Evidence map›Paper›PMID 28152281›Full record

ArticlePediatric pulmonology2017

Glutathione-S-transferase P1 may predispose children to a decline in pulmonary function after stem cell transplant.

Julie Stark, Jamie Renbarger, James Slaven, Zhangsheng Yu, Jenny Then, Jodi Skiles, Stephanie Davis

Abstract read
In one paragraph

Article in Pediatric pulmonology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. Article
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.

Julie StarkDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana.
Jamie RenbargerDepartment of Hematology/Oncology, Indiana University School of Medicine, Indianapolis, Indiana.
James SlavenDepartment of Biostatics, Indiana University School of Medicine, Indianapolis, Indiana.
Zhangsheng YuDepartment of Biostatics, Indiana University School of Medicine, Indianapolis, Indiana.
Jenny ThenDepartment of Hematology/Oncology, Indiana University School of Medicine, Indianapolis, Indiana.
Jodi SkilesDepartment of Hematology/Oncology, Indiana University School of Medicine, Indianapolis, Indiana.
Stephanie DavisDepartment of Pediatrics, Section of Pediatric Pulmonology, Allergyand Sleep Medicine, Indiana University School of Medicine, Indianapolis, Indiana.

Funding

Indiana University Center for Pediatric PharmacologyU54HD071598 · NICHD · INDIANA UNIVERSITY INDIANAPOLIS · PI RENBARGER, JAMIE L · 2011 to 2015
$3.8M
NICHD NIH HHS U54 HD071598
6 · The paper itself

Abstract

rationalePulmonary complications after hematopoietic stem cell transplant (SCT) are associated with increased mortality. Genetic markers for those at risk for pulmonary impairment post-SCT have not been widely investigated.

methodsForty-nine patients were retrospectively selected from a single institution's biorepository with linked clinical data. All subjects performed pre-SCT PFTs. Genotyping was conducted using the Infinium Exome-24 BeadChip. Four single nucleotide polymorphisms (SNPs) were selected (rs1800871, rs1695, rs1800629, rs12477314) and evaluated for association with PFT parameters as change over time from baseline. Associations between SNPs and PFT parameters were assessed and adjusted for the following confounding variables: age, gender, and race.

resultsUsing the recessive genetic model, patients with one or two minor alleles for the glutathione S-transferase P1 (GSTP1) SNP rs1695 had a lower decline in FEV

conclusionsOur findings suggest that GSTP1 genotype may be associated with lung function during the first year post-SCT. Identifying and investigating genes that predispose patients to pulmonary complications after SCT may allow for more personalized patient management based on pre-emptive genetic testing. The glutathione S-transferase gene merits further investigation.

Indexed as

Genetic Predisposition to DiseaseStem Cell TransplantationAdolescentChildFemaleGenetic TestingGenotypeGlutathione S-Transferase piHumansMalePolymorphism, Single NucleotideRespiratory Function TestsRetrospective StudiesGlutathione S-Transferase piGSTP1 protein, humanbiomarkersgenetics/genome-wide association studies (GWAS)lung pathologypulmonary function testing (PFT)

Identifiers

PMID28152281
PMCPMC5716628

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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.