Evidence map›Paper›PMID 21423661›Full record

ArticlePloS one2011

Identifying a window of vulnerability during fetal development in a maternal iron restriction model.

Camelia Mihaila, Jordan Schramm, Frederick G Strathmann, Dawn L Lee, Robert M Gelein, Anne E Luebke, Margot Mayer-Pröschel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.5field-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

25 citing papers in PubMed, 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

7 authors at 1 institution in 1 country.

Camelia MihailaDepartment of Biomedical Genetics, University of Rochester, Rochester, New York, United States of America.
Jordan Schramm
Frederick G Strathmann
Dawn L Lee
Robert M Gelein
Anne E Luebke
Margot Mayer-Pröschel
University of Rochester · US

Funding

The University of Rochester's Clinical and Translational Science InstituteTL1RR024135 · NCRR · UNIVERSITY OF ROCHESTER · PI PEARSON, THOMAS ARTHUR · 2006 to 2011
$3.7M
STOCHASTIC MODELING OF MULTI TYPE CELL SYSTEMSR01NS039511 · NINDS · UNIVERSITY OF UTAH · PI HYRIEN, OLLIVIER · 2001 to 2011
$3.2M
Molecular biology of cochlear efferent receptorsR01DC003086 · NIDCD · UNIVERSITY OF ROCHESTER · PI LUEBKE, ANNE E · 2001 to 2009
$2.5M
Integrated multidisciplinary approach for analyzing diffuse myelination disordersR01HD059739 · NICHD · UNIVERSITY OF ROCHESTER · PI MAYER-PROSCHEL, MARGOT · 2010 to 2010
$921k
NCRR NIH HHS TL1 RR024135NICHD NIH HHS R01 HD059739NICHD NIH HHS R01HD059739NIDCD NIH HHS R01 DC003086NINDS NIH HHS R01 NS039511NINDS NIH HHS R01NS39511
6 · The paper itself

Abstract

It is well acknowledged from observations in humans that iron deficiency during pregnancy can be associated with a number of developmental problems in the newborn and developing child. Due to the obvious limitations of human studies, the stage during gestation at which maternal iron deficiency causes an apparent impairment in the offspring remains elusive. In order to begin to understand the time window(s) during pregnancy that is/are especially susceptible to suboptimal iron levels, which may result in negative effects on the development of the fetus, we developed a rat model in which we were able to manipulate and monitor the dietary iron intake during specific stages of pregnancy and analyzed the developing fetuses. We established four different dietary-feeding protocols that were designed to render the fetuses iron deficient at different gestational stages. Based on a functional analysis that employed Auditory Brainstem Response measurements, we found that maternal iron restriction initiated prior to conception and during the first trimester were associated with profound changes in the developing fetus compared to iron restriction initiated later in pregnancy. We also showed that the presence of iron deficiency anemia, low body weight, and changes in core body temperature were not defining factors in the establishment of neural impairment in the rodent offspring.Our data may have significant relevance for understanding the impact of suboptimal iron levels during pregnancy not only on the mother but also on the developing fetus and hence might lead to a more informed timing of iron supplementation during pregnancy.

Indexed as

Iron DeficienciesModels, BiologicalAnemia, Iron-DeficiencyAnimalsAnimals, NewbornCochlear NerveEvoked Potentials, Auditory, Brain StemFemaleFetal DevelopmentHumansIron, DietaryMaleNeural ConductionPregnancyPrenatal Exposure Delayed EffectsRatsIron, Dietary

Identifiers

PMID21423661
PMCPMC3057971
OpenAlexW1972638997

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.