Evidence map›Paper›PMID 33476335›Full record

ArticlePLoS medicine2021

Associations of maternal dietary inflammatory potential and quality with offspring birth outcomes: An individual participant data pooled analysis of 7 European cohorts in the ALPHABET consortium.

Ling-Wei Chen, Adrien M Aubert, Nitin Shivappa, Jonathan Y Bernard, Sara M Mensink-Bout, Aisling A Geraghty, John Mehegan, Matthew Suderman, Kinga Polanska, Wojciech Hanke and 11 more

Abstract readMulticenter Study
In one paragraph

Article in PLoS medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Ling-Wei ChenHRB Centre for Health and Diet Research, School of Public Health, Physiotherapy, and Sports Science, University College Dublin, Dublin, Republic of Ireland.ORCID 0000-0002-2661-8752
Adrien M AubertUniversité de Paris, Centre for Research in Epidemiology and StatisticS (CRESS), Inserm, Inrae, Paris, France.
Nitin ShivappaCancer Prevention and Control Program, Arnold School of Public Health, University of South Carolina, Columbia, South Carolina, United States of America.ORCID 0000-0003-0441-8896
Jonathan Y BernardUniversité de Paris, Centre for Research in Epidemiology and StatisticS (CRESS), Inserm, Inrae, Paris, France.ORCID 0000-0002-6418-983X
Sara M Mensink-BoutThe Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.ORCID 0000-0002-5381-6287
Aisling A GeraghtyUCD Perinatal Research Centre, School of Medicine, University College Dublin, National Maternity Hospital, Dublin, Republic of Ireland.ORCID 0000-0003-0861-7630
John MeheganHRB Centre for Health and Diet Research, School of Public Health, Physiotherapy, and Sports Science, University College Dublin, Dublin, Republic of Ireland.ORCID 0000-0002-4229-3599
Matthew SudermanMRC Integrative Epidemiology Unit, University of Bristol, Bristol, United Kingdom.ORCID 0000-0002-2715-9930
Kinga PolanskaNofer Institute of Occupational Medicine, Lodz, Poland.ORCID 0000-0002-3212-2307
Wojciech HankeNofer Institute of Occupational Medicine, Lodz, Poland.ORCID 0000-0001-7162-2569
Elzbieta TrafalskaDepartment of Hygiene and Epidemiology, Medical University of Lodz, Lodz, Poland.ORCID 0000-0002-1937-0090
Caroline L ReltonMRC Integrative Epidemiology Unit, University of Bristol, Bristol, United Kingdom.
Sarah R CrozierMRC Lifecourse Epidemiology Unit (University of Southampton) Southampton General Hospital, Southampton, United Kingdom.ORCID 0000-0002-9524-1127
Nicholas C HarveyMRC Lifecourse Epidemiology Unit (University of Southampton) Southampton General Hospital, Southampton, United Kingdom.ORCID 0000-0002-8194-2512
Cyrus CooperMRC Lifecourse Epidemiology Unit (University of Southampton) Southampton General Hospital, Southampton, United Kingdom.ORCID 0000-0003-3510-0709
Liesbeth DuijtsThe Generation R Study Group, Erasmus MC, University Medical Center, Rotterdam, the Netherlands.ORCID 0000-0001-6731-9452
Barbara HeudeUniversité de Paris, Centre for Research in Epidemiology and StatisticS (CRESS), Inserm, Inrae, Paris, France.ORCID 0000-0002-1565-1629
James R HébertCancer Prevention and Control Program, Arnold School of Public Health, University of South Carolina, Columbia, South Carolina, United States of America.ORCID 0000-0002-0677-2672
Fionnuala M McAuliffeUCD Perinatal Research Centre, School of Medicine, University College Dublin, National Maternity Hospital, Dublin, Republic of Ireland.
Cecily C KelleherHRB Centre for Health and Diet Research, School of Public Health, Physiotherapy, and Sports Science, University College Dublin, Dublin, Republic of Ireland.ORCID 0000-0001-9548-4914
Catherine M PhillipsHRB Centre for Health and Diet Research, School of Public Health, Physiotherapy, and Sports Science, University College Dublin, Dublin, Republic of Ireland.ORCID 0000-0003-4916-4463

Funding

Biotechnology and Biological Sciences Research Council BB/P028179/1Biotechnology and Biological Sciences Research Council BB/P028187/1Department of Health 10/33/04Medical Research Council G0400491Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_21000Medical Research Council MC_PC_21001Medical Research Council MC_U147585819Medical Research Council MC_U147585824Medical Research Council MC_U147585827Medical Research Council MC_UP_A620_1014Medical Research Council MC_UP_A620_1015Medical Research Council MC_UU_12011/1Medical Research Council MC_UU_12011/2
6 · The paper itself

Abstract

backgroundAdverse birth outcomes are major causes of morbidity and mortality during childhood and associate with a higher risk of noncommunicable diseases in adult life. Maternal periconception and antenatal nutrition, mostly focusing on single nutrients or foods, has been shown to influence infant birth outcomes. However, evidence on whole diet that considers complex nutrient and food interaction is rare and conflicting. We aim to elucidate the influence of whole-diet maternal dietary inflammatory potential and quality during periconceptional and antenatal periods on birth outcomes. METHODS AND

findingsWe harmonized and pooled individual participant data (IPD) from up to 24,861 mother-child pairs in 7 European mother-offspring cohorts [cohort name, country (recruitment dates): ALSPAC, UK (1 April 1991 to 31 December 1992); EDEN, France (27 January 2003 to 6 March 2006); Generation R, the Netherlands (1 April 2002 to 31 January 2006); Lifeways, Ireland (2 October 2001 to 4 April 2003); REPRO_PL, Poland (18 September 2007 to 16 December 2011); ROLO, Ireland (1 January 2007 to 1 January 2011); SWS, United Kingdom (6 April 1998 to 17 December 2002)]. Maternal diets were assessed preconceptionally (n = 2 cohorts) and antenatally (n = 7 cohorts). Maternal dietary inflammatory potential and quality were ranked using the energy-adjusted Dietary Inflammatory Index (E-DII) and Dietary Approaches to Stop Hypertension (DASH) index, respectively. Primary outcomes were birth weight and gestational age at birth. Adverse birth outcomes, i.e., low birth weight (LBW), macrosomia, small-for-gestational-age (SGA), large-for-gestational-age (LGA), preterm and postterm births were defined according to standard clinical cutoffs. Associations of maternal E-DII and DASH scores with infant birth outcomes were assessed using cohort-specific multivariable regression analyses (adjusted for confounders including maternal education, ethnicity, prepregnancy body mass index (BMI), maternal height, parity, cigarettes smoking, and alcohol consumption), with subsequent random-effects meta-analyses. Overall, the study mothers had a mean ± SD age of 29.5 ± 4.9 y at delivery and a mean BMI of 23.3 ± 4.2 kg/m2. Higher pregnancy DASH score (higher dietary quality) was associated with higher birth weight [β(95% CI) = 18.5(5.7, 31.3) g per 1-SD higher DASH score; P value = 0.005] and head circumference [0.03(0.01, 0.06) cm; P value = 0.004], longer birth length [0.05(0.01, 0.10) cm; P value = 0.010], and lower risk of delivering LBW [odds ratio (OR) (95% CI) = 0.89(0.82, 0.95); P value = 0.001] and SGA [0.87(0.82, 0.94); P value < 0.001] infants. Higher maternal prepregnancy E-DII score (more pro-inflammatory diet) was associated with lower birth weight [β(95% CI) = -18.7(-34.8, -2.6) g per 1-SD higher E-DII score; P value = 0.023] and shorter birth length [-0.07(-0.14, -0.01) cm; P value = 0.031], whereas higher pregnancy E-DII score was associated with a shorter birth length [-0.06(-0.10, -0.01) cm; P value = 0.026] and higher risk of SGA [OR(95% CI) = 1.18(1.11, 1.26); P value < 0.001]. In male, but not female, infants higher maternal prepregnancy E-DII was associated with lower birth weight and head circumference, shorter birth length, and higher risk of SGA (P-for-sex-interaction = 0.029, 0.059, 0.104, and 0.075, respectively). No consistent associations were observed for maternal E-DII and DASH scores with gestational age, preterm and postterm birth, or macrosomia and LGA. Limitations of this study were that self-reported dietary data might have increased nondifferential measurement error and that causality cannot be claimed definitely with observational design.

conclusionsIn this cohort study, we observed that maternal diet that is of low quality and high inflammatory potential is associated with lower offspring birth size and higher risk of offspring being born SGA in this multicenter meta-analysis using harmonized IPD. Improving overall maternal dietary pattern based on predefined criteria may optimize fetal growth and avert substantial healthcare burden associated with adverse birth outcomes.

Indexed as

Maternal Nutritional Physiological PhenomenaPregnancy OutcomeEuropeFemaleFetal DevelopmentFetal Growth RetardationHumansInfant, NewbornInfant, Small for Gestational AgeInflammationMalePregnancySex Factors

Identifiers

PMID33476335
PMCPMC7819611

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