Evidence map›Paper›PMID 26503813›Full record

ArticleThe pharmacogenomics journal2016

NUDT15 gene polymorphism related to mercaptopurine intolerance in Taiwan Chinese children with acute lymphoblastic leukemia.

D-C Liang, C-P Yang, H-C Liu, T-H Jaing, S-H Chen, I-J Hung, T-C Yeh, T-H Lin, C-L Lai, C-Y Lai and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in The pharmacogenomics journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 4 pooled it
9.9field-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

54 citing papers in PubMed, 4 syntheses or guidelines pooled it, 82 citations in OpenAlex.

  1. Association ofHaematologica · 2024
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Review
  7. Article
  8. Higher prevalence ofFrontiers in pharmacology · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Frontiers in pediatrics · 2022
    Article
  13. Article
  14. Article
  15. Review
  16. Importance ofJournal of personalized medicine · 2021
    Review
  17. Article
  18. Article
  19. The application of clinical genetics · 2021
    Article
  20. 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 4 institutions in 1 country.

D-C LiangDivision of Pediatric Hematology-Oncology, Mackay Children's Hospital and Mackay Medical College, Taipei, Taiwan.
C-P YangDivision of Pediatric Hematology-Oncology, Chang Gung Children's Hospital, Taoyuan, Taiwan.
H-C LiuDivision of Pediatric Hematology-Oncology, Mackay Children's Hospital and Mackay Medical College, Taipei, Taiwan.
T-H JaingDivision of Pediatric Hematology-Oncology, Chang Gung Children's Hospital, Taoyuan, Taiwan.
S-H ChenDivision of Pediatric Hematology-Oncology, Chang Gung Children's Hospital, Taoyuan, Taiwan.
I-J HungDivision of Pediatric Hematology-Oncology, Chang Gung Children's Hospital, Taoyuan, Taiwan.
T-C YehDivision of Pediatric Hematology-Oncology, Mackay Children's Hospital and Mackay Medical College, Taipei, Taiwan.
T-H LinDivision of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, Taipei, Taiwan.
C-L LaiDivision of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, Taipei, Taiwan.
C-Y LaiChang Gung University, Taoyuan, Taiwan.
L-Y ShihChang Gung University, Taoyuan, Taiwan.
Chang Gung Children's Hospital · TWChang Gung University · TWMackay Medical College · TWChang Gung Memorial Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A recent study identified a variant of the NUDT15 gene (rs116855232 C>T) associated with intolerance to thiopurine in Korean patients with Crohn's disease. This study prompted us to substantiate the finding in a Taiwanese population. Four hundred and four children with acute lymphoblastic leukemia (ALL), and 100 adults with chronic immune thrombocytopenic purpura or localized lymphoma having normal bone marrow were examined. Two candidate gene approaches, pyrosequencing for NUDT15 and TaqMan assay for thiopurine methyltransferase (TPMT) genotyping (rs1142345 A>G), were performed. We showed a risk allele frequency of NUDT15 of 11.6% in children with ALL and 15.5% in adults. By contrast, the risk allele frequency of TPMT was only 1.6% in children with ALL and 0.5% in adults. The high frequency of risk variant for NUDT15, but not the very low frequency of risk variant for TPMT, was closely associated with the intolerance to mercaptopurine in children with ALL in Taiwan, contrast to that of European descent. In regard to NUDT15 polymorphism, the maximal tolerable daily doses of mercaptopurine in homozygotes, heterozygotes and wild-type groups were 9.4 mg m

Indexed as

Pharmacogenomic VariantsPolymorphism, GeneticAge FactorsAntimetabolites, AntineoplasticChildChild, PreschoolDisease-Free SurvivalFemaleGene FrequencyGenetic Association StudiesHeterozygoteHomozygoteHumansInfantInfant, NewbornKaplan-Meier EstimateAntimetabolites, AntineoplasticMercaptopurineNudix HydrolasesNUDT15 protein, humanPyrophosphatases

Identifiers

PMID26503813
OpenAlexW2340010050

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.