Literature DB >> 35994490

Maternal dietary folate intake with folic acid supplements and wheeze and eczema in children aged 2 years in the Japan Environment and Children's Study.

Hideyuki Masuda1, Sumitaka Kobayashi1, Chihiro Miyashita1, Sachiko Itoh1, Yu Ait Bamai1, Yasuaki Saijo2, Yoshiya Ito3, Reiko Kishi1, Atsuko Ikeda-Araki1,4.   

Abstract

Maternal intake of folic acid supplements is reportedly associated with the risk of early-onset allergies in offspring. However, only a few studies have considered the intake of both folic acid supplements and dietary folate. Here, the relationship between maternal intake of folic acid supplements and allergic symptoms such as wheeze and eczema in offspring was analyzed while considering dietary folate intake. We examined 84,361 mothers and 85,114 children in the Japan Environment and Children's Study. The participants were divided into three groups depending on maternal folic acid supplementation ("no use," "occasional use," and "daily use"). Each group was then subdivided into three groups based on total folic acid and dietary folate intake. Outcomes were determined considering the wheeze and eczema status of each child at the age of 2 years. The status was based on the International Study of Asthma and Allergies in Childhood. It was found that 22.1% of the mothers took folic acid supplements daily. In contrast, 56.3% of the mothers did not take these supplements. Maternal intake of folic acid supplements was not associated with wheeze and eczema in the offspring. In contrast, only dietary folate intake was positively associated with wheeze at the age of 2 (adjusted odds ratio, 1.103; 95% confidence interval, 1.003-1.212). However, there is no scientific evidence of a biological mechanism that clarifies this result. Potential confounders such as other nutrition, outdoor/indoor air pollution, and genetic factors may have affected the results. Therefore, further studies on the association between maternal intake of folic acid and allergic symptoms at the age of 3 or above are needed to confirm the results of this study. Trial registration UMIN Clinical Trials Registry (number: UMIN000030786).

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Year:  2022        PMID: 35994490      PMCID: PMC9394831          DOI: 10.1371/journal.pone.0272968

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.752


Introduction

Folic acid, a B vitamin, plays an important role in erythropoiesis and DNA methylation. It also decreases the risk of neural tube defects [1-3]. Folic acid deficiency (serum folic acid < 5 ng/mL) causes serious health impairments, including neuropsychiatric disorders [4]. Hence, 68 countries have a mandatory folic acid fortification in food [5]. However, Japan has no such mandate. The dietary folate intake recommendation by the Ministry of Health, Labour and Welfare in Japan for adults is 240 μg/day. Moreover, to reduce the risk of neural tube closure in the fetus, women who are in the pre-pregnancy stage and in the first trimester of pregnancy are recommended to take in 400 μg/day folic acid derived from supplements [6]. In addition, dietary folate intake (240 μg/day) is recommended in the second/third trimester of pregnancy as additional intake [6]. However, in a Japanese study from 2017, only 45.1% of pregnant women used folic acid supplements [7]. Moreover, on average, dietary folate intake is 243 μg/day in Japanese pregnant women [8]. Thus, the current recommendations for the intake of folic acid supplements and dietary folate during pregnancy in Japan are insufficient. Dietary folate and supplementary folic acid differ in their chemical structures and contain polyglutamic and monoglutamic acid, respectively. The major difference between them is their absorption rate in the digestive tract during the metabolism of polyglutamic to monoglutamic acid [9]. Allergies such as asthma and atopic dermatitis are major public health problems worldwide. A nationwide cohort study in Japan showed that approximately 13%–14% of children at the age of 3 suffer from wheeze or eczema [10]. Maternal risk factors for allergies have been reported by some studies; these include maternal gestational smoking, maternal stressful events, and maternal obesity [11-13]. Additionally, cohort studies have reported that folic acid supplementation during pregnancy is a risk factor for allergies in offspring [14-18]. In the Norwegian Mother and Child Cohort Study, folic acid supplementation in the first trimester of pregnancy increased the relative risk (RR) of wheeze (RR, 1.06; 95% confidence interval [CI], 1.03–1.10) compared with no supplementation [14]. In the Prevention and Incidence of Asthma and Mite Allergy birth cohort study, Bekkers et al. found that the risk of contracting wheeze in children at 1 year of age (prevalence ratio, 1.20; 95% CI, 1.04–1.39) was higher with the use of folic acid-containing supplements than with the use of folic acid-lacking supplements [15]. Moreover, in the Generation R study, a folate concentration of ≥16.21 nmol/L in plasma during pregnancy increased the risk of atopic dermatitis in offspring (odds ratio [OR], 1.16; 95% CI, 1.03–1.32) compared with lower concentrations (≤10.30 nmol/L) [16]. Nevertheless, only a few studies have analyzed the association between folic acid supplementation and allergies in offspring considering dietary folate intake. In the Generation 1 Cohort Study in Australia, high maternal intake of folic acid supplements during late pregnancy was associated with a higher risk of asthma in children at 3.5 years of age (RR, 1.26; 95% CI, 1.09–1.47) compared with no supplement intake. However, maternal intake of dietary folate was not associated with asthma in offspring [17]. Furthermore, Parr et al. considered total folic acid intake (dietary and supplemental) and observed that a folate-rich diet combined with at least 400 μg/day folic acid supplement intake (total ≥ 578 μg/day) increased the relative risk of childhood asthma (RR,1.23; 95% CI, 1.06–1.44) compared with low intake (total ≤ 146 μg/day) in the Norwegian Mother and Child Cohort Study [18]. Dietary folate and supplemental folic acid are absorbed as monoglutamate and converted to polyglutamate in tissue [9]; there is no significant difference in their in-vivo functions. Therefore, the effects of dietary folate intake must be considered to evaluate the contribution of folic acid supplementation during pregnancy to allergic risk in offspring. In previous studies, allergic symptoms such as asthma, wheeze, and atopic dermatitis in offspring were associated with the maternal intake of folic acid [14-18]. In this study, we evaluated the association between folic acid supplements and dietary folate intake during pregnancy and wheeze and eczema, which are early symptoms of asthma and atopic dermatitis in offspring.

Materials and methods

The Japan Environment and Children’s Study (JECS) protocol was reviewed and approved by the Institutional Review Board on Epidemiological Studies of the Ministry of the Environment and the Ethics Committees of all participating institutions. Details of the JECS have been described previously [19,20]. In brief, the JECS is a nationwide birth cohort study in Japan that elucidated environmental factors that affect the health and development of children. The JECS recruited approximately 100,000 participants during pregnancy between January 2011 and March 2014. Written informed consent was obtained from parents or guardians. In this study, we used the jecs-ta-20190930 dataset, which contains data on 104,062 fetal records. In total, 18,948 records were excluded for the following reasons: stillbirth; miscarriage; unanswered birth questions; and non-responses to questionnaires during the second/third trimester, questionnaires regarding children aged 2 years, questionnaires about folic acid intake (supplemental or dietary), and queries regarding both symptoms (wheeze and eczema). Finally, data from 85,114 records were used in the analysis (Fig 1).
Fig 1

Flow chart of the participant selection.

Exposure was defined as the self-reported use of folic acid supplements and dietary folate intake in the past month obtained from a questionnaire distributed during the second/third trimester. The intake of folic acid supplements was divided into three groups: mothers who did not take folic acid supplements were included in the “no use” group; mothers who occasionally took the supplements were included in the “occasional use” group; and mothers who took them at least once a day were included in the “daily use” group. Dietary folate intake (μg/day) after conception was calculated using a semiquantitative food frequency questionnaire (FFQ) [21]. In brief, the FFQ asked the participants about the frequency of consumption of 172 food and beverage items, from never to seven or more times per day for food, and ten or more glasses per day for beverages. Thereafter, the intake of 53 nutrients was calculated. The folic acid intake (μg) was divided into three groups (<240, 240–479, and ≥480 μg/day) based on the standards issued by the Ministry of Health, Labour and Welfare of Japan and a previous report from the JECS [6,22]. Outcomes were wheeze and eczema in offspring at the age of 2. These were defined using a questionnaire based on the ISAAC [23-25]. A partially modified version of the validated Japanese ISAAC questionnaire for children aged 6–7 years was used [10]. Wheeze was defined as a positive response to the following questions: “Have you had wheezing or whistling in the chest at any time in the past?” and “Have you had wheezing or whistling in the chest in the last 12 months?”. Eczema was defined as a positive response to the following questions: “Have you ever had a recurring itchy rash for at least 6 months? If yes: Have you had this itchy rash at any time in the last 12 months? If yes: Has this itchy rash at any time affected any of the following places: the folds of the elbows, behind the knees, in front of the ankles, under the buttocks, or around the neck, ears, or eyes?”. Maternal and offspring characteristics, such as folic acid intake (supplemental and dietary) and wheeze and eczema symptoms were examined. First, we examined the associations with folic acid supplement and dietary folate intake separately. For folic acid supplement intake, “no use” was selected as a reference, whereas for dietary folate intake, “240–479 μg/day” was selected as the reference range based on the recommended consumption of folate per day for individuals during the first trimester (240 μg/day) and second/third trimester (480 μg/day) of pregnancy [6]. Second, to examine the interaction of maternal folic acid supplementation and dietary folate intake, we combined folic supplementation and dietary folate intake to find the association with symptoms among offspring. In this analysis, “no use” and” 240–479 μg/day” were selected as the reference [8]. The ORs and their 95% CIs were determined using crude and multivariate logistic regression analyses. To analyze the adjusted OR (aOR), multivariate logistic regression analyses were performed after adjusting for maternal age (≤24, 25–34, and ≥35 years), sex (male/female), gestational age (<37, ≥37 to <42, and ≥42 weeks), maternal and paternal education (junior high school/high school/technical junior college, technical [vocational] college/associate degree/bachelor’s degree/graduate degree [Master’s/Doctorate]), history of maternal allergy (yes/no), maternal smoking during pregnancy (no smoking/passive smoking/active smoking), maternal alcohol consumption during pregnancy (yes/no), maternal body mass index (BMI) before pregnancy (<18.5, ≥18.5 to <25.0, ≥25.0 to <30.0, and ≥30.0), parity (primipara/multipara), breastfeeding term (0 months, ≥1.00 to <6.00 months, ≥6.00 to <13.00 months, and ≥13.00 months), and nursery school and day-care center for children aged 1 or 2 years (yes/no). These factors were selected based on previous studies that reported an association between folic acid intake during pregnancy and allergies in offspring [14-18]. All analyses were performed using SPSS Statistics version 22 (IBM Corp., Armonk, NY, USA).

Results

Table 1 shows the characteristics of the 84,361 mothers. Mothers in the “daily use” group constituted 22.1% of all participants, whereas those in the “no use” group equaled 56.3%. Mothers in the “daily use” group exhibited the following parameters more often than those in the “no use” group: older maternal age, high parental education, no smoking, no alcohol consumption, existing allergies, singleton, and appropriate BMI. Compared with those in the “<240 μg/day” group, mothers in the “240–479 μg/day” group (40.6% of all participants) more often exhibited older maternal age, high maternal and paternal education, no smoking, existing allergies, primipara, and an appropriate BMI. However, a high frequency of alcohol consumption was exhibited by the “240–479 μg/day” group.
Table 1

Characteristics of the participants (mother).

All participantsFolic acid supplementFolate (μg) diet per day
(total = 84,361 mothers)n (%)n (%)
n%No useOccasional useDaily use<240240–479≥480
Maternal age Mean (SD) 31.4 (4.9)
≤24 years 7,1688.54,911 (10.3%)1,381 (7.6%)876 (4.7%)4,884 (10.9%)1,971 (5.8%)313 (6.0%)
25–34 years 53,57063.530,194 (63.6%)11,872 (65.1%)11,504 (61.8%)29,115 (64.9%)21,357 (62.4%)3,098 (59.0%)
≥35 years 23,6222812,397 (26.1%)4,976 (27.3%)6,249 (33.5%)10,894 (24.3%)10,891 (31.8%)1,837 (35.0%)
No answer 1<0.01
Education (mother) Junior high/high school/technical college 30,18235.818,477 (39.0%)5,820 (32.1%)5,885 (31.7%)17,911 (40.1%)10,591 (31.0%)1,680 (32.1%)
Professional school/junior college/university/graduate school 53,86463.828,848 (61.0%)12,333 (67.9%)12,683 (68.3%)26,791 (59.9%)23,523 (69.0%)3,550 (67.9%)
No answer 3150.4
Education (father) Junior high/high school/technical college 37,31544.222,678 (48.2%)7,379 (40.8%)7,258 (39.3%)21,066 (47.4%)13,988 (41.2%)2,261 (43.5%)
Professional school/junior college/university/graduate school 46,29154.924,358 (51.8%)10,702 (59.2%)11,231 (60.7%)23,357 (52.6%)19,992 (58.8%)2,942 (56.5%)
No answer 7550.9
Allergy (mother) No 35,96442.621,021 (44.4%)7,361 (40.5%)7,582 (40.9%)19,589 (43.8%)14,184 (41.6%)2,191 (41.9%)
Yes 48,0815726,307 (55.6%)10,796 (59.5%)10,978 (59.1%)25,154 (56.2%)19,893 (58.4%)3,034 (58.1%)
No answer 3160.4
Smoking (during pregnancy) No smoking 45,38653.824,138 (51.7%)10,182 (56.9%)11,066 (60.3%)22,821 (51.8%)19,693 (58.2%)2,972 (57.6%)
Passive smoking 34,41040.820,438 (43.8%)7,144 (39.9%)6,828 (37.2%)19,271 (43.7%)13,130 (39.0%)2,009 (38.9%)
Active smoking 3,0963.72,069 (4.4%)570 (3.2%)457 (2.5%)1,960 (4.4%)958 (2.8%)178 (3.5%)
No answer 1,4691.7
Alcohol consumption (during pregnancy) No 81,44796.545,647 (96.8%)17,667 (97.6%)18,133 (98.0%)43,420 (97.5%)32,991 (97.0%)5,036 (96.5%)
Yes 2,3022.71,497 (3.2%)430 (2.4%)375 (2.0%)1,113 (2.5%)1,008 (3.0%)181 (3.5%)
No answer 6120.7
Parity Primipara 35,48542.117,043 (36.1%)8,612 (47.8%)9,830 (53.4%)20,633 (46.4%)13,142 (38.7%)1,710 (32.8%)
Multipara 48,12957.130,129 (63.9%)9,422 (52.2%)8,578 (46.6%)23,829 (53.6%)20,804 (61.3%)3,496 (67.2%)
No answer 7470.9
Body mass index (before pregnancy) <18.5 13,64416.27,582 (16.0%)2,967 (16.3%)3,095 (16.6%)7,420 (16.5%)5,442 (15.9%)782 (14.9%)
≥18.5 and <25.0 62,18773.73,4678 (73.0%)13,608 (74.7%)13,901 (74.6%)32,766 (73.0%)25,537 (74.6%)3,884 (74.0%)
≥25.0 and <30.0 6,5687.83,961 (8.3%)1,304 (7.2%)1,303 (7.0%)3,601 (8.0%)2,514 (7.3%)453 (8.6%)
≥30.0 1,9502.31,276 (2.7%)347 (1.9%)327 (1.8%)1,100 (2.5%)723 (2.1%)127 (2.4%)
No answer 120.01
Total 84,36110047,503 (56.3%)18,229 (21.6%)18,629 (22.1%)44,894 (53.2%)34,219 (40.6%)5,248 (5.2%)

SD, standard deviation.

SD, standard deviation. Table 2 presents the characteristics of the offspring. Among all children, 24.0% had wheeze and 13.0% had eczema. Male sex, premature birth, high birth weight, short-term breastfeeding, children commuting to nursery schools and day-care centers, and children without pets exhibited a high wheeze frequency. Furthermore, eczema was more prevalent in the male sex, with high birth weight, long-term breastfeeding, a regular commute to a day-care center, and ownership of pets. The characteristics of the mother were closely linked with a high frequency of symptoms in the offspring. Offspring with low paternal education, maternal allergies, as well as those whose mothers exhibited high alcohol consumption, multipara, and high BMI generally exhibited a high wheeze frequency. In addition, offspring with high maternal and paternal education, maternal allergies, as well as those whose mothers exhibited high alcohol consumption and multipara exhibited a high eczema frequency (S1 Table).
Table 2

Characteristics of the participants (children).

All participantsWheezeEczema
(total = 85114 children)n (%)n (%)
n%YesNoYesNo
Sex Male 4360951.211633 (57.0%)31698 (49.4%)6207 (56.0%)37222 (50.5%)
Female 4150448.88785 (43.0%)32467 (50.6%)4878 (44.0%)36471 (49.5%)
No answer 10
Gestational age (months) <37 44525.21299 (6.4%)3177 (4.9%)550 (5.0%)3884 (5.3%)
≥37 and <42 8031394.419040 (93.4%)60784 (94.9%)10497 (94.9%)69500 (94.5%)
≥42 1890.239 (0.2%)147 (0.2%)18 (0.2%)171 (0.2%)
No answer 1600.2
Multiple birth singleton 8359898.220039 (98.1%)63037 (98.2%)10880 (98.1%)72388 (98.2%)
multitone 15161.8380 (1.9%)1128 (1.8%)206 (1.9%)1305 (1.8%)
Birth weight (g) <2500 75598.91916 (9.4%)5593 (8.7%)895 (8.1%)6639 (9.0%)
≥2500 and <4000 766249018279 (89.8%)57873 (90.4%)10043 (90.8%)66274 (90.1%)
≤4000 7240.9171 (0.8%)548 (0.9%)117 (1.1%)605 (0.8%)
No answer 2070.2
Birth year 2011 83139.82068 (10.1%)6195 (9.7%)1033 (9.3%)7230 (9.8%)
2012 2405528.35693 (27.9%)18212 (28.4%)2971 (26.8%)20997 (28.5%)
2013 3013035.47312 (35.8%)22632 (35.3%)4030 (36.4%)25989 (35.3%)
2014 2261626.65436 (26.2%)17126 (26.7%)3052 (27.5%)19477 (26.4%)
Breastfeeding term (months) 0 20992.5513 (2.6%)1573 (2.5%)232 (2.1%)1857 (2.6%)
≥1.00 and <6.00 1458817.13866 (19.3%)10605 (16.8%)1685 (15.5%)12837 (17.7%)
≥6.00 and <13.00 5282462.112543 (62.6%)39965 (63.3%)6904 (63.4%)45737 (63.1%)
≥13.00 1415816.63107 (15.5%)10982 (17.4%)2074 (19.0%)12015 (16.6%)
No answer 14451.7
Nursery school and day care center for children No 4097448.16028 (29.9%)34774 (55.0%)4935 (45.1%)35870 (49.4%)
Yes 4293750.414156 (70.1%)28432 (45.0%)5996 (54.9%)36787 (50.6%)
No answer 12031.4
History of pet ownership (~1.5 y) No 6919981.316397 (82.9%)52379 (83.6%)9069 (84.1%)59871 (83.4%)
Yes 1372516.13373 (17.1%)10267 (16.4%)1709 (15.9%)11952 (16.6%)
No answer 21902.6
Total 85,11410020,419 (24.0)64,165 (75.4)11,086 (13.0)73,693 (86.6)
The association between folic acid intake and wheeze or eczema in children was assessed using logistic regression analysis (Table 3). The risk of wheeze increased in the “≥480 μg/day” group compared with that in the “240–479 μg/day” group (aOR 1.113; 1.037–1.194). In addition, the risk of wheeze decreased in the “<240 μg/day” group compared with that in the “240–479 μg/day” group (aOR 0.942; 0.909–0.977). The risk of eczema in offspring was low when the intake of dietary folate was low (<240 μg/day) compared with the risk when the intake of dietary folate was 240–479 μg/day (aOR 0.915; 0.876–0.956). However, the risk of eczema did not increase in the “≥480 μg/day” group compared with that in the “240–479 μg/day” group (aOR 1.009; 0.925–1.101).
Table 3

Exposure to folic acid supplement or dietary folate and allergy.

n%WheezeEczema
CrudeaAdjustedbCrudeaAdjustedb
OR95% CIOR95% CIOR95% CIOR95% CI
Folic acid supplement No use 47,89456.3RefRefRefRef
Occasional use 18,36821.60.9750.937–1.0141.0190.976–1.0631.0911.038–1.147*1.0781.023–1.136*
Daily use 18,85222.10.8740.839–0.909*0.9750.933–1.0181.0080.958–1.0601.0160.963–1.071
Dietary folate (μg/day) <240 45,26053.20.9460.915–0.978*0.9420.909–0.977*0.890.854–0.928*0.9150.876–0.956*
240–479 34,54040.6RefRefRefRef
≥480 5,3146.21.1491.076–1.227*1.1131.037–1.194*1.0190.938–1.1081.0090.925–1.101

CI, confidence interval; OR, odds ratio.

aCrude is non-adjusted.

bAdjusted is adjusted for maternal age, sex, gestational age, education (mother and father), allergy (mother), smoking (during pregnancy), alcohol consumption (during pregnancy), body mass index (before pregnancy), parity, breastfeeding term, nursery school and day-care center for children.

CI, confidence interval; OR, odds ratio. aCrude is non-adjusted. bAdjusted is adjusted for maternal age, sex, gestational age, education (mother and father), allergy (mother), smoking (during pregnancy), alcohol consumption (during pregnancy), body mass index (before pregnancy), parity, breastfeeding term, nursery school and day-care center for children. Finally, the association between the combined folic acid supplemental/dietary folic acid intake and wheeze or eczema in children was analyzed (Table 4). In the “no use” group, the OR of wheeze varied depending on the dietary folate intake (“<240 μg/day”: aOR 0.943; 0.900–0.988; “≥480 μg/day”: aOR 1.103; 1.003–1.212). Moreover, daily use of folic acid supplement at a concentration of <240 μg/day decreased the risk of wheeze (aOR 0.906; 0.849–0.966). Regarding eczema, no intake of folic acid supplements or intake of these supplements at a concentration of <240 μg/day decreased the risk of eczema compared with “240–479 μg/day” (aOR 0.880; 0.830–0.933). Moreover, “daily use and <240 μg/day” decreased the risk of eczema (aOR 0.914; 0.845–0.988). Collectively, the lack of dietary folate intake decreased the ORs of symptoms. However, maternal folic acid supplementation did not alter the risk of symptoms.
Table 4

Folic acid (supplement and diet) and allergies.

WheezeEczema
CrudeaAdjustedbCrudeaAdjustedb
Folic acid supplementDietary folate (μg/day)n(%)OR95% CIOR95% CIOR95% CIOR95% CI
No use <240 26,22730.80.9470.906–0.989*0.9430.900–0.988*0.8540.808–0.903*0.880.830–0.933*
240–479 18,73422.0RefRefRefRef
≥480 2,9333.41.1091.015–1.211*1.1031.003–1.212*1.0180.910–1.1401.0290.915–1.157
Occasional use <240 9,65011.30.9290.877–0.984*0.970.911–1.0320.9890.921–1.0631.0150.942–1.094
240–479 7,6349.00.9530.896–1.0141.0060.941–1.0751.0240.949–1.1061.0130.935–1.097
≥480 1,0841.31.1851.034–1.358*1.1340.978–1.3161.0430.875–1.2440.9710.805–1.170
Daily use <240 9,38311.00.810.763–0.859*0.9060.849–0.966*0.8870.824–0.956*0.9140.845–0.988*
240–479 8,1729.60.8860.833–0.942*0.9860.923–1.0530.9770.905–1.0540.9950.920–1.077
≥480 1,2971.51.0310.906–1.1731.1070.964–1.2720.9960.845–1.1730.9990.843–1.185

CI, confidence interval; OR, odds ratio.

aCrude is non-adjusted.

bAdjusted is adjusted for maternal age, sex, gestational age, education (mother and father), allergy (mother), smoking (during pregnancy), alcohol consumption (during pregnancy), body mass index (before pregnancy), parity, breastfeeding term, nursery school and day-care center for children.

CI, confidence interval; OR, odds ratio. aCrude is non-adjusted. bAdjusted is adjusted for maternal age, sex, gestational age, education (mother and father), allergy (mother), smoking (during pregnancy), alcohol consumption (during pregnancy), body mass index (before pregnancy), parity, breastfeeding term, nursery school and day-care center for children.

Discussion

We observed that high maternal intake of dietary folate was a risk factor for wheeze and eczema in children at 2 years of age. Conversely, folic acid supplements were not associated with wheeze and eczema in the offspring. To the best of our knowledge, this is the first study in Japan to demonstrate the association between maternal intake of folic acid supplements and allergic symptoms in offspring while considering dietary folate intake separately. Previous studies have reported various results. Bekkers et al. defined exposure as folic acid supplement intake during pregnancy (yes/no). Supplement intake increased the risk of wheeze in the first year [15]. Haberg et al. defined exposure as maternal supplementation before/after the 12th week (yes/no) and observed that supplementation increases the risk of wheeze in the first trimester of pregnancy [14]. Kiefte-de Jong et al. defined exposure as supplement intake in the first trimester (yes/no) and observed no association [16]. All these studies evaluated the association between maternal intake of folic acid supplement only and allergies. However, the periods when data were collected differed among these studies. Two out of three studies showed the association between maternal folic acid intake and allergies in offspring [14-16]. Moreover, Parr et al. considered the total amount of folic acid and showed that high folic acid intake increases the relative risk of asthma in children compared with low intake [18]. They did not show the influence by each folic acid supplement and dietary folate. Whitrow et al. considered folic acid and folate intake as continuous variables similar to exposure and showed an association between high maternal folic acid supplement intake and allergies. The exposure in the study by Whitrow et al. is the most similar to that in our study [17]. However, conversely, we found no association between maternal intake of supplements and symptoms in offspring, but high maternal dietary folate intake was associated with wheeze in offspring. However, the definition of exposure in previous reports differed from that in this study. Moreover, to the best of our knowledge, only a few studies have analyzed the risk of symptoms in offspring by maternal dietary folate. Here, high dietary folate intake was associated with allergies in children aged 2 years, whereas supplement intake was not. Currently, there is no report on the mechanism of allergy development depending on dietary folate or supplement intake. Furthermore, there is no scientific evidence of a biological mechanism of allergies in offspring caused only by dietary folate intake. Therefore, we considered that the intake of other nutrients with folic acid may have contributed to an increased risk of allergies. The BMI of the “≥480 μg/day” group was higher than that of the “<240 μg/day” and “240–479 μg/day” groups (Table 1), indicating a difference in dietary habits and high-calorie food intake. Omega-3 fatty acid and vitamin D intake during pregnancy is perceived to decrease allergies [26,27]. Thus, we examined their contribution and performed further analyses adjusted with omega-3 fatty acids and vitamin D intake determined using the FFQ. Consequently, the OR shifted towards 1 (S2 Table). It remains unclear whether maternal nutrient intake, except for folic acid, increases the risk of symptoms in offspring. A comprehensive analysis is needed to elucidate the association between maternal intake of nutrients and symptoms in offspring. The major strength of this study is that an extensive study cohort was utilized (~100,000 mothers). Furthermore, 85,114 children were divided into nine groups according to dietary and supplemental folic acid intake by mothers. The amount of consumed dietary folate was based on the FFQ, which is widely used in nutrient intake calculations. Folic acid fortification is not commonly implemented in Japan. Therefore, it is not necessary to consider whether the folic acid values calculated using the FFQ will be misclassified owing to the addition of folic acid supplements. We believe that this was advantageous in this assessment. However, this study had several limitations. In this study, we excluded 18,948 participants because of the lack of information about folate intake and/or prevalence of wheeze and eczema. Thus, we were not able to compare if there was any bias on folate intake or the prevalence percentage between participants included and excluded. However, we compared basic characteristics such as maternal age, education, as well as the prevalence of wheeze and eczema reported in previous studies of the JECS, indicating that there was no difference in participant characteristics, the prevalence of wheeze and eczema in children, and the percentage of folic acid supplements intake [10,28,29]. Therefore, the analyzed population is not likely to be biased with respect to the original population. Second, maternal folic acid supplement intake information only considers its usage and not its quantity. Third, children in the “wheeze” group exhibited “multipara” and “nursery school and day-care center for children (yes)” (Table 2), probably owing to the confusion between respiratory disease caused by infection from a sibling/friend and wheeze. Forth, genetic factors, such as methylenetetrahydrofolate reductase polymorphism C677T (MTHFR-C677T), were not considered. Maternal MTHFR-C677T may be associated with allergies in offspring through folic acid intake [30]. Finally, there are other risk factors that may cause wheeze and eczema. Potential confounders could not be sufficiently considered in this study, such as indoor and/or outdoor air pollution. For example, previous studies reported that environmental factors such as PM2.5 are known risk factors that increase allergies [31-33]. Regarding indoor environments, allergens such as dust mites are well known factors associated with allergies [34], so that these potential confounding factors could be considered in further studies.

Conclusions

Maternal intake of folic acid supplements is not associated with wheeze and eczema in children at the age of 2. However, high concentrations of dietary folate (≥480 μg/day) increase the risk of wheeze compared with low concentrations (240–479 μg/day) after adjustment. Nonetheless, the mechanisms that explain these results remain unclear; these observations may be attributed to other nutrients and/or calories. This study showed an association between maternal dietary folate intake and allergic symptoms at the age of 2. However, this association represents weak evidence to reconsider intake recommendations. Thus, we suggest the intake of both dietary and supplemental folic acid to avoid neural tube defects. Further studies on the association between the maternal intake of folic acid and allergic symptoms at the age of 3 or above considering potential confounders such as other nutrition, outdoor/indoor air pollution, and genetic factors are needed to confirm the results of this study.

Characteristics of the participants (mothers and children).

(DOCX) Click here for additional data file.

Folic acid (supplement and diet) and the allergies adjusted with omega-3 fatty acid and vitamin D intake.

†Adjusted is adjusted for maternal age, sex of child, fetus week number, education (mother and father), allergy (mother), smoking (during pregnancy), alcohol consumption (during pregnancy), body mass index (before pregnancy), parity, breastfeeding term, nursery school and baby farm, omega-3 fatty acid intake (< 1.6 g/day, ≥ 1.6 g/day), vitamin D intake (< 8.5 μg/day, ≥ 8.5 μg/day). The intake of omega-3 fatty acid and vitamin D was classified based on the maternal standard issued by the Ministry of Health, Labor, and Welfare in Japan (2020). ‡OR, odds ratio; §CI, confidence interval. (DOCX) Click here for additional data file. 10 May 2022
PONE-D-22-10468
Maternal dietary folate intake with folic acid supplement use and childhood wheeze and eczema in the Japan Environment and Children's Study
PLOS ONE Dear Dr. Araki, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. ============================== Numerous advantages of the authors’ manuscript over the studies so far published include the largest-ever sample size and the full consideration of potential confounders, which was highly appreciated by Reviewer 3. Taken together, I would like to encourage the authors to revise the manuscript while making clearer the following points that the three reviewers have kindly raised. Let me summarize as follows. 1. Perhaps the significance of the findings is more strongly upheld if the authors discuss more on the rationale of, and the consequences of, the adjustment for numerous covariates (Reviewer 1). Confounding by maternal education and smoking may be of a particular relevance with this regard considering the points addressed in the paper recommended by Reviewer 2. 2. Please rephrase the hypothesis the authors posed; “maternal intake of supplement along with dietary folate intake” is a bit too vague. I suppose that, because of this unclarity, Reviewer 1 has felt that readers are not carefully guided to the analysis plan. Also, the additional analysis (LL. 234 and onward) sounds abrupt to me as this analysis was not originally planned. 3. Please re-check the consistency and clarity of the text (Reviewer 2). An example include “however” in LL 225 and “however” in the following sentence. ============================== Please submit your revised manuscript by Jun 24 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. Please include the following items when submitting your revised manuscript:
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For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols. We look forward to receiving your revised manuscript. Kind regards, Kenji J Tsuchiya, MD, PhD Academic Editor PLOS ONE Journal Requirements: When submitting your revision, we need you to address these additional requirements. 1. Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf 2. You indicated that you had ethical approval for your study. In your Methods section, please ensure you have also stated whether you obtained consent from parents or guardians of the minors included in the study or whether the research ethics committee or IRB specifically waived the need for their consent. 3.  One of the noted authors is a group or consortium "Japan Environment and Children’s Study (JECS) Group". In addition to naming the author group, please list the individual authors and affiliations within this group in the acknowledgments section of your manuscript. Please also indicate clearly a lead author for this group along with a contact email address. 4. We note that you have included the phrase “data not shown” in your manuscript. Unfortunately, this does not meet our data sharing requirements. PLOS does not permit references to inaccessible data. We require that authors provide all relevant data within the paper, Supporting Information files, or in an acceptable, public repository. Please add a citation to support this phrase or upload the data that corresponds with these findings to a stable repository (such as Figshare or Dryad) and provide and URLs, DOIs, or accession numbers that may be used to access these data. Or, if the data are not a core part of the research being presented in your study, we ask that you remove the phrase that refers to these data. 5. Please include captions for your Supporting Information files at the end of your manuscript, and update any in-text citations to match accordingly. Please see our Supporting Information guidelines for more information: http://journals.plos.org/plosone/s/supporting-information. 6. Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice. [Note: HTML markup is below. Please do not edit.] Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: No Reviewer #2: Yes Reviewer #3: Yes ********** 2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes Reviewer #3: Yes ********** 3. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes Reviewer #2: No Reviewer #3: Yes ********** 4. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes Reviewer #3: Yes ********** 5. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: The long effect of maternal intake of dietary folate and folic acid supplement on health of offspring is worthy of assessment because folic acid supplement has become popular for pregnant women around the world. Unfortunately, the evidence from the population remains limited. This study focused on maternal dietary folate intake with folic acid supplement use and childhood wheeze and eczema, and found something interesting. However, some technical issues should be addressed further. 1. It is unclear why the authors selected wheeze and eczema as indicator for allergy. Maybe more review should be included in the part of introduction. 2. An important technical flaw is that authors did not provide strategy of statistical analysis for data in details. If possible, add it please. 3. Due to lots of potential confounders, how did authors consider them? It could be one of limitation of this study. 4. The data used here was from a cohort project. Lots of participants were excluded due to various reasons. Is there any difference between the participants included and those excluded? If yes, whether is the association biased? Maybe something more should be done about this issue. 5. In this study, whether or not other allergens during childhood are considered, which could confound this association between maternal folate or folic acid and allergy of offspring. Pls say something more in discussion. 6. Conclusion should be done with caution because of confounders and weak association from the table 4. Reviewer #2: In general, this is a good manuscript aiming to understand the relationship between folic acid intake, wheeze and eczema. The authors used data from nearly 100,000 mother-child pairs whose folic acid intake was self-reported. This is a main limitiation of the study that should be stressed. Please give more details on the instrument for dietary data collection (FFQ) Please consider, if possible, the adherence to recommendation on folic acid use during pregnancy. Have the authors information on the timing of folic acid intake (before pregnancy or after the conception). This is also important to understand the effect of the duration of folic acid intake. (please consider the following 10.3390/ijerph17020638). I would also suggest a double-check of the text for revising minor errors and typos. Reviewer #3: This is an excellent work. The authors found that high maternal intake of dietary folate was a risk factor for wheeze and eczema in children at 2 years of age, but folic acid supplements were not associated with wheeze and eczema in the offspring. The strength of this work is the nationwide birth cohort study with huge sample with 84,361 mothers and 85,114 children. Some minor suggestions or comments are as follows: 1. TITLE. I suggest the authors to modify the current title to a more accurate and attractive one such as "Maternal dietary folate intake with folic acid supplement use and wheeze and eczema in children aged 2 years in Japan: A nationwide cohort study". 2. About the limitations in DISCUSSION. Another two aspects should be mentioned: (1) The authors didn't consider the indoor and outdoor environmental factors. The authors mentioned "These factors (covariates) were selected based on previous studies that reported an association between folic acid intake during pregnancy and allergies in offspring", but the environmental factors have been widely considered to be the risk factors for childhood allergic sympotms/diseases. Some references include: -- Onset and remission of childhood wheeze and rhinitis across China - associations with early life indoor and outdoor air pollution. Environment International 2019, 123: 61-69. -- Preconceptional, prenatal and postnatal exposure to outdoor and indoor environmental factors on allergic diseases/symptoms in preschool children. Chemosphere 2016, 152: 459-467 (2) As the authors mentioned in ABSTRACT that "The study does not provide evidence that pregnant women should be denied folic acid intake owing to the increased risk early onset allergies in offspring", further/future studies focusing on the its association with allergic diseases, asthma or rhinitis, in elder preschool children aged 3-6 years are necessary to confirm the conclusions of the present work. ********** 6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. 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21 Jun 2022 We would like to thank you for the reviewers for the valuable comments that have helped us to substantially improve the manuscript. For a point-by-point response to these comments, please refer to the followings, and the text marked in yellow is the corrected part. Pages and lines are referring clean version of the manuscript. RESPONSES TO THE COMMENTS OF REVIEWER 1 1. It is unclear why the authors selected wheeze and eczema as indicator for allergy. Maybe more review should be included in the part of introduction. Response: We thank you for this pertinent comment. In previous studies, allergic symptoms such as asthma, wheeze, and atopic dermatitis have been associated with the maternal intake of folic acid. Therefore, we used wheeze and eczema, which are early symptoms of asthma and atopic dermatitis, as the outcomes. Per your comment, we have revised the following text in the Introduction (p. 5, line 103): In previous studies, allergic symptoms such as asthma, wheeze, and atopic dermatitis in offspring were associated with the maternal intake of folic acid [14-18]. In this study, we evaluated the association between folic acid supplements and dietary folate intake during pregnancy and wheeze and eczema, which are early symptoms of asthma and atopic dermatitis in offspring. 2. An important technical flaw is that authors did not provide strategy of statistical analysis for data in details. If possible, add it please. Response: In accordance with your comment, we have revised the following text in the Material and Methods (p. 7, line 151): First, we examined the associations with folic acid supplement and dietary folate intake separately. For folic acid supplement intake, “no use” was selected as a reference, whereas for dietary folate intake, “240–479 µg/day” was selected as the reference range based on the recommended consumption of folate per day for individuals during the first trimester (240 µg/day) and second/third trimester (480 µg/day) of pregnancy [6]. Second, to examine the interaction of maternal folic acid supplementation and dietary folate intake, we combined folic supplementation and dietary folate intake to find the association with symptoms among offspring. In this analysis, “no use” and” 240–479 µg/day” were selected as the reference [8]. 3. Due to lots of potential confounders, how did authors consider them? It could be one of limitation of this study. Response: There may have been potential confounders such as maternal/paternal genetic factors, indoor/outdoor air pollution, and other allergens. We have added the following limitation in the Discussion. (p. 15, line 297): Finally, there are other risk factors that may cause wheeze and eczema. Potential confounders could not be sufficiently considered in this study, such as indoor and/or outdoor air pollution. For example, previous studies reported that environmental factors such as PM2.5 are known risk factors that increase allergies [31-33]. Regarding indoor environments, allergens such as dust mites are well known factors associated with allergies [34], so that these potential confounding factors could be considered in further studies. 4. The data used here was from a cohort project. Lots of participants were excluded due to various reasons. Is there any difference between the participants included and those excluded? If yes, whether is the association biased? Maybe something more should be done about this issue. Response: We excluded 18,948 participants because of the lack of information about folate intake and/or prevalence of wheeze and eczema. Thus, we were not able to compare if there was any bias of folate intake or a prevalence percentage between participants included and excluded. However, there was no difference in participant characteristics, the prevalence of wheeze, and eczema in children, and the percentage of folic acid supplement intake was compared with that of previous studies of JECS. We have added the following sentence to the limitations. (p. 15, line 282): In this study, we excluded 18,948 participants because of the lack of information about folate intake and/or prevalence of wheeze and eczema. Thus, we were not able to compare if there was any bias on folate intake or the prevalence percentage between participants included and excluded. However, we compared basic characteristics such as maternal age, education, as well as the prevalence of wheeze and eczema reported in previous studies of the JECS, indicating that there was no difference in participant characteristics, the prevalence of wheeze and eczema in children, and the percentage of folic acid supplements intake [10, 28, 29]. Therefore, the analyzed population is not likely to be biased with respect to the original population. 5. In this study, whether or not other allergens during childhood are considered, which could confound this association between maternal folate or folic acid and allergy of offspring. Pls say something more in discussion. Response: As per our reply to your 3rd comment, we have added the following sentences to the limitations regarding other allergens during childhood. (p. 15, line 297): Finally, there are other risk factors that may cause wheeze and eczema. Potential confounders could not be sufficiently considered in this study, such as indoor and/or outdoor air pollution. For example, previous studies reported that environmental factors such as PM2.5 are known risk factors that increase allergies [31-33]. Regarding indoor environments, allergens such as dust mites are well known factors associated with allergies [34], so that these potential confounding factors could be considered in further studies. 6. Conclusion should be done with caution because of confounders and weak association from the table 4. Response: There was the possibility that some confounders affected the results shown in Table 4. In further studies, more confounders such as nutrients, environmental, and genetic factors must be considered. We have added the following sentences to the conclusion. (p. 16, line 312): However, this association represents weak evidence to reconsider intake recommendations. Thus, we suggest the intake of both dietary and supplemental folic acid to avoid neural tube defects. Further studies on the association between the maternal intake of folic acid and allergic symptoms at the age of 3 or above considering potential confounders such as other nutrition, outdoor/indoor air pollution, and genetic factors are needed to confirm the results of this study. RESPONSES TO THE COMMENTS OF REVIEWER 2 We thank you for the insightful comments, which have helped us to substantially improve the manuscript. 1. Please give more details on the instrument for dietary data collection (FFQ) Response: We thank you for this pertinent comment. In accordance with the comment, we have added the following text to the Materials and Methods (p. 6, line 134): In brief, the FFQ asked the participants about the frequency of consumption of 172 food and beverage items, from never to seven or more times per day for food, and ten or more glasses per day for beverages. Thereafter, the intake of 53 nutrients was calculated. 2. Please consider, if possible, the adherence to recommendation on folic acid use during pregnancy. Have the authors information on the timing of folic acid intake (before pregnancy or after the conception). This is also important to understand the effect of the duration of folic acid intake. (please consider the following 10.3390/ijerph17020638). I would also suggest a double-check of the text for revising minor errors and typos. Response: Thank you for your comment. We agree with your recommendation and have added the following sentences to the conclusion. (p. 16, line 312): “However, this association represents weak evidence to reconsider intake recommendations. Thus, we suggest the intake of both dietary and supplemental folic acid to avoid neural tube defects.” We could not consider the timing and duration of folic acid intake, which is an important issue to consider in future research. In addition, we thank you for your suggestion to double-check the manuscript. We rechecked the manuscript and fixed grammatical and typographical errors as needed. RESPONSES TO THE COMMENTS OF REVIEWER 3 We thank you for the insightful comments, which have helped us to substantially improve the manuscript. 1. TITLE. I suggest the authors to modify the current title to a more accurate and attractive one such as "Maternal dietary folate intake with folic acid supplement use and wheeze and eczema in children aged 2 years in Japan: A nationwide cohort study". Response: We thank you for this pertinent comment. In accordance with the comment, we have revised the title as follows: "Maternal dietary folate intake with folic acid supplements and wheeze and eczema in children aged 2 years in the Japan Environment and Children’s Study." As a part of a nationwide cohort study, we were recommended to include “Japan Environment and Children’s Study” in the title. 2. About the limitations in DISCUSSION. Another two aspects should be mentioned: (1) The authors didn't consider the indoor and outdoor environmental factors. The authors mentioned "These factors (covariates) were selected based on previous studies that reported an association between folic acid intake during pregnancy and allergies in offspring", but the environmental factors have been widely considered to be the risk factors for childhood allergic sympotms/diseases. Some references include: -- Onset and remission of childhood wheeze and rhinitis across China - associations with early life indoor and outdoor air pollution. Environment International 2019, 123: 61-69. -- Preconceptional, prenatal and postnatal exposure to outdoor and indoor environmental factors on allergic diseases/symptoms in preschool children. Chemosphere 2016, 152: 459-467 Response: There may have been potential confounders such as maternal/paternal genetic factors, indoor/outdoor air pollution, and other allergens. We have added the following limitation to the Discussion. (p. 15, line 297): Finally, there are other risk factors that may cause wheeze and eczema. Potential confounders could not be sufficiently considered in this study, such as indoor and/or outdoor air pollution. For example, previous studies reported that environmental factors such as PM2.5 are known risk factors that increase allergies [31-33]. Regarding indoor environments, allergens such as dust mites are well known factors associated with allergies [34], so that these potential confounding factors could be considered in further studies. (2) As the authors mentioned in ABSTRACT that "The study does not provide evidence that pregnant women should be denied folic acid intake owing to the increased risk early onset allergies in offspring", further/future studies focusing on the its association with allergic diseases, asthma or rhinitis, in elder preschool children aged 3-6 years are necessary to confirm the conclusions of the present work. Response: We agree with the comment. We have incorporated this suggestion throughout the abstract and conclusion. (p. 2, line 42): In contrast, only dietary folate intake was positively associated with wheeze at the age of 2 (adjusted odds ratio, 1.103; 95% confidence interval, 1.003–1.212). However, there is no scientific evidence of a biological mechanism that clarifies this result. Potential confounders such as other nutrition, outdoor/indoor air pollution, and genetic factors may have affected the results. Therefore, further studies on the association between maternal intake of folic acid and allergic symptoms at the age of 3 or above are needed to confirm the results of this study. (p. 16, line 313): Thus, we suggest the intake of both dietary and supplemental folic acid to avoid neural tube defects. Further studies on the association between the maternal intake of folic acid and allergic symptoms at the age of 3 or above considering potential confounders such as other nutrition, outdoor/indoor air pollution, and genetic factors are needed to confirm the results of this study. Submitted filename: Response_to_Reviewers.docx Click here for additional data file. 29 Jul 2022 Maternal dietary folate intake with folic acid supplements and wheeze and eczema in children aged 2 years in the Japan Environment and Children’s Study PONE-D-22-10468R1 Dear Dr. Araki, We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements. Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication. An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. 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If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation. Reviewer #1: All comments have been addressed Reviewer #2: All comments have been addressed Reviewer #3: All comments have been addressed ********** 2. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Yes Reviewer #2: Yes Reviewer #3: Yes ********** 3. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes Reviewer #3: Yes ********** 4. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes Reviewer #2: Yes Reviewer #3: Yes ********** 5. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes Reviewer #3: Yes ********** 6. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: (No Response) Reviewer #2: (No Response) Reviewer #3: This manuscript was improved according to the reviewers' comments. The quality is now fine. I suggest to accept this work for publication. ********** 7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: No Reviewer #2: No Reviewer #3: No ********** 12 Aug 2022 PONE-D-22-10468R1 Maternal dietary folate intake with folic acid supplements and wheeze and eczema in children aged 2 years in the Japan Environment and Children’s Study Dear Dr. Ikeda-Araki: I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org. If we can help with anything else, please email us at plosone@plos.org. Thank you for submitting your work to PLOS ONE and supporting open access. Kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Kenji J Tsuchiya Academic Editor PLOS ONE
  30 in total

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3.  Foetal exposure to maternal stressful events increases the risk of having asthma and atopic diseases in childhood.

Authors:  Roberto de Marco; Giancarlo Pesce; Paolo Girardi; Pierpaolo Marchetti; Marta Rava; Paolo Ricci; Alessandro Marcon
Journal:  Pediatr Allergy Immunol       Date:  2012-09-09       Impact factor: 6.377

4.  House dust mite and cockroach exposure are strong risk factors for positive allergy skin test responses in the Childhood Asthma Management Program.

Authors:  K Huss; N F Adkinson; P A Eggleston; C Dawson; M L Van Natta; R G Hamilton
Journal:  J Allergy Clin Immunol       Date:  2001-01       Impact factor: 10.793

Review 5.  Folate and DNA methylation: a review of molecular mechanisms and the evidence for folate's role.

Authors:  Krista S Crider; Thomas P Yang; Robert J Berry; Lynn B Bailey
Journal:  Adv Nutr       Date:  2012-01-05       Impact factor: 8.701

6.  Prenatal and postnatal exposures to ambient air pollutants associated with allergies and airway diseases in childhood: A retrospective observational study.

Authors:  Wei Liu; Chen Huang; Jiao Cai; Qingyan Fu; Zhijun Zou; Chanjuan Sun; Jialing Zhang
Journal:  Environ Int       Date:  2020-06-22       Impact factor: 9.621

7.  The international study of asthma and allergies in childhood (ISAAC): phase three rationale and methods.

Authors:  P Ellwood; M I Asher; R Beasley; T O Clayton; A W Stewart
Journal:  Int J Tuberc Lung Dis       Date:  2005-01       Impact factor: 2.373

8.  Periconceptional folic acid intake and disturbing factors: A single-center study in Japan.

Authors:  Shunsuke Kamura; Aiko Sasaki; Kohei Ogawa; Kiyoko Kato; Haruhiko Sago
Journal:  Congenit Anom (Kyoto)       Date:  2021-11-16       Impact factor: 1.409

9.  Folic acid supplements in pregnancy and early childhood respiratory health.

Authors:  S E Håberg; S J London; H Stigum; P Nafstad; W Nystad
Journal:  Arch Dis Child       Date:  2008-12-03       Impact factor: 3.791

Review 10.  Absorption and blood/cellular transport of folate and cobalamin: Pharmacokinetic and physiological considerations.

Authors:  David H Alpers
Journal:  Biochimie       Date:  2015-11-14       Impact factor: 4.079

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