Evidence map›Paper›PMID 15834437›Full record

ArticleBone marrow transplantation2005

The hemochromatosis C282Y allele: a risk factor for hepatic veno-occlusive disease after hematopoietic stem cell transplantation.

A R Kallianpur, L D Hall, M Yadav, D W Byrne, T Speroff, R S Dittus, J L Haines, B W Christman, M L Summar

Abstract read
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In one paragraph

Article in Bone marrow transplantation, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. C282Y polymorphism in the HFE gene is associated with risk of breast cancer.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
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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.

A R KallianpurDivision of General Internal Medicine and Public Health, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37212, USA. Asha.Kallianpur@vanderbilt.edu
L D Hall
M Yadav
D W Byrne
T Speroff
R S Dittus
J L Haines
B W Christman
M L Summar

Funding

Chemotherapy Toxicity: Reduction via Urea Cycle SupportR01CA092313 · NCI · VANDERBILT UNIVERSITY · PI CHRISTMAN, BRIAN W · 2001 to 2004
$1.1M
COMMON POLYMORPHISM EFFECTS ON UREA CYCLE FUNCTIONR01ES009915 · NIEHS · VANDERBILT UNIVERSITY · PI SUMMAR, MARSHALL L · 1999 to 2001
$362k
AHRQ HHS HS-55198NCI NIH HHS CA-92313NCRR NIH HHS RR00095NIEHS NIH HHS ES-09915
6 · The paper itself

Abstract

Hepatic veno-occlusive disease (HVOD) is a serious complication of hematopoietic stem cell transplantation (HSCT). Since the liver is a major site of iron deposition in HFE-associated hemochromatosis, and iron has oxidative toxicity, we hypothesized that HFE genotype might influence the risk of HVOD after myeloablative HSCT. We determined HFE genotypes in 166 HSCT recipients who were evaluated prospectively for HVOD. We also tested whether a common variant of the rate-limiting urea cycle enzyme, carbamyl-phosphate synthetase (CPS), previously observed to protect against HVOD in this cohort, modified the effect of HFE genotype. Risk of HVOD was significantly higher in carriers of at least one C282Y allele (RR=3.7, 95% CI 1.2-12.1) and increased progressively with C282Y allelic dose (RR=1.7, 95% CI 0.4-6.8 in heterozygotes; RR=8.6, 95% CI 1.5-48.5 in homozygotes). The CPS A allele, which encodes a more efficient urea cycle enzyme, reduced the risk of HVOD associated with HFE C282Y. We conclude that HFE C282Y is a risk factor for HVOD and that CPS polymorphisms may counteract its adverse effects. Knowledge of these genotypes and monitoring of iron stores may facilitate risk-stratification and testing of strategies to prevent HVOD, such as iron chelation and pharmacologic support of the urea cycle.

Indexed as

Mutation, MissenseAdultAllelesBreast NeoplasmsCarbamoyl-Phosphate Synthase (Ammonia)FemaleGenetic Predisposition to DiseaseGenotypeHematologic NeoplasmsHematopoietic Stem Cell TransplantationHemochromatosisHepatic Veno-Occlusive DiseaseHumansIronMaleMiddle AgedCarbamoyl-Phosphate Synthase (Ammonia)Iron

Identifiers

PMID15834437

What OpenQuestion holds

Textmetadata
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.