Evidence map›Paper›PMID 26880023›Full record

ArticleNeurotoxicology2016

Associations between prenatal mercury exposure and early child development in the ALSPAC study.

Jean Golding, Steven Gregory, Yasmin Iles-Caven, Joseph Hibbeln, Alan Emond, Caroline M Taylor

Open access · hybridAbstract read
In one paragraph

Article in Neurotoxicology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 7% of its field
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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Prenatal Mercury Exposure and Neurodevelopment up to the Age of 5 Years: A Systematic Review.International journal of environmental research and public health · 2022
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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

6 authors at 2 institutions in 2 countries.

Jean GoldingCentre for Child and Adolescent Health, School of Social & Community Medicine, University of Bristol, Bristol, UK. Electronic address: jean.golding@bristol.ac.uk.
Steven GregoryCentre for Child and Adolescent Health, School of Social & Community Medicine, University of Bristol, Bristol, UK. Electronic address: Steven.Gregory@bristol.ac.uk.
Yasmin Iles-CavenCentre for Child and Adolescent Health, School of Social & Community Medicine, University of Bristol, Bristol, UK. Electronic address: cdylic@bristol.ac.uk.
Joseph HibbelnNational Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, USA. Electronic address: jhibbeln@mail.nih.gov.
Alan EmondCentre for Child and Adolescent Health, School of Social & Community Medicine, University of Bristol, Bristol, UK. Electronic address: alan.emond@bristol.ac.uk.
Caroline M TaylorCentre for Child and Adolescent Health, School of Social & Community Medicine, University of Bristol, Bristol, UK. Electronic address: Caroline.M.Taylor@bristol.ac.uk.
University of Bristol · GBNational Institute on Alcohol Abuse and Alcoholism · US

Funding

Essential Fatty Acids In Psychiatric DisordersZIAAA000115 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI HIBBELN, JOSEPH · 2009 to 2020
$7.8M
Intramural NIH HHSMedical Research Council G9815508Medical Research Council MC_PC_15018Wellcome Trust 102215Wellcome Trust 102215/2/13/2Wellcome Trust 104077/Z/14/Z
6 · The paper itself

Abstract

introductionThere is evidence that high levels of mercury exposure to the pregnant woman can result in damage to the brain of the developing fetus. However there is uncertainty as to whether lower levels of the metal have adverse effects on the development of the infant and whether components of fish consumption and/or the selenium status of the woman is protective.

methodsIn this study we analysed data from the Avon Longitudinal Study of Parents and Children (ALSPAC) (n=2875-3264) to determine whether levels of total blood mercury of pregnant women collected in the first half of pregnancy are associated with the development of the offspring at ages 6, 18, 30 and 42 months. The developmental measures used maternal self-reported scales for individual types of development (fine and gross motor, social and communication skills) and total scores. Multiple and logistic regression analyses treated the outcomes both as continuous and as suboptimal (the lowest 15th centile). The statistical analyses first examined the association of prenatal mercury exposure with these developmental endpoints and then adjusted each for a number of social and maternal lifestyle factors; finally this model was adjusted for the blood selenium level.

resultsTotal maternal prenatal blood mercury and selenium ranged from 0.17 to 12.76 and 17.0 to 324μg/L respectively. We found no evidence to suggest that prenatal levels of maternal blood mercury were associated with adverse development of the child, even when the mother had consumed no fish during pregnancy. In general, the higher the mercury level the more advanced the development of the child within the range of exposure studied. For example, the fully adjusted effect sizes for total development at 6 and 42 months were +0.51 [95%CI +0.05, +1.00] and +0.43 [95%CI +0.08, +0.78] points per SD of mercury. For the risk of suboptimal development the ORs at these ages were 0.90 [95%CI 0.80, 1.02] and 0.88 [95%CI 0.77, 1.02]. In regard to the associations between blood mercury and child development there were no differences between the mothers who ate fish and those who did not, thus implying that the benefits were not solely due to the beneficial nutrients in fish.

conclusionsWe found no evidence of adverse associations between maternal prenatal blood mercury and child development between 6 and 42 months of age. The significant associations that were present were all in the beneficial direction.

Indexed as

Age FactorsChild, PreschoolDevelopmental DisabilitiesFemaleFood ContaminationHumansInfantLongitudinal StudiesMaleMaternal ExposureMercury CompoundsOutcome Assessment, Health CarePregnancyPrenatal Exposure Delayed EffectsRetrospective StudiesSeleniumMercury CompoundsSeleniumALSPACChild DevelopmentFishMaternal blood mercuryPrenatal exposureSelenium

Identifiers

PMID26880023
PMCPMC4819890
OpenAlexW2263108505

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.