Evidence map›Paper›PMID 24323870›Full record

ArticleBirth defects research. Part B, Developmental and reproductive toxicology2013

Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype.

Karen L Soldano, Melanie E Garrett, Heidi L Cope, J Michael Rusnak, Nathen J Ellis, Kaitlyn L Dunlap, Marcy C Speer, Simon G Gregory, Allison E Ashley-Koch

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In one paragraph

Article in Birth defects research. Part B, Developmental and reproductive toxicology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 95% 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

3 citing papers in PubMed, 5 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 3 institutions in 1 country.

Karen L SoldanoCenter for Human Genetics, Duke University Medical Center, Durham, North Carolina.
Melanie E Garrett
Heidi L Cope
J Michael Rusnak
Nathen J Ellis
Kaitlyn L Dunlap
Marcy C Speer
Simon G Gregory
Allison E Ashley-Koch
Center for Human Genetics · USDuke University Hospital · USDuke Medical Center · US

Funding

The Hereditary Basis of Neural Tube DefectsR01NS039818 · NINDS · DUKE UNIVERSITY · PI ASHLEY-KOCH, ALLISON E · 1999 to 2008
$6.8M
NINDS NIH HHS NS039818NINDS NIH HHS R01 NS039818
6 · The paper itself

Abstract

Neural tube defects (NTDs) are caused by improper neural tube closure during the early stages of embryonic development. NTDs are hypothesized to have a complex genetic origin and numerous candidate genes have been proposed. The nitric oxide synthase 3 (NOS3) G594T polymorphism has been implicated in risk for spina bifida, and interactions between that single nucleotide polymorphism (SNP) and the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism have also been observed. To evaluate other genetic variation in the NO pathway in the development of NTDs, we examined all three NOS genes: NOS1, NOS2, and NOS3. Using 3109 Caucasian samples in 745 families, we evaluated association in the overall dataset and within specific phenotypic subsets. Haplotype tagging SNPs in the NOS genes were tested for genetic association with NTD subtypes, both for main effects as well as for the presence of interactions with the MTHFR C677T polymorphism. Nominal main effect associations were found with all subtypes, across all three NOS genes, and interactions were observed between SNPs in all three NOS genes and MTHFR C677T. Unlike the previous report, the most significant associations in our dataset were with cranial subtypes and the AG genotype of rs4795067 in NOS2 (p = 0.0014) and the interaction between the rs9658490 G allele in NOS1 and MTHFR 677TT genotype (p = 0.0014). Our data extend the previous findings by implicating a role for all three NOS genes, independently and through interactions with MTHFR, in risk not only for spina bifida, but all NTD subtypes.

Indexed as

Polymorphism, Single NucleotideGenotypeHaplotypesHumansMethylenetetrahydrofolate Reductase (NADPH2)Neural Tube DefectsNitric Oxide SynthaseNitric Oxide Synthase Type INitric Oxide Synthase Type IINitric Oxide Synthase Type IIIPhenotypeMethylenetetrahydrofolate Reductase (NADPH2)Nitric Oxide SynthaseNitric Oxide Synthase Type INitric Oxide Synthase Type IINitric Oxide Synthase Type IIINOS1 protein, humanNOS2 protein, humanNOS3 protein, humananencephalyMTHFRneural tube defectNOS1NOS2NOS3NTDspina bifida

Identifiers

PMID24323870
PMCPMC4169175
OpenAlexW1700732248

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Registered trials

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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.