Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-25T06:25:27.827Z Has data issue: false hasContentIssue false

Fish consumption prior to pregnancy and pregnancy outcomes in the National Birth Defects Prevention Study, 1997–2011

Published online by Cambridge University Press:  17 October 2018

Renata H Benjamin*
Affiliation:
Department of Epidemiology, Human Genetics and Environmental Sciences, University of Texas Health Science Center at Houston (UTHealth) School of Public Health, 1200 Pressler Street, Houston, TX77030, USA
Laura E Mitchell
Affiliation:
Department of Epidemiology, Human Genetics and Environmental Sciences, University of Texas Health Science Center at Houston (UTHealth) School of Public Health, 1200 Pressler Street, Houston, TX77030, USA
Mark A Canfield
Affiliation:
Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, TX, USA
Adrienne T Hoyt
Affiliation:
Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, TX, USA
Dejian Lai
Affiliation:
Department of Biostatistics, UTHealth School of Public Health, Houston, TX, USA
Tunu A Ramadhani
Affiliation:
Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, TX, USA
Suzan L Carmichael
Affiliation:
Department of Pediatrics, Stanford University, Stanford, CA, USA
Amy P Case
Affiliation:
Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, TX, USA
D Kim Waller
Affiliation:
Department of Epidemiology, Human Genetics and Environmental Sciences, University of Texas Health Science Center at Houston (UTHealth) School of Public Health, 1200 Pressler Street, Houston, TX77030, USA
the National Birth Defects Prevention Study
Affiliation:
Department of Epidemiology, Human Genetics and Environmental Sciences, University of Texas Health Science Center at Houston (UTHealth) School of Public Health, 1200 Pressler Street, Houston, TX77030, USA Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, TX, USA Department of Biostatistics, UTHealth School of Public Health, Houston, TX, USA Department of Pediatrics, Stanford University, Stanford, CA, USA
*
*Corresponding author: Email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Objective

To evaluate the relationships between maternal fish consumption and pregnancy outcomes in a large, population-based sample of women in the USA.

Design

We collected average fish consumption prior to pregnancy using a modified version of the semi-quantitative Willett FFQ. We estimated adjusted OR (aOR) and 95 % CI for associations between different levels of fish consumption and preterm birth (<37 weeks), early preterm birth (<32 and <35 weeks) and small-for-gestational-age infants (SGA; <10th percentile).

Setting

The National Birth Defects Prevention Study (NBDPS).

Subjects

Control mother–infant pairs with estimated delivery dates between 1997 and 2011 (n 10 919).

Results

No significant associations were observed between fish consumption and preterm birth or early preterm birth (aOR = 0·7–1·0 and 0·7–0·9, respectively). The odds of having an SGA infant were elevated (aOR = 2·1; 95 % CI 1·2, 3·4) among women with daily fish consumption compared with women consuming fish less than once per month. No associations were observed between other levels of fish consumption and SGA (aOR = 0·8–1·0).

Conclusions

High intake of fish was associated with twofold higher odds of having an SGA infant, while moderate fish consumption prior to pregnancy was not associated with preterm or SGA. Our study, like many other studies in this area, lacked information regarding preparation methods and the specific types of fish consumed. Future studies should incorporate information on nutrient and contaminant contents, preparation methods and biomarkers to assess these relationships.

Type
Research paper
Copyright
© The Authors 2018 

Fish, including both freshwater and saltwater fish and shellfish species, provide high-quality protein and nutrients, including long-chain n-3 PUFA (DHA and EPA)( Reference Coletta, Bell and Roman 1 Reference Mahaffey, Clickner and Jeffries 3 ). DHA and EPA are important for fetal neural and retinal development and they may reduce inflammatory processes, increase vasodilation, reduce platelet aggregation and influence the onset of labour through prostaglandin synthesis( Reference Coletta, Bell and Roman 1 , Reference Jensen 2 , Reference Kris-Etherton, Harris and Appel 4 ). However, fish may also contain contaminants, such as methylmercury and persistent organic pollutants, which may adversely affect fetal development and impact pregnancy outcomes( Reference Oken and Bellinger 5 ).

Preterm and small-for-gestational-age (SGA) infants are at increased risk of morbidity, mortality and long-term developmental deficits( 6 , 7 ). Growth restriction and preterm delivery can sometimes be attributed to known causes, such as medical conditions and gestation of multiples; however, the aetiology remains unclear in many cases and novel approaches to prevention are needed. Recent studies( Reference Rogers, Emmett and Ness 8 Reference Olsen and Secher 15 ) suggest that consuming fish during pregnancy may increase birth weight and help to protect against preterm birth; however, concerns remain about the effects of contaminants found in fish on fetal health. These concerns are heightened by several recent studies that have reported associations between high consumption of specific types of fish and increased risk of preterm birth or SGA( Reference Halldorsson, Meltzer and Thorsdottir 16 Reference Mohanty, Siscovick and Williams 18 ).

Most of the studies that have assessed the associations between fish intake and pregnancy outcomes have been conducted in coastal European countries (Norway, Spain, France and Denmark), where fish consumption habits are different from those in the USA( Reference Guldner, Monfort and Rouget 9 , Reference Olsen, Osterdal and Salvig 10 , Reference Haugen, Meltzer and Brantsaeter 13 Reference Mendez, Plana and Guxens 17 ). Per capita fish consumption in Norway is twice as high as that in the USA and inland farmed fish, including tilapia and catfish, make up a larger proportion of the domestic fish supply in the USA than in Europe( 19 ). Prior US studies examining the relationships between fish consumption and birth outcomes have focused on specific populations: one was a clinical trial of women at high risk for preterm birth( Reference Klebanoff, Harper and Lai 11 ) and two were cohorts of predominantly non-Hispanic white women (66–88 %) living in specific geographic regions (Boston and Washington State)( Reference Mohanty, Siscovick and Williams 18 , Reference Oken, Kleinman and Olsen 20 , Reference Mohanty, Thompson and Burbacher 21 ). Results from European studies and prior US studies may not generalize to the US population as a whole.

The objective of the present study was to evaluate associations between fish consumption and preterm birth or SGA in a diverse sample of US women. To do so, we used data from the National Birth Defects Prevention Study (NBDPS), which surveyed a population-based sample of women as part of a case–control study of birth defects. Only control participants, who delivered an infant without a major structural birth defect, were included in the current analyses. To our knowledge, ours is the largest US study to examine the relationship between maternal fish intake and preterm birth and SGA.

Methods

Population and design

The NBDPS was a multisite, population-based, case–control study of birth defects with ten participating sites across the USA (Arkansas, California, Georgia/Centers for Disease Control and Prevention, Iowa, Massachusetts, New Jersey, New York, North Carolina, Texas and Utah)( Reference Yoon, Rasmussen and Lynberg 22 ). Controls were unmatched, live-born infants without a major birth defect, randomly selected from hospital records or vital records, who were born during the same time period and from the same geographic area as cases. Mothers were interviewed via a computer-assisted telephone interview between 6 weeks and 2 years after delivery( Reference Yoon, Rasmussen and Lynberg 22 ). Interviews were conducted between 1997 and 2013 for infants with estimated due dates between 1997 and 2011. Participation rates were 67 % among case mothers and 65 % among control mothers.

The NBDPS used a shortened version of the semi-quantitative Willett FFQ developed for the Nurse’s Health Study to collect information on average maternal diet in the year prior to pregnancy, including information on how often women ate a 85–140 g (3–5 oz) serving of fish( Reference Willett, Sampson and Stampfer 23 ). The questionnaire had sixteen possible responses for the frequency of fish consumption, ranging from never/less than once per month to six times or more per day.

The NBDPS maternal interview collected information about the infant including sex, date of birth and due date. For our primary analysis, preterm delivery was defined as a birth occurring at less than 37 weeks of gestation. For additional sensitivity analyses, early preterm birth was defined as a delivery occurring before 35 weeks of gestation and before 32 weeks of gestation. Since this was a secondary analysis of an existing study, we had limited power to evaluate early preterm delivery. However, since research suggests that associations between fish or fish oil consumption and preterm birth may differ between early and late preterm birth( Reference Brantsaeter, Englund-Ogge and Haugen 14 ), we sought to evaluate whether the associations between fish consumption levels and preterm birth differed when restricting preterm to earlier gestational ages. Infant birth weight was collected from medical records or birth certificates. SGA was defined as an infant with a birth weight below the 10th percentile for the infant’s sex and gestational age compared with a reference population (2011 US birth certificate data)( Reference Duryea, Hawkins and McIntire 24 ). Cut-offs for the 10th percentiles of birth weight were determined separately for each infant sex; and within each sex, they were determined separately for each week in gestation. While birth weight curves specific to maternal race/ethnicity and parity have been used in some studies, prior studies of fish consumption and SGA have used birth weight curves specific to infant sex and gestational age only. To compare our results with prior findings, we chose to use comparable birth weight measures.

Eligibility criteria

NBDPS control participants who delivered a live-born singleton infant were eligible for inclusion in the present analyses. Mother–infant pairs were excluded if fish consumption data were missing or if the mother had type 1 or type 2 diabetes prior to pregnancy. Women with diabetes diagnosed prior to pregnancy were excluded from analyses because it is strongly associated with both preterm birth and large for gestational age( Reference Colstrup, Mathiesen and Damm 25 , Reference McCance 26 ); moreover, with <1 % of births among women with type 1 diabetes( Reference Peng, Ehrlich and Crites 27 ), there would not be an adequate number of exposed women to assess confounding. For the SGA analyses, mother–infant pairs were also excluded if the infant’s birth weight or sex was not provided or if the infant’s gestational age fell outside the range of gestational ages for which a 10th percentile standard was available, i.e. <24 or >42 weeks at delivery.

Statistical analyses

To facilitate comparisons with existing literature, we categorized the sixteen fish consumption categories from the FFQ as follows: less than once per month, 1–3 times per month, once per week, 2–6 times per week, and once per day or more. The following potential confounders were selected a priori ( 6 , 7 , Reference Goldenberg, Culhane and Iams 28 , Reference Carmichael, Yang and Shaw 29 ) from variables collected in the NBDPS interview and categorized as follows: maternal race/ethnicity (non-Hispanic white; non-Hispanic black; US-born Hispanic; foreign-born Hispanic; US-born other; foreign-born other), maternal age (16–19, 20–29, 30–39 and 40–49 years), maternal education (≤12 years/high school or General Educational Development; 13–15 years/some college or associate degree; ≥16 years/college degree or higher), maternal pre-pregnancy BMI (<18·5, 18·5–<25·0, 25·0–<30·0 and ≥30·0 kg/m2), household income (<$US 20 000; $US 20 000–50 000; >US $50 000), household size (1–2 people; 3–4 people; 5–6 people; ≥7 people), smoking (no smoking in pregnancy v. any smoking in pregnancy), alcohol use (no alcohol use in periconceptional period v. alcohol use in the periconceptional period), gestational diabetes (no gestational diabetes v. diabetes during pregnancy), hypertension (no hypertension; hypertension with medication; hypertension without medication), parity (0, 1, 2 and ≥3 prior live births), maternal height (quartiles), as well as average daily intake of energy, carbohydrates, total fat, protein, Fe and Zn in the year prior to pregnancy, calculated from the FFQ( Reference Willett, Sampson and Stampfer 23 ) and divided into quartiles of intake to allow for non-linear relationships. Hispanic and other (predominantly Asian) race/ethnicity were divided into US-born and foreign-born because the rates of preterm birth and SGA differ between the groups( Reference Gould, Madan and Qin 30 , Reference Gagnon, Zimbeck and Zeitlin 31 ). Furthermore, the associations are in opposite directions, with foreign-born Asian mothers at increased risk and foreign-born Hispanic mothers at decreased risk of adverse outcomes compared with US-born mothers( Reference Gagnon, Zimbeck and Zeitlin 31 ). Non-Hispanic white and black mothers were not further divided by nativity due to the low proportion of foreign-born mothers in these groups. The distribution of potential confounders was assessed for differences across fish consumption levels by χ 2 tests.

Crude OR (cOR) estimates for the association between each outcome and fish consumption categories were calculated by simple logistic regression. We used 95 % CI to assess whether the odds of having a preterm delivery or an SGA infant differed by level of fish intake using women who reported eating fish less than once per month or never as the reference group. We used logistic regression and the change in estimate method to identify confounders for inclusion in the adjusted model. The initial full multivariable logistic regression model contained indicator variables for four levels of fish intake and all covariates that were described above and that were associated with the outcome (P<0·25) in simple logistic regression. The final model estimating adjusted OR (aOR) and 95 % CI for each outcome contained the levels of fish intake and those covariates that resulted in a 10 % or greater change in one of the aOR for fish consumption when they were dropped from the full model. Additional sensitivity analyses were conducted looking at the association between fish consumption and early preterm births (<32 weeks and <35 weeks of gestation) and SGA restricted to full-term infants only.

We assessed interactions between the level of fish intake and the following covariates: maternal race/ethnicity and maternal education. Interaction terms were retained in the multivariable model if the group of interaction terms was significantly associated with the outcome (likelihood ratio test P<0·05). We checked model fit for the final models using the Hosmer and Lemeshow goodness-of-fit test (P<0·05 indicating poor fit). All analyses were conducted using the statistical software package SAS version 9.4. Finally, we assessed how robust the association estimates were to unmeasured confounding by conducting a sensitivity analysis looking at the strength of association that an unmeasured confounder would need to have with both the exposure and the outcome to explain the observed association (E-value)( Reference VanderWeele and Ding 32 ). The E-value aids in assessment of causality in observational studies that may be affected by confounding by quantifying the strength of association an unmeasured confounder would need to have to explain the results: a large value implies a strongly associated unmeasured confounder would need to be present, while a small value implies a weakly associated unmeasured confounder could explain the observed association( Reference VanderWeele and Ding 32 ).

Results

There were 11 829 control mothers included in the NBDPS with estimated due dates between 1997 and 2011, of whom 11 451 (97 %) delivered singletons with a gestational age of at least 20 weeks and were eligible for inclusion in the current analyses. Mothers missing fish consumption data (n 461) or with pre-existing type 1 or type 2 diabetes (n 71) were excluded, leaving 10 919 mother–infant pairs for the preterm analysis. Infants were additionally excluded from the SGA analysis if they were missing birth weight (n 145), infant sex (n 10) or had a gestational age outside the gestational age range of 24 to 42 weeks (n 48). These exclusions left 10 716 mother–infant pairs for the SGA analysis. Overall, 853 (7·8 %) infants were preterm and 828 (7·7 %) were SGA, while forty-six (0·4 %) infants were both preterm and SGA.

Women reported 3·3 servings of fish per month on average and 31·6 % (n 3446) of women reported eating no fish or eating it less than once per month (Table 1). Maternal sociodemographic characteristics differed across fish consumption categories (χ 2 P<0·05, Table 1). Women in the highest consumption group were more likely to be black, foreign-born Hispanic or foreign born-other (self-reported race as Asian, Native American or other) compared with women in the lowest consumption group, who were more likely to be white or US-born Hispanic. Women in the highest and lowest consumption groups were more likely to have a high-school education or less compared with women with moderate consumption (1–3 times per month, once per week or 2–6 times per week). Women who consumed fish 1–3 times per month, once per week or 2–6 times per week were more likely to have a college degree than women who consumed fish daily or less than once per month.

Table 1 Maternal sociodemographic characteristics associated with fish consumption frequency in the National Birth Defects Prevention Study, 1997–2011

Preterm birth

The percentage of infants born preterm ranged from 6·7 to 7·6 % among women eating fish once per week, 2–6 times per week or once per day or more, compared with 8·2 % of infants born preterm among women reporting fish consumption less than once per month (Table 2). After assessing potential confounding (variables assessed are shown in the online supplementary material, Table S1), maternal race/ethnicity was the only variable retained in the adjusted model and no significant interactions were found (P = 0·31 and 0·38). After adjustment, we observed no association between fish consumption levels and preterm birth (aOR = 0·7–1·0). Restricting to early preterm births (<32 weeks and <35 weeks) v. full-term births (≥37 weeks), results were similar in both analyses. Results for early preterm birth are presented for <35 weeks only due to sample size limitations (Table 2). We observed no association between fish consumption and early preterm delivery <35 weeks (aOR = 0·7–0·9). OR were not reported for the highest consumption category because this group contained fewer than five early preterm infants.

Table 2 Crude and adjusted OR for the associations between levels of fish consumption and preterm birth (<37 weeks of gestational age) or early preterm birth (<35 weeks of gestational age) in the National Birth Defects Prevention Study, 1997–2011

cOR, crude OR; aOR, adjusted OR; NR, not reported; Ref., reference category.

* Observations missing maternal race/ethnicity (n 48) were excluded from analysis.

Multivariable logistic regression models adjusted for maternal race/ethnicity.

Average number of 85–140 g (3–5 oz) servings of fish eaten per month, week or day during the year prior to pregnancy.

§ Observations with gestational age 35–36 weeks at delivery (n 536) were excluded from analysis.

OR not reported due to small cell size.

Small for gestational age

The percentage of SGA infants among fish consumers ranged from 7·1 to 20·4 % compared with 8·0 % among women reporting fish consumption less than once per month (Table 3). After assessing potential confounding (variables assessed are shown in the online supplementary material, Table S2), the final adjusted model included maternal race/ethnicity and maternal education and no significant interactions were found between fish consumption and either covariate (P = 0·69 and 0·99). Adjusted odds of having an SGA infant for women who ate fish 1–3 times per month (aOR = 0·9; 95 % CI 0·8, 1·1), once per week (aOR = 1·0; 95 % CI 0·8, 1·2) or 2–6 times per week (aOR = 0·8; 95 % CI 0·7, 1·1) were not significantly different compared with women who ate fish less than once per month (Table 3). Consuming fish once per day or more was associated with increased odds of having an SGA infant (aOR = 2·1; 95 % CI 1·2, 3·4) compared with fish consumption less than once per month. Adjustment for confounders had the greatest impact in the highest consumption category, lowering the OR from 2·9 to 2·1 (Table 3).

Table 3 Crude and adjusted OR for the associations between levels of fish consumption and small-for-gestational-age infants (SGA; birth weight <10th percentile for gestational age and infant sex) among all infants and restricted to full-term infants (37–42 weeks of gestational age) in the National Birth Defects Prevention Study, 1997–2011

cOR, crude OR; aOR, adjusted OR; Ref., reference category.

* Observations missing birth weight (n 145), infant sex (n 10), with gestational age outside the range (<24 or >42 weeks) with reference values (n 48) or missing maternal race/ethnicity or maternal education (n 89) were excluded from analysis.

Multivariable logistic regression model adjusted for maternal race/ethnicity and maternal education.

Average number of 85–140 g (3–5 oz) servings of fish eaten per month, week or day during the year prior to pregnancy.

§ Observations with gestational age <37 weeks at delivery (n 826) were excluded from analysis.

Restricting the SGA analysis to term deliveries (≥37 weeks) resulted in nearly identical estimates as the analysis of all SGA births. The highest fish consumption level was associated with elevated odds of having an SGA infant (aOR = 2·2; 95 % CI 1·3, 3·6; Table 3). aOR for the other consumption categories were nearly identical to estimates for the full sample and ranged from 0·8 to 1·0.

Based on the sensitivity analysis calculating the E-value of the robustness to unmeasured confounding, an unmeasured confounder would have to be associated with both the outcome and the exposure by a ratio of 3·6 above and beyond adjustment for the measured confounders to fully explain the observed 2·1-fold higher odds of SGA among daily fish consumers. An unmeasured confounder associated with both the exposure and outcome by a ratio of 1·7 or higher above and beyond the measured confounders could move the confidence interval to include the null.

Discussion

Our finding of an average of 3·3 servings (85–140 g (3–5 oz)) of fish per month is similar to other studies of US women that reported fish consumption of 85–100 g (3·0–3·5 oz) per week( 33 , Reference Papanikolaou, Brooks and Reider 34 ). A higher proportion of women in the present study reported consuming fish less than once per month (31·6 %) than in European studies, where 8–18 % of women reported no fish consumption( Reference Rogers, Emmett and Ness 8 , Reference Guldner, Monfort and Rouget 9 , Reference Halldorsson, Meltzer and Thorsdottir 16 ).

A recent meta-analysis that pooled data from nineteen European birth cohorts found an 11–13 % reduction in preterm birth among women eating fish twice per week or more compared with women eating fish once per week or less( Reference Leventakou, Roumeliotaki and Martinez 12 ). Studies that have categorized fish consumption in a similar manner to our study reported OR for preterm birth of 0·84 for twice per week v. once per week or less( Reference Haugen, Meltzer and Brantsaeter 13 ) and 0·65 for twice per week or more v. less than once per month( Reference Guldner, Monfort and Rouget 9 ). While our association estimates of a 10–30 % decrease in the odds of preterm birth among women eating fish twice per week or more were similar in magnitude to these European studies, our study lacked the precision needed to find an association of this magnitude. In contrast to most of the previous studies, one recent US study reported an increased risk of preterm birth among women consuming lean fish more than once per week( Reference Mohanty, Siscovick and Williams 18 ). We did not observe an increased risk of preterm birth among high consumers in our study; however, we were unable to evaluate lean fish consumption specifically.

Women reporting daily fish consumption had twice the odds of having an SGA infant compared with women who reported eating fish less than once per month; however, this estimate was based on twenty-one SGA infants and only a small proportion of women reported consumption levels this high. These findings should be replicated in future studies by including a high consumption category. Several prior studies have found an elevated risk of SGA among women consuming high levels of fatty fish( Reference Halldorsson, Meltzer and Thorsdottir 16 ), shellfish (oysters, mussels, shrimp, prawns, lobster and crab)( Reference Guldner, Monfort and Rouget 9 ), crustaceans (a component of shellfish: shrimp, prawns, lobster and crab)( Reference Mendez, Plana and Guxens 17 ) and canned tuna( Reference Mendez, Plana and Guxens 17 ). The aOR estimates for SGA among women consuming shellfish, crustaceans and canned tuna twice per week or more were of similar magnitude to our findings (aOR = 2·14, 2·45 and 2·49, respectively)( Reference Guldner, Monfort and Rouget 9 , Reference Mendez, Plana and Guxens 17 ). As shellfish and canned tuna are among the most commonly eaten fish types in the USA( Reference Mahaffey, Clickner and Jeffries 3 ), they may also have been the most commonly eaten types of fish among the women in our study who reported daily consumption of fish.

Evidence of a relationship between high maternal fish consumption and decreased birth weight has also been previously reported in the USA. Mohanty et al. used a different outcome measure, low birth weight (<2500 g), and reported a 2·2-fold higher risk among women consuming lean fish more than once per week compared with non-consumers( Reference Mohanty, Thompson and Burbacher 21 ). While we were unable to evaluate lean fish consumption specifically and replicate this finding in our study, lean fish, including canned light tuna, breaded fish products and catfish, are also commonly eaten species in the USA( Reference Mahaffey, Clickner and Jeffries 3 ).

Our study was limited by collecting fish consumption using a single question in the FFQ. A previous study demonstrated that a one-item FFQ about fish consumption correlated more closely with plasma DHA concentrations and comparably correlated with methylmercury intake compared with a four- or thirty-six-item FFQ( Reference Oken, Guthrie and Bloomingdale 35 ). Longer FFQ were found to provide no advantage over one-item FFQ in ranking intakes of fish, DHA and methylmercury( Reference Oken, Guthrie and Bloomingdale 35 ). As in many previous studies, we were unable to assess which types of fish were consumed by women in the highest consumption group and how preparation methods may have impacted nutrient and contaminant contents. Since both fish and shellfish are sources of nutrients and possibly contaminants, more detailed consumption and preparation data should be collected in future studies. Additionally, since we performed a secondary analysis of data from a study of birth defects in which the critical window for development of the outcome occurs early in pregnancy, the present study queried average fish consumption during the year prior to conception. Prior studies of fish consumption and pregnancy outcomes vary widely in the timing of collection of fish consumption data, with studies collecting FFQ data in the first trimester( Reference Guldner, Monfort and Rouget 9 , Reference Mohanty, Siscovick and Williams 18 , Reference Mohanty, Thompson and Burbacher 21 ), second trimester( Reference Klebanoff, Harper and Lai 11 , Reference Haugen, Meltzer and Brantsaeter 13 , Reference Brantsaeter, Englund-Ogge and Haugen 14 , Reference Halldorsson, Meltzer and Thorsdottir 16 ), third trimester( Reference Rogers, Emmett and Ness 8 ), or at multiple points in pregnancy( Reference Olsen, Osterdal and Salvig 10 , Reference Olsen and Secher 15 , Reference Mendez, Plana and Guxens 17 ). It is possible that some women in the present study may have changed their consumption habits during pregnancy. Recently Razzaghi and Tinker reported no differences in seafood consumption between pregnant and non-pregnant US women using both detailed 30 d fish intake data and 24 h dietary recalls collected in the National Health and Nutrition Examination Survey from 1999 to 2006( Reference Razzaghi and Tinker 36 ). Additionally, women were asked to recall their average consumption during the year prior to pregnancy, which may have introduced recall bias. Finally, there may be residual confounding or bias affecting our observed associations. Our calculated E-value of 3·6 indicates that only a strong unmeasured confounder could fully explain the association observed between daily fish consumption and SGA. None of the potential confounders we did evaluate were associated this strongly with the outcome. While our results are fairly robust to unmeasured confounding and we assessed a number of potential confounders in our analyses, we cannot rule out the possibility that women who reported daily fish consumption may have had other co-occurring health behaviours or dietary patterns that were not assessed and may be driving the results.

The strengths of our study include the large sample size and the diverse study population from multiple regions across the USA. We assessed the association between high fish consumption and SGA infants. Previous studies that have grouped fish consumption by quartiles may have masked elevated risk in high consumers by grouping them with moderate consumers. We would not have observed an association between high fish consumption and SGA if we had grouped women consuming fish 2–6 times per week with the highest consumers (once per day or more). Additionally, as our sample was based on NBDPS controls, none of the infants in our analyses had chromosomal abnormalities or other major structural birth defects, which can impact gestational age at birth and birth weight, and we were able to assess potential confounding by other dietary components calculated from the FFQ.

To the best of our knowledge, the present study is the first US one to observe an elevated risk of SGA among women reporting daily fish consumption. The elevated risk of SGA we observed among high fish consumers should be confirmed and future studies should collect more detailed data on fish consumption to investigate whether a specific component or contaminant is associated with SGA. Currently the US Food and Drug Administration recommends that when eating fish from commercial sources, women of childbearing age and pregnant women should eat 2–3 servings of fish lower in methylmercury (‘best choices’) or 1 serving of fish with moderate methylmercury content (‘good choices’), while avoiding fish with high mercury content( 37 ). Our results are consistent with the Food and Drug Administration’s recommendation in suggesting that, with respect to the risk of preterm birth and SGA, moderate intake of fish may be beneficial and high intake may be harmful. These results add to the body of evidence that women of childbearing age should be counselled on appropriate fish consumption for a healthy pregnancy.

Acknowledgements

Financial support: This publication was supported in part through a cooperative agreement (U01DD000494) between the Centers for Disease Control and Prevention (CDC) and the Texas Department of State Health Services (DSHS). Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the CDC or the Texas DSHS. Conflict of interest: None. Authorship: R.H.B. was involved in study design, literature review, data analysis and manuscript writing. L.E.M., M.A.C., T.A.R., S.A.C. and A.P.C. were involved in study design and manuscript revisions. A.T.H. replicated analyses and was involved in manuscript revisions. D.L. supervised statistical methods and reviewed the manuscript. D.K.W. was the senior investigator involved in study design, analysis and manuscript revisions. Ethics of human subject participation: This study was conducted according to the guidelines laid down in the Declaration of Helsinki and all procedures involving human subjects were approved by the Institutional Review Board for each centre. Approval for this secondary analysis was granted by The University of Texas Health Science Center at Houston Committee for the Protection of Human Subjects.

Supplementary material

To view supplementary material for this article, please visit https://doi.org/10.1017/S1368980018002641

References

1. Coletta, JM, Bell, SJ & Roman, AS (2010) Omega-3 fatty acids and pregnancy. Rev Obstet Gynecol 3, 163171.Google Scholar
2. Jensen, CL (2006) Effects of n-3 fatty acids during pregnancy and lactation. Am J Clin Nutr 83, 6 Suppl., 1452S1457S.Google Scholar
3. Mahaffey, KR, Clickner, RP & Jeffries, RA (2008) Methylmercury and omega-3 fatty acids: co-occurrence of dietary sources with emphasis on fish and shellfish. Environ Res 107, 2029.Google Scholar
4. Kris-Etherton, PM, Harris, WS & Appel, LJ (2002) Fish consumption, fish oil, omega-3 fatty acids, and cardiovascular disease. Circulation 106, 27472757.Google Scholar
5. Oken, E & Bellinger, DC (2008) Fish consumption, methylmercury and child neurodevelopment. Curr Opin Pediatr 20, 178183.Google Scholar
6. Institute of Medicine (2007) Preterm Birth: Causes, Consequences, and Prevention. Washington DC: The National Academies Press; available at http://www.nap.edu/catalog/11622.html.Google Scholar
7. Centers for Disease Control and Prevention (2006) QuickStats: Percentage of small-for-gestational-age births, by race and Hispanic ethnicity – United States, 2005. https://www.cdc.gov/mmwr/preview/mmwrhtml/mm5750a5.htm (accessed October 2017).Google Scholar
8. Rogers, I, Emmett, P, Ness, A et al. (2004) Maternal fish intake in late pregnancy and the frequency of low birth weight and intrauterine growth retardation in a cohort of British infants. J Epidemiol Community Health 58, 486492.Google Scholar
9. Guldner, L, Monfort, C, Rouget, F et al. (2007) Maternal fish and shellfish intake and pregnancy outcomes: a prospective cohort study in Brittany, France. Environ Health 6, 33.Google Scholar
10. Olsen, SF, Osterdal, ML, Salvig, JD et al. (2006) Duration of pregnancy in relation to seafood intake during early and mid pregnancy: prospective cohort. Eur J Epidemiol 21, 749758.Google Scholar
11. Klebanoff, MA, Harper, M, Lai, Y et al. (2011) Fish consumption, erythrocyte fatty acids, and preterm birth. Obstet Gynecol 117, 10711077.Google Scholar
12. Leventakou, V, Roumeliotaki, T, Martinez, D et al. (2014) Fish intake during pregnancy, fetal growth, and gestational length in 19 European birth cohort studies. Am J Clin Nutr 99, 506516.Google Scholar
13. Haugen, M, Meltzer, HM, Brantsaeter, AL et al. (2008) Mediterranean-type diet and risk of preterm birth among women in the Norwegian Mother and Child Cohort Study (MoBa): a prospective cohort study. Acta Obstet Gynecol Scand 87, 319324.Google Scholar
14. Brantsaeter, AL, Englund-Ogge, L, Haugen, M et al. (2017) Maternal intake of seafood and supplementary long chain n-3 poly-unsaturated fatty acids and preterm delivery. BMC Pregnancy Childbirth 17, 41.Google Scholar
15. Olsen, SF & Secher, NJ (2002) Low consumption of seafood in early pregnancy as a risk factor for preterm delivery: prospective cohort study. BMJ 324, 15.Google Scholar
16. Halldorsson, TI, Meltzer, HM, Thorsdottir, I et al. (2007) Is high consumption of fatty fish during pregnancy a risk factor for fetal growth retardation? A study of 44,824 Danish pregnant women. Am J Epidemiol 166, 687696.Google Scholar
17. Mendez, MA, Plana, E, Guxens, M et al. (2010) Seafood consumption in pregnancy and infant size at birth: results from a prospective Spanish cohort. J Epidemiol Community Health 64, 216222.Google Scholar
18. Mohanty, AF, Siscovick, DS, Williams, MA et al. (2016) Periconceptional seafood intake and pregnancy complications. Public Health Nutr 19, 17951803.Google Scholar
19. Food and Agriculture Organization of the United Nations (2016) The State of World Fisheries and Aquaculture, 2016. http://www.fao.org/3/a-i5555e.pdf (accessed July 2017).Google Scholar
20. Oken, E, Kleinman, KP, Olsen, SF et al. (2004) Associations of seafood and elongated n-3 fatty acid intake with fetal growth and length of gestation: results from a US pregnancy cohort. Am J Epidemiol 160, 774783.Google Scholar
21. Mohanty, AF, Thompson, ML, Burbacher, TM et al. (2015) Periconceptional seafood intake and fetal growth. Paediatr Perinat Epidemiol 29, 376387.Google Scholar
22. Yoon, PW, Rasmussen, SA, Lynberg, MC et al. (2001) The National Birth Defects Prevention Study. Public Health Rep 116, 3240.Google Scholar
23. Willett, WC, Sampson, L, Stampfer, MJ et al. (1985) Reproducibility and validity of a semiquantitative food frequency questionnaire. Am J Epidemiol 122, 5165.Google Scholar
24. Duryea, EL, Hawkins, JS, McIntire, DD et al. (2014) A revised birth weight reference for the United States. Obstet Gynecol 124, 1622.Google Scholar
25. Colstrup, M, Mathiesen, ER, Damm, P et al. (2013) Pregnancy in women with type 1 diabetes: have the goals of St. Vincent declaration been met concerning foetal and neonatal complications? J Matern Fetal Neonatal Med 26, 16821686.Google Scholar
26. McCance, DR (2015) Diabetes in pregnancy. Best Pract Res Clin Obstet Gynaecol 29, 685699.Google Scholar
27. Peng, TY, Ehrlich, SF, Crites, Y et al. (2017) Trends and racial and ethnic disparities in the prevalence of pregestational type 1 and type 2 diabetes in Northern California: 1996–2014. Am J Obstet Gynecol 216, 177.e1e8.Google Scholar
28. Goldenberg, RL, Culhane, JF, Iams, JD et al. (2008) Epidemiology and causes of preterm birth. Lancet 371, 7584.Google Scholar
29. Carmichael, SL, Yang, W, Shaw, GM et al. (2013) Maternal dietary nutrient intake and risk of preterm delivery. Am J Perinatol 30, 579588.Google Scholar
30. Gould, JB, Madan, A, Qin, C et al. (2003) Perinatal outcomes in two dissimilar immigrant populations in the United States: a dual epidemiologic paradox. Pediatrics 111, e676e682.Google Scholar
31. Gagnon, AJ, Zimbeck, M, Zeitlin, J et al. (2009) Migration to western industrialised countries and perinatal health: a systematic review. Soc Sci Med 69, 934946.Google Scholar
32. VanderWeele, TJ & Ding, P (2017) Sensitivity analysis in observational research: introducing the E-value. Ann Intern Med 167, 268274.Google Scholar
33. US Department of Agriculture & US Department of Health and Human Services (2010) Dietary Guidelines for Americans, 2010, 7th ed, Washington, DC: US Government Printing Office; available at https://health.gov/dietaryguidelines/dga2010/dietaryguidelines2010.pdf Google Scholar
34. Papanikolaou, Y, Brooks, J, Reider, , C et al. (2014) US adults are not meeting recommended levels for fish and omega-3 fatty acid intake: results of an analysis using observational data from NHANES 2003–2008. Nutr J 13, 31.Google Scholar
35. Oken, E, Guthrie, LB, Bloomingdale, A et al. (2014) Assessment of dietary fish consumption in pregnancy: comparing one-, four-, and thirty-six-item questionnaires. Public Health Nutr 17, 19491959.Google Scholar
36. Razzaghi, H & Tinker, SC (2014) Seafood consumption among pregnant and non-pregnant women of childbearing age in the United States, NHANES 1999–2006. Food Nutr Res 11, 58.Google Scholar
37. US Food and Drug Administration & US Environmental Protection Agency (2017) Eating Fish: What Pregnant Women and Parents Should Know.https://www.fda.gov/downloads/Food/FoodborneIllnessContaminants/Metals/UCM536321.pdf (accessed July 2017).Google Scholar
Figure 0

Table 1 Maternal sociodemographic characteristics associated with fish consumption frequency in the National Birth Defects Prevention Study, 1997–2011

Figure 1

Table 2 Crude and adjusted OR for the associations between levels of fish consumption and preterm birth (<37 weeks of gestational age) or early preterm birth (<35 weeks of gestational age) in the National Birth Defects Prevention Study, 1997–2011

Figure 2

Table 3 Crude and adjusted OR for the associations between levels of fish consumption and small-for-gestational-age infants (SGA; birth weight <10th percentile for gestational age and infant sex) among all infants and restricted to full-term infants (37–42 weeks of gestational age) in the National Birth Defects Prevention Study, 1997–2011

Supplementary material: File

Benjamin et al. supplementary material

Tables S1-S2

Download Benjamin et al. supplementary material(File)
File 30.6 KB