Evidence map›Paper›PMID 32805249›Full record

ArticleEnvironmental research2020

Prenatal exposure to organophosphate pesticides and brain morphology and white matter microstructure in preadolescents.

Michiel A van den Dries, Sander Lamballais, Hanan El Marroun, Anjoeka Pronk, Suzanne Spaan, Kelly K Ferguson, Matthew P Longnecker, Henning Tiemeier, Mònica Guxens

Open access · greenAbstract read
In one paragraph

Article in Environmental research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
5.8field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

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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

9 authors at 4 institutions in 3 countries.

Michiel A van den DriesErasmus MC, University Medical Center Rotterdam, Department of Child and Adolescent Psychiatry, Rotterdam, 3015 CN, the Netherlands; Erasmus MC, University Medical Center Rotterdam, The Generation R Study Group, Rotterdam, 3015 CN, the Netherlands.
Sander LamballaisErasmus MC, University Medical Center Rotterdam, The Generation R Study Group, Rotterdam, 3015 CN, the Netherlands; Erasmus MC, University Medical Center Rotterdam, Department of Epidemiology, Rotterdam, 3015 CN, the Netherlands; Erasmus MC, University Medical Center Rotterdam, Department of Clinical Genetics, Rotterdam, 3015 CN, the Netherlands.
Hanan El MarrounErasmus MC, University Medical Center Rotterdam, Department of Child and Adolescent Psychiatry, Rotterdam, 3015 CN, the Netherlands; Erasmus MC, University Medical Center Rotterdam, Department of Pediatrics, Rotterdam, 3015 CN, the Netherlands; Department of Psychology, Education and Child Studies, Erasmus School of Social and Behavioral Sciences, Erasmus University Rotterdam, 3062 PA, the Netherlands.
Anjoeka PronkDepartment of Risk Analysis for Products in Development, TNO, Utrecht, 3584 CB, the Netherlands.
Suzanne SpaanDepartment of Risk Analysis for Products in Development, TNO, Utrecht, 3584 CB, the Netherlands.
Kelly K FergusonEpidemiology Branch, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Durham, North Carolina, NC, 27709, USA.
Matthew P LongneckerRamboll, Raleigh, North Carolina, NC, 27612, USA.
Henning TiemeierErasmus MC, University Medical Center Rotterdam, Department of Child and Adolescent Psychiatry, Rotterdam, 3015 CN, the Netherlands; Department of Social and Behavioral Sciences, Harvard T. H. Chan School of Public Health, Boston, MA, 02115, USA.
Mònica GuxensErasmus MC, University Medical Center Rotterdam, Department of Child and Adolescent Psychiatry, Rotterdam, 3015 CN, the Netherlands; ISGlobal, Barcelona, 08003, Spain; Pompeu Fabra University, Barcelona, 08002, Spain; Spanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Instituto de Salud Carlos III, 28029, Spain. Electronic address: monica.guxens@isglobal.org.
Erasmus MC · NLHarvard University · USNational Institutes of Health · USUniversitat Pompeu Fabra · ES

Funding

The Training Program in Reproductive, Perinatal, and Pediatric Life Course EpidemiologyT32HD104612 · NICHD · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Sonia Hernandez-Diaz, Henning Tiemeier · 2021 to 2026
$2.2M
Early exposures and neurodevelopmental, behavioral, and health outcomesUG3DA045251 · NIDA · UNIVERSITY OF CHICAGO · PI LAHEY, BENJAMIN B · 2017 to 2018
$718k
NICHD NIH HHS T32 HD104612NIDA NIH HHS UG3 DA045251NIEHS NIH HHS HHSN273201500003CNIEHS NIH HHS HHSN273201500003O
6 · The paper itself

Abstract

backgroundPrenatal exposure to organophosphate (OP) pesticides associate with impaired neurodevelopment in humans and animal models. However, much uncertainty exists about the brain structural alterations underlying these associations. The objective of this study was to determine whether maternal OP pesticide metabolite concentrations in urine repeatedly measured during gestation are associated with brain morphology and white matter microstructure in 518 preadolescents aged 9-12 years.

methodData came from 518 mother-child pairs participating in the Generation R Study, a population-based birth cohort from Rotterdam, the Netherlands. Maternal urine concentrations were determined for 6 dialkylphosphates (DAPs) including 3 dimethyl (DM) and 3 diethyl (DE) alkyl phosphate metabolites, collected at early, mid, and late pregnancy. At child's age 9-12 years, magnetic resonance imaging was performed to obtain T1-weighted images for brain volumes and surface-based cortical thickness and cortical surface area, and diffusion tensor imaging was used to measure white matter microstructure through fractional anisotropy (FA) and mean diffusivity (MD). Linear regression models were fit for the averaged prenatal exposure across pregnancy.

resultsDM and DE metabolite concentrations were not associated with brain volumes, cortical thickness, and cortical surface area. However, a 10-fold increase in averaged DM metabolite concentrations across pregnancy was associated with lower FA (B = -1.00, 95%CI = -1.80, -0.20) and higher MD (B = 0.13, 95%CI = 0.04, 0.21). Similar associations were observed for DE concentrations.

conclusionsThis study provides the first evidence that OP pesticides may alter normal white matter microstructure in children, which could have consequences for normal neurodevelopment. No associations were observed with structural brain morphology, including brain volumes, cortical thickness, and cortical surface area.

Indexed as

PesticidesPrenatal Exposure Delayed EffectsWhite MatterBrainChildDiffusion Tensor ImagingFemaleHumansNetherlandsOrganophosphatesPregnancyOrganophosphatesPesticidesBrain morphologyMRIOrganophosphate pesticidesPrenatal exposureWhite matter microstructure

Identifiers

PMID32805249
PMCPMC7657967
OpenAlexW3049354877

What OpenQuestion holds

Textmetadata
LicenceTDM
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.