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Article

The Consumption of Food-Based Iodine in the Immediate Pre-Pregnancy Period in Madrid Is Insufficient. San Carlos and Pregnancy Cohort Study

by
Verónica Melero
1,†,
Isabelle Runkle
1,†,
Nuria Garcia de la Torre
1,2,
Paz De Miguel
1,3,
Johanna Valerio
1,
Laura del Valle
1,
Ana Barabash
1,2,3,
Concepción Sanabria
1,
Inmaculada Moraga
1,
Cristina Familiar
1,
Alejandra Durán
1,3,
Maria Jose Torrejón
4,
Jose Angel Diaz
1,3,
Martin Cuesta
1,
Jorge Grabiel Ruiz
1,
Inés Jiménez
1,
Mario Pazos
1,
Miguel Angel Herraiz
5,
Nuria Izquierdo
5,
Noelia Pérez
5,
Pilar Matia
1,3,
Natalia Perez-Ferre
1,3,
Clara Marcuello
1,3,
Miguel Angel Rubio
1,3 and
Alfonso Luis Calle-Pascual
1,2,3,*add Show full author list remove Hide full author list
1
Endocrinology and Nutrition Department, Hospital Clínico Universitario San Carlos and Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain
2
Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), 28029 Madrid, Spain
3
Medicina II Department, Facultad de Medicina, Universidad Complutense de Madrid, 28040 Madrid, Spain
4
Clinical Laboratory Department, Hospital Clínico Universitario San Carlos and Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain
5
Gynecology and Obstetrics Department, Hospital Clínico Universitario San Carlos and Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Nutrients 2021, 13(12), 4458; https://doi.org/10.3390/nu13124458
Submission received: 18 November 2021 / Revised: 12 December 2021 / Accepted: 12 December 2021 / Published: 14 December 2021
(This article belongs to the Section Nutrition in Women)
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Abstract

:
A pre-gestational thyroid reserve of iodine is crucial to guarantee the increased demand for thyroid hormone production of early pregnancy. An iodine intake ≥150 µg/day is currently recommended. The objective of this study was to assess average pre-gestational food-based iodine consumption in pregnant women at their first prenatal visit (<12 gestational weeks), and its association with adverse materno-fetal events (history of miscarriages, early fetal losses, Gestational Diabetes, prematurity, caesarean sections, and new-borns large/small for gestational age). Between 2015–2017, 2523 normoglycemic women out of 3026 eligible had data in the modified Diabetes Nutrition and Complication Trial (DNCT) questionnaire permitting assessment of pre-gestational food-based iodine consumption, and were included in this study. Daily food-based iodine intake was 123 ± 48 µg, with 1922 (76.1%) not reaching 150 µg/day. Attaining this amount was associated with consuming 8 weekly servings of vegetables (3.84; 3.16–4.65), 1 of shellfish (8.72; 6.96–10.93) and/or 2 daily dairy products (6.43; 5.27–7.86). Women who reached a pre-gestational intake ≥150 µg had lower rates of hypothyroxinemia (104 (17.3%)/384 (21.4%); p = 0.026), a lower miscarriage rate, and a decrease in the composite of materno-fetal adverse events (0.81; 0.67–0.98). Reaching the recommended iodine pre-pregnancy intake with foods could benefit the progression of pregnancy.

1. Introduction

Thyroid hormone (TH) is essential for embryo/fetal development [1,2]. Up until the 16–18th week of gestation, the only source of TH in the embryo/fetus is the maternal thyroid [1,3,4]. To meet the needs of pregnancy, the maternal thyroid must increase free T4 (FT4) secretion, particularly in the 1st trimester of gestation. During this time, circulating FT4 maternal levels actually rise, with a maximum between 7–11 gestational weeks (GW), in spite of passing TH to the embryo, and increasing levels of thyroid hormone binding protein. An insufficient production of TH by the maternal thyroid can result in severe neurocognitive delay [1]. Maternal thyroid hypofunction, albeit mild, is also associated with both maternal and fetal complications in pregnancy and the peripartum period. These include preterm delivery, early stage fetal losses, miscarriages, perinatal death/stillbirths, postpartum hemorrhage, fetal distress during labor, preeclampsia and higher risk of caesarean section [4,5].
Iodine is essential for TH synthesis [4,6]. Adequate iodine stores as well as an increase in iodine intake are needed to permit the physiological increase in maternal thyroid FT4 secretion characteristic of early stages of pregnancy [1]. However, dietary iodine deficiency is a relevant problem worldwide [7,8,9]. In fact, iodine deficit is still the most important cause of preventable neurocognitive dysfunction and motor disability in offspring [8,10,11,12,13,14,15]. To prevent iodine deficiency, the WHO recommends a daily iodine intake of 150 µg from foods and from iodized salt in non-pregnant adults, increasing to 250 µg/day during gestation, the latter requiring the use of iodine supplements as recommended by the WHO in some regions [16]. The importance of pre-gestational iodine ingestion has been shown by a study in which the use of iodized salt for a minimum of 2 years before pregnancy, enabling adequate thyroid stores of iodine, permitted better Thyroid stimulating Hormone (TSH) and/or FT4 levels than those found not only in women presenting an insufficient iodine intake before and throughout pregnancy, but also in women starting iodine supplements during pregnancy, without having assured adequate pre-gestation iodine consumption [17].
In the general population, and in women of childbearing age, the main sources of iodine are foods rich in iodine and iodized salt [18,19]. Among the former are fish, shellfish and seaweeds, as well as dairy products and several vegetables [13,20,21,22,23,24,25,26]. Although the use of iodized salt is recommended by the WHO, not all countries have established on-going campaigns to encourage its systematic use. Spain is an example of a country where a campaign was carried out for only a few months, more than 20 years ago. Although the WHO classified Spain as a country with a mild iodine deficiency in 2004 [27], it is currently considered an iodine-sufficient country [28,29]. However, iodine consumption varies in different regions [28,30,31,32,33,34].
Yet according to the results of a recent population-based study [35], the median urinary iodine in Spanish women between 18 and 50 years of age ranges from 114–119 µg/day, reflecting an adequate iodine intake (≥150 µg), since 90% of ingested iodine is excreted in the urine [36] but it may not be enough for women of childbearing age, especially in a pre-pregnancy situation. Furthermore, more than 30% of the women studied had a urinary iodine level below 50 µg/day, and less than 45% consumed iodized salt. To compound the problem, the use of iodized salt does not guarantee an adequate supply of iodine either. A recent FACUA (Federación de Asociaciones de Consumidores y Usuarios de Andalucía) [37] report, an Andalusian consumer organization (data not available) analysed 20 different classes of iodized salt. Most had a lower iodine content than what was given on the label. Iodine intake can therefore not be assured even when iodized salt is regularly used, highlighting the importance of food-based iodine consumption.
The primary objective of this study is to evaluate the average pre-gestational food-based iodine consumption in pregnant women studied at the onset of gestation. The results would permit knowing the number of women reaching the recommended pre-gestational daily iodine intake of 150 of µg with foods alone. The first secondary objective is to determine the eating pattern(s) associated with achieving the aforementioned daily food-based iodine consumption. The second one is to assess whether there is an association between not attaining said food-based iodine intake and the development of adverse materno-fetal outcomes.

2. Material and Methods

2.1. Experimental Design and Ethic Statement

The Hospital Clínico San Carlos is a public hospital located in the central area of Madrid. The hospital provides healthcare for a reference population of 445,000 inhabitants. Prenatal screening consultations of all pregnant women in the reference population are located in the hospital, where the women undergo the first ultrasound and the screening test to detect the risk of chromosomal alterations between 9 and 12 gestational weeks (GW). The current study involves the participants of our hospital-based cohort of pregnant women screened for gestational diabetes mellitus (GDM), from January 2015 to December 2017 (the San Carlos Cohort for the prevention of GDM ISRCTN84389045, ISRCTN13389832 and ISRCTN16896947).
It was approved by the Clinical Trials Committee of the Hospital Clínico San Carlos (CI 13/296-E, CI16/442-E, and CI 16/316), and conducted according to Declaration of Helsinki). All women signed the informed consent at the onset of the trial.

2.2. Participants

Women participating in the study met the following inclusion criteria: a fasting blood glucose (FBG) < 92 mg/dL, an age ≥ 18 years. Exclusion criteria were: having a multiple gestation, a gestational age (GW) > GW14 and/or intolerance/allergy to nuts or extra virgin olive oil (EVOO), or any medical conditions or pharmacological therapy that could compromise the follow-up program.
A total of 3026 consecutive women, who attended the prenatal screening visit before GW12, with a singleton pregnancy and without prior fertility treatment or known diseases, were initially eligible for the study. Women with pre-gestational thyroid disease and/or pre-gestational levothyroxine treatment (n = 135) and women without valid data available from the semi-quantitative questionnaire of frequency of food consumption (n = 368) were excluded. A total of 2523 women were included for analysis. The clinical characteristics of the included women are shown in Table 1.

2.3. AΠssessment of Food-Based Iodine Consumption

The semi-quantitative questionnaire used to register the number of weekly servings from different food groups was an adaptation of the Diabetes Nutrition and Complication trial (DNCT) questionnaire [38]. The DNCT questionnaire consists of 15 items, 3 of which provide information on physical activity (the physical activity score), and 12 of which evaluate food-frequency consumption (the Nutrition score). The questionnaire permits 3 options, with Option A (value +1) the most favourable, Option B (value 0) expresses an intermediate value, and Option C (value −1) the least favourable. In addition to evaluating eating patterns categorically, the number of weekly servings from 20 different food groups and minutes/week of sports activity of at least moderate intensity were collected. The questionnaire includes vegetables, fruits, nuts, white fish, fatty fish, canned fish, and shellfish. However, the specific subtype of food was not registered. Hence, to more precisely estimate iodine consumption, the following approximation was carried out. A total of 200 women chosen consecutively were evaluated to calculate the average iodine intake from the servings of each food group. For this survey, the first 50 consecutive women attending the prenatal clinic consultation before GW12 at the beginning of each quarter of the calendar year were included to reflect the seasonal character of many fruits, vegetables, fish, and shellfish. Food subtypes were specified. Foods whose iodine content was low, and contributed less than 1% of total iodine intake, were not tabulated in the study. Once the average composition of a serving from each food group was estimated, the calculation of iodine content was made using data from the Spanish Consumer Office, and tables of composition of iodine in food as reference [39,40]. Data are provided in Supplementary Table S1. The use of iodine supplements and the intake of iodized salt were not included for the estimation of pre-gestational food-based iodine consumption.
Simultaneously, the 14-point Mediterranean Diet Adherence Screener (MEDAS) questionnaire [41] was applied. Both questionnaires were conducted by a trained dietician at the first gestational visit, between 9 and 12 GW. At this time, participants retrospectively described their pre-pregnancy diet and physical activity. From these 2 questionnaires, the MEDAS and Nutrition scores were obtained. Both the MEDAS and DNCT questionnaires had been previously used in studies on the prevention of gestational diabetes.

2.4. Data Collection

At the first visit, sociodemographic information such as age, ethnicity, educational level, employment status, and parity was collected. A family history of metabolic disease (type 2 DM, and each component of the metabolic syndrome), smoking habit, and habitual consumption of iodized salt, as well as the use of supplements with iodine (with or without folic acid), were recorded as clinical data. In addition, daily food-based iodine consumption in the pre-pregnancy period was also registered at this first appointment. Anthropometric data, such as current body weight (taken with light clothes and without shoes) and height (taken without shoes), to obtain body mass index (BMI) were collected. Declared body weight was also registered. Blood pressure was measured with an adequate armlet (Omron 705IT, Omron Global, Kyoto, Japan) when the participants had been seated for 10 min.

2.5. Follow-Up during Gestation

To evaluate the relationship between food-based iodine intake and materno-fetal adverse events, the following parameters were evaluated: a prior history of miscarriages and fetal losses occurring before GW18, prematurity (new-borns before GW37), development of pre-eclampsia (blood pressure greater than 140 mmHg and albuminuria from GW20 on) and diagnosis of gestational diabetes mellitus (GDM) applying the IADPSG diagnostic criteria, the form of delivery as vaginal or caesarean section, the number of newborns small for gestational age (SGA) and large for gestational age (LGA) considered as <10 percentile and >90 percentile, respectively, were analysed in this study. The composite materno-fetal adverse outcomes (CMFAO) variable analysed the risk of suffering from any adverse event previously described (miscarriage history, early fetal loss, preeclampsia, prematurity, caesarean section, GDM and SGA/LGA new-borns) and its association with reaching a food-based intake of ≥150 µg of iodine/day in pre-pregnancy women.
A diagnosis of hypothyroidism and/or hypothyroxinemia was also registered. Gestational subclinical hypothyroidism was defined as a TSH level ≥ 2.5 µIU/mL, and hypothyroxinemia as a FT4 ≥ 7.5 pg/mL during the first trimester of pregnancy.

2.6. Biochemical Data

To evaluate the biochemical markers corresponding with the baseline characteristics of women, an early-morning blood sample was collected after an 8–10 h fast. For this study, the following parameters were determined: fasting serum glucose (glucose oxidase); fasting serum insulin; homeostasis assessment model for insulin resistance (HOMA); total cholesterol and triglyceride levels (enzymatic); thyroid function was assessed by determining circulating TSH and FT4 levels.
Fasting serum glucose was measured with a method standardized by the International Federation of Clinical Chemistry and Laboratory Medicine, using ion-exchange high-performance liquid chromatography in gradient, with a Tosoh G8 analyser (Tosoh Co., Tokyo, Japan). Fasting serum insulin (FSI) was measured by a chemiluminescence immunoassay in an IMMULITE 2000 Xpi (Siemens, Healthcare Diagnostics, Munich, Germany). Homeostasis assessment model for insulin resistance (HOMA) was calculated as glucose (mmol/L) × insulin (µUI/mL)/22.7). Total cholesterol and triglyceride levels (enzymatic) were analysed. TSH was measured by a 3rd generation sandwich-chemiluminescence immunoassay with magnetic particles using human TSH mouse monoclonal antibodies in a DXI-800® (Beckman–Coulter). The manufacturer’s stated normal range for non-pregnant adults is 0.38–5.33 μIU/mL, with a sensitivity of 0.01 μIU/mL, intraassay coefficient of variation (CV) < 10%, and range 0.01–50.0 μIU/mL. Intra-assay CVs are 4.9% for a concentration of 0.69 μIU/mL, 5.8% for 5.47 μIU/mL, and 6.2% for 29 μIU/mL. FT4 was measured by a 2-step competitive-chemiluminescence immunoassay with paramagnetic particles, in a DXI-800® (Beckman Coulter). The manufacturer’s stated normal range for non-pregnant adults is 5.8–16.4 pg/mL, with a sensitivity of 2.5 pg/mL, range: 2.5–60 pg/mL. Intra-assay CVs are 7.8% for a concentration of 8.5 pg/mL, 5.7% for 22.9 pg/mL and 4.3% for 43 pg/mL. To determine total cholesterol and triglycerides, a colorimetric method with CHOD-PAP and GPO-PAP, respectively, was used.
An External Quality Guarantee Program of the SEQC (Sociedad Española de Química Clínica) evaluates the quality of the methods monthly.

3. Statistical Analysis

Data are expressed as Mean + SD, median (Q1–Q3) or as number and percentage. For the comparison of continuous variables, Fisher’s test was used for unpaired data, and the chi-square test was used for categorical variables. Pre-gestational food-based iodine consumption was analysed. The use of iodine supplements and/or the consumption of iodized salt were not included in the analysis. Results were divided into 2 groups above and below the daily recommendation for pre-gestational consumption (150 µg/day). To explore the relationship between each lifestyle habit and consumption of at least 150 µg/day of iodine, a generalized linear binary logistic regression model was performed. The dependent variable was used to analyse a minimum iodine consumption of 150 µg/day versus a lower one. The reference value was 0 when iodine intake was less than 150 µg, whereas an intake ≥150 µg/day was taken as value 1. Twenty items were selected, according to their iodine content, as predictors of reaching an iodine consumption of at least 150 µg/day. The consumption of sixteen foods were analysed: vegetables, nuts, EVOO, fatty fish, canned fish, white fish, seafood, whole grains, dairy products (skimmed, semi-skimmed, whole and fortified), processed meats, mayonnaise, and dark chocolate. One item was for sports activity (registered in minutes of moderate physical activity) and 3 items for physical activity score. Nutrition score (12 items) and MEDAS score (14 items) were analysed. For each of the selected items, servings per week and the minutes per week of sports activity, were graduated on an increasing scale with the scores of the questionnaires used. Missing values were excluded from the analysis. The associations between food-based iodine intake per day as categorical variables (>150 µg/day vs. <150 µg/day) and gestational adverse outcomes were studied by the chi-squared test. The magnitude of association between food-based iodine per day intake >150 µg/day vs. <150 µg/day, with the latter as reference group, and gestational outcomes were evaluated using the odds ratio (OR) and 95% confidence interval (95%CI). Analysis was adjusted for age, parity, and smoking status.

4. Results

The mean daily iodine intake in the analysed women was 123 ± 48 µg/day, and the median (Q1–Q3) was 119 (90–140) µg/day. Of the 2523 analysed women, 1922 (76.1%) did not reach the recommended 150 µg of daily iodine intake from foods alone. Women who did not reach 150 µg of food-based iodine per day were younger, were more often multiparous, and had a lower educational status as compared to those who did. The former were more often active smokers, either up to the moment they became aware of pregnancy, or prior to as well as during pregnancy. The percentage of women with hypothyroxinemia was higher in those who did not reach the food-based iodine cut-off point. The consumption of iodized salt was also lower in the group of women who did not reach the daily 150 µg of food-based iodine. No significant differences were observed between both groups when comparing the other variables studied. These data are shown in Table 2.
The number of the predictive cut-off points of weekly servings of each food analysed, the scores of the MEDAS and DNCT questionnaires in association with a daily iodine intake of 150 µg are shown in Table 3.
After applying the binary logistic regression model, the probability of meeting the recommended iodine intake of 150 µg/day (OR; 95% CI) was associated with the consumption of at least 1 weekly serving of shellfish (8.72; 6.96–10.93), 2 daily servings of dairy products (6.43; 5.27–7.86), 8 weekly servings of vegetables (3.84; 3.16–4.65), 3 weekly servings of canned fish (3.07; 2.50–3.77), and/or 7 weekly servings of semi-skimmed dairy (3.02; 2.51–3.65). The MEDAS and Nutrition Score also yielded significant results when they were associated with the consumption of at least 150 µg of daily iodine intake. The physical activity score and the practise of at least 150 min weekly of sports-related activities was also statistically significant (2.45; 1.38–4.35). The results are displayed in Figure 1.
There was a tendency towards a lower rate of maternal-fetal adverse events among women who reached the recommended daily food-based iodine intake of 150 µg. There was a significantly lower rate of early fetal loss before GW18 in women who reached the aforementioned daily iodine intake when compared to those who did not ((3.1%) vs. (4.0%) respectively; p = 0.042). Furthermore, the rate of the composite variable of maternal-fetal adverse events was significantly lower in women who achieved the recommended pre-gestational iodine intake based on foods versus those who did not (205 (34.1%) vs. 747 (38.9%) respectively; p = 0.018). These data are shown in Table 4.
Women with a pre-pregnancy daily food-based iodine consumption of at least 150 µg showed a decrease in the rates of fetal losses < 18 GW (OR; 0.77; 0.39–1.03) as compared with those with a lower iodine food-based intake. In addition, the former women presented a 19% reduction in the risk of suffering at least one adverse event (composite variable) as compared with the latter, with an OR of 0.81 (0.81; 0.67–0.98). The data are given in Figure 2.

5. Discussion

A high percentage of the women in the current study (76.1%) did not reach the recommended pre-gestational level of iodine intake (≥150 µg) with foods alone. Additionally, only 38.6% of these women would have increased their iodine consumption through the pre-gestational use of iodized salt. Furthermore, less than 9% of women initiated iodine supplements before gestation. A recent survey conducted in the Norwegian population also detected a low food-based iodine intake in close to 50% of the women of fertile age studied [42]. Another Norwegian study assessing the food-based iodine consumption found that 74% of women had an average of food-based iodine intake lower than recommended during pregnancy [43], and less than 5% reached the daily iodine consumption recommended by the WHO in pregnancy [16] in the absence of iodine supplementation [44]. However, to our knowledge, the current study is the first to evaluate the average food-based iodine intake in the immediate pre-gestational period. Furthermore, pre-gestational iodine consumption corresponded with early pregnancy iodine intake in the vast majority of women studied, with iodine supplementation starting only upon diagnosis of pregnancy based on food and iodized salt consumption; almost half of the women we have studied would not have attained the recommended level of pre-gestational iodine intake.
Approximately 25% of the women analysed in the current study did reach adequate levels of pre-gestational iodine consumption through dietary foods. In these women, at least 8 weekly servings of vegetables, 3 servings of canned fish, 1 serving of shellfish and/or 2 daily servings of dairy products contributed the most towards attaining a daily iodine intake ≥ 150 µg. The importance of assuring food-based iodine consumption is highlighted by the variability in the iodine content of that has been detected in available iodized salt products [37]. In fact, both packaging and weather conditions can substantially reduce the iodine content of commercially available iodized salt [45]. In addition, estimation of an individual’s salt consumption can be difficult, since the exact amount of salt an individual uses is variable, and quantification challenging. However, our study indicates that requisite pre-gestational iodine intake can be assured with foods alone, without depending on the use of “theoretically” iodized salt. Programs recommending universal consumption of iodized salt are extremely important, particularly if quality controls of the marketed on-the-shelf product are in place [46].
A higher percentage of the analysed women with an adequate food-based iodine intake regularly performed moderate physical activity. The group with a higher food-based iodine consumption could therefore have a healthier lifestyle. In fact, the women who performed physical exercise on a regular basis included less smokers, had a healthier diet, and a greater food-based iodine consumption than those who did not regularly exercise.
The women who assured the requisite pre-gestational iodine intake with foods presented a lower rate of spontaneous miscarriage, and a lower rate of the composite variable of adverse materno-fetal events than those who did not. Iodine deficiency during pregnancy has been found to be related with materno-fetal complications, such as higher rates of Neonatal Intensive Care Unit (NICU) admissions and preterm delivery [47]. Moderate iodine deficiency is associated with a higher risk of miscarriage, preterm labor and low birth weight. Similar studies, using food-based iodine as reference, also detected that iodine deficiency is associated with a decrease in fetal growth, a higher risk of suffering preterm delivery and low fecundity and preeclampsia [44]. Even studies in mildly iodine-deficient regions have found that an adequate iodine status during pregnancy can decrease the rates of perinatal/infant mortality [48]. However, to our knowledge, the current study is the first to detect an association between an adequate food-based iodine consumption in the pre-pregnancy period and a reduction in the rate of the materno-fetal adverse events.
Assuring a sufficient food-based iodine intake could be beneficial for pregnancy by permitting an adequate maternal thyroid response to pregnancy. Women with iodine insufficiency, albeit mild, do not present the physiological increase in circulating FT4 levels seen early in pregnancy [1]. In fact, in conditions of iodine insufficiency, FT4 levels can be low, without a corresponding rise in TSH levels, although the latter can also occur [1]. Furthermore, several authors have found isolated hypothyroxinemia, when occurring early in pregnancy, to be associated with adverse maternal/fetal outcomes [4,17,49,50,51,52,53,54,55]. In the current study, we detected a higher rate of low FT4 levels in the women who did not attain a pregestational (and therefore early gestational) food-based iodine intake of 150 µg or higher as compared with those who did (384 (21.4%) versus 104 (17.3%), p = 0.026, respectively). Hypothyroxinemia is likely an important contributor to the negative effect of a lower food-based iodine intake on the evolution of gestation [56].
Our study has limitations. Although urinary iodine is the most accurate way to determine iodine consumption, considering that the study was carried out at the first gestational visit, when the women studied were already using iodine supplements, this data would not reflect pre-pregnancy iodine consumption. Secondly, food frequency questionnaires can be inaccurate, particularly when retrospective. However, the questionnaire used was previously validated, and applied by a trained professionals. Lastly, the calculation of the iodine content was estimated based on the average iodine content of foods, number and size of servings, all of which are subject to variability and only 200 women, 50 per quarter, were studied for a detailed analysis of the specific food subtypes consumed. However, region-specific micronutrient food content tables were used. The intake of iodized salt was not included for the estimation of pre-gestational food-based iodine consumption. The iodine content of iodized salt is highly variable and is not reflected in the labelling. The salt consumption in general population is also extremely variable, taking into account also that >78% women work outside the home and do not make meals in their own home. This would make it very difficult to quantify accurately the consumption of iodine from iodized salt. Our study only considers the food-based iodine content, which more accurately reflects the importance of long-term iodine consumption prior to pregnancy. Although the rate of insufficient pregestational iodine intake could be reduced, this rate would still be important.

6. Conclusions

The current study finds that the pre-gestational food-based iodine consumption in our population is insufficient to assure an adequate iodine status in the absence of additional iodine sources. Fewer than 25% of the pregnant women evaluated had attained the recommended intake of ≥150 µg daily before pregnancy with foods alone. The women that achieved this level of food-based iodine consumption showed a reduced risk for spontaneous miscarriage, as well as for a composite of adverse materno-fetal events when compared with those eating foods with a lower iodine content. We believe that an optimal consumption of iodine-containing foods in women of childbearing age could help guarantee an adequate maternal iodine reserve, favoring a normal progression of pregnancy. Therefore, an iodine-sufficient diet should be encouraged in these women. Further studies are needed to assess whether this type of diet confers additional benefits to offspring.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/nu13124458/s1, Table S1: Estimation of Iodine content in food items used for calculation of iodine intake from the adapted DNCT questionnaire.

Author Contributions

Conceptualization, V.M., I.R., P.D.M., M.A.R. and A.L.C.-P.; methodology V.M., J.V., L.d.V., N.G.d.l.T., A.B., A.L.C.-P. and M.J.T.; Investigation, C.S., I.M., C.F., A.D., M.J.T., J.A.D., M.C., J.G.R., I.J., M.P., M.A.H., N.I., N.P., P.M., N.P.-F., C.M., M.A.R. and A.L.C.-P.; Data curation, L.d.V. and A.L.C.-P.; Writing—original draft preparation, V.M., N.G.d.l.T., I.R. and A.L.C.-P.; Writing—review and editing, I.R. and A.L.C.-P.; Supervision, A.L.C.-P. and P.D.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by grants from the Instituto de Salud Carlos III/MICINN of Spain under grant number PI20/01758, and European Regional Development Fund (FEDER)‘‘A way to build Europe’’ and Sociedad de Endocrinología, Nutrición y Diabetes de la Comunidad de Madrid (SENDIMAD) under grant number IPI/2018/NR5. The design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, and approval of the manuscript; and decision to submit the manuscript for publication are the responsibilities of the authors alone and independent of the funders.

Data Availability Statement

The data presented in this study are available in supplementary metadata. The data presented in this study are available on request from the corresponding author.

Acknowledgments

We wish to acknowledge our deep appreciation to the administrative personnel and nurses and dieticians from the Laboratory Department (Marisol Sanchez Orta, María Dolores Hermoso Martín, María Victoria Saez de Parayuelo) and the Pregnancy and Diabetes Unit and to all members of the Endocrinology and Nutrition and Obstetrics and Gynecology departments of the San Carlos Clinical Hospital.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. De Escobar, G.M.; Obregon, M.J.; Del Rey, F.E. Role of thyroid hormone during early brain development. Eur. J. Endocrinol. 2004, 151, U25–U37. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Williams, G.R. Neurodevelopmental and neurophysiological actions of thyroid hormone. J. Neuroendocr. 2008, 20, 784–794. [Google Scholar] [CrossRef] [PubMed]
  3. Taylor, P.N.; Lazarus, J.H. Hypothyroidism in pregnancy. Endocrinol. Metab. Clin. N. Am. 2019, 48, 547–556. [Google Scholar] [CrossRef] [PubMed]
  4. Korevaar, T.I.M.; Medici, M.; Visser, T.J.; Peeters, R.P. Thyroid disease in pregnancy: New insights in diagnosis and clinical management. Nat. Rev. Endocrinol. 2017, 13, 610–622. [Google Scholar] [CrossRef]
  5. Krassas, G.E.; Poppe, K.; Glinoer, D. Thyroid function and human reproductive health. Endocr. Rev. 2010, 31, 702–755. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. van der Spek, A.H.; Fliers, E.; Boelen, A. The classic pathways of thyroid hormone metabolism. Mol. Cell. Endocrinol. 2017, 458, 29–38. [Google Scholar] [CrossRef]
  7. Andersson, M.; Karumbunathan, V.; Zimmermann, M.B. Global Iodine status in 2011 and trends over the past decade. J. Nutr. 2012, 142, 744–750. [Google Scholar] [CrossRef] [PubMed]
  8. World Health Organization. Assessment of Iodine Deficiency Disorders and Monitoring Their Elimination: A Guide for Programme Managers, 3rd ed.; World Health Organization: Geneva, Switzerland, 2007; pp. 1–108. ISBN 978-92-4-159582-7. [Google Scholar]
  9. Zimmermann, M.B.; Andersson, M. Global endocrinology: Global perspectives in endocrinology: Coverage of iodized salt programs and Iodine status in 2020. Eur. J. Endocrinol. 2021, 185, R13–R21. [Google Scholar] [CrossRef]
  10. Bath, S.C.; Steer, C.D.; Golding, J.; Emmett, P.; Rayman, M.P. Effect of inadequate Iodine status in UK pregnant women on cognitive outcomes in their children: Results from the avon longitudinal study of parents and children (ALSPAC). Lancet 2013, 382, 331–337. [Google Scholar] [CrossRef]
  11. Hynes, K.L.; Otahal, P.; Hay, I.; Burgess, J. Mild Iodine deficiency during pregnancy is associated with reduced educational outcomes in the offspring: 9-year follow-up of the gestational Iodine cohort. J. Clin. Endocrinol. Metab. 2013, 98, 1954–1962. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Murcia, M.; Espada, M.; Julvez, J.; Llop, S.; Lopez-Espinosa, M.-J.; Vioque, J.; Basterrechea, M.; Riaño-Galan, I.; González-Safont, L.; Alvarez-Pedrerol, M.; et al. Iodine intake from supplements and diet during pregnancy and child cognitive and motor development: The INMA mother and child cohort study. J. Epidemiol. Community Health 2018, 72, 216–222. [Google Scholar] [CrossRef]
  13. Zimmermann, M.B. Iodine deficiency. Endocr. Rev. 2009, 30, 376–408. [Google Scholar] [CrossRef] [Green Version]
  14. Choudhry, H. Nasrullah Iodine consumption and cognitive performance: Confirmation of adequate consumption. Food Sci. Nutr. 2018, 6, 1341–1351. [Google Scholar] [CrossRef]
  15. Toloza, F.J.K.; Motahari, H.; Maraka, S. Consequences of severe Iodine deficiency in pregnancy: Evidence in humans. Front. Endocrinol. 2020, 11. [Google Scholar] [CrossRef]
  16. WHO Secretariat; Andersson, M.; De Benoist, B.; Delange, F.; Zupan, J. Prevention and control of Iodine deficiency in pregnant and lactating women and in children less than 2-years-old: Conclusions and recommendations of the technical consultation. Public Health Nutr. 2007, 10, 1606–1611. [Google Scholar] [CrossRef] [Green Version]
  17. Moleti, M.; Di Bella, B.; Giorgianni, G.; Mancuso, A.; De Vivo, A.; Alibrandi, A.; Trimarchi, F.; Vermiglio, F. Maternal thyroid function in different conditions of Iodine nutrition in pregnant women exposed to mild-moderate Iodine deficiency: An observational study. Clin. Endocrinol. 2011, 74, 762–768. [Google Scholar] [CrossRef]
  18. Candido, A.C.; Morais, N.D.S.D.; Dutra, L.V.; Pinto, C.A.; Franceschini, S.D.C.C.; Alfenas, R.D.C.G. Insufficient Iodine intake in pregnant women in different regions of the world: A systematic review. Arch. Endocrinol. Metab. 2019, 63, 306–311. [Google Scholar] [CrossRef] [Green Version]
  19. Alvarez-Pedrerol, M.; Ribas, N.; García, R.; Rodriguez, A.; Soriano, D.; Guxens, M.; Mendez, M.; Sunyer, J. Iodine sources and Iodine levels in pregnant women from an area without known Iodine deficiency. Clin. Endocrinol. 2010, 72, 81–86. [Google Scholar] [CrossRef]
  20. Zimmermann, M.; Trumbo, P.R. Lodine. Adv. Nutr. 2013, 4, 262–264. [Google Scholar] [CrossRef]
  21. Fuge, R.; Johnson, C.C. Iodine and human health, the role of environmental geochemistry and diet, a review. Appl. Geochem. 2015, 63, 282–302. [Google Scholar] [CrossRef]
  22. Haldimann, M.; Alt, A.; Blanc, A.; Blondeau, K. Iodine content of food groups. J. Food Compos. Anal. 2005, 18, 461–471. [Google Scholar] [CrossRef]
  23. van der Reijden, O.L.; Zimmermann, M.B.; Galetti, V. Iodine in dairy milk: Sources, concentrations and importance to human health. Best Pr. Res. Clin. Endocrinol. Metab. 2017, 31, 385–395. [Google Scholar] [CrossRef]
  24. U.S. Department of Agriculture; Food and Drug Administration (FDA); Office of Dietary Supplements, NIH. USDA, FDA, ODS-NIH Database for the Iodine Content of Common Foods Release (2020). Available online: https://www.ars.usda.gov/northeast-area/beltsville-md-bhnrc/beltsville-human-nutrition-research-center/methods-and-application-of-food-composition-laboratory/mafcl-site-pages/Iodine/ (accessed on 11 October 2021).
  25. Herrick, K.A.; Perrine, C.G.; Aoki, Y.; Caldwell, K.L. Iodine status and consumption of key iodine sources in the U.S. population with special attention to reproductive age women. Nutrients 2018, 10, 874. [Google Scholar] [CrossRef] [Green Version]
  26. WHO. Guideline: Fortification of Food-Grade Salt with Iodine for the Prevention and Control of Iodine Deficiency Disorders; World Health Organization: Geneva, Switzerland, 2014; pp. 1–43. ISBN 978-92-4-150792-9. [Google Scholar]
  27. WHO. Iodine Status Worldwide: WHO Global Database on Iodine Deficiency; World Health Organization: Geneva, Switzerland, 2004; pp. 1–58. ISBN 92-4-159200-1. [Google Scholar]
  28. Ministerio de Sanidad y consume, Sociedad Española de Endocrinología y Nutrición (SEEN). Déficit de Yodo en España. Situación Actual. Available online: https://www.mscbs.gob.es/profesionales/saludPublica/prevPromocion/maternoInfantil/docs/yodoSEEN.pdf (accessed on 17 October 2021).
  29. Iodine Global Network (IGN). Global Scorecard of Iodine Nutrition in 2021. Available online: https://www.ign.org/cm_data/IGN_Global_Scorecard_2021_7_May_2021.pdf (accessed on 11 November 2021).
  30. Vila, L.; Lucas, A.; Donnay, S.; de la Vieja, A.; Wengrovicz, S.; Santiago, P.; Bandrés, O.; Velasco, I.; Garcia-Fuentes, E.; Ares, S.; et al. Iodine nutrition status in Spain needs for the future. Endocrinol. Diabetes Y Nutr. 2020, 67, 61–69. [Google Scholar] [CrossRef]
  31. Rego-Iraeta, A.; Pérez-Fdez, R.; Cadarso-Suárez, C.; Tomé, M.; Fdez-Mariño, A.; Mato, J.; Botana, M.; Solache, I. Iodine nutrition in the adult population of galicia (Spain). Thyroid 2007, 17, 161–167. [Google Scholar] [CrossRef]
  32. Olmedo, P.; García, E.; Gutiérrez, C.; Serrano, M.; Moreno, M.; Ureña, T.; Santiago, P. Assessment of Iodine nutritional status in the general population in the province of Jaén. Endocrinol. Nutr. 2015, 62, 373–379. [Google Scholar] [CrossRef]
  33. Vila, L.; Serra-Prat, M.; de Castro, A.; Palomera, E.; Casamitjana, R.; Legaz, G.; Barrionuevo, C.; Muñoz, J.A.; García, A.J.; Lal-Trehan, S.; et al. Iodine nutritional status in pregnant women of two historically different Iodine-deficient areas of Catalonia, Spain. Nutrition 2011, 27, 1029–1033. [Google Scholar] [CrossRef] [PubMed]
  34. Vila, L. Prevention and control of Iodine deficiencies in Spain. Rev. Esp. Salud Pública 2008, 82, 371–377. [Google Scholar] [CrossRef] [Green Version]
  35. Soriguer, F.; García-Fuentes, E.; Gutierrez-Repiso, C.; Rojo-Martínez, G.; Velasco, I.; Goday, A.; Bosch-Comas, A.; Bordiú, E.; Calle, A.; Carmena, R.; et al. Iodine intake in the adult population. [email protected] study. Clin. Nutr. 2012, 31, 882–888. [Google Scholar] [CrossRef]
  36. Zimmermann, M.B.; Andersson, M. Assessment of Iodine nutrition in populations: Past, present, and future. Nutr. Rev. 2012, 70, 553–570. [Google Scholar] [CrossRef]
  37. FACUA-Consumidores En Acción. Available online: https://www.facua.org/ (accessed on 17 November 2021).
  38. Ruiz-Gracia, T.; Duran, A.; Fuentes, M.; Rubio, M.A.; Runkle, I.; Carrera, E.F.; Torrejón, M.J.; Bordiú, E.; del Valle, L.; de la Torre, N.G.; et al. Lifestyle patterns in early pregnancy linked to gestational diabetes mellitus diagnoses when using IADPSG criteria. The St Carlos gestational study. Clin. Nutr. 2016, 35, 699–705. [Google Scholar] [CrossRef]
  39. Ministerio de Agricultura y Pesca, Alimentación y Medio Ambiente. Informe Del Consumo de Alimentación En España. 2016; pp. 1–225. Available online: https://www.mapa.gob.es/images/es/informe_del_consumo_de_alimentos_en_espana_2016_web_tcm30-419484 (accessed on 17 November 2021).
  40. Mataix Verdú, F.J. Tabla de Composición de Alimentos, 5th ed.; Editorial Universidad de Granada: Granada, Spain, 2011; ISBN 9788433849809. [Google Scholar]
  41. Schröder, H.; Fitó, M.; Estruch, R.; Martínez-González, M.A.; Corella, D.; Salas-Salvadó, J.; Lamuela-Raventós, R.; Ros, E.; Salaverría, I.; Fiol, M.; et al. A short screener is valid for assessing mediterranean diet adherence among older spanish men and women. J. Nutr. 2011, 141, 1140–1145. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Carlsen, M.H.; Andersen, L.F.; Dahl, L.; Norberg, N.; Hjartåker, A. New Iodine food composition database and updated calculations of Iodine intake among Norwegians. Nutrients 2018, 10, 930. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Trumbo, P.; Yates, A.A.; Schlicker, S.; Poos, M. Dietary reference intakes for Vitamin A, Vitamin K, Arsenic, Boron, Chromium, Copper, Iodine, Iron, Manganese, Molybdenum, Nickel, Silicon, Vanadium, and Zinc. J. Am. Diet Assoc. 2001, 101, 294–301. [Google Scholar] [CrossRef]
  44. Abel, M.H.; Caspersen, I.H.; Sengpiel, V.; Jacobsson, B.; Meltzer, H.M.; Magnus, P.; Alexander, J.; Brantsæter, A.L. Insufficient maternal Iodine intake is associated with subfecundity, reduced foetal growth, and adverse pregnancy outcomes in the Norwegian mother, father and child cohort study. BMC Med. 2020, 18, 211. [Google Scholar] [CrossRef] [PubMed]
  45. Diosady, L.L.; Alberti, J.O.; Mannar, M.G.V.; Fitzgerald, S. Stability of Iodine in iodized salt used for correction of Iodine-deficiency disorders. II. Food Nutr. Bull. 1998, 19, 240–250. [Google Scholar] [CrossRef]
  46. Dold, S.; Zimmermann, M.B.; Jukic, T.; Kusic, Z.; Jia, Q.; Sang, Z.; Quirino, A.; Luis, T.O.L.S.; Fingerhut, R.; Kupka, R.; et al. Universal salt iodization provides sufficient dietary iodine to achieve adequate iodine nutrition during the first 1000 days: A cross-sectional multicenter study. J. Nutr. 2018, 148, 587–598. [Google Scholar] [CrossRef]
  47. Gargari, S.S.; Fateh, R.; Bakhshali-Bakhtiari, M.; Saleh, M.; Mirzamoradi, M.; Bakhtiyari, M. Maternal and neonatal outcomes and determinants of Iodine deficiency in third trimester of pregnancy in an Iodine sufficient area. BMC Pregnancy Childbirth 2020, 20, 174–179. [Google Scholar] [CrossRef]
  48. Zimmermann, M.B. The effects of Iodine deficiency in pregnancy and infancy. Paediatr. Périnat. Epidemiol. 2012, 26, 108–117. [Google Scholar] [CrossRef]
  49. Tehrani, F.R.; Nazarpour, S.; Behboudi-Gandevani, S. Isolated maternal hypothyroxinemia and adverse pregnancy outcomes: A systematic review. J. Gynecol. Obstet. Hum. Reprod. 2021, 50, 102057. [Google Scholar] [CrossRef]
  50. Cleary-Goldman, J.; Malone, F.D.; Messerlian, G.; Sullivan, L.; Canick, J.; Porter, T.F.; Luthy, D.; Gross, S.; Bianchi, D.W.; D′Alton, M.E. Maternal thyroid hypofunction and pregnancy outcome. Obstet. Gynecol. 2008, 112, 85–92. [Google Scholar] [CrossRef] [PubMed]
  51. Dosiou, C.; Medici, M. Management of endocrine disease: Isolated maternal hypothyroxinemia during pregnancy: Knowns and unknowns. Eur. J. Endocrinol. 2017, 176, R21–R38. [Google Scholar] [CrossRef] [PubMed]
  52. Gong, X.; Liu, A.; Sun, H.; Li, C.; Yu, X.; Fan, C.; Shan, Z.; Teng, W.; Li, Y.; Li, Y. The impact of isolated maternal hypothyroxinemia during the first and second trimester of gestation on pregnancy outcomes: An intervention and prospective cohort study in China. J. Endocrinol. Investig. 2018, 42, 599–607. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Alexander, E.K.; Pearce, E.N.; Brent, G.A.; Brown, R.S.; Chen, H.; Dosiou, C.; Grobman, W.A.; Laurberg, P.; Lazarus, J.; Mandel, S.J.; et al. 2017 Guidelines of the American Thyroid Association for the diagnosis and management of thyroid disease during pregnancy and the postpartum. Thyroid 2017, 27, 315–389. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Pop, V.J.; Brouwers, E.P.; Wijnen, H.; Oei, G.; Essed, G.G.; Vader, H.L. Low concentrations of maternal thyroxin during early gestation: A risk factor of breech presentation? BJOG Int. J. Obstet. Gynaecol. 2004, 111, 925–930. [Google Scholar] [CrossRef]
  55. Yang, X.; Yu, M.Y.; Zhang, C.; Zhang, Y.; Chen, M.Z.; Dubois, L.; Huang, H.-F.; Fraser, W.D.; Fan, J. The association between isolated maternal hypothyroxinemia in early pregnancy and preterm birth. Thyroid 2020, 30, 1724–1731. [Google Scholar] [CrossRef]
  56. Runkle, I.; de Miguel, M.P.; Barabash, A.; Cuesta, M.; Diaz, Á.; Duran, A.; Familiar, C.; García de la Torre, N.; Herraiz, M.A.; Izquierdo, N.; et al. Early levothyroxine treatment for subclinical hypothyroidism or hypothyroxinemia in pregnancy: The st carlos gestational and thyroid protocol. Front. Endocrinol. 2021, 12, 743057. [Google Scholar] [CrossRef]
Nutrients 13 04458 g001 550
Figure 1. Probability of reaching a pre-gestational food-based iodine intake ≥ 150 µg/day and its association with specific food and servings. OR: Odds ratio; CI: confidence interval; EVOO: extra virgin olive oil; MEDAS: Mediterranean Diet Adherence Screener. All servings are weekly except for the consumption of EVOO and dairy products (without specifying fat content) which are daily.
Figure 1. Probability of reaching a pre-gestational food-based iodine intake ≥ 150 µg/day and its association with specific food and servings. OR: Odds ratio; CI: confidence interval; EVOO: extra virgin olive oil; MEDAS: Mediterranean Diet Adherence Screener. All servings are weekly except for the consumption of EVOO and dairy products (without specifying fat content) which are daily.
Nutrients 13 04458 g001
Nutrients 13 04458 g002 550
Figure 2. Risk for suffering at least one maternal-fetal adverse event and its association with the recommended daily iodine intake of 150 µg. GDM: Gestational Diabetes Mellitus. CMFAO: Composite Materno-foetal Adverse outcomes: at least one event of miscarriage history, early foetal loss, preeclampsia, prematurity, caesarean section, GDM and SGA: small for gestational age/LGA: large for gestational age newborns. OR: Odds ratio; CI: confidence interval.
Figure 2. Risk for suffering at least one maternal-fetal adverse event and its association with the recommended daily iodine intake of 150 µg. GDM: Gestational Diabetes Mellitus. CMFAO: Composite Materno-foetal Adverse outcomes: at least one event of miscarriage history, early foetal loss, preeclampsia, prematurity, caesarean section, GDM and SGA: small for gestational age/LGA: large for gestational age newborns. OR: Odds ratio; CI: confidence interval.
Nutrients 13 04458 g002
Table
Table 1. Baseline characteristics of the women studied.
Table 1. Baseline characteristics of the women studied.
N2523
Age32.64 ± 5.19
Family history of: Type 2 diabetes/MetS(>2 components)113 (4.5%)/560 (22.2%)
History of Prior Miscarriage838 (33.2%)
Ethnicity: Caucasian/Hispanic1530 (60.6%)/789 (31.3%)
Primiparous/multiparous1081 (42.8%)/1432 (56.7%)
University or Technical degree1646 (65.3%)
Works outside of the home1969 (78%)
Smoker: until pregnancy/currently320 (12.7%)/208 (8.2%)
BW (kg)63.8 ± 11.4
BMI (kg/m2)24.14 ± 4.09
SBP (mmHg)108.83 ± 10.34
DBP (mmHg)67.17 ± 8.79
FSG (mg/dL)80.31 ± 6.07
FSI (mlU/L)18.29 ± 21.15
HOMA-IR3.65 ± 4.28
Cholesterol (mg/dL)173.02 ± 30.96
Triglycerides (mg/dL)81.48 ± 37.83
TSH (µIU/mL)2.04 ± 1.53
FT4 (pg/mL)8.64 ± 1.49
Pre-pregnancy Nutrition Score0.32 ± 3.12
Pre-pregnancy MEDAS score4.89 ± 1.74
Pre-pregnancy Physical activity score−1.83 ± 0.96
Pre-pregnancy supplements:
Iodine supplement22 (0.9%)
Folic acid + iodine supplement198 (7.8%)
Pregnancy supplements:
Iodine supplement127 (5.0%)
Folic acid + iodine supplement1313 (52.0%)
Use of iodized salt 1021 (40.5%)
Data are Mean ± SD or number (%). METS: Metabolic Syndrome. BW: body weight; BMI: body mass index; SBP: systolic blood pressure; DBP: diastolic blood pressure; FSG: fasting serum glucose; FSI: fasting serum insulin; HOMA-IR: Homeostatic model assessment; MEDAS Score: 14-point Mediterranean Diet Adherence Screener; TSH: thyroid stimulating hormone; FT4: free thyroxin.
Table
Table 2. Characteristics of the women studied according to pre-gestational food-based iodine consumption.
Table 2. Characteristics of the women studied according to pre-gestational food-based iodine consumption.
Iodine Intake < 150 µg/DayIodine Intake ≥ 150 µg/Dayp
N1922 (76.1%)602 (23.9%)
Age 32.4 ± 5.333.4 ± 4.8 0.000
Miscarriage/GDM History670 (34.9%)/61 (3.2%)202 (33.5%)/24 (4.0%)0.906
Caucasian Ethnicity1166 (60.7%)364 (60.6%)0.166
Primipary820 (42.8%)261 (43.5%)0.044
University degree1214 (63.3%)432 (71.8%)0.003
Salaried work1496 (77.9%)474 (78.7%)0.507
Family history of MetS382 (19.9%)121 (21.1%)0.792
Smoker until/during pregnancy255 (13.3%)/171 (8.9%)65 (10.8%)/37 (6.1%)0.010
Body Weight (Kg)61.9 ± 11.5 61.5 ± 10.4 0.465
BMI (Kg/m2)23.4 ± 4.1 23.1 ± 3.8 0.073
sBP (mm Hg)108.9 ± 10.4108.9 ± 10.10.915
dBP (mm Hg)67.1 ± 8.967.3 ± 8.50.710
FSG (mg/dl)80 ± 680 ± 60.435
FPI (µIU/mL)18 ± 2118 ± 210.124
HOMA-IR3.64 ± 4.303.69 ± 4.250.777
Total Cholesterol (mg/dl)172 ± 30175 ± 330.914
Triglycerides (mg/dl)81 ± 3484 ± 460.092
TSH µIU/mLTSH > 2.5 µIU/mL2.13 ± 1.41 530 (27.6%)2.02 ± 1.41 162 (27.0%)0.1660.411
FT4 pg/mLFT4 < 7.5 pg/mL8.56 ± 1.57 384 (21.4%)8.67 ± 1.47 104 (17.3%)0.1700.026
Use of Iodized salt742 (38.6%)280 (46.5%)0.006
GDM: gestational diabetes mellitus; MetS: metabolic syndrome; BMI: body mass index; sBP: systolic blood pressure; dBP: diastolic blood pressure; FSG: fasting serum glucose; FPI: fasting plasma insulin; HOMA-IR: Homeostatic model assessment; TSH: thyroid stimulating hormone; FT4: free thyroxine. The consumption of iodized salt was not included in the analysis of pre-gestational food-based iodine consumption.
Table
Table 3. Rate of pre-gestational individual foods consumption and exercise per group of pre-gestational food-based iodine intake.
Table 3. Rate of pre-gestational individual foods consumption and exercise per group of pre-gestational food-based iodine intake.
Iodine Intake < 150 µg/DayIodine Intake ≥ 150 µg/Dayp
≥8 servings of vegetable 406/1922 (21.1%)305/602 (50.7%)0.000
≥2 servings of nuts580/1922 (30.2%)264/602 (43.9%)0.000
Consumption of EVOO1544/1922 (80.3%)541/602 (89.9%)0.000
≥2 servings of oily fish 470/1922 (24.5%)238/602 (39.5%)0.000
≥3 servings of canned oily fish 302/1922 (15.7%)219/602 (36.4%)0.000
≥1 serving of white fish 1262/1922 (65.7%)508/602 (84.4%)0.000
≥1 serving of shellfish 168/1922 (8.7%)274/602 (45.5%)0.000
≥2 servings of whole grain cereals527/1921 (27.4%)217/602 (36.0%)0.000
≥4 servings of fat-free dairy products 576/1922 (30.0%)306/602 (50.8%)0.000
≥7 servings of low-fat dairy products 569/1922 (29.6%)337/602 (56.0%)0.000
≥5 servings of full-fat dairy products 900/1922 (46.8%)404/602 (67.1%)0.000
≥7 servings of fortified dairy products248/1921 (12.9%)133/602 (22.1%)0.000
≥2 servings of dairy products 476/1921 (24.8%)409/602 (67.9%)0.000
≤1 servings of processed red meat 1583/1922 (82.4%)532/601 (88.2%)0.000
>0 serving of mayonnaise serving1265/1921 (65.9%)436/602 (72.4%)0.001
≥6 servings of dark chocolate serving70/1922 (3.6%)42/602 (7.0%)0.001
≥150 min of sports activity 28/1921 (1.5%)21/600 (3.5%)0.001
≥−1 Physical activity Score583/1919 (30.4%)232/601 (38.6%)0.000
≥1 Nutrition score791/1914 (41.3%)404/599 (67.4%)0.000
≥6 MEDAS score574/1832 (31.3%)267/570 (46.8%)0.000
EVOO: extra virgin olive oil; MEDAS: 14-points Mediterranean Diet Adherence Screener; All servings are weekly except for the consumption of EVOO and dairy products (those without specifying fat content), which are daily.
Table
Table 4. Maternal-fetal adverse outcomes by pre-gestational food-based iodine intake.
Table 4. Maternal-fetal adverse outcomes by pre-gestational food-based iodine intake.
Iodine Intake < 150 µg/DayIodine Intake ≥ 150 µg/Dayp
History of prior miscarriage672/1922 (35.1%)201/602 (33.4%)0.296
Fetal loss < 18 GW in current pregnancy68/1922 (4.0%)18/602 (3.1%)0.042
Prematurity104/1854 (5.6%)28/584 (4.9%)0.077
Preeclampsia28/1854 (1.5%)7/584 (1.2%)0.374
GDM367/1854 (19.8%)109/584 (18.7%)0.326
Non-instrumental vaginal delivery1118/1854 (60.3%)364/584 (62.3%)0.230
Caesarean section402/1854 (21.7%)124/584 (21.2%)0.764
SGA/LGA401/1854 (21.6%)104/584 (17.8%)0.280
CMFAO747/1922 (38.9%)205/602 (34.1%)0.018
GDM: gestational diabetes mellitus; SGA: small for gestational age; LGA: large for gestational age; CMFAO: Composite materno-foetal Adverse outcomes. The consumption of iodized salt was not included in the analysis of pre-gestational food-based iodine consumption.
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Melero, V.; Runkle, I.; Garcia de la Torre, N.; De Miguel, P.; Valerio, J.; del Valle, L.; Barabash, A.; Sanabria, C.; Moraga, I.; Familiar, C.; et al. The Consumption of Food-Based Iodine in the Immediate Pre-Pregnancy Period in Madrid Is Insufficient. San Carlos and Pregnancy Cohort Study. Nutrients 2021, 13, 4458. https://doi.org/10.3390/nu13124458

AMA Style

Melero V, Runkle I, Garcia de la Torre N, De Miguel P, Valerio J, del Valle L, Barabash A, Sanabria C, Moraga I, Familiar C, et al. The Consumption of Food-Based Iodine in the Immediate Pre-Pregnancy Period in Madrid Is Insufficient. San Carlos and Pregnancy Cohort Study. Nutrients. 2021; 13(12):4458. https://doi.org/10.3390/nu13124458

Chicago/Turabian Style

Melero, Verónica, Isabelle Runkle, Nuria Garcia de la Torre, Paz De Miguel, Johanna Valerio, Laura del Valle, Ana Barabash, Concepción Sanabria, Inmaculada Moraga, Cristina Familiar, and et al. 2021. "The Consumption of Food-Based Iodine in the Immediate Pre-Pregnancy Period in Madrid Is Insufficient. San Carlos and Pregnancy Cohort Study" Nutrients 13, no. 12: 4458. https://doi.org/10.3390/nu13124458

APA Style

Melero, V., Runkle, I., Garcia de la Torre, N., De Miguel, P., Valerio, J., del Valle, L., Barabash, A., Sanabria, C., Moraga, I., Familiar, C., Durán, A., Torrejón, M. J., Diaz, J. A., Cuesta, M., Ruiz, J. G., Jiménez, I., Pazos, M., Herraiz, M. A., Izquierdo, N., ... Calle-Pascual, A. L. (2021). The Consumption of Food-Based Iodine in the Immediate Pre-Pregnancy Period in Madrid Is Insufficient. San Carlos and Pregnancy Cohort Study. Nutrients, 13(12), 4458. https://doi.org/10.3390/nu13124458

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