Evidence map›Paper›PMID 20237949›Full record

ArticleJournal of neuro-oncology2010

Genetic variants of folate and methionine metabolism and PCNSL incidence in a German patient population.

Delia Kurzwelly, Stefan Knop, Markus Guenther, Juergen Loeffler, Agnieszka Korfel, Eckhard Thiel, Holger Hebart, Matthias Simon, Michael Weller, Michael Linnebank and 1 more

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In one paragraph

Article in Journal of neuro-oncology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 4 pooled it
1.6field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 4 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Association ofThe American journal of clinical nutrition · 2017
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Association ofJournal of Cancer · 2024
    Article
  7. Review
  8. Article
  9. Genes · 2021
    Review
  10. Article
  11. Article
  12. 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

11 authors at 7 institutions in 3 countries.

Delia KurzwellyDivision of Clinical Neurooncology, Department of Neurology, University of Bonn, Sigmund-Freud-Str. 25, Bonn, Germany.
Stefan Knop
Markus Guenther
Juergen Loeffler
Agnieszka Korfel
Eckhard Thiel
Holger Hebart
Matthias Simon
Michael Weller
Michael Linnebank
Ulrich Herrlinger
University of Bonn · DEUniversitätsklinikum Würzburg · DEUniversity Hospital of Zurich · CHCharité - Universitätsmedizin Berlin · DEFranklin University · USKlinikum Stuttgart · DEUniversity of Education Schwaebisch Gmuend · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Functional genetic polymorphisms involved in folate and methionine metabolism play an important role in both DNA synthesis and methylation, and affect the risk of various malignancies including lymphoproliferative disorders such as systemic non-Hodgkin's lymphoma. In a retrospective analysis of 185 immunocompetent patients with primary central nervous system lymphoma (PCNSL) and 212 population controls we therefore investigated eight genetic polymorphisms affecting methionine metabolism for potential association with the development of PCNSL. We observed underrepresentation of the G-allele of the methyltetrahydrofolate homocysteine S-methyltransferase (MTR) c.2756A > G (D919G) missense polymorphism among PCNSL patients (P = 0.045; odds ratio (OR) = 0.65; 0.43-0.99). Furthermore, for the methylenetetrahydrofolate reductase (MTHFR) c.1298A > C (E429A) polymorphism the mutated C-allele was found more frequently among PCNSL patients than among population controls (P = 0.026; OR = 1.57; 1.05-2.34). There were no associations of the other polymorphisms investigated (MTHFR c.677C > T, transcobalamin 2 (Tc2) c.776C > G, cystathionin beta-synthase (CBS) c.844_855ins68, reduced folate carrier-1 (RFC-1) c.80G > A, thymidylate synthase (TYMS) 28-bp repeat, and dihydrofolate reductase (DHFR) c.594 + 59del19 bp) and the presence of PCNSL. This analysis is the largest to date to evaluate associations between genetic variants of folate and methionine metabolism and PCNSL. Our results suggest the hypothesis that folate and methionine metabolism is relevant to susceptibility to PCNSL.

Indexed as

AdultAgedAged, 80 and overCentral Nervous System NeoplasmsFemaleFolic AcidGenetic Predisposition to DiseaseGenotypeGermanyHumansIncidenceLymphomaMaleMethionineMiddle AgedPolymorphism, Single NucleotideFolic AcidMethionine

Identifiers

PMID20237949
OpenAlexW2041110979

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.