Evidence map›Paper›PMID 18365141›Full record

ArticleInternational journal of hematology2008

Decreased risk of acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation in patients with the 5,10-methylenetetrahydrofolate reductase 677TT genotype.

Kyoko Sugimoto, Makoto Murata, Makoto Onizuka, Yoshihiro Inamoto, Seitaro Terakura, Yachiyo Kuwatsuka, Taku Oba, Koichi Miyamura, Yoshihisa Kodera, Tomoki Naoe

Abstract read
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In one paragraph

Article in International journal of hematology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
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  4. Article
  5. Article
  6. Article
  7. Role of non-HLA gene polymorphisms in graft-versus-host disease.International journal of hematology · 2013
    Review
  8. Genomic studies of GVHD-lessons learned thus far.Bone marrow transplantation · 2013
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
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

10 authors at 2 institutions in 1 country.

Kyoko SugimotoDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan.
Makoto MurataDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan. mmurata@med.nagoya-u.ac.jp.
Makoto OnizukaDepartment of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Yoshihiro InamotoDepartment of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Seitaro TerakuraDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan.
Yachiyo KuwatsukaDepartment of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Taku ObaDepartment of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Koichi MiyamuraDepartment of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Yoshihisa KoderaDepartment of Hematology, Japanese Red Cross Nagoya First Hospital, Nagoya, Japan.
Tomoki NaoeDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan.
Nagoya University · JPTokai University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polymorphism in 5,10-methylenetetrahydrofolate reductase (MTHFR), a central enzyme in folate metabolism, has been shown to affect the sensitivity of patients to folate-based drugs such as methotrexate. In this study, we investigated whether a common single nucleotide polymorphism at position 677 in the donor or recipient's MTHFR gene affects the risk for acute graft-versus-host disease (GVHD) following allogeneic hematopoietic stem cell transplantation (HSCT) from HLA-identical sibling donors when the recipient receives prophylactic treatment with methotrexate for GVHD. MTHFR genotypes were determined in 159 recipients with a hematological disease and their donors using polymerase chain reaction-restriction fragment length polymorphism analysis of genomic DNA. The 677TT genotype, which encodes an enzyme with approximately 30% of the activity of the wild-type (677CC), was observed in 13% of patients and in 8% of normal donors. Multivariate analyses demonstrated a significant association between 677TT genotype in patients and a lower incidence of grade I-IV acute GVHD (relative risk, 0.35; 95% confidence interval, 0.13-0.95; P = 0.040). There was no association between the incidence of acute GVHD and the donor MTHFR genotypes. These results suggest that greater immunosuppression by methotrexate due to low MTHFR enzyme activity decreases the risk of acute GVHD in recipients of allogeneic HSCT.

Indexed as

Hematopoietic Stem Cell TransplantationLiving DonorsPolymorphism, GeneticAcute DiseaseAdolescentAdultFemaleGenotypeGraft vs Host DiseaseHematologic DiseasesHumansImmunosuppression TherapyImmunosuppressive AgentsMaleMethotrexateMethylenetetrahydrofolate Reductase (NADPH2)Immunosuppressive AgentsMethotrexateMethylenetetrahydrofolate Reductase (NADPH2)

Identifiers

PMID18365141
OpenAlexW2073673533

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.