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Article

Associations of Food and Nutrient Intake with Serum Hepcidin and the Risk of Gestational Iron-Deficiency Anemia among Pregnant Women: A Population-Based Study

by
Noor Rohmah Mayasari
1,
Chyi-Huey Bai
2,3,
Tzu-Yu Hu
1,
Jane C.-J. Chao
1,
Yi Chun Chen
1,
Ya Li Huang
2,3,
Fan-Fen Wang
4,
Alexey A. Tinkov
5,6,
Anatoly V. Skalny
6,7 and
Jung-Su Chang
1,8,9,10,*
1
School of Nutrition and Health Sciences, College of Nutrition, Taipei Medical University, Taipei 110, Taiwan
2
School of Public Health, College of Public Health, Taipei Medical University, Taipei 110, Taiwan
3
Department of Public Health, School of Medicine, College of Medicine, Taipei Medical University, Taipei 110, Taiwan
4
Department of Internal Medicine, Yangming Branch, Taipei City Hospital, Taipei 11146, Taiwan
5
Laboratory of Ecobiomonitoring and Quality Control, Yaroslavl State University, 150003 Yaroslavl, Russia
6
Laboratory of Molecular Dietetics, IM Sechenov First Moscow State Medical University (Sechenov University), 119435 Moscow, Russia
7
Laboratory of Medical Elementology, KG Razumovsky Moscow State University of Technologies and Management, 109004 Moscow, Russia
8
Graduate Institute of Metabolism and Obesity Sciences, College of Nutrition, Taipei Medical University, Taipei 110, Taiwan
9
Nutrition Research Center, Taipei Medical University Hospital, Taipei 110, Taiwan
10
Chinese Taipei Society for the Study of Obesity (CTSSO), Taipei 110, Taiwan
*
Author to whom correspondence should be addressed.
Nutrients 2021, 13(10), 3501; https://0-doi-org.brum.beds.ac.uk/10.3390/nu13103501
Submission received: 31 August 2021 / Revised: 25 September 2021 / Accepted: 28 September 2021 / Published: 3 October 2021
(This article belongs to the Special Issue Maternal Nutrition in Pregnancy)
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Abstract

:
Hepcidin is a regulator of iron metabolism. Diet affects the body’s iron status, but how it influences hepcidin concentrations and the risk of gestational iron-deficiency anemia (IDA) remains unclear. We investigated relationships of food and nutrient intake with serum hepcidin levels in relation to the iron status at a population scale. A retrospective cross-sectional study was conducted based on data obtained from the Nationwide Nutrition and Health Survey in pregnant women, Taiwan (2017~2020). In total, 1430 pregnant women aged 20~45 years with a singleton pregnancy were included. Data from blood biochemistry, 24-h dietary recall, and a food frequency questionnaire were collected during a prenatal checkup. Adjusted multivariate linear and logistic regression analyses were employed to measure the beta coefficient (ß) and 95% confidence interval (CI) of serum hepcidin and the odds ratio (OR) of IDA. In IDA women, serum hepcidin levels were positively correlated with the intake frequency of Chinese dim sum and related foods (β = 0.037 (95% CI = 0.015~0.058), p = 0.001) and dark leafy vegetables (β = 0.013 (0.001~0.025), p = 0.040), but they were negatively correlated with noodles and related products (β = −0.022 (−0.043~−0.001), p = 0.038). An adjusted multivariate logistic regression analysis showed that dietary protein [OR: 0.990 (0.981~1.000), p = 0.041], total fiber [OR: 0.975 (0.953~0.998), p = 0.031], and rice/rice porridge [OR: 1.007 (1.00~1.014), p = 0.041] predicted gestational IDA. Total carbohydrates [OR: 1.003 (1.000~1.006), p = 0.036], proteins [OR: 0.992 (0.985~0.999), p = 0.028], gourds/shoots/root vegetables [OR: 1.007 (0.092~1.010), p = 0.005], and to a lesser extent, savory and sweet glutinous rice products [OR: 0.069 (0.937~1.002), p = 0.067] and dark leafy vegetables [OR: 1.005 (0.999~1.011), p = 0.088] predicted IDA. The risk of IDA due to vegetable consumption decreased with an increasing vitamin C intake (p for trend = 0.024). Carbohydrates and vegetables may affect the gestational iron status through influencing hepcidin levels. Vitamin C may lower the risk of gestational IDA due to high vegetable consumption.

1. Introduction

Iron-deficiency (ID) anemia (IDA) is recognized as the most widespread nutritional deficiency affecting 56 million pregnant women worldwide [1]. Globally, trends and prevalences of gestational anemia vary significantly across regions and countries [2]. The prevalence of anemia among pregnant women ranges from 56% in Central and West Africa and 52% in South Asia to 22% in high-income countries [2]. In North America, the prevalence of gestational ID is very low (7.3%) in the first trimester but significantly increases in the second (23.7%) and third trimesters (39.2%) [3]. This corresponds to a progressive rise in gestational IDA in the first, second, and third trimesters: 2.7%, 2.2%, and 10.8%, respectively [3]. However, a recent survey showed an increasing trend of gestational ID (23.8%) in the first trimester in 2021 [4]. Gestational IDA is associated with the risk of maternal mortality and both cognitive and behavioral abnormalities of neonates [5,6].
Iron bioavailability in pregnancy is controlled by the hepcidin hormone. Hepcidin, a negative master iron regulator, controls iron homeostasis through proteolytic degradation of ferroportin, the only known mammalian iron exporter [7]. Currently, how the hepcidin level is regulated during pregnancy remains unclear. Outside of pregnancy, hepcidin is downregulated by low body iron storage, hypoxia, and anemia (e.g., erythropoietic activity), and it is upregulated by inflammation or high iron stores [7,8]. In healthy pregnancies, maternal hepcidin concentrations are gradually downregulated in the second and third trimesters, and they are nearly undetectable by late pregnancy [7,9,10,11]. Decreasing circulating hepcidin levels during the gestational stages indicates maternal iron deprivation, and it is vital for the maintenance of proper maternal and embryonic iron homeostasis [12]. Low levels of serum hepcidin enhances maternal dietary iron absorption and the transfer of dietary iron across the placenta, resulting in enhancement of the neonatal iron status [13]. In contrast, high gestational hepcidin levels decrease dietary iron absorption and impair the efficacy of maternal iron supplementation, as well as the transfer of maternal iron to the fetus, leading to restricted iron bioavailability of the fetus. Overall, low levels of maternal hepcidin may allow a supply of iron into the circulation-placenta-neonate axis and facilitate iron endowment to the fetus [7].
A few studies investigated the relationship of diet with the hepcidin-iron axis [14,15,16,17], but none of them focused on pregnancy. Foods such as vegetables and carbohydrates can potentially affect hepcidin levels [14,16,17,18], but results are inconsistent. Vegetables such as dark leafy vegetables and bamboo shoots have an iron-inhibitory effect, presumably due to phytate- or phenolic compound-mediated iron-chelating effects [19,20]. A study found that adolescent girls who had the highest intake of green leafy vegetables (e.g., amaranth) had significantly higher levels of serum hepcidin and ferritin compared to those with the lowest intake [16]. Administration of T. occidentalis leaves led to modest increases in hemoglobin (Hb) and hepatic iron levels and hepcidin messenger (m)RNA expression in animals with a diet-induced ID [14]. In contrast, supplementation with moringa leaf to rats with diet-induced ID resulted in increased serum iron levels but decreased hepatic hepcidin and ferroportin expressions [17]. Vegetables are also polyphenol-rich foods, and polyphenols may regulate hepcidin levels. For example, studies showed that quercetin [21] and myricetin [22] suppress hepcidin synthesis via the bone morphogenetic protein 6 (BMP6)/mothers against decapentaplegic homolog 4 (SMAD4) signaling pathways. In contrast, an animal study showed that a quercetin injection decreased the non-heme iron absorption rate, possibly through downregulating ferroportin, but it enhanced hepcidin synthesis [23]. Carbohydrate-containing foods such as cereals and brown/milled rice may inhibit iron absorption due to the presence of phytates and fiber [24,25]. Ascorbic acid (vitamin C) can prevent the iron-chelating effects of dietary fiber or phenolic compounds in vegetables and carbohydrate-rich foods, and it can also stimulate iron uptake by inhibiting hepcidin expression [26].
ID is still the most common cause of anemia in pregnant women. Currently, how foods and nutrients affect maternal hepcidin levels and the risk of gestational IDA remain largely unknown. By studying a nationwide representative population, the broad aim of this study was to investigate the relationships of food and nutrient intake with serum hepcidin and the risk of gestational IDA at a population scale among pregnant women in Taiwan.

2. Materials and Methods

2.1. Study Design and Population

This study was a retrospective cross-sectional study based on data obtained from the Nationwide Nutrition and Health Survey in pregnant women, which was conducted in Taiwan in 2017~2019 (Pregnant NAHSIT 2017~2019). Stratified probability sampling was used to stratify the sample population into four strata: northern, central, southern, and eastern regions. For each stratum, at least two medical facilities were selected according to the number of prenatal examinations each year. Pregnant women were recruited at the prenatal care center, and they had to meet all of the following criteria to be eligible for the study: (1) aged 15 years or older, (2) with a Taiwanese residency and able to speak fluent Chinese or Taiwanese, (3) had received a maternal health handbook, and (4) agreed to participate and provided a copy of signed written informed consent (N = 1502). In Taiwan, prenatal care checkups are based on recommendations in the maternal health handbook in the interval of 13~17 weeks for the first trimester, 22~26 weeks for the second trimester, and >29 weeks for the third trimester. In this study, 72 participants were excluded due to being underage (n = 7), having multiple pregnancies (n = 33), and lacking information on blood biochemistry or dietary data (n = 32). In total, 1430 respondents were included in the analysis. All participants provided written informed consent. The study was approved by the Institutional Review Board of Taipei Medical University (no. TMU-JIRB N201707039) and was therefore performed in accordance with ethical standards laid down in the Declaration of Helsinki.

2.2. Data Collection

In brief, pregnant NAHSIT 2017–2019 included three components: (1) a self-reported questionnaire consisting of socioeconomic data, health history, and use of prenatal supplements; (2) a face-to-face interview to obtain habitual dietary intake; and (3) blood biochemistry. A self-reported baseline questionnaire included information such as age, pre-pregnancy body-mass index (pBMI), region, trimester, parity, and reported use of prenatal dietary supplements (e.g., multivitamins, vitamin B12, folate, and iron). The pBMI (kg/m2) was calculated from self-reported pre-pregnancy body weight and body height. Dietary data were collected by a 24-h recall and food frequency questionnaire (FFQ) during face-to-face interviews by an experienced dietitian. Blood samples were collected during a prenatal visit to assess the iron status.

2.3. 24-h Dietary Recall and FFQ

Participants were required to recall all foods or beverages consumed in the past 24 h, and portion sizes were estimated by an experienced dietitian using food models, picture aids, and household utensils. Detailed information on the food consumed (e.g., cooking methods, type of meal, mealtime, snacking, and place) was also recorded. Nutrient intake was calculated using the online software Cofit Pro (Cofit Healthcare, Taipei, Taiwan) based on the Taiwan Food Nutrient Database.
The interviewer-administrated FFQ developed in this study consisted of 59 food items. The FFQ was modified from the NAHSIT Taiwanese FFQ, which originally consisted of 64 food items [27]. In this study, food items were assembled into 33 food groups based on the similarity of food characteristics and nutritional contents (Supplementary Table S1). Similar foods were listed close to each other to prevent redundant collection [27]. Participants were asked to recall their usual frequency of each food item during the past month. The frequency of consumption was reported as how often each food was consumed: (1) how many times per day, (2) how many times per week, or (3) how many times per month. The mean consumption of each food group was presented as times/month. A validation study showed that the Taiwanese FFQ for Chinese-speaking people in Taiwan is reproducible and provides a useful measure of habitual intake over a 6-month period [27]. The FFQ also exhibited acceptable reproducibility and validity in assessing most food and nutrient intake levels among pregnant women in China [28].
Initially, 33 food groups were included in the statistical analysis. Since the broad aim of this study was to investigate foods that may influence levels of hepcidin, a master iron regulator, we first performed a multivariate linear regression analysis to investigate the relationship between individual food groups and serum hepcidin levels. Fifteen food items were removed from further analysis due to having no correlation with serum hepcidin levels. The 18 food groups selected for the further investigation included rice/rice porridge/related products; noodles/related products; breakfast cereals/oats/related products; Chinese dim sum/related foods; sweet buns/bean buns/related products; savory and sweet glutinous rice; light-colored vegetables; dark leafy vegetables; gourds and root vegetables; legumes; total vegetables; fresh fruits; 100% pure fruit juice/vegetable juice; canned fruits/dried fruits/jam; fish/shellfish/seafood; roe and processed seafood products; poultry meat; and liver/organs/blood products (Table 2). The FFQ provides the number of frequencies of food intake each month. In this study, the FFQ could not provide nutrient intake estimation. We used a 24-h recall to estimate nutrient intake.

2.4. Laboratory Examination

All participants underwent blood collection by venipuncture at a medical facility. Hemoglobin (Hb) was measured by a complete blood cell count using a hematology analyzer (Sysmex, Kobe, Japan). Serum ferritin was measured by a chemiluminescence immunoassay by Beckman Coulter Unicel DxC 800 (Beckman Coulter, Brea, CA, USA). Transferrin saturation (TS) was calculated by dividing serum iron by the total iron-binding capacity (TIBC). Serum iron was measured by a ferrozine-based colorimetric assay and TIBC by an immunoturbidimetric method with a Beckman Coulter Unicel DxC 800 (Beckman Coulter). Serum hepcidin levels were measured with a human hepcidin DuoSet enzyme-linked immunosorbent assay (ELISA) (R&D Systems, Minneapolis, MN, USA), according to the manufacturer’s instructions. Variation in the intra- and inter-assay coefficients of serum hepcidin was <10%.

2.5. Definitions

According to the World Health Organization (WHO), ID is defined as TS of <16% [29] and serum ferritin of <15 ng/mL [30]. The Center of Disease Control and Prevention (CDC) defines Hb levels of <11.0 g/dL in the first and third trimesters of pregnancy and <10.5 g/dL in the second trimester as anemia [31]. Gestational IDA is defined as (1) an Hb level of <11 g/dL in the first and third trimesters and <10.5 g/dL in the second trimester, (2) TS of <16%, and (3) serum ferritin of <15 ng/mL. Trimesters (Ts) are defined according to guidelines of the Ministry of Health and Welfare, Taiwan: (1) T1 as the first 17 weeks of pregnancy following the last normal menstrual period, (2) T2 as weeks 18~28, and (3) T3 as weeks 29~40.

2.6. Statistical Analysis

Serum hepcidin levels were stratified into quartiles (Qs), with Q1 being the lowest and Q4 being the highest values. Continuous variables are presented as the mean ± standard deviation (SD), and categorical variables are presented as a number (percentage). Since our data provided a sufficiently large sample population, the linear regression required no assumption of a normal distribution [32]. Total energy intake using a residual method was adjusted for in this study [33]. A general linear model and Chi-squared test were used to analyze the p for trend between variables for continuous data and categorical data, respectively. Adjusted multivariate linear and logistic regression analyses were employed to measure the beta coefficient (ß) and 95% confidence interval (CI) of serum hepcidin and the odds ratio (OR) of IDA, using nutrient intake levels and food groups as predictors. The significance level for the p for trend and p value was defined as <0.05. Data were analyzed using SPSS vers. 21 (IBM, Armonk, NY, USA) and GraphPad Prism 5 (GraphPad Software, San Diego, CA, USA).

3. Results

3.1. Maternal Baseline Characteristics Stratified by Quartiles (Qs) of Serum Hepcidin Levels

Table 1 shows baseline characteristics of the study participants, according to serum hepcidin levels. Compared to those with the lowest (Q1) serum hepcidin levels, pregnant women with the highest serum hepcidin (Q4) were older, heavier, had the highest proportions of living in the northern area of Taiwan (38.1%), a primiparous rate (59.7%), in trimester 1 (49.9%), and used total prenatal supplements (90.9%) and folate supplements (55.7%) (all p for trend <0.01) (Table 1). Blood biochemical analyses showed that serum hepcidin levels were positively correlated with all iron biomarkers of Hb, %TS, and serum ferritin (all p for trend <0.001). In contrast, serum hepcidin levels were negatively correlated with the prevalence of anemia (16%), IDA (0%), and ID (0.3%), except for the prevalence of non-IDA anemia (16%), which was positively correlated with serum hepcidin levels (all p for trend <0.001) (Table 1).

3.2. Associations between Maternal Nutrient/Food Intake and Serum Hepcidin Levels

We next investigated relationships between food and nutrient intake and serum hepcidin levels among pregnant women. Table 2 shows that serum hepcidin levels were positively correlated with intake levels of dietary fiber (Q1: 1.5 ± 8.6 g vs. Q4: 3.0 ± 9.4 g), vitamin C (Q1: 67.7 ± 100.3 g vs. Q4: 86.0 ± 145.2 g), 100% pure fruit juice or fruit/vegetable juice (Q1: 5.4 ± 8.6 times/month vs. Q4: 7.3 ± 12.9 times/month), and canned fruits/dried fruits/jam (Q1: 2.3 ± 9.6 times/month vs. Q4: 4.4 ± 14.5 times/month) (all p for trend <0.05). In contrast, negative linear trends were found between serum hepcidin levels and consumption frequencies of breakfast cereals/oats/related products (Q1: 2.9 ± 9.3 times/month vs. Q4: 1.4 ± 8.5 times/month), sweet buns/bean buns/related products (Q1: 3.2 ± 6.2 times/month vs. Q4: 2.1 ± 5.1 times/month), light-colored vegetables (Q1: 23.4 ± 21.3 times/month vs. Q4: 21.2 ± 19.2 times/month), gourds/shoots/root vegetables (Q1: 29.3 ± 26.2 times/month vs. Q4: 25.4 ± 22.8 times/month), legumes (Q1: 4.0 ±7.9 times/month vs. Q4: 2.7 ± 4.8 times/month), and fish/shellfish/seafood (Q1: 20.9 ± 20.1 times/month vs. Q4: 19.1 ± 18.0 times/month) (all p for trend <0.05) (Table 2).

3.3. Potential Foods and Nutrients That Affect Serum Hepcidin Levels

We next performed a multivariate linear regression analysis to investigate the predictive effects of nutrients and foods on serum hepcidin levels stratified by the iron status (Table 3). For all women, serum hepcidin levels were positively associated with intake frequency levels of savory/sweet glutinous rice products (β = 0.677 (95% CI: 0.330~1.024), p < 0.001), canned fruits/dried fruits/jam (β = 0.157 (0.009~0.304), p = 0.037), and liver/organs/blood products (β = 0.332 (0.139~0.526), p = 0.001) but negatively correlated with breakfast cereals/oats/related products (β = −0.187 (−0.370~−0.003), p = 0.046), gourds/shoots/root vegetables (β = −0.071 (−0.133~−0.010), p = 0.022), and to a lesser extent, light-colored vegetables (β = −0.075 (−0.150~0.001), p = 0.052), after adjusting for covariates (age, pBMI, region, parity, total supplement use, and trimester) (Table 3: all women).
Among non-IDA pregnant women, intake frequency levels of savory/sweet glutinous rice products (β = 0.662 (0.218~1.107), p = 0.004), roe/processed seafood products (β = 1.223 (0.0.321~2.124), p = 0.008), and liver/organs/blood products (β = 0.489 (0.189~0.790), p = 0.001) were positively correlated with serum hepcidin levels, but intake of breakfast cereals/oats/related products (β = −0.295 (−0.567~−0.023), p = 0.034) was negatively correlated with serum hepcidin levels (Table 3: non-IDA). For ID women, the intake frequency of dark leafy vegetables (β = 0.012 (0.000~0.023), p = 0.006) was positively correlated with serum hepcidin levels (Table 3: ID). Among IDA women, serum hepcidin levels were positively associated with the intake frequency of Chinese dim sum/related foods (β = 0.037 (0.015~0.058), p = 0.001) and dark leafy vegetables (β = 0.013 (0.001~0.025), p = 0.040), but negatively correlated with noodles/related products (β = −0.022 (−0.043~−0.001), p = 0.038) (Table 3: IDA).

3.4. Predictive Effects of Nutrients and Food Groups on Gestational ID and IDA

Figure 1 shows that after adjusting for age, pBMI, region, parity, total supplement use, and trimester, protein [OR: 0.990 (0.981~1.000), p = 0.041], total dietary fiber [OR: 0.975 (0.953~0.998), p = 0.031], rice/rice porridge [OR: 1.007 (1.00~1.014), p = 0.041], and to a lesser extent, dietary iron [OR: 0.970 (0.953~0.098), p = 0.073] independently predicted gestational IDA. Factors independently associated with ID were total carbohydrates [OR: 1.003 (1.000~1.006), p = 0.036], proteins [OR: 0.992 (0.985~0.999), p = 0.028], gourds/shoots/root vegetables [OR: 1.007 (0.092~1.010), p = 0.005], and borderline associations were observed with savory/sweet glutinous rice products [OR: 0.069 (0.937~1.002), p = 0.067] and dark leafy vegetables [OR: 1.005 (0.999~1.011), p = 0.088], after adjusting for covariates (age, pBMI, region, parity, total supplement use (%), and trimester).
Figure 2A shows that individuals with the highest intake levels of dark leafy vegetables (T3) and the lowest intake levels of vitamin C (T1) had the highest risk for IDA, and the risk decreased with increasing vitamin C consumption; OR = 2.47 (1.32~4.6), 1.17 (0.63~2.18), and 1.31 (0.70~2.44) for T1, T2, and T3, respectively (p for trend = 0.024). A similar relationship was observed for individuals with the highest intake levels of gourds/shoots/root vegetables (T3) and vitamin C; OR = 1.92 (1.00~3.68), 1.23 (0.65~2.30), 1.31 (0.68~2.50) for vitamin C at T1, T2, and T3, respectively (Figure 2B).

4. Discussion

Hepcidin is the master regulator of iron homeostasis, but its regulation during pregnancy remains unclear. As far as we are aware, this is among the first study to investigate associations of intake of foods and nutrients with hepcidin levels. Using cross-sectional data from 1456 pregnant women who participated in the Nationwide Nutrition and Health Survey in pregnant women in Taiwan (2017~2020) (Pregnant NAHSIT 2017~2020), we found that serum hepcidin was inversely correlated with trimester and the prevalences of ID and IDA. This suggests that as pregnancy progress, serum hepcidin levels decrease as circulating iron cannot meet the demand of erythropoiesis. Low hepcidin levels can enhance dietary iron absorption and iron bioavailability across the placenta to support fetal development. Food-hepcidin relationships seem to be dependent on the iron status of pregnant women. Total carbohydrates, carbohydrate-rich foods (rice/rice porridge), and vegetables (dark leafy vegetables, and gourds/shoots/root vegetables) predicted the risk of ID or IDA. In contrast, dietary protein, total dietary fiber, and to a lesser extent, dietary iron protected against gestational IDA. Increased intake of vitamin C may lower the risk of IDA associated with high vegetable intake (dark leafy vegetables and gourds/shoots/root vegetables).
The present study found that dark leafy vegetables were positively correlated with hepcidin levels. To put our results into perspective, we observed that one frequency increase in dark leafy vegetable consumption increased serum hepcidin levels by 0.013 and 0.012 ng/mL in pregnant women with IDA and ID, respectively (all p < 0.005). Vegetables are polyphenol-rich foods. The literature shows that polyphenols may either up- or downregulate hepcidin expression. Zen and colleagues found that genistein stimulates hepcidin expression via enhanced signal transduction and activator of transcription 3 (STAT3) in HepG2 cells [34]. An animal study revealed that quercetin inhibited intestinal non-heme iron absorption via decreasing duodenal divalent metal transporter 1 (DMT1), duodenal cytochrome B (Dcytb), and ferroportin but increasing hepcidin expression in the liver and spleen [23]. In contrast, Mu et al. found that myricetin potently inhibited hepcidin expression, and this effect was mediated by BMP/SMAD signaling [22]. An in vivo study showed that epigallocatechin-3-gallate (EGCG) inhibited interleukin (IL)-6-induced hepcidin [35]. Overall, polyphenols may influence the relationship between vegetable consumption and the risk of gestational ID/IDA.
Vitamin C may also play a role in vegetable consumption and the IDA risk. The risk of IDA was 2.47- and 1.92-fold higher among pregnant women who consumed the lowest vitamin C (T1) but highest levels of dark leafy vegetables (T3: 49 times/month) and gourds/shoots/root vegetables (T3: 55 times/month), respectively, compared to those who consumed the lowest levels. The risk decreased with increasing vitamin C consumption (T3: 194 mg/day) for women with the highest intake of dark leafy vegetables (T3) and gourds/shoots/root vegetables (T3). Ghatpande el at. found that low consumption of vitamin C-rich fruits was associated with lower levels of circulating iron [16]. Vegetables contain a high amount of dietary iron. The bioavailability of plant-based iron depends upon the content of promoters (vitamin C) and inhibitors (phytates, tannins, and polyphenols) [16]. Plant iron is the non-heme iron, ferric iron (Fe3+), which needs to be reduced to the soluble ferrous iron (Fe2+) for absorption. This is achieved by the combined actions of Dcytb, a ferrireductase that is present on apical membranes of duodenal enterocytes and dietary reducing agents, such as vitamin C [36]. Importantly, vitamin C may directly enhance iron bioavailability by inhibiting hepcidin mRNA expression [37].
Another interesting finding was the correlations among carbohydrate-rich foods, hepcidin, and gestational ID/IDA. The present study found that one frequency increase in Chinese dim sum and related foods was associated with a 0.037 increase in hepcidin levels, but one frequency increase in noodles and related products was correlated with a 0.022 decrease in hepcidin (all p < 0.005). The adjusted logistic regression showed that total carbohydrate intake [OR: 1.003 (1.000~1.006), p = 0.036] predicted the ID risk, and the intake frequency of rice/rice porridge [OR: 1.007 (1.00~1.014), p = 0.041] predicted gestational IDA. According to the food classification, Chinese dim sum and related foods and rice/rice porridge are classified as foods with a high glycemic index (GI), but noodles and related products are classified as foods with a low GI [38,39]. Dickinson et al. found that among young lean healthy subjects, consumption of high-GI foods was associated with increased oxidative stress and both acute and chronic low-grade inflammation [40]. There is general agreement in the literature that the presence of oxidative stress and inflammation stimulates hepcidin over-synthesis, which in turn, leads to functional ID and IDA [6.7]. Our previous study showed that an altered carbohydrate/fat ratio predicted functional IDA among overweight and obese women [41]. Animal studies showed that a high-fructose diet induces a systemic iron deficiency and hepatic iron overload, possibly by inflammation-mediated hepcidin-ferroportin alterations [42]. Since lowering maternal hepcidin is essential for transporting bioavailable iron to the placenta [9], future studies need to clarify the underlying mechanisms between the type of carbohydrate foods consumed and hepcidin levels among pregnant women.
Several limitations of this study should be recognized when interpreting the results. Because NAHSIT-Pregnant is a cross-sectional survey, the present study could not assess temporality or causality in any of the associations we found. Our analysis included only one 24-h set of recall data, which might not accurately reflect the usual intake of each individual but does provide a valid means for estimating the intake of the group. Our findings also largely rely on self-reported dietary data, which may be subject to recall bias or systematic underreporting of energy intake, particularly in those who are overweight or obese in late pregnancy [43]. In addition, we were unable to account for the effects of pregnancy-related nausea and vomiting that typically occur in the first trimester on dietary intake; thus, it is possible that self-reported dietary intake was overestimated in this subgroup. Failure to account for total energy intake can obscure associations between nutrient intake levels and disease risk or may even reverse the direction of the association. Thus, the current study adjusted for the total energy intake as a way to control confounding dietary factors [33]. Over-reporting of food intake in FFQs was observed in pregnant women [44]. However, the FFQ is considered to be one of the most appropriate dietary methods used in large-scale epidemiological studies, and it provides useful information on dietary patterns [45]. Despite these limitations, the present study had several strengths. The main strength of the current study was the use of a nationwide representative sample of pregnant women in Taiwan, which also provided a sufficiently large sample population. This suggests that our estimates may have good precision and/or reliability. The present study also included various parameters, which allowed us to adjust for several potential confounding variables that are known to affect gestational IDA, such as age, pre-pregnancy BMI, parity, total supplement use (%), and trimester.

5. Conclusions

Intake frequency of carbohydrate-rich foods and vegetables may affect the gestational iron status through influencing hepcidin levels. Specifically, the increased consumption of total carbohydrate intake, especially refined carbohydrates may increase the risk of gestational ID and IDA. By contrast, complex carbohydrates foods (e.g., breakfast cereals, oats, and related products) may protect against gestational ID and IDA through downregulating hepcidin levels to enhance iron delivery to the fetus. A high intake of vegetables may also increase the risk, but this effect can be suppressed by the addition of vitamin C in the diet. Additional studies are needed to confirm the food-hepcidin-ID/IDA relationship among pregnant women living in countries with different cultural contexts and food preferences. Overall, dietary strategies that incorporate hepcidin-modulating foods may help prevent gestational ID or IDA.

Supplementary Materials

The following are available online at https://0-www-mdpi-com.brum.beds.ac.uk/article/10.3390/nu13103501/s1, Table S1: Food items and food groups included in the multiple linear regression analysis of gestational serum hepcidin levels.

Author Contributions

J.-S.C., C.-H.B., J.C.-J.C., Y.C.C., Y.L.H., F.-F.W., A.A.T. and A.V.S. designed the search strategy and interpreted the results. N.R.M. and T.-Y.H. performed the data analysis. J.-S.C. and N.R.M. drafted the paper and approved the submitted paper. J.-S.C. performed critical revision of the manuscript for important intellectual content. All authors have read and agreed to the published version of the manuscript.

Funding

Jung-Su Chang was supported by grants from Taipei Medical University Hospital (110TMU-TMUH-109) and the Ministry of Science and Technology, Taiwan (MOST 110-2320-B-038-046).

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Review Board (or Ethics Committee) of the Taipei Medical University Institutional Review Board (TMU-JIRB N201707039, date of approval: 2017/09/05).

Informed Consent Statement

Not applicable.

Data Availability Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Acknowledgments

All the authors would like to thank the Ministry of Health and Welfare of Taiwan that allowed us to retrieve data of the NAHSIT 2017–2019, pregnant women.

Conflicts of Interest

No potential conflicts of interest are reported by the authors.

References

  1. World Health Organization (WHO). The Global Prevalence of Anaemia in 2011; WHO Document Production Services: Genewa, Switzerland, 2015. [Google Scholar]
  2. Stevens, G.A.; Finucane, M.M.; De-Regil, L.M.; Paciorek, C.J.; Flaxman, S.R.; Branca, F.; Peña-Rosas, J.P.; Bhutta, Z.A.; Ezzati, M.; Nutrition Impact Model Study Group. Global, regional, and national trends in haemoglobin concentration and prevalence of total and severe anaemia in children and pregnant and non-pregnant women for 1995–2011: A systematic analysis of population-representative data. J. Lancet Glob. Health 2013, 1, e16–e25. [Google Scholar] [CrossRef] [Green Version]
  3. O’Brien, K.O.; Ru, Y. Iron status of North American pregnant women: An update on longitudinal data and gaps in knowledge from the United States and Canada. Am. J. Clin. Nutr. 2017, 106, 1647S–1654S. [Google Scholar] [CrossRef] [Green Version]
  4. Teichman, J.; Nisenbaum, R.; Lausman, A.; Sholzberg, M. Suboptimal iron deficiency screening in pregnancy and the impact of socioeconomic status in a high-resource setting. Blood Adv. 2021. [Google Scholar] [CrossRef] [PubMed]
  5. Breymann, C.; Auerbach, M. Iron deficiency in gynecology and obstetrics: Clinical implications and management. Hematol. Am. Soc. Hematol. Educ. Program 2017, 2017, 152–159. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Khaskheli, M.-N.; Baloch, S.; Sheeba, A.; Baloch, S.; Khaskheli, F.K. Iron deficiency anaemia is still a major killer of pregnant women. Pak. J. Med. Sci. 2016, 32, 630–634. [Google Scholar] [CrossRef] [PubMed]
  7. Fisher, A.L.; Nemeth, E. Iron homeostasis during pregnancy. Am. J. Clin. Nutr. 2017, 106, 1567s–1574s. [Google Scholar] [CrossRef] [PubMed]
  8. Ganz, T.; Nemeth, E. Hepcidin and iron homeostasis. Biochim. Biophys. Acta 2012, 1823, 1434–1443. [Google Scholar] [CrossRef] [Green Version]
  9. Sangkhae, V.; Ganz, T.; Nemeth, E. Maternal Hepcidin Suppression Is Essential for Healthy Pregnancy. Blood 2020, 136, 43–44. [Google Scholar] [CrossRef]
  10. Bah, A.; Pasricha, S.-R.; Jallow, M.W.; Sise, E.A.; Wegmuller, R.; Armitage, A.E.; Drakesmith, H.; Moore, S.E.; Prentice, A.M. Serum Hepcidin Concentrations Decline during Pregnancy and May Identify Iron Deficiency: Analysis of a Longitudinal Pregnancy Cohort in The Gambia. J. Nutr. 2017, 147, 1131–1137. [Google Scholar] [CrossRef] [Green Version]
  11. Santen, S.v.; Kroot, J.J.C.; Zijderveld, G.; Wiegerinck, E.T.; Spaanderman, M.E.A.; Swinkels, D.W. The iron regulatory hormone hepcidin is decreased in pregnancy: A prospective longitudinal study. Clin. Chem. Lab. Med. 2013, 51, 1395–1401. [Google Scholar] [CrossRef]
  12. Sangkhae, V.; Fisher, A.L.; Chua, K.J.; Ruchala, P.; Ganz, T.; Nemeth, E. Maternal hepcidin determines embryo iron homeostasis in mice. Blood 2020, 136, 2206–2216. [Google Scholar] [CrossRef]
  13. Koenig, M.D.; Tussing-Humphreys, L.; Day, J.; Cadwell, B.; Nemeth, E. Hepcidin and iron homeostasis during pregnancy. Nutrients 2014, 6, 3062–3083. [Google Scholar] [CrossRef] [PubMed]
  14. Hamlin, F.; Latunde-Dada, G.O. Iron bioavailability from a tropical leafy vegetable in anaemic mice. Nutr. Metab. 2011, 8, 9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Zehra, A.; Saleh Abdullah, S.M.; Saboor, M. Moinuddin. Effect of Intravenous Iron Supplementation on Hepcidin Levels in Iron Deficient Pregnant Females in Second and Third Trimester. Indian J. Hematol. Blood Transfus. 2017, 33, 396–401. [Google Scholar] [CrossRef] [PubMed]
  16. Ghatpande, N.S.; Apte, P.P.; Naik, S.S.; Kulkarni, P.P. Fruit and Vegetable Consumption and Their Association With the Indicators of Iron and Inflammation Status Among Adolescent Girls. J. Am. Coll. Nutr. 2019, 38, 218–226. [Google Scholar] [CrossRef] [PubMed]
  17. Saini, R.K.; Manoj, P.; Shetty, N.P.; Srinivasan, K.; Giridhar, P. Dietary iron supplements and Moringa oleifera leaves influence the liver hepcidin messenger RNA expression and biochemical indices of iron status in rats. Nutr. Res. 2014, 34, 630–638. [Google Scholar] [CrossRef]
  18. Sim, M.; Dawson, B.; Landers, G.; Wiegerinck, E.T.; Swinkels, D.W.; Townsend, M.-A.; Trinder, D.; Peeling, P. The effects of carbohydrate ingestion during endurance running on post-exercise inflammation and hepcidin levels. Eur. J. Appl. Physiol. 2012, 112, 1889–1898. [Google Scholar] [CrossRef] [PubMed]
  19. Cercamondi, C.I.; Icard-Vernière, C.; Egli, I.M.; Vernay, M.; Hama, F.; Brouwer, I.D.; Zeder, C.; Berger, J.; Hurrell, R.F.; Mouquet-Rivier, C. A Higher Proportion of Iron-Rich Leafy Vegetables in a Typical Burkinabe Maize Meal Does Not Increase the Amount of Iron Absorbed in Young Women. J. Nutr. 2014, 144, 1394–1400. [Google Scholar] [CrossRef]
  20. Karanja, P.N.; Kenji, G.M.; Njoroge, S.M.; Sila, D.N.; Onyango, C.A.; Koaze, H.; Baba, N. Compositional Characteristics of Young Shoots of Selected Bamboo Species Growing in Kenya and Their Potential as Food Source. J. Food Nutr. Res. 2015, 3, 607–612. [Google Scholar] [CrossRef]
  21. Tang, Y.; Li, Y.; Yu, H.; Gao, C.; Liu, L.; Chen, S.; Xing, M.; Liu, L.; Yao, P. Quercetin prevents ethanol-induced iron overload by regulating hepcidin through the BMP6/SMAD4 signaling pathway. J. Nutr. Biochem. 2014, 25, 675–682. [Google Scholar] [CrossRef]
  22. Mu, M.; An, P.; Wu, Q.; Shen, X.; Shao, D.; Wang, H.; Zhang, Y.; Zhang, S.; Yao, H.; Min, J.; et al. The dietary flavonoid myricetin regulates iron homeostasis by suppressing hepcidin expression. J. Nutr. Biochem. 2016, 30, 53–61. [Google Scholar] [CrossRef]
  23. Lesjak, M.; Balesaria, S.; Skinner, V.; Debnam, E.S.; Srai, S.K.S. Quercetin inhibits intestinal non-haem iron absorption by regulating iron metabolism genes in the tissues. Eur. J. Nutr. 2019, 58, 743–753. [Google Scholar] [CrossRef] [Green Version]
  24. Pabón de Rozo, M.; VanCampen, D.; Miller, D.D. Effects of some carbohydrates on iron absorption. Arch. Latinoam. Nutr. 1986, 36, 688–700. [Google Scholar] [PubMed]
  25. Trinidad, T.P.; Mallillin, A.C.; Sagum, R.S.; Briones, D.P.; Encabo, R.R.; Juliano, B.O. Iron absorption from brown rice/brown rice-based meal and milled rice/milled rice-based meal. Int. J. Food Sci. Nutr. 2009, 60, 688–693. [Google Scholar] [CrossRef] [PubMed]
  26. 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]
  27. Lee, M.-S.; Pan, W.-H.; Liu, K.-L.; Yu, M.-S.J.A.P.j.o.c.n. Reproducibility and validity of a Chinese food frequency questionnaire used in Taiwan. Asia Pac. J. Clin. Nutr. 2006, 15, 127–286. [Google Scholar]
  28. Zhang, H.; Qiu, X.; Zhong, C.; Zhang, K.; Xiao, M.; Yi, N.; Xiong, G.; Wang, J.; Yao, J.; Hao, L.J.N.j. Reproducibility and relative validity of a semi-quantitative food frequency questionnaire for Chinese pregnant women. Nutr. J. 2015, 14, 56. [Google Scholar] [CrossRef] [Green Version]
  29. World Health Organization. Iron Deficiency Anaemia: Assessment, Prevention and Control: A Guide for Programme Managers; World Health Organization: Geneva, Switzerland, 2001. [Google Scholar]
  30. Breymann, C. Iron Deficiency Anemia in Pregnancy. Semin. Hematol. 2015, 52, 339–347. [Google Scholar] [CrossRef]
  31. Centers for Disease Contol and Prevention. (CDC) criteria for anemia in children and childbearing-aged women. MMWR Morb. Mortal. Wkly. Rep. 1989, 38, 400–404. [Google Scholar]
  32. Lumley, T.; Diehr, P.; Emerson, S.; Chen, L. The importance of the normality assumption in large public health data sets. J. Annu. Rev. Public Health 2002, 23, 151–169. [Google Scholar] [CrossRef]
  33. Willett, W.C.; Howe, G.R.; Kushi, L.H.J.T.A.j.o.c.n. Adjustment for total energy intake in epidemiologic studies. Am. J. Clin. Nutr. 1997, 65, 1220S–1228S. [Google Scholar] [CrossRef]
  34. Zhen, A.W.; Nguyen, N.H.; Gibert, Y.; Motola, S.; Buckett, P.; Wessling-Resnick, M.; Fraenkel, E.; Fraenkel, P.G. The small molecule, genistein, increases hepcidin expression in human hepatocytes. Hepatology 2013, 58, 1315–1325. [Google Scholar] [CrossRef] [Green Version]
  35. Kim, Y.-J.; Kim, K.-S.; Lim, D.; Yang, D.J.; Park, J.-I.; Kim, K.W.; Jeong, J.-H.; Choi, H.-S.; Kim, D.-K. Epigallocatechin-3-Gallate (EGCG)-Inducible SMILE Inhibits STAT3-Mediated Hepcidin Gene Expression. Antioxidants 2020, 9, 514. [Google Scholar] [CrossRef]
  36. Lesjak, M.; K S Srai, S. Role of Dietary Flavonoids in Iron Homeostasis. Pharmaceuticals 2019, 12, 119. [Google Scholar] [CrossRef] [Green Version]
  37. Chiu, P.F.; Ko, S.Y.; Chang, C.C. Vitamin C affects the expression of hepcidin and erythropoietin receptor in HepG2 cells. J. Ren. Nutr. Off. J. Counc. Ren. Nutr. Natl. Kidney Found. 2012, 22, 373–376. [Google Scholar] [CrossRef]
  38. Foster-Powell, K.; Holt, S.H.; Brand-Miller, J.C. International table of glycemic index and glycemic load values: 2002. Am. J. Clin. Nutr. 2002, 76, 5–56. [Google Scholar] [CrossRef] [Green Version]
  39. Lin, M.-H.A.; Wu, M.-C.; Lu, S.; Lin, J. Glycemic index, glycemic load and insulinemic index of Chinese starchy foods. World J. Gastroenterol. 2010, 16, 4973–4979. [Google Scholar] [CrossRef] [PubMed]
  40. Dickinson, S.; Hancock, D.P.; Petocz, P.; Ceriello, A.; Brand-Miller, J. High-glycemic index carbohydrate increases nuclear factor-kappaB activation in mononuclear cells of young, lean healthy subjects. Am. J. Clin. Nutr. 2008, 87, 1188–1193. [Google Scholar] [CrossRef] [PubMed]
  41. Chang, J.-S.; Chen, Y.-C.; Owaga, E.; Palupi, K.C.; Pan, W.-H.; Bai, C.-H. Interactive Effects of Dietary Fat/Carbohydrate Ratio and Body Mass Index on Iron Deficiency Anemia among Taiwanese Women. Nutrients 2014, 6, 3929–3941. [Google Scholar] [CrossRef] [Green Version]
  42. Wang, C.; Wang, X.; Song, G.; Xing, H.; Yang, L.; Han, K.; Chang, Y.Z.J.J.o.F.B. A high-fructose diet in rats induces systemic iron deficiency and hepatic iron overload by an inflammation mechanism. J. Food Biochem. 2021, 45, e13578. [Google Scholar] [PubMed]
  43. Moran, L.J.; McNaughton, S.A.; Sui, Z.; Cramp, C.; Deussen, A.R.; Grivell, R.M.; Dodd, J.M. The characterisation of overweight and obese women who are under reporting energy intake during pregnancy. BMC Pregnancy Childbirth 2018, 18, 204. [Google Scholar] [CrossRef] [PubMed]
  44. 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]
  45. 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] [PubMed] [Green Version]
Nutrients 13 03501 g001 550
Figure 1. Adjusted odds ratio (OR) and 95% confidence intervals (CI) of gestational iron deficiency (ID) and ID anemia (IDA) with various intake levels of nutrients (A) and foods (B) among all pregnant women after adjusting for age, pre-pregnancy body-mass index, region, parity, total supplement use (%), and trimester. p value/p for trend as * p ≤ 0.05.
Figure 1. Adjusted odds ratio (OR) and 95% confidence intervals (CI) of gestational iron deficiency (ID) and ID anemia (IDA) with various intake levels of nutrients (A) and foods (B) among all pregnant women after adjusting for age, pre-pregnancy body-mass index, region, parity, total supplement use (%), and trimester. p value/p for trend as * p ≤ 0.05.
Nutrients 13 03501 g001
Nutrients 13 03501 g002 550
Figure 2. Odd ratio (OR) and 95% confidence interval (CI) of iron-deficiency anemia (IDA) for the interactive effect of vitamin C and dark leafy vegetables (A) and gourds/shoots/root vegetables (B) after adjusting for age, pre-pregnancy body-mass index, region, parity, total supplement use (%), and trimester. p value/p for trend as * p ≤ 0.05, ** p ≤ 0.01.
Figure 2. Odd ratio (OR) and 95% confidence interval (CI) of iron-deficiency anemia (IDA) for the interactive effect of vitamin C and dark leafy vegetables (A) and gourds/shoots/root vegetables (B) after adjusting for age, pre-pregnancy body-mass index, region, parity, total supplement use (%), and trimester. p value/p for trend as * p ≤ 0.05, ** p ≤ 0.01.
Nutrients 13 03501 g002
Table
Table 1. Maternal baseline characteristics according to quartiles of serum hepcidin levels (N = 1430).
Table 1. Maternal baseline characteristics according to quartiles of serum hepcidin levels (N = 1430).
VariableSerum Hepcidin Level, Quartilesp for Trend a
Q1 (n = 355)Q2 (n = 360)Q3 (n = 358)Q4 (n = 357)
Basic characteristic
Age (years)31.7 ± 5.032.9 ± 4.632.8 ± 4.632.9 ± 4.60.002
Pre-pregnancy body-mass index (kg/m2)22.1 ± 3.922.8 ± 4.022.7 ± 4.123.0 ± 4.10.006
Region <0.001
Northern (n, %)95 (26.8)115 (31.9)132 (36.9)136 (38.1)
Central (n, %)79 (22.3)95 (26.4)88 (24.6)67 (18.8)
Southern (n, %)67 (18.9)65 (18.1)80 (22.3)74 (20.7)
Eastern (n, %)114 (32.1)85 (23.6)58 (16.2)80 (22.4)
Trimester <0.001
First trimester (n, %)43 (12.1)36 (10.0)97 (27.1)178 (49.9)
Second trimester (n, %)112 (31.5)84 (23.3)145 (40.5)122 (34.2)
Third trimester (n, %)200 (56.3)240 (66.7)116 (32.4)57 (16.0)
Parity <0.001
Primiparous (n, %)158 (44.6)191 (53.2)215 (60.2)212 (59.7)
Reported use of prenatal dietary supplements
Total supplement use (n, %)259 (73.4)291 (82.7)320 (90.4)321 (90.9)<0.001
Multivitamin-mineral (n, %)199 (56.5)220 (63.2)246 (69.5)216 (61.4)0.071
Vitamin B (n, %)47 (13.5)61 (17.4)74 (21.1)73 (20.9)0.005
Folate (n, %)138 (39.2)145 (41.4)165 (47.3)195 (55.7)<0.001
Iron (n, %)33 (9.5)44 (12.6)33 (9.3)37 (10.6)0.988
Blood biochemistry
Serum hepcidin (ng/mL)0.3 ± 0.32.4 ± 1.419.8 ± 10.673.2 ± 24.6<0.001
TS (%)10.1 ± 7.512.8 ± 7.920.8 ± 9.322.2 ± 9.1<0.001
Hb (g/dL)11.2 ± 1.811.5 ± 1.712.2 ± 2.012.1 ± 2.0<0.001
Serum ferritin (ng/mL)8.0 ± 6.010.3 ± 4.423.8 ± 14.650.0 ± 33.7<0.001
Iron abnormality
Anemia (n, %)142 (40.0)104 (28.9)51 (14.2)57 (16.0)<0.001
Non-IDA anemia (n, %)10 (2.8)12 (3.3)39 (10.9)57 (16.0)<0.001
IDA (n, %)132 (37.2)92 (25.6)12 (3.4)0 (0.0)<0.001
Iron deficiency (n, %)293 (82.5)263 (73.1)49 (13.7)1 (0.3)<0.001
ap for trend was performed by a general linear model for categorical variables and a one-way ANOVA for continuous variables. Continuous data are presented as the mean ± standard deviation (SD); categorical data are presented as the number (percentage of the same group). Hepcidin quartiles: quartile 1 (Q1) ≤0.80 ng/mL; quartile 2 (Q2) >0.81–≤5.66 ng/mL; quartile 3 (Q3) >5.67–≤40.05 ng/mL; quartile 4 (Q4) ≥40.00 ng/mL. Abbreviation: TS, transferrin saturation; Hb, hemoglobin; IDA, iron-deficiency anemia. Definitions, anemia: first trimester Hb <11 g/dL, second trimester Hb <10.5 g/dL, third trimester Hb <11 g/dL; IDA: serum ferritin ˂15 ng/mL and transferrin saturation <16%, and first trimester Hb <11 g/dL, second trimester Hb <10.5 g/dL, third trimester Hb <11 g/dL, ID: serum ferritin <15 ng/mL and transferrin saturation <16%.
Table
Table 2. Nutrient and food intake frequencies among pregnant women according to quartile levels of serum hepcidin (N = 1430).
Table 2. Nutrient and food intake frequencies among pregnant women according to quartile levels of serum hepcidin (N = 1430).
VariableHepcidin-Level, Quartilesp for Trend a
Quartile 1 (n = 355)Quartile 2 (n = 360)Quartile 3 (n = 358)Quartile 4 (n = 357)
Nutrient intake b
Carbohydrates (g)14.3 ± 48.713.6 ± 45.311.3 ± 43.39.7 ± 45.00.141
Protein (g)5.0 ± 17.76.5 ± 18.27.8 ± 16.96.8 ± 16.00.099
Fat (g)−8.0 ± 19.8−7.9 ± 17.4−7.6 ± 18.1−6.4 ± 18.90.255
Dietary fiber (g)1.5 ± 8.62.2 ± 8.22.0 ± 7.33.0 ± 9.40.04
Dietary Fe (mg)2.0 ± 4.92.8 ± 6.82.2 ± 4.73.0 ± 8.60.108
Dietary B9 (µg)74.2 ± 83.076.8 ± 83.176.2 ± 84.078.2 ± 108.30.594
Dietary B12 (µg)2.9 ± 10.32.5 ± 7.32.2 ± 5.92.9 ± 9.60.941
Dietary vitamin C (mg)67.7 ± 100.366.8 ± 108.080.8 ± 119.086.0 ± 145.20.014
Food group b (frequency: times/month)
Rice and rice porridge38.6 ± 23.236.4 ± 21.736.0 ± 23.035.8 ± 21.60.096
Noodles and related products15.5 ± 13.415.0 ± 12.016.0 ± 12.216.1 ± 12.90.303
Breakfast cereals, oats, and related products2.9 ± 9.31.7 ± 7.02.0 ± 8.31.4 ± 8.50.029
Chinese dim sum and related foods9.0 ± 11.69.6 ± 11.810.0 ± 12.310.5 ± 13.40.144
Sweet buns, bean buns, and related products3.2 ± 6.22.8 ± 8.01.6 ± 4.62.1 ± 5.10.002
Savory and sweet glutinous rice products0.9 ± 3.30.9 ± 3.10.67 ± 2.81.3 ± 6.80.512
Light-colored vegetables23.4 ± 21.324.1 ± 22.021.3 ± 18.021.2 ± 19.20.05
Dark leafy vegetables26.4 ± 20.829.8 ± 23.426.6 ± 21.024.9 ± 18.70.121
Gourds, shoots, and root vegetables29.3 ± 26.230.1 ± 27.526.0 ± 22.925.4 ± 22.80.007
Legumes4.0 ± 7.93.6 ± 7.53.1 ± 5.52.7 ± 4.80.007
Total vegetables47.2 ± 27.648.9 ± 29.844.8 ± 28.045.2 ± 27.60.135
Fresh fruits32.6 ± 20.932.2 ± 21.329.4 ± 18.530.1 ± 20.00.029
100% pure fruit juice or fruit/vegetable juice5.4 ± 8.65.4 ± 9.54.8 ± 6.67.3 ± 12.90.033
Canned fruits, dried fruits, and jam2.3 ± 9.62.1 ± 7.81.8 ± 7.94.4 ± 14.50.016
Fish, shellfish, and seafood20.9 ± 20.121.5 ± 19.617.7 ± 16.419.1 ± 18.00.043
Roe and processed seafood products0.6 ± 2.30.5 ± 2.760.4 ± 2.00.7 ± 2.70.845
Poultry meat17.1 ± 15.417.4 ± 15.616.7 ± 14.415.6 ± 13.10.14
Liver, organs, and blood products2.8 ± 8.53.0 ± 7.22.6 ± 5.93.9 ± 9.60.123
a p for trend was assessed by a one-way ANOVA. All data are presented as the mean ± standard deviation (SD). b Nutrient intake and food group were adjusted for total energy using residual methods. Hepcidin quartiles: quartile 1 (Q1) ≤0.80 ng/mL; quartile 2 (Q2) >0.81–≤5.66 ng/mL; quartile 3 (Q3) >5.67–≤40.05 ng/mL; quartile 4 (Q4) ≥40.00 ng/mL.
Table
Table 3. Adjusted beta coefficient (ß) and 95% confidence interval (CI) of gestational serum hepcidin levels for nutrients and food groups among pregnant women.
Table 3. Adjusted beta coefficient (ß) and 95% confidence interval (CI) of gestational serum hepcidin levels for nutrients and food groups among pregnant women.
All Pregnant Women (N = 1430)Non-Iron Deficiency/Iron-Deficiency Anemia (Non-ID/IDA) Pregnant Women (N = 824)Iron Deficiency (ID) Pregnant Women (N = 606)Iron Deficiency Anemia (IDA) Pregnant Women (N = 236)
ß (95% CI)p Value aß (95% CI)p Value aß (95% CI)p Value aß (95% CI) p Value a
Nutrient intake b
  Carbohydrates (g)−0.027 (−0.061–0.007)0.122−0.016 (−0.068–0.036)0.5540.000 (−0.006–0.005)0.891−0.001 (−0.004–0.002)0.531
 Protein (g)0.023 (−0.067–0.113)0.617−0.051 (−0.188–0.086)0.465−0.004 (−0.019–0.011)0.574−0.004 (−0.014–0.005)0.382
 Fat (g)0.071 (−0.014–0.155)0.1000.069 (−0.059–0.196)0.2910.003 (−0.011–0.018)0.652−0.002 (−0.010–0.007)0.711
 Dietary fiber (g)0.121 (−0.063–0.306)0.1980.184 (−0.093–0.460)0.192−0.010 (−0.042–0.021)0.5250.001 (−0.038–0.040)0.969
 Dietary Fe (mg)0.203 (−0.032–0.439)0.0910.209 (−0.104–0.522)0.191−0.029 (−0.080–0.021)0.255−0.026 (−0.080–0.027)0.333
 Dietary folate (µg)0.008 (−0.009–0.025)0.3380.006 (−0.018–0.031)0.602−0.002 (−0.005–−0.001)0.243−0.002 (−0.005–0.001)0.201
 Dietary vitamin B12 (µg)0.117 (−0.002–0.355)0.0520.268 (−0.014–0.550)0.062−0.011 (−0.039–0.018)0.451−0.017 (−0.047–0.012)0.254
 Dietary vitamin C (mg)0.014 (0.001–0.026)0.0410.014 (−0.004–0.031)0.136−0.000 (−0.003–0.002)0.9420.001 (−0.002–0.004)0.560
Food group b (frequency: times/month)
 Rice and rice porridge−0.035 (−0.103–0.034)0.318−0.023 (−0.126–0.080)0.658−0.009 (−0.021–0.002)0.123−0.006 (−0.016–0.004)0.233
 Noodles and related products0.071 (−0.051–0.192)0.2550.070 (−0.113–−0.253)0.453−0.008 (−0.029–0.012)0.421−0.022 (−0.043–−0.001)0.038
 Breakfast cereals, oats, and related products−0.187 (−0.370–−0.003)0.046−0.295 (−0.567–−0.023)0.0340.027 (−0.005–0.058)0.0970.005 (−0.026–0.037)0.737
 Chinese dim sum and related foods0.033 (−0.090–0.156)0.6030.063 (−0.123–0.249)0.5050.007 (−0.014–0.028)0.5060.037 (0.015–0.058)0.001
 Sweet buns, bean buns, and related products0.097 (−0.347–0.152)0.445−0.160 (−0.614–0.294)0.489−0.019 (−0.055–0.016)0.286−0.001 (−0.027–0.026)0.969
 Savory and sweet glutinous rice products0.677 (0.330–1.024)<0.0010.662 (0.218–1.107)0.004−0.007 (−0.091–0.076)0.8620.017 (−0.064–0.097)0.683
 Light–colored vegetables−0.075 (−0.150–0.001)0.052−0.079 (−0.201–0.042)0.2010.003 (−0.009–0.015)0.6020.003 (−0.011–0.017)0.693
 Dark leafy vegetables−0.061 (−0.133–0.012)0.101−0.079 (−0.195–0.037)0.1810.012 (0.000–0.023)0.0060.013 (0.001–0.025)0.04
 Gourds, shoots, and root vegetables−0.071 (−0.133–−0.010)0.022−0.066 (−0.165–0.033)0.1900.004 (−0.006–0.014)0.403−0.009 (−0.018–0.001)0.076
 Legumes−0.129 (−0.362–0.104)0.276−0.045 (−0.456–0.366)0.831−0.015 (−0.049–0.019)0.375−0.009 (−0.052–0.033)0.666
 Total vegetables−0.024 −0.079–0.030)0.376−0.022 (−0.105–0.060)0.5950.007 (−0.002–0.016)0.1050.003 (−0.006–0.012)0.541
 Fresh fruits−0.046 (−0.122–0.030)0.237−0.022 (−0.142–0.098)0.7160.008 (0.005–0.020)0.2200.003 (−0.009–0.015)0.637
 100% pure fruit juice or fruit/vegetable juice0.140 (−0.017–0.298)0.080.173 (−0.057–0.404)0.1400.018 (−0.010–0.046)0.198−0.010 (−0.035–0.014)0.392
 Canned fruits, dried fruits, and jam0.157 (0.009–0.304)0.0370.176 (−0.018–0.370)0.076−0.014 (−0.046–0.019)0.415−0.005 (−0.042–0.032)0.8
 Fish, shellfish, and seafood−0.014 (−0.097–0.068)0.733−0.001 (−0.132–0.130)0.991−0.014 (−0.046–0.019)0.415−0.002 (−0.015–0.011)0.764
 Roe and processed seafood products0.434 (−0.153–1.022)0.1471.223 (0.321–2.124)0.008−0.021 (−0.118–0.077)0.678−0.015 (−0.099–0.070)0.731
 Poultry meat−0.076 (−0.180–0.028)0.151−0.083 (−0.249–0.082)0.323−0.010 (−0.027–0.006)0.226−0.007 (−0.022–0.008)0.378
 Liver, organs, and blood products0.332 (0.139–0.526)0.0010.489 (0.189–0.790)0.0010.001 (−0.033–0.030)0.9270.012 (−0.029–0.053)0.558
a Adjusted for age, pre-pregnancy body-mass index, region, parity, total supplement use (%), and trimester. b Nutrient intake and food group were adjusted for total energy using residual method.
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Mayasari, N.R.; Bai, C.-H.; Hu, T.-Y.; Chao, J.C.-J.; Chen, Y.C.; Huang, Y.L.; Wang, F.-F.; Tinkov, A.A.; Skalny, A.V.; Chang, J.-S. Associations of Food and Nutrient Intake with Serum Hepcidin and the Risk of Gestational Iron-Deficiency Anemia among Pregnant Women: A Population-Based Study. Nutrients 2021, 13, 3501. https://0-doi-org.brum.beds.ac.uk/10.3390/nu13103501

AMA Style

Mayasari NR, Bai C-H, Hu T-Y, Chao JC-J, Chen YC, Huang YL, Wang F-F, Tinkov AA, Skalny AV, Chang J-S. Associations of Food and Nutrient Intake with Serum Hepcidin and the Risk of Gestational Iron-Deficiency Anemia among Pregnant Women: A Population-Based Study. Nutrients. 2021; 13(10):3501. https://0-doi-org.brum.beds.ac.uk/10.3390/nu13103501

Chicago/Turabian Style

Mayasari, Noor Rohmah, Chyi-Huey Bai, Tzu-Yu Hu, Jane C.-J. Chao, Yi Chun Chen, Ya Li Huang, Fan-Fen Wang, Alexey A. Tinkov, Anatoly V. Skalny, and Jung-Su Chang. 2021. "Associations of Food and Nutrient Intake with Serum Hepcidin and the Risk of Gestational Iron-Deficiency Anemia among Pregnant Women: A Population-Based Study" Nutrients 13, no. 10: 3501. https://0-doi-org.brum.beds.ac.uk/10.3390/nu13103501

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