Evidence map›Paper›PMID 27872059›Full record

ArticleBlood2017

Genome-wide minor histocompatibility matching as related to the risk of graft-versus-host disease.

Paul J Martin, David M Levine, Barry E Storer, Edus H Warren, Xiuwen Zheng, Sarah C Nelson, Anajane G Smith, Bo K Mortensen, John A Hansen

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 3 pooled it
9.3field-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

50 citing papers in PubMed, 3 syntheses or guidelines pooled it, 113 citations in OpenAlex.

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  12. Novel Aspects of Immunogenetics and Post-Transplant Events in Kidney Transplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Paul J MartinDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA.ORCID 0000-0001-9051-1215
David M LevineDepartment of Biostatistics, University of Washington, Seattle, WA.
Barry E StorerDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA.
Edus H WarrenDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA.
Xiuwen ZhengDepartment of Biostatistics, University of Washington, Seattle, WA.
Sarah C NelsonDepartment of Biostatistics, University of Washington, Seattle, WA.
Anajane G SmithDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA.
Bo K MortensenDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA.
John A HansenDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA.
Fred Hutch Cancer Center · USUniversity of Washington · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
Whole Genome Association Analysis of Hematopoietic Cell Transplant (HCT) OutcomeR01HL105914 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI MARTIN, PAUL J · 2011 to 2019
$9.8M
Whole Genome Association Analysis of Hematopoietic Cell Transplant OutcomeR01HL087690 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HANSEN, JOHN ANDREW · 2006 to 2008
$4.1M
NCI NIH HHS P30 CA015704NHLBI NIH HHS R01 HL087690NHLBI NIH HHS R01 HL105914
6 · The paper itself

Abstract

The risk of acute graft-versus-host disease (GVHD) is higher after allogeneic hematopoietic cell transplantation (HCT) from unrelated donors as compared with related donors. This difference has been explained by increased recipient mismatching for major histocompatibility antigens or minor histocompatibility antigens. In the current study, we used genome-wide arrays to enumerate single nucleotide polymorphisms (SNPs) that produce graft-versus-host (GVH) amino acid coding differences between recipients and donors. We then tested the hypothesis that higher degrees of genome-wide recipient GVH mismatching correlate with higher risks of GVHD after allogeneic HCT. In HLA-genotypically matched sibling recipients, the average recipient mismatching of coding SNPs was 9.35%. Each 1% increase in genome-wide recipient mismatching was associated with an estimated 20% increase in the hazard of grades III-IV GVHD (hazard ratio [HR], 1.20; 95% confidence interval [CI], 1.05-1.37;

Indexed as

Hematopoietic Stem Cell TransplantationAdolescentAdultAllelesChildChild, PreschoolFemaleGenome-Wide Association StudyGraft vs Host DiseaseHistocompatibility TestingHLA AntigensHumansInfantInfant, NewbornMaleMinor Histocompatibility AntigensHLA AntigensMinor Histocompatibility Antigens

Identifiers

PMID27872059
PMCPMC5301826
OpenAlexW2549979982

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.