Leukemia Research
Volume 34, Issue 12 , Pages 1596-1600, December 2010

MTHFR C677T polymorphisms and childhood acute lymphoblastic leukemia: A meta-analysis

  • Jing Wang

      Affiliations

    • Department of Hematology, the Affiliated DrumTower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing 210008, Jiangsu PR China
  • ,
  • Ping Zhan

      Affiliations

    • Department of Respiratory Medicine, Nanjing Chest Hospital, Nanjing, PR China
  • ,
  • Bing Chen

      Affiliations

    • Department of Hematology, the Affiliated DrumTower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing 210008, Jiangsu PR China
  • ,
  • Rongfu Zhou

      Affiliations

    • Department of Hematology, the Affiliated DrumTower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing 210008, Jiangsu PR China
  • ,
  • Yonggong Yang

      Affiliations

    • Department of Hematology, the Affiliated DrumTower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing 210008, Jiangsu PR China
  • ,
  • Jian Ouyang

      Affiliations

    • Department of Hematology, the Affiliated DrumTower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing 210008, Jiangsu PR China
    • Corresponding Author InformationCorresponding author. Tel.: +86 25 83105211; fax: +86 25 83105211.

Received 4 January 2010; received in revised form 19 March 2010; accepted 20 March 2010. published online 07 March 2011.

Abstract 

To date, case–control studies on the association between methylenetetrahydrofolate reductase (MTHFR) C677T and childhood acute lymphoblastic leukemia have provided either controversial or inconclusive results. To clarify the effect of MTHFR C677T on the risk of childhood acute lymphoblastic leukemia, a meta-analysis of all case–control observational studies was performed. Heterogeneity (I2=65%, P<0.0001) for C677T among the studies was extreme. The random effects (RE) model showed that the 677T allele was not associated with a decreased susceptibility risk of childhood acute lymphoblastic leukemia compared with the C allele [OR=0.96, 95% confidence interval (CI) (0.88–1.04), P=0.34]. The contrast of homozygotes, recessive model and dominant model produced the same pattern of results as the allele contrast. Although MTHFR C677T was associated with increased risks of colorectal cancer, leukemia, and gastric cancer, our pooled data suggest no evidence for a major role of MTHFR C677T in the carcinogenesis of childhood acute lymphoblastic leukemia.

Keywords: MTHFR polymorphisms, Acute lymphoblastic leukemia, Meta-analysis

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PII: S0145-2126(10)00175-X

doi:10.1016/j.leukres.2010.03.034

Leukemia Research
Volume 34, Issue 12 , Pages 1596-1600, December 2010