”. ICCs (p < 0.01) for “healthy” pattern and “processed foods and dairy” pattern were 0.76 for and 0.71 for reproducibility, and 0.36 and 0.37 for validity, respectively. Cross-classification and Bland–Altman analysis showed good agreement for reproducibility and validity; κw values showed moderate agreement for reproducibility and low agreement for validity. In conclusion, the FeP-FFQ showed good indicators of reproducibility and validity to identify dietary patterns related to iron intake among pregnant women.

Graphical Abstract

1. Introduction

Anemia is a health problem that affects over 1.5 billion people worldwide, and its prevalence is higher among >5-year-old children and pregnant women [1]. Thus, it is considered one of the leading global public health challenges. In Mexico, the health of women of reproductive age is affected by conditions such as high blood pressure (6.8% in women aged 20–39 years), hypercholesterolemia (18.6% in women aged 20–39 years), overweight (26.9% in adolescents; 36.3% in women aged 20–49 years) and obesity (14.1% in adolescents, 38.5% in women aged 20–49 years). The prevalence of anemia among women between 12–49 years of age is 17.5% for non-pregnant women while it is almost twice as high for pregnant women (34.9%) [2]. During pregnancy, anemia is associated with intrauterine growth restriction, low birthweight [3], perinatal death, and maternal mortality from hemorrhage [4].
According to the World Health Organization (WHO), anemia during pregnancy is defined as <11.0 g/dL hemoglobin concentrations during the first and third trimesters and <10.5 g/dL during the second trimester [5,6]. Among pregnant women, the world prevalence of anemia is 40.1% [7], and it can be as higher as 56% among low and middle-income countries [8], with iron deficiency being the most common cause.
During pregnancy, iron is essential because it is a crucial component of hemoglobin for oxygen supply, and it is necessary for diverse enzymatic reactions [9]. Thus, requirements and intestinal absorption are increased due to the expansion of red blood cell numbers and the transfer of higher iron quantities to the placental structures and fetus, especially during the second and third trimesters of pregnancy [4].
Iron intake is an important modifiable factor affecting iron status during pregnancy [10]. Pregnant women’s iron levels depend on different aspects: the quantity consumed through foods and supplements, the gestational trimester, body iron stores (requirement of at least 500 mg [11]), and iron-type (heme and non-heme). However, the consumed iron absorption process is the factor that most affects body iron bioavailability and homeostasis [12,13].
Non-heme iron absorption is affected by promoters like vitamin C, vitamin A and peptides containing cysteine and fiber, and inhibitors such as tannins, phytates, polyphenols, phosphorus, and calcium [14]. In contrast, heme iron is inhibited only in the presence of calcium [12].
Because nutrients are not consumed separately but in combination, it is crucial to consider pregnant women’s diet in its entirety when dietary factors associated with iron status are investigated [15]. For this purpose, analyzing dietary patterns is highly useful because these consider the whole diet, how the foods are consumed, and their different combinations. Therefore, their use might overcome the limitations of studying foods and nutrients individually and their associations between dietary intake and iron status [16].
An initial nutriments screening of pregnant women is needed to assess the prevalence of anemia during pregnancy. The Food Frequency Questionnaire (FFQ) is the most used tool to assess diet because it provides long-term diet intake data [15,17]. Numerous studies have used FFQs to establish diverse macro-and micro-nutrient dietary patterns. However, very few have reported the validity and reproducibility of FFQ to determine iron-related dietary patterns [18].
Therefore, this study aimed to design and validate a FFQ to identify iron-related dietary patterns among pregnant women.

2. Materials and Methods

2.1. Study Participants

The research was conducted in Guadalajara, Mexico, from March to September 2018, including pregnant women between 20 and 40 years of age, in either their second or third trimester of pregnancy and attending outpatient service at the Maternal and Child Hospital “Esperanza López Mateos”, a public hospital providing attention to pregnant adolescents and low-income women without social security. Exclusion criteria were women with multiple pregnancies, chronic disease diagnostic, or pregnancy complications (specifically, preeclampsia and gestational diabetes; gastrointestinal disorders were nor considered as exclusion criteria).
A convenience sampling with consecutive cases was used. The recommended sample size for the validity of semiquantitative food frequency questionnaires is 110 participants, approximately, considering a power of 80% and α = 0.5 [19]. Based on this, 140 participants were included at the beginning of the study, considering possible follow-up losses.

2.2. Study Design

The participants completed the qualitative Food Frequency Questionnaire through an interview to identify iron-related dietary patterns (FeP-FFQ) at baseline (FeP-FFQ1), which could be at either their 2nd or 3rd gestational trimester. During this first interview, sociodemographic and anthropometric data were collected, and participants were trained on how to complete a three-day diet record (3DDR), with two weekdays and one weekend day. The training was provided during the first interview and consisted of explaining how to fill out the diaries with five steps: the time and place of the meal, name of the dish, dish ingredients, type of ingredient (e.g., whole milk, light milk), amount consumed. These steps were also written on the diet record form along with an entry example. Participants were also instructed on standard cooking measures (tablespoon, teaspoon, cups). At the end of the training, participants were asked to write down one entry example to verify the instructions were clear and clarify questions. Participants were also instructed to take pictures of their reported meals and drinks whenever possible. They were asked to submit their 3DDR at their next interview and were contacted by phone in advance to verify they had no questions. One month later, the participants submitted their 3DDR and it was verified that they had been completed correctly; at this point in time they also completed the second FeP-FFQ (FeP-FFQ2).

2.3. FeP-FFQ Development and Application

The FeP-FFQ is an adaptation of Beck et al.’s [18] qualitative Fe-FFQ. Foods rich in iron, calcium, vitamin C, vitamin A, and fiber were added, considering those of frequent consumption in Mexico. Following Zhou’s [20] suggestion, foods with at least 3% of the daily iron recommended intake for Mexican pregnant women were included (SAME [21]). The qualitative FeP-FFQ includes a total of 76 items divided into ten categories: vegetables; fruits; grains and starchy foods; legumes; meat, poultry, cured meats and eggs; fish and seafood; dairy; snacks, sweets and desserts; alcoholic beverages; and other beverages. Participants were asked how often they ate each food during pregnancy, with nine answer options: never or rarely, 1–3 times/month, once a week, 2–4 times/week, 5–6 times/week, once a day, 2–3 times/day, 4–6 times/day, and ≥7 times/day.

2.4. Measurements

Procedures for data collection are presented below.

2.4.1. Sociodemographic, Anthropometric Data and Iron Status

Sociodemographic (e.g., age, sex, civil status, education, socioeconomic status) and anthropometric (e.g., pregestational weight, current weight, height) data were collected at the moment participants were recruited, when they could be at either the 2nd or 3rd trimester of pregnancy. Data were collected through a questionnaire designed for this study and applied by a trained nutritionist. Socioeconomic status was evaluated and classified using the AMAI (Mexican Association of Market Intelligence and Opinion Agencies) [22] scores. Weight was measured using a Tanita scale, model TBF-300A with a 0.1 kg precision, and height was measured with a Seca portable stadiometer, model 213. Age was calculated from the participants’ birthdates. Current and pregestational body mass indexes (BMI) were calculated by dividing weight in kilograms by height in meters squared. Current BMI was classified using the Atalah curves for the Latin-American population [23]. Hemoglobin status data were obtained from the medical records at the 3rd trimester of pregnancy.

2.4.2. Diet Records

During the first interview, women received the 3DDR form, were instructed on how to fill it correctly, and were asked to submit it four weeks later, during their second appointment. Each participant filled two diet records of weekdays and one of a weekend day, specifying mealtime, place, and time of consumption. They were asked to write down the name of the dish and each ingredient and the type of food (e.g., whole milk, skim milk, lactose-free milk); and when possible, to take photos of all meals and drinks consumed during the three reported days. During the second appointment, 3DDRs were collected and screened for missing information. Subsequently, all foods in the records were counted, added up, and categorized manually according to the 76 items in the FeP-FFQ. For analysis purposes, when participants reported consuming two different food items of the same group at the same mealtime (e.g., strawberries and orange), it was registered as a two-time consumption of the food group, except for water, which was registered as one intake for every 250 mL consumed during a day. For dishes where the participants provided recipes, ingredients were assigned individually to the corresponding FeP-FFQ item. Some of the foods reported in the 3DDR did not match any of the FeP-FFQ items, which were excluded from analyses.

2.5. Statistical Analysis

Descriptive analytics were performed for quantitative variables and are presented as means and standard deviations (SD), while qualitative variables are presented as frequencies and percentages.
To evaluate the reproducibility and relative validity of each FeP-FFQ item, the intake frequency was adjusted for each participant and each food consumed by using the midpoint as the level of consumption. Then values were converted to weekly intake frequency (e.g., 1–3 times/month = 2 times/month = 0.5 times/week). These weekly values were later converted to a 3-day consumption frequency to align with the 3DDR (e.g., 0.5 times/week divided by seven and multiplied by 3 = 0.21 times in 3 days). Additionally, all food items reported in the 3DDRs were categorized into the 76 items of the FeP-FFQ.

2.5.1. Identification of the Most Frequently Consumed Food Items

To identify dietary patterns, first, the most frequently consumed food items were identified by obtaining the means and standard deviations of the consumption frequency of each food item from the 3DDR, FeP-FFQ1, and FeP-FFQ2. Food items not identified as frequent consumption in the 3DDR and both FeP-FFQ were excluded from the factor analyses. Thirty-two out of the 76 items emerged as of higher frequency of consumption.

2.5.2. Identification of Dietary Patterns from the FeP-FFQs and the Diet Records

Spearman correlation was performed to measure the reproducibility of the most frequently consumed food items from the questionnaire (FeP-FFQ1 and FeP-FFQ2), while for relative validity, Pearson’s linear correlation was used for the consumption frequency of each item in the FeP-FFQ1 and 3DDR. Paired t-tests were used to compare food items’ intake frequency mean differences: FeP-FFQ1 vs. FeP-FFQ2 for reproducibility; and FeP-FFQ1 vs. 3DDR for relative validity, with a significant p-value of <0.05. The effect size was obtained for the significant differences between the questionnaires using the formula: effect size r = √t2/(t2 + df) (where t = t statistic produced by paired t-test and df = degrees of freedom). An effect size of 0.1 indicates a small effect, 0.3 a medium effect, and ≥0.5 a large effect [22].
Subsequently, a factor analysis with varimax rotation was used for FeP-FFQ1, FeP-FFQ2, and 3DDR to identify dietary patterns. The Kaiser–Meyer–Olkin measure of sampling adequacy and Bartlett’s test p values were used to determine the presence of relationships between variables in the factor analysis, with values of >0.5 and <0.05, respectively.
The relative validity and reproducibility of dietary patterns derived from FeP-FFQ1 were examined by calculating Pearson linear correlation coefficients, ICC, and cross-classification between diet pattern scores obtained from FeP-FFQ1 and the 3DDR (relative validity), and FeP-FFQ1 and FeP-FFQ2 (reproducibility).
Finally, diet pattern scores were divided into tertiles and reproducibility (FeP-FFQ1 vs. FeP-FFQ2) and validity (FeP-FFQ vs. 3DDR) analyses were complemented with the Bland–Altman method and weighted Kappa Cohen coefficient to assess the level of agreement between methods based on Landis and Koch [24] classification, where κw values between 0.21 and 0.40 indicate fair agreement, between 0.41 and 0.60 moderate agreement, between 0.61 and 0.80 good agreement, and >0.81 very good agreement.
All statistical analyses were performed using IBM-SPSS software version 21.

3. Results

3.1. Participant Characteristics

A total of 140 women were initially invited to participate and completed the first FeP-FFQ; 30 were excluded because they did not complete all the required questionnaires; therefore, 110 participants completed the study. Participant characteristics are detailed in Table 1. Mean age was 26.89 years (SD 5.58). The mean monthly family income was 409.82 USD (SD 315.52), and from this, 199.42 USD (SD 77.84) is used as a monthly food stipend. Most of the participants live in free union (54.5%), have an education level of secondary school (46.4%), are housewives (80.9%), have a family composed of a mother, father, and children (73.6%), and are low-middle class (31.8%). The mean pregestational BMI was 26.0 kg/m2 (SD 5.7), and the majority of participants were classified as “normal weight” (43.6%). In contrast, the mean current BMI was 28.8 kg/m2 (SD 5.6) and “overweight” was the most common classification among participants (35.5%).

3.2. Food Intake Frequency

From the three questionnaires (FeP-FFQ1, FeP-FFQ2 y 3DDR), 32 food items with the most frequent consumption were obtained (Table 2). Mean consumption fluctuated between 15.54 (for water) to 0.90 (for sausages and ham) times/3 days. Slight differences in frequency of consumption were found for the 32 items between FeP-FFQ2 and 3DDR compared to FeP-FFQ1. On the other hand, the mean intake frequency reported was higher in both FeP-FFQs than in the 3DDR for the 32 food items except water and beef. For most items, consumption frequency was significantly different between FeP-FFQ1 and 3DDR. This contrasts with the comparison between both FeP-FFQs, where significant differences were only found for 10 out of 32 items. Through paired t-tests, it was found that the consumption frequency was overestimated for FeP-FFQ1 in 19 out of 32 items (59.4% of the foods) compared to the 3DDR (p < 0.01): corn tortilla, tomato, citrus fruits, lime, stone fruits, homemade beans, banana and fried plantain, apple, lettuce, carrot, melon, watermelon, sour cream, rice, yogurt (drinking yogurt included), pasta soup, papaya, ice-cream/sorbet/popsicles, and beef.

3.3. Identification of Dietary Patterns

The Kaiser–Meyer–Olkin measure of sampling adequacy was 0.761 for FeP-FFQ1, 0.640 for FeP-FFQ2, and 0.491 for 3DDR (>0.5 acceptable), and Bartlett’s test p values were all 0.001 (<0.001 acceptable). Identified dietary patterns were: (a) “healthy” dietary patterns consisting of chilies, lime, onion, banana, apple, citrus fruits, melon, stone fruits, carrot and papaya; and (b) “industrialized food and dairy” pattern including soda, ice-cream, rice, pasta soup, sausages, and cheese (Table 3). The dietary patterns obtained from the FeP-FFQ1, FeP-FFQ2, and 3DDR explained 31.81%, 27.84%, and 17.24% of the variance in the food intake scores for each dietary pattern, respectively.

3.4. Reproducibility and Validity of Dietary Patterns

Pearson correlation coefficients for the reproducibility of the dietary pattern scores from the factorial analysis between FeP-FFQ1 and FeP-FFQ2 suggested good reproducibility: 0.60 for the “healthy” pattern and 0.55 for the “industrialized food and dairy” pattern (p < 0.01); while the ICC were 0.76 and 0.71 (<0.01), respectively. Validity correlations of the dietary pattern scores between FeP-FFQ1 and 3DDR were: 0.11 for the “healthy” pattern (p > 0.05) and 0.20 for the “industrialized food and dairy” pattern (p < 0.05). ICC for the validity of the dietary pattern scores were 0.36 for the “healthy” pattern and 0.37 for the “industrialized food and dairy” pattern (p < 0.01). Cross-classification of the reproducibility of dietary pattern scores found 58.2% of participants classified in the same third for “healthy” and 51.9% for “industrialized food and dairy” pattern. A low percentage was classified in the opposite third for the “healthy” pattern (5.5%) and 11.9% for the “industrialized food and dairy” pattern.
Moreover, a fair and significant agreement for the validity of both patterns was found (κw = 0.12 for ”healthy” and κw = 0.14 for “industrialized food and dairy”); and a moderate and significant agreement for reproducibility of the “healthy” pattern (κw = 0.47) and “industrialized food and dairy” pattern (κw = 0.32).
Bland–Altman plots compare reproducibility between FeP-FFQ1 and FeP-FFQ2; and validity between FeP-FFQ1 and 3DDR of dietary patterns scores (Figure 1 and Figure 2, respectively). The x-axis shows dietary pattern mean score, and the y-axis, the difference between scores, FeP-FFQ1 vs. FeP-FFQ2 for reproducibility and FeP-FFQ1 vs. 3DDR for validity.
It is noteworthy that the means for reproducibility and validity of both patterns was equal to zero. This allows identifying the agreement magnitude visually between both methods, in this case, of FeP-FFQ and 3DDR. Dotted lines show the agreement limits between both methods, and they are situated at ±1.96 SD from the mean agreement. The plot shows that most dietary pattern scores fall within the agreement limits.

4. Discussion

This study shows the relative reproducibility and validity of a qualitative food frequency questionnaire to identify iron-related dietary patterns (FeP-FFQ) among Mexican pregnant women. This is relevant considering the high prevalence of anemia among Mexican pregnant women (34.9%) [2], which is similar to the global prevalence (36.5%) [1] and because this prevalence doubled from 2012 to 2018, going from 17.9% to 34.9% [2]. Moreover, the anemia prevalence among Mexican pregnant women is significantly higher than in non-pregnant women, highlighting the importance of having a tool that helps to evaluate the iron-related dietary patterns among this population.

4.1. Reproducibility and Validity of FeP-FFQ

The FeP-FFQ showed sufficient reproducibility and validity indicators in the food items to identify iron-related dietary patterns in pregnant women. Moreover, this affirmation is supported by the obtained reproducibility coefficients (r > 0.3) for the items most frequently consumed. Other studies have reported correlation coefficients similar to those in this study [15,18,26,27]. Regarding the time interval in the administration of the questionnaires, it should be noted that in the present study, an interval of one month was used between the administration of FeP-FFQ1 and FeP-FFQ2, obtaining reproducibility coefficients greater than those expected. In contrast, the studies by Rodríguez [27] y Glabska [15] used wider intervals (one year and six weeks, respectively) to evaluate questionnaire reproducibility. The obtained coefficients were similar to those in this study (r > 0.3). On the other hand, the variability of the obtained coefficients could be explained by diverse factors: (a) the statistical analyses used: in this study, only the Spearman method with qualitative variables of frequency intake was used, while Baer [28] used the Pearson method quantitatively and adjusted to the total energy intake. (b) Participants characteristics: the present study included women between 20 and 40 years of age, although studies in other countries have included adolescent pregnant women; thus, the differences observed between these populations could be explained by the differences in the diet of adolescents [26,29].
The FeP-FFQ obtained validity correlation coefficients of >0.3 for the most frequently consumed items, similar to the values reported by Robinson [30], Galante [31], and Brunst [32]. However, other studies have reported slightly higher validity coefficients (r > 0.6) [29,33,34]. These differences could be attributed to diverse factors: the design of the questionnaire, including the number of items, seasonality, and time-frame can contribute to the coefficients’ variability between studies; the variability in the methodology used, for example, the reference standard used as a method for validation may also contribute [35,36,37]. The reference standards most commonly used are diet records (DR), 24h-R, and the biochemical markers [17,27,35,36,38]. Generally, 24h-R and DR cannot represent the habitual consumption of the period of interest since they often contain errors and underestimate the intake of nutrients by almost 20% [36]. Therefore, correlation coefficients between both methods for most foods and nutrients are between 0.4 and 0.7 [36]. Nevertheless, DRs are deemed the best comparison method available [19]. The present study used one DR as the reference standard, a method used by different studies that obtained similar validity coefficients [15,18,26,29,30,39,40,41,42].

4.2. Reproducibility and Validity of Dietary Patterns

Dietary patterns offer information about the characteristic combinations of the foods consumed by individuals or groups. The methodology to define them is relatively new and has become increasingly popular in nutrition epidemiology to evaluate a diet as an alternative to nutrient-based analyses [43,44,45,46,47,48]. The factorial analysis uses reported information from different instruments to identify common underlying dimensions (factors or patterns), where food intake or several foods are integrated through scores [43,46,47]. Subsequently, these are labeled, but this method can be subjective; sometimes it tends to confuse the population because it is done based on the foods patterns [46].
In the present study, the first dietary pattern was labeled “healthy”, similar to the patterns reported by some other studies [18,45,47,49]. “Industrialized food and dairy” was the label for the second pattern, which was not found in similar studies screened by the authors [18,43,44,45,46,47,48,49]. Few studies have examined the validity and reproducibility of dietary patterns obtained through factorial analysis [48].
In this study, Pearson correlation coefficients for reproducibility of the dietary pattern scores were 0.60 for the “healthy” pattern and 0.55 for the “industrialized food and dairy” pattern. These results are very similar to the ones reported in another three studies analyzing reproducibility of dietary pattern scores [43,45,48]; however, these studies did not analyze iron-related dietary patterns.
Validity correlation coefficients obtained in this study were “good”, with 0.11 for the “healthy” dietary pattern and 0.20 for the “industrialized food and dairy” pattern. Other studies have reported higher dietary pattern scores correlation values for validity [18,43,44,45,46,47,48]. For example, Beck et al. [18] reported reproducibility and validity coefficients higher than those in the present study. These discrepancies could be attributed to the population characteristics. Our study included pregnant women from 20 to 40 years of age, mainly with secondary school studies and a medium-low socioeconomic status, while Beck [18] included women between 18 and 44 years of age, not pregnant, with high education studies and high socioeconomic status. In this regard, Teixeira y col. [50] reported that age, education level, and socioeconomic status were directly associated with Brazilian pregnant women’s dietary patterns; furthermore, they suggested there is a need for additional resources to allow vulnerable mothers to have an adequate diet during pregnancy.
The present research is the first study of its type that complemented its results with ICC for the reproducibility and validity of both patterns. However, the values for validity (“healthy” = 0.36 and “industrialized food and dairy” = 0.37) were not as good as the ones for reproducibility (“healthy” = 0.76 and “industrialized food and dairy” = 0.71). Because correlation coefficients can underestimate the level of agreement with actual intake between the reference method and the new method [35,51], this study additionally used the Bland–Altman analysis to evaluate the level of agreement between methods. The mean difference of the scores for both dietary patterns was equal to zero, similar to the result reported by Beck et al. [18] for their validated dietary patterns.
The “healthy” and “industrialized food and dairy” dietary patterns scores for FeP-FFQs and 3DDR were classified into tertiles. Both patterns were classified for the same third: 58.2% and 51.9%, and opposite third: 5.5% and 11.9%, respectively. Similar results were reported by Beck [18], finding that “healthy” and “sandwich and drinks” patterns classified in the same third: 52.17% and 54.78%; and opposite third: 52.17% and 54.78%, respectively.
In our study, weighted Cohen’s kappa coefficient was used to quantify the relative importance between agreements and different levels of disagreement [52]. The agreement for relative validity was fair and significant for both dietary patterns, in contrast to the moderate agreement for validity found by Beck [15]. On the other hand, both dietary patterns showed a moderate reproducibility, similar to the one reported by Beck [18]. It is noteworthy that the use of weighted Cohen’s kappa is controversial, given that its magnitude depends on the number of categories used and the weights applied, since the maximum weight is given to perfect agreement and proportionally lower weights according to the level of agreement [51,53].

4.3. Limitations and Strengths

This study presents some limitations, which are listed next. The use of 3DDR as a reference standard for validity could have been biased if the participants made mistakes in their reported intake; regardless, participants were trained to minimize these potential mistakes. Additionally, it has been reported that people tend to change their habitual intake when they know they are under evaluation [19], which may cause the wrong estimation of the actual intake. Nonetheless, it was decided to use this method because it minimizes potential memory biases of the 24h-R and reduces the time of administration, though they must be screened in detail through interviews. A card with the nine consumption frequencies suggested by Walter Willet [19] was used to minimize errors and reduce time during the FeP-FFQ application. This card was provided to every participant, and they indicated the frequency of intake of each food item.
Another limitation could be that all of the 32 food items most frequently consumed were included in the factorial analysis, which is different from the one used in other studies, which tend to group all consumed foods into categories [45,47,49,54,55]. However, it has been described that consuming 15 to 20 food items per week is possible for most people, even though optimal health can be achieved when a variety of 30 or more food items are consumed per week [56]. Including 32 food items in the analysis allows identifying poor dietary patterns through to the most healthy patterns. In the present study, biochemical markers were not included due to lack of feasibility to obtain serum ferritin and C-reactive protein as primary indicators for iron deficiency. A further study is planned to investigate if the identified dietary patterns are related to iron deficiency biochemical markers.
Lastly, in this study specific nutrients known to affect the absorption of iron, such as phytic acid/phytates, polyphenols/tannins, proteins from soya beans, and calcium [57], were not considered for analysis.
The strengths of this study are as follows: the FeP-FFQ included food items that have been identified as facilitators or inhibitors of iron absorption and the sources of this nutrient, which provides a complete picture of its consumption. In addition, to the best of our knowledge, the FeP-FFQ is the first tool designed specifically to determine iron-related dietary patterns, also reporting the reproducibility and validity of these dietary patterns for its use among pregnant women. Although a previous similar study was identified15, this was conducted among women aged 18 to 44 years from New Zealand, and it did not focus on identifying iron-related dietary patterns for pregnant women.

5. Conclusions

The FeP-FFQ showed good indicators of reproducibility and validity; therefore, this instrument could contribute to identifying iron-related dietary patterns among pregnant women since it provides an efficient way to evaluate iron intake qualitatively and the influence of other diet components on iron absorption (facilitators and inhibitors). In addition, this instrument could be helpful to determine how the combination of foods and drinks might affect iron status and thus, be able to provide practical clinical and public health information on the prevention of iron deficiency in pregnant Mexican women.
Because the application of the FeP-FFQ is easy, it will allow further studies to analyze the relationships between dietary patterns, iron status, and its risk factors among pregnant women and the baby. Likewise, because this tool is quick to be applied, simple, and relatively inexpensive, it might be helpful in epidemiological studies to determine the iron intake of pregnant women qualitatively, contributing to the early detection of risk factors related to iron deficiency and anemia prevention among Mexican pregnant women, and in consequence, reduction in health expenses.
Moreover, the implementation of this tool could also be helpful to develop and/or evaluate programs and public policies aiming at the optimal iron status of populations and, therefore, healthier pregnancies and babies. Further studies might explore the associations between dietary patterns and iron-deficiency anemia, through biomarkers, for a complete picture of the validity of this tool.

Author Contributions

Conceptualization, M.L.N.-P., M.F.B.-O., B.V. and G.M.-O.; Data curation, M.L.N.-P.; Formal analysis, M.L.N.-P., J.F.-B. and G.M.-O.; Investigation, M.L.N.-P.; Methodology, M.L.N.-P., M.F.B.-O., J.F.-B., B.V., N.P.R.-R. and G.M.-O.; Project administration, G.M.-O.; Resources, G.M.-O.; Supervision, J.F.-B. and N.P.R.-R.; Writing—original draft, M.L.N.-P. and N.P.R.-R.; Writing—review and editing, M.F.B.-O., J.F.-B., B.V., N.P.R.-R. and G.M.-O. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the National Council of Science and Technology (CONACYT) scholarship (number 814898) and the National System of Researchers (SNI) support (file no. 62046 and no. 22064; CVU-794213 and CVU-267588).

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki, and approved by the Bioethics Committee of the Maternal and Child Hospital “Esperanza López Mateos” (registry number 24/HMIELM-JAL/2019) and the Health Sciences University Center’s Ethics, Research and Biosafety Committees (reference no. CI-07018).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Not applicable.

Acknowledgments

We would like to thank Enrique Romero Velarde for his contributions to the development of this work and Jorge Castro Albarrán for his support in the development of the fieldwork at the Mother & Child Hospital “López Mateos”. We would also like to thank nutritionists Jazmín Camacho y Yair Adonaí Sánchez Nuño for their support, both at the recruitment of participants and data collection. Special thanks to all the participants in this study, for without them, this study could not have been possible.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. World Health Organization. Anaemia in Women and Children. Available online: https://www.who.int/data/gho/data/themes/topics/anaemia_in_women_and_children (accessed on 15 May 2022).
  2. Shamah-Levy, T.; Vielma-Orozco, E.; Heredia-Hernández, O.; Romero-Martínez, M.; Mojica-Cuevas, J.; Cuevas-Nasu, L.; Santaella-Castell, J.A.; Rivera-Dommarco, J. Encuesta Nacional de Salud y Nutrición 2018-19: Resultados Nacionales; Instituto Nacional de Salud Pública: Cuernavaca, México, 2020. [Google Scholar]
  3. Breymann, C. Iron deficiency anemia in pregnancy. In Seminars in Hematology; Elsevier: Amsterdam, The Netherlands, 2015; Volume 52, pp. 339–347. [Google Scholar] [CrossRef]
  4. Ramakrishnan, U. Functional Consequences of Nutritional Anemia during Pregnancy and Early Childhood; CRC Press, LLC: Boca Raton, FL, USA, 2001; pp. 43–68. [Google Scholar]
  5. World Health Organization. Haemoglobin Concentrations for the Diagnosis of Anaemia and Assessment of Severity; World Health Organization: Geneva, Switzerland, 2011; Available online: https://apps.who.int/iris/handle/10665/85839. (accessed on 22 May 2018).
  6. Resnik, R.; Lockwood, C.J.; Moore, T.; Greene, M.F.; Copel, J.; Silver, R.M. Creasy and Resnik’s Maternal-Fetal Medicine: Principles and Practice E-Book; Elsevier Health Sciences: Amsterdam, The Netherlands, 2018. [Google Scholar]
  7. World Health Organization. Global Health Observatory Data Repository/World Health Statistics. Available online: https://apps.who.int/gho/data/node.main.ANEMIAPREGNANTWOMAN?lang=en (accessed on 30 May 2018).
  8. Black, R.E.; Victora, C.G.; Walker, S.P.; Bhutta, Z.A.; Christian, P.; de Onis, M.; Ezzati, M.; Grantham-McGregor, S.; Katz, J.; Martorell, R.; et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet 2013, 382, 427–451. [Google Scholar] [CrossRef]
  9. Demuth, I.R.; Martin, A.; Weissenborn, A. Iron supplementation during pregnancy-A cross-sectional study undertaken in four German states. BMC Pregnancy Childbirth 2018, 18, 491. [Google Scholar] [CrossRef] [PubMed]
  10. World Health Organization. Nutritional Anaemias: Tools for Effective Prevention and Control. Available online: https://apps.who.int/iris/rest/bitstreams/1091289/retrieve (accessed on 4 June 2018).
  11. Cao, C.; O’Brien, K.O. Pregnancy and iron homeostasis: An update. Nutr. Rev. 2013, 71, 35–51. [Google Scholar] [CrossRef] [PubMed]
  12. Fernández-Ballart, J.D. Iron metabolism during pregnancy. Clin. Drug Investig. 2000, 19, 9–19. [Google Scholar] [CrossRef]
  13. Msemo, O.A.; Bygbjerg, I.C.; Møller, S.L.; Nielsen, B.B.; Ødum, L.; Perslev, K.; Lusingu, J.P.A.; Kavishe, R.A.; Minja, D.T.R.; Schmiegelow, C. Prevalence and risk factors of preconception anemia: A community-based cross-sectional study of rural women of reproductive age in northeastern Tanzania. PLoS ONE 2018, 13, e0208413. [Google Scholar] [CrossRef]
  14. Kaufer-Horwitz, M.; Pérz-Lizaur, A.B.; Arroyo, P. Nutriología Médica; Panamericana: Singapore, 2015. [Google Scholar]
  15. Głąbska, D.; Guzek, D.; Ślązak, J.; Włodarek, D. Assessing the validity and reproducibility of an iron dietary intake questionnaire conducted in a group of young Polish women. Nutrients 2017, 9, 199. [Google Scholar] [CrossRef] [Green Version]
  16. Beck, K.L. Iron Deficiency in Young Women: Causes, Consequences and Solutions: A Thesis Presented in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy in Nutritional Science at Massey University. Ph.D. Thesis, Massey University, Albany, New Zealand, 2013. [Google Scholar]
  17. Fayet, F.; Flood, V.; Petocz, P.; Samman, S. Relative and biomarker-based validity of a food frequency questionnaire that measures the intakes of vitamin B12, folate, iron, and zinc in young women. Nutr. Res. 2011, 31, 14–20. [Google Scholar] [CrossRef]
  18. Beck, K.L.; Kruger, R.; Conlon, C.A.; Heath, A.-L.M.; Coad, J.; Matthys, C.; Jones, B.; Stonehouse, W. The relative validity and reproducibility of an iron food frequency questionnaire for identifying iron-related dietary patterns in young women. J. Acad. Nutr. Diet. 2012, 112, 1177–1187. [Google Scholar] [CrossRef]
  19. Willett, W.; Lenart, E. Nutritional Epidemiology, 3rd ed.; New York Oxford University Press: New York, NY, USA, 2013; pp. 96–141. [Google Scholar] [CrossRef]
  20. Zhou, G.; Gan, Y.; Miao, M.; Hamilton, K.; Knoll, N.; Schwarzer, R. The role of action control and action planning on fruit and vegetable consumption. Appetite 2015, 91, 64–68. [Google Scholar] [CrossRef]
  21. Pérez-Lizaur, A.B.; Palacios-González, B.; Castro-Becerra, A.L.; Flores-Galicia, I. SMAE: Sistema Mexicano de Alimentos Equivalentes, 4th ed.; Porrúa: Ciudad de México, Mexico, 2014; ISBN 9786070079283. [Google Scholar]
  22. Cohen, J.A. Power primer. Psychol. Bull. 1992, 112, 155–159. [Google Scholar] [CrossRef]
  23. Atalah, E.; Castillo, C.; Castro, R.A.A. Propuesta de un nuevo estándar de evaluación nutricional en embarazadas. Rev. Med. Chile 1997, 15, 1429–1436. [Google Scholar]
  24. Landis, J.R.; Koch, G.G. The measurement of observer agreement for categorical data. Biometrics 1977, 33, 159–174. [Google Scholar] [CrossRef] [Green Version]
  25. Asociación Mexicana de Agencias de Inteligencia de Mercado y Opinión Pública. Índice de Niveles Socioeconómicos. Available online: https://www.amai.org/NSE/index.php (accessed on 10 January 2018).
  26. Heath, A.L.; Skeaff, C.M.; Gibson, R.S. The relative validity of a computerized food frequency questionnaire for estimating intake of dietary iron and its absorption modifiers. Eur. J. Clin. Nutr. 2000, 54, 592–599. [Google Scholar] [CrossRef] [Green Version]
  27. Trinidad-Rodríguez, I.; Fernández-Ballart, J.; Cucó-Pastor, G.; Biarnés-Jordà, E.; Arija-Val, V. Validación de un cuestionario de frecuencia de consumo alimentario corto: Reproducibilidad y validez. Nutr. Hosp. 2008, 23, 242–252. [Google Scholar]
  28. Baer, H.J.; Blum, R.E.; Rockett, H.R.H.; Leppert, J.; Gardner, J.D.; Suitor, C.W.; A Colditz, G. Use of a food frequency questionnaire in American Indian and Caucasian pregnant women: A validation study. BMC Public Health 2005, 5, 135. [Google Scholar] [CrossRef] [Green Version]
  29. Brown, J.E.; Buzzard, I.M.; Jacobs, D.R., Jr.; Hannan, P.J.; Kushi, L.H.; Barosso, G.M.; Schmid, L.A. A food frequency questionnaire can detect pregnancy-related changes in diet. J. Am. Diet. Assoc. 1996, 96, 262–266. [Google Scholar] [CrossRef]
  30. Robinson, S.; Godfrey, K.; Osmond, C.; Cox, V.; Barker, D. Evaluation of a food frequency questionnaire used to assess nutrient intakes in pregnant women. Eur. J. Clin. Nutr. 1996, 50, 302–308. [Google Scholar] [PubMed]
  31. Galante, A.P.; Colli, C. Development and use of an on-line semiquantitative food-frequency questionnaire to evaluate calcium and iron intake. Rev. Bras. Epidemiol. 2008, 11, 402–410. [Google Scholar] [CrossRef]
  32. Brunst, K.; Kannan, S.; Ni, Y.-M.; Gennings, C.; Ganguri, H.; Wright, R. Validation of a Food Frequency Questionnaire for Estimating Micronutrient Intakes in an Urban US Sample of Multi-Ethnic Pregnant Women. Matern. Child Health J. 2015, 20, 250–260. [Google Scholar] [CrossRef] [Green Version]
  33. Forsythe, H.E.; Gage, B. Use of a multicultural food-frequency questionnaire with pregnant and lactating women. Am. J. Clin. Nutr. 1994, 59, 203S–206S. [Google Scholar] [CrossRef]
  34. Zhou, S.J.; Schilling, M.J.; Makrides, M. Evaluation of an iron specific checklist for the assessment of dietary iron intake in pregnant and postpartum women. Nutrition 2005, 21, 908–913. [Google Scholar] [CrossRef] [PubMed]
  35. Cade, J.; Thompson, R.; Burley, V.; Warm, D. Development, validation and utilisation of food-frequency questionnaires–a review. Public Health Nutr. 2002, 5, 567–587. [Google Scholar] [CrossRef] [Green Version]
  36. Thompson, F.; Byers, T. Manual de Instrumentos de Evaluación Dietética; INCAP/MDE156: Guatemala, 2006; ISBN 9993968072. [Google Scholar]
  37. Serra-Majem, L.; Andersen, L.F.; Henríque-Sánchez, P.; Doreste-Alonso, J.; Sánchez-Villegas, A.; Ortiz-Andrelluchi, A.; Negri, E.; La Vecchia, C. Evaluating the quality of dietary intake validation studies. Br. J. Nutr. 2009, 102 (Suppl. S1), S3–S9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Baranowski, T. 24-hour recall and diet record methods. In Nutritional Epidemiology, 3rd ed.; Oxford University Press: New York, NY, USA, 2013; Volume 40, pp. 49–69. [Google Scholar] [CrossRef]
  39. Erkkola, M.; Karppinen, M.; Javanainen, J.; Räsänen, L.; Knip, M.; Virtanen, S.M. Validity and reproducibility of a food frequency questionnaire for pregnant Finnish women. Am. J. Epidemiol. 2001, 154, 466–476. [Google Scholar] [CrossRef] [PubMed]
  40. Matthys, C.; Pynaert, I.; Roe, M.; Fairweather-Tait, S.J.; Heath, A.-L.; De Henauw, S. Validity and reproducibility of a computerised tool for assessing the iron, calcium and vitamin C intake of Belgian women. Eur. J. Clin. Nutr. 2004, 58, 1297–1305. [Google Scholar] [CrossRef] [Green Version]
  41. Pynaert, I.; Matthys, C.; De Bacquer, D.; De Backer, G.; De Henauw, S. Evaluation of a 2-day food record to determine iron, calcium and vitamin C intake in young Belgian women. Eur. J. Clin. Nutr. 2008, 62, 104–110. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Shateinstein, B.; Xu, H.; Luo, Z.C.; Fraser, W. Relative validity of a Food frequency questionnaire for pregnant women. Can. J. Diet. Pract. Res. 2011, 72, 60–69. [Google Scholar] [CrossRef] [PubMed]
  43. Hu, F.B. Dietary pattern analysis: A new direction in nutritional epidemiology. Curr. Opin. Lipidol. 2002, 13, 3–9. [Google Scholar] [CrossRef]
  44. Togo, P.; Heitmann, B.L.; Sørensen, T.I.A.; Osler, M. Consistency of food intake factors by different dietary assessment methods and population groups. Br. J. Nutr. 2003, 90, 667–678. [Google Scholar] [CrossRef] [Green Version]
  45. Khani, B.R.; Ye, W.; Terry, P.; Wolk, A. Reproducibility and validity of major dietary patterns among Swedish women assessed with a food-frequency questionnaire. J. Nutr. 2004, 134, 1541–1545. [Google Scholar] [CrossRef]
  46. Crozier, S.R.; Inskip, H.M.; Godfrey, K.M.; Robinson, S.M. Dietary patterns in pregnant women: A comparison of food-frequency questionnaires and 4 d prospective diaries. Br. J. Nutr. 2008, 99, 869–875. [Google Scholar] [CrossRef] [Green Version]
  47. Ambrosini, G.L.; O’Sullivan, T.A.; De Klerk, N.H.; Mori, T.A.; Beilin, L.J.; Oddy, W.H. Relative validity of adolescent dietary patterns: A comparison of a FFQ and 3 d food record. Br. J. Nutr. 2011, 105, 625–633. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Nanri, A.; Shimazu, T.; Ishihara, J.; Takachi, R.; Mizoue, T.; Inoue, M.; Tsugane, S. Reproducibility and validity of dietary patterns assessed by a food frequency questionnaire used in the 5-year follow-up survey of the Japan Public Health Center-Based Prospective Study. J. Epidemiol. 2012, 22, 205–215. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Shi, Z.; Hu, X.; Yuan, B.; Pan, X.; Dai, Y.; Holmboe-Ottesen, G. Association between dietary patterns and anaemia in adults from Jiangsu Province in Eastern China. Br. J. Nutr. 2006, 96, 906–912. [Google Scholar] [CrossRef] [Green Version]
  50. Teixeira, J.A.; Castro, T.G.; Grant, C.C.; Wall, C.R.; da Silva Castro, A.L.; Francisco, R.P.V.; Vieira, S.E.; Saldiva, S.R.D.M.; Marchioni, D.M. Dietary patterns are influenced by sociodemographic conditions of women in childbearing age: A cohort study of pregnant women. BMC Public Health 2018, 18, 301. [Google Scholar] [CrossRef] [PubMed]
  51. Bland, J.M.; Altman, D. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1986, 327, 307–310. [Google Scholar] [CrossRef]
  52. Masson, L.F.; Mcneill, G.; Tomany, J.O.; Simpson, J.; Peace, H.; Wei, L.; Grubb, D.; Bolton-Smith, C. Statistical approaches for assessing the relative validity of a food-frequency questionnaire: Use of correlation coefficients and the kappa statistic. Public Health Nutr. 2003, 6, 313–321. [Google Scholar] [CrossRef] [PubMed]
  53. Cohen, J. Weighted kappa: Nominal scale agreement provision for scaled disagreement or partial credit. Psychol. Bull. 1968, 70, 213. [Google Scholar] [CrossRef]
  54. Hu, F.B.; Rimm, E.; Smith-Warner, S.A.; Feskanich, D.; Stampfer, M.J.; Ascherio, A.; Sampson, L.; Willett, W.C. Reproducibility and validity of dietary patterns assessed with a food-frequency questionnaire. Am. J. Clin. Nutr. 1999, 69, 243–249. [Google Scholar] [CrossRef] [Green Version]
  55. Okubo, H.; Murakami, K.; Sasaki, S.; Kim, M.K.; Hirota, N.; Notsu, A.; Fukui, M.; Date, C. Relative validity of dietary patterns derived from a self-administered diet history questionnaire using factor analysis among Japanese adults. Public Health Nutr. 2010, 13, 1080–1089. [Google Scholar] [CrossRef]
  56. Hodgson, J.M.; Hsu-Hage, B.H.; Wahlqvist, M.L. Food variety as a quantitative descriptor of food intake. Ecol. Food Nutr. 1994, 32, 137–148. [Google Scholar] [CrossRef]
  57. Milman, N.T. A review of nutrients and compounds, which promote or inhibit intestinal iron absorption: Making a platform for dietary measures that can reduce iron uptake in patients with genetic haemochromatosis. J. Nutr. Metab. 2020, 2020, 7373498. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Bland–Altman plots for dietary patterns reproducibility between FeP-FFQ1 and FeP-FFQ2: (A) “healthy” pattern agreement, (B) “industrialized food and dairy” pattern agreement. The solid line represents the mean difference, and the dotted lines represent the agreement limits (SD ±1.96).
Figure 1. Bland–Altman plots for dietary patterns reproducibility between FeP-FFQ1 and FeP-FFQ2: (A) “healthy” pattern agreement, (B) “industrialized food and dairy” pattern agreement. The solid line represents the mean difference, and the dotted lines represent the agreement limits (SD ±1.96).
Nutrients 14 02313 g001
Figure 2. Bland–Altman plots for dietary patterns validity between FeP-FFQ1 and 3DDR: (A) “healthy” pattern agreement, (B) “industrialized food and dairy” pattern agreement. The solid line represents the mean difference, and the dotted lines represent the agreement limits (SD ±1.96).
Figure 2. Bland–Altman plots for dietary patterns validity between FeP-FFQ1 and 3DDR: (A) “healthy” pattern agreement, (B) “industrialized food and dairy” pattern agreement. The solid line represents the mean difference, and the dotted lines represent the agreement limits (SD ±1.96).
Nutrients 14 02313 g002
Table 1. Participants’ sociodemographic, anthropometric characteristics and iron status (n = 110).
Table 1. Participants’ sociodemographic, anthropometric characteristics and iron status (n = 110).
Sociodemographic Characteristicsn (%)
Civil statusMarried33 (30)
Free union60 (54.5)
Single16 (14.5)
Divorced1 (1)
Education levelNone0 (0)
Knows how to write and read1 (0.9)
Elementary school12 (10.9)
Secondary school51 (46.4)
High school36 (37.2)
Bachelor degree9 (8.2)
Graduate degree1 (0.9)
OccupationHousewife89 (80.9)
Paid job19 (17.3)
Student2 (1.8)
Socioeconomic status *AB (high class)3 (2.7)
C+ (middle-high class)5 (4.5)
C (middle class)19 (17.3)
C− (middle-low class)22 (20)
D+ (low-middle class)35 (31.8)
D (low class)26 (23.6)
E (extreme poverty)0 (0)
Anthropometric characteristics
Height (m)Mean (SD)1.6 (0.1)
Pregestational weight (kg) **Mean (SD)66.1 (15.2)
Pregestational BMI ***Mean (SD)26.0 (5.7)
Pregestational BMI statusLow11 (10)
Normal48 (43.6)
Overweight25 (22.7)
Obese26 (23.6)
Current weight (kg)Mean (SD)73.2 (15.2)
Current BMIMean (SD)28.8 (5.6)
Current BMI status ****Low10 (9.1)
Normal35 (31.8)
Overweight39 (35.5)
Obese26 (23.6)
Iron status
Hemoglobin (g/dL) *****Mean (SD)12.15 (1.04)
Hemoglobin status *****Anemia (≤11.0)16 (14.5)
Normal (≥11.1)94 (85.5)
SD: standard deviation; BMI: body mass index. * Obtained and classified using the AMAI (Mexican Association of Market Intelligence and Opinion Agencies) scores [25]. ** Obtained by selfreport at the initial interview. *** Calculated from the selfreported pregestational weight. **** Atalah E, Castillo C, Castro R, Aldea A. Propuesta de un nuevo estándar de evaluación nutricional en embarazadas. Rev Med Chile 1997; 15: 1429–1436 [23]. ***** Hb status from the 3rd trimester of pregnancy.
Table 2. Estimated intake and comparisons between FeP-FFQ1, FeP-FFQ2 & 3DDR (n = 110).
Table 2. Estimated intake and comparisons between FeP-FFQ1, FeP-FFQ2 & 3DDR (n = 110).
Frequency of Intake over 3 Days
Mean ± SD
Difference
Mean ± SD
Correlation Coefficients ®
ItemsFeP-FFQ1FeP-FFQ23DDRFeP-FFQ1 vs. 3DDRFeP-FFQ1 vs. FeP-FFQ2FeP-FFQ1 vs. 3DDRFeP-FFQ1 vs. FeP-FFQ2
Water15.54 ± 6.0715.62 ± 5.6920.30 ± 8.56−4.84 ± 8.20 **b−0.17 ± 5.730.41 **0.52 **
Corn tortilla6.07 ± 3.565.78 ± 3.494.30 ± 1.781.77 ± 3.41 **a0.28 ± 3.190.33 **0.59 **
Tomato4.91 ± 4.963.94 ± 4.112.78 ± 1.522.12 ± 5.17 **a0.96 ± 4.56 *0.010.50 **
Citrus fruits c4.20 ± 4.572.72 ± 3.381.92 ± 1.542.28 ± 4.80 **a1.48 ± 3.94 **a0.010.54 **
Lime d4.06 ± 5.123.05 ± 3.721.36 ± 1.372.69 ± 4.91 **a1.00 ± 3.42 *0.28 *0.74 **
Onion3.40 ± 3.723.16 ± 3.162.51 ± 1.650.89 ± 3.92 *0.24 ± 3.840.090.38 **
Milk3.32 ± 3.553.09 ± 2.632.73 ± 1.760.59 ± 3.380.23 ± 3.200.34 **0.49 **
Stone fruits e3.08 ± 3.912.13 ± 3.270.76 ± 0.992.31 ± 3.80 **b0.94 ± 3.43 *0.23 *0.55 **
Homemade beans2.64 ± 2.752.25 ± 2.171.45 ± 1.251.19 ± 2.83 **a0.39 ± 2.08 *0.150.68 **
Chilies f2.64 ± 3.322.10 ± 2.472.17 ± 1.840.46 ± 3.180.53 ± 2.920.35 **0.52 **
Banana and fried plantain2.46 ± 3.571.94 ± 2.701.19 ± 1.091.27 ± 3.74 **a0.52 ± 3.71−0.000.32 **
Apple2.21 ± 3.621.62 ± 3.110.65 ± 0.861.56 ± 3.59 **a0.59 ± 2.49 *0.150.73 **
Lettuce1.86 ± 2.351.36 ± 2.020.76 ± 0.981.09 ± 2.51 **a0.49 ± 2.56 *0.040.31 **
Carrot1.69 ± 2.531.21 ± 1.370.74 ± 0.990.95 ± 2.57 **a0.48 ± 2.910.150.23 **
Soda1.62 ± 2.551.89 ± 2.751.35 ± 1.490.27 ± 2.15−0.27 ± 2.090.54 **0.69 **
Eggs1.58 ± 2.121.36 ± 2.021.51 ± 1.060.07 ± 2.030.22 ± 2.190.33 **0.17 **
Melon1.53 ± 3.800.93 ± 2.280.34 ± 0.561.19 ± 3.78 **a0.60 ± 2.84 *0.120.66 **
Watermelon1.41 ± 3.540.45 ± 0.900.22 ± 0.471.18 ± 3.52 **a0.96 ± 3.35 *0.110.33 **
Sour cream1.39 ± 1.581.29 ± 1.490.86 ± 0.960.52 ± 1.67 **a0.10 ± 1.140.21 *0.72 **
Rice1.35 ± 1.510.94 ± 0.560.69 ± 0.870.65 ± 1.66 **a0.41 ± 1.47 *0.100.25 *
Yogurt g1.26 ± 1.281.12 ± 1.370.43 ± 0.670.82 ± 1.23 **b0.14 ± 1.040.34 **0.69
Pasta soup1.19 ± 1.631.11 ± 1.280.55 ± 0.730.63 ± 1.68 **a0.07 ± 1.680.150.34 **
Potato1.15 ± 1.551.00 ± 0.960.87 ± 0.910.28 ± 1.78 **0.15 ± 1.070.020.73 **
Mexican sweet bread1.13 ± 1.830.83 ± 0.830.75 ± 0.930.37 ± 1.98 *0.29 ± 1.650.090.43 **
Cookies1.12 ± 1.990.95 ± 1.340.56 ± 1.980.55 ± 2.82 *0.16 ± 1.940.000.37 **
Poultry1.09 ± 1.620.88 ± 0.820.81 ± 0.770.28 ± 1.770.21 ± 1.700.040.16 **
Cheese1.07 ± 1.540.96 ± 1.550.66 ± 0.860.40 ± 1.79 *0.10 ± 0.74−0.030.88 **
Papaya1.00 ± 2.020.82 ± 1.940.31 ± 0.630.69 ± 2.04 **a0.17 ± 1.940.130.51 **
Ice-cream, sorbet, popsicles0.93 ± 1.810.67 ± 1.210.09 ± 0.310.83 ± 1.80 **a0.26 ± 1.530.150.54 **
Grains0.91 ± 1.870.70 ± 1.150.45 ± 0.690.46 ± 1.79 *0.20 ± 1.650.30 **0.48 **
Beef0.90 ± 0.610.82 ± 0.571.70 ± 1.28−0.79 ± 1.32 **b0.08 ± 0.600.170.47 **
Sausages and ham0.90 ± 1.320.97 ± 1.330.95 ± 0.95−0.58 ± 1.52−0.07 ± 1.170.140.61 **
* Significant values (p < 0.05); ** Significant values (p < 0.01); ® † Spearman correlation coefficients; a Medium effect size (0.3–0.49); b Large effect size (≥0.5) [20]. c Includes orange or mandarin, guava, lemon, pineapple, grapefruit, and strawberries; d used in flavor water, salads, broths, meat); e Such as mango and peach; f Fresh, dried, minced or whole; g Drinking yogurt included.
Table 3. Factor loadings for the two identified dietary patterns by administration of FeP-FFQ1, FeP-FFQ2, and 3DDR (n = 110).
Table 3. Factor loadings for the two identified dietary patterns by administration of FeP-FFQ1, FeP-FFQ2, and 3DDR (n = 110).
Dietary Pattern
HealthyIndustrialized Food and Dairy
ItemsFeP-FFQ1FeP-FFQ23DDRFeP-FFQ1FeP-FFQ23DDR
Melon0.840.770.48
Watermelon0.780.190.29 0.39−0.24
Banana and fried plantain0.760.340.35 −0.42
Citrus fruits0.750.670.50 0.39
Stone fruits0.750.720.37 0.23
Grains0.630.44 0.25 −0.46
Apple0.620.830.69
Potato0.60 0.230.56
Lime0.590.660.56 0.21
Tomato0.510.66 0.39 0.52
Eggs0.49 0.20
Onion0.480.53 0.70
Papaya0.470.300.30−0.260.31
Homemade beans0.420.38
Lettuce0.390.73 0.22
Carrot0.380.710.32
Rice0.360.33 0.350.450.27
Corn tortilla0.340.24 0.42 0.33
Milk0.280.25 0.48 −0.42
Chilies (fresh, minced, dried, whole)0.270.320.44 0.44
Ice cream, sorbet, popsicles0.22 0.340.440.29
Beef0.20 0.39 0.40
Soda −0.260.380.540.40
Pasta soup 0.770.340.21
Sausages and ham 0.660.610.20
Cheese 0.630.39−0.30
Sour cream 0.250.440.52
Mexican sweet bread −0.220.210.48
Cookies 0.400.150.41
Yogurt 0.330.420.40
Poultry 0.600.31
Water 0.250.32
Notes: Correlations < 0.15 excluded to enable ease in interpretation.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Navarro-Padilla, M.L.; Bernal-Orozco, M.F.; Fernández-Ballart, J.; Vizmanos, B.; Rodríguez-Rocha, N.P.; Macedo-Ojeda, G. The Reproducibility and Relative Validity of a Food Frequency Questionnaire for Identifying Iron-Related Dietary Patterns in Pregnant Women. Nutrients 2022, 14, 2313. https://doi.org/10.3390/nu14112313

AMA Style

Navarro-Padilla ML, Bernal-Orozco MF, Fernández-Ballart J, Vizmanos B, Rodríguez-Rocha NP, Macedo-Ojeda G. The Reproducibility and Relative Validity of a Food Frequency Questionnaire for Identifying Iron-Related Dietary Patterns in Pregnant Women. Nutrients. 2022; 14(11):2313. https://doi.org/10.3390/nu14112313

Chicago/Turabian Style

Navarro-Padilla, Mayra Lizeth, María Fernanda Bernal-Orozco, Joan Fernández-Ballart, Barbara Vizmanos, Norma Patricia Rodríguez-Rocha, and Gabriela Macedo-Ojeda. 2022. "The Reproducibility and Relative Validity of a Food Frequency Questionnaire for Identifying Iron-Related Dietary Patterns in Pregnant Women" Nutrients 14, no. 11: 2313. https://doi.org/10.3390/nu14112313

APA Style

Navarro-Padilla, M. L., Bernal-Orozco, M. F., Fernández-Ballart, J., Vizmanos, B., Rodríguez-Rocha, N. P., & Macedo-Ojeda, G. (2022). The Reproducibility and Relative Validity of a Food Frequency Questionnaire for Identifying Iron-Related Dietary Patterns in Pregnant Women. Nutrients, 14(11), 2313. https://doi.org/10.3390/nu14112313

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop