Evidence map›Paper›PMID 24896769›Full record

ArticleJournal of exposure science & environmental epidemiology

Infant toenails as a biomarker of in utero arsenic exposure.

Matthew A Davis, Zhigang Li, Diane Gilbert-Diamond, Todd A Mackenzie, Kathryn L Cottingham, Brian P Jackson, Joyce S Lee, Emily R Baker, Carmen J Marsit, Margaret R Karagas

Open access · greenAbstract read
In one paragraph

Article in Journal of exposure science & environmental epidemiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
6.2field-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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 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

10 authors at 2 institutions in 1 country.

Matthew A Davis1] Children's Environmental Health and Disease Prevention Research Center at Dartmouth, Hanover, New Hampshire, USA [2] Institute for Quantitative Biomedical Sciences Graduate Program, Dartmouth College, Hanover, New Hampshire, USA.
Zhigang Li1] Children's Environmental Health and Disease Prevention Research Center at Dartmouth, Hanover, New Hampshire, USA [2] Section of Biostatistics and Epidemiology, Department of Community and Family Medicine, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Diane Gilbert-Diamond1] Children's Environmental Health and Disease Prevention Research Center at Dartmouth, Hanover, New Hampshire, USA [2] Section of Biostatistics and Epidemiology, Department of Community and Family Medicine, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Todd A Mackenzie1] Section of Biostatistics and Epidemiology, Department of Community and Family Medicine, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA [2] Department of Medicine, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Kathryn L Cottingham1] Children's Environmental Health and Disease Prevention Research Center at Dartmouth, Hanover, New Hampshire, USA [2] Department of Biological Sciences, Dartmouth College, Hanover, New Hampshire, USA.
Brian P Jackson1] Children's Environmental Health and Disease Prevention Research Center at Dartmouth, Hanover, New Hampshire, USA [2] Trace Element Analysis Core Laboratory, Dartmouth College, Hanover, New Hampshire, USA.
Joyce S LeeRhode Island Child Health Study, Providence, Rhode Island, USA.
Emily R Baker1] Children's Environmental Health and Disease Prevention Research Center at Dartmouth, Hanover, New Hampshire, USA [2] Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Carmen J Marsit1] Children's Environmental Health and Disease Prevention Research Center at Dartmouth, Hanover, New Hampshire, USA [2] Rhode Island Child Health Study, Providence, Rhode Island, USA [3] Department of Pharmacology and Toxicology, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Margaret R Karagas1] Children's Environmental Health and Disease Prevention Research Center at Dartmouth, Hanover, New Hampshire, USA [2] Section of Biostatistics and Epidemiology, Department of Community and Family Medicine, Geisel School of Medicine at Dartmouth, Hanover, New Hampshire, USA.
Dartmouth College · USProvidence College · US

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
VARIATION IN BIOACCUMULATION AND BIOMAGNIFICATION OF METALS IN NORTHERN US LAKESP42ES007373 · NIEHS · DARTMOUTH COLLEGE · PI CHEN, CELIA Y · 1995 to 2019
$52.0M
Relation Between In-utero Vitamin D and Immune Function in Early Childhood P20GM104416 · NIGMS · DARTMOUTH COLLEGE · PI KARAGAS, MARGARET RITA · 2013 to 2022
$23.7M
Project 3: Placental Biomarkers of Exposure and Outcome (Marsit)P01ES022832 · NIEHS · DARTMOUTH COLLEGE · PI KARAGAS, MARGARET RITA · 2013 to 2018
$4.7M
Environment, Imprinting, and NeurodevelopmentR01ES022223 · NIEHS · EMORY UNIVERSITY · PI CHEN, JIA, MARSIT, CARMEN JOSEPH · 2013 to 2017
$4.3M
Training Program for Quantitative Population Sciences in CancerR25CA134286 · NCI · DARTMOUTH COLLEGE · PI KARAGAS, MARGARET RITA, TOSTESON, TOR D · 2009 to 2018
$3.0M
Epigenetics in Neurodevelopment and Mental HealthR01MH094609 · NIMH · DARTMOUTH COLLEGE · PI MARSIT, CARMEN JOSEPH · 2011 to 2015
$2.3M
Project 4: Determining How Arsenic Modulates Hedgehog Signaling During DevelopmenP20ES018175 · NIEHS · DARTMOUTH COLLEGE · PI KARAGAS, MARGARET RITA · 2010 to 2012
$892k
The United States Complementary and Alternative Medicine MarketK01AT006162 · NCCIH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVIS, MATTHEW A · 2010 to 2014
$706k
NCCIH NIH HHS K01 AT006162NCCIH NIH HHS K01AT006162NCI NIH HHS P30 CA023108NCI NIH HHS R25 CA134286NCI NIH HHS R25CA134286NIEHS NIH HHS P01 ES022832NIEHS NIH HHS P20 ES018175NIEHS NIH HHS P42 ES007373NIEHS NIH HHS R01 ES022223NIGMS NIH HHS P20 GM104416NIMH NIH HHS R01 MH094609
6 · The paper itself

Abstract

A growing body of evidence suggests that in utero and early-life exposure to arsenic may have detrimental effects on children, even at the low to moderate levels common in the United States and elsewhere. In a sample of 170 mother-infant pairs from New Hampshire, we determined infant exposure to in utero arsenic by evaluating infant toenails as a biomarker using inductively coupled plasma mass spectrometry. Infant toenail arsenic concentration correlated with maternal postpartum toenail concentrations (Spearman's correlation coefficient 0.34). In adjusted linear models, a doubling of maternal toenail arsenic concentration was associated with a 53.8% increase in infant toenail arsenic concentration as compared with 20.4% for a doubling of maternal urine arsenic concentration. In a structural equation model, a doubling of the latent variable integrating maternal toenail and urine arsenic concentrations was associated with a 67.5% increase in infant toenail arsenic concentration. A similar correlation between infant and maternal postpartum toenail concentrations was observed in a validation cohort of 130 mother-infant pairs from Rhode Island. In utero exposure to arsenic occurs through maternal water and dietary sources, and infant toenails appear to be a reliable biomarker for estimating arsenic exposure during the critical window of gestation.

Indexed as

Maternal ExposureArsenicBiomarkersFemaleFetusHumansInfantMaleMass SpectrometryNailsPregnancyArsenicBiomarkers

Identifiers

PMID24896769
PMCPMC4141012
OpenAlexW2010880959

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.