Evidence map›Paper›PMID 27267668›Full record

ReviewMolecular and cellular endocrinology2016

One carbon metabolism in pregnancy: Impact on maternal, fetal and neonatal health.

Satish C Kalhan

Open access · greenAbstract readReview
In one paragraph

Review in Molecular and cellular endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed, 2 pooled it
7.8field-weighted citation impact, top 2% 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

83 citing papers in PubMed, 2 syntheses or guidelines pooled it, 124 citations in OpenAlex.

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23 more citing papers are in PubMed but not listed here.

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

1 author at 1 institution in 1 country.

Satish C KalhanDepartment of Molecular Medicine, Cleveland Clinic Lerner College of Medicine of Case Western Reserve University, Department of Pathobiology, Lerner Research Institute, NE-40, Cleveland Clinic, 9500 Euclid Av, Cleveland, OH, 44195, USA. Electronic address: sck@case.edu.
Cleveland Clinic Lerner College of Medicine · US

Funding

Zosuquidar trihydrochloride for acute myeloid leukemia &refractory anemiaM01RR000080 · NCRR · UNIVERSITY HOSPITALS OF CLEVELAND · PI DEARBORN, DORR GELLATLY · 1985 to 2007
$22.2M
Glutamine Metabolism in the Human NewbornR01HD042154 · NICHD · CLEVELAND CLINIC LERNER COM-CWRU · PI KALHAN, SATISH C · 2003 to 2007
$1.7M
Sulfur Amino Acid Metabolism in NAFLDR01DK079937 · NIDDK · CLEVELAND CLINIC LERNER COM-CWRU · PI KALHAN, SATISH C · 2009 to 2010
$1.1M
Maternal One Carbon Metabolism and Low Birth Weight InfantR21HD073880 · NICHD · CLEVELAND CLINIC LERNER COM-CWRU · PI KALHAN, SATISH C · 2013 to 2014
$391k
NCRR NIH HHS M01 RR000080NICHD NIH HHS R01 HD042154NICHD NIH HHS R21 HD073880NIDDK NIH HHS R01 DK079937
6 · The paper itself

Abstract

One carbon metabolism or methyl transfer, a crucial component of metabolism in all cells and tissues, supports the critical function of synthesis of purines, thymidylate and methylation via multiple methyl transferases driven by the ubiquitous methyl donor s-adenosylmethionine. Serine is the primary methyl donor to the one carbon pool. Intracellular folates and methionine metabolism are the critical components of one carbon transfer. Methionine metabolism requires vitamin B12, B6 as cofactors and is modulated by endocrine signals and is responsive to nutrient intake. Perturbations in one carbon transfer can have profound effects on cell proliferation, growth and function. Epidemiological studies in humans and experimental model have established a strong relationship between impaired fetal growth and the immediate and long term consequences to the health of the offspring. It is speculated that during development, maternal environmental and nutrient influences by their effects on one carbon transfer can impact the health of the mother, impair growth and reprogram metabolism of the fetus, and cause long term morbidity in the offspring. The potential for such effects is underscored by the unique responses in methionine metabolism in the human mother during pregnancy, the absence of transsulfuration activity in the fetus, ontogeny of methionine metabolism in the placenta and the unique metabolism of serine and glycine in the fetus. Dietary protein restriction in animals and marginal protein intake in humans causes characteristic changes in one carbon metabolism. The impact of perturbations in one carbon metabolism on the health of the mother during pregnancy, on fetal growth and the neonate are discussed and their possible mechanism explored.

Indexed as

MethylationAnimalsCarbonFemaleFetal DevelopmentFetal Growth RetardationFetusHealth StatusHumansPregnancyPrenatal Nutritional Physiological PhenomenaProtein DeficiencyVitamin B DeficiencyCarbonFetusGrowthHomocysteineOne carbon metabolismPregnancyProtein restriction

Identifiers

PMID27267668
PMCPMC5014566
OpenAlexW2415830539

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.