British Journal of Haematology · 2001 · 145 citations · 11 references
Life SciencesGeneticsMolecular GeneticsCancer GeneticsMedical GeneticsPediatric GeneticsGenetic DisordersGenetic Risk AssessmentPediatric Cancer GeneticsPediatric LeukemiasLeukemia RiskMetabolism Enzyme PolymorphismsMethylenetetrahydrofolate Reductase PolymorphismsSubjectsThiopurine S-methyltransferase Polymorphism
We have determined the prevalence of methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C in 71 children (< or = 15 years) with acute lymphoblastic leukaemia (ALL) and in 71 control subjects. Odds ratio (OR) for ALL linked to MTHFR C677T was 0.4 (95% CI 0.2-0.8); for heterozygotes it was 0.5 (95% CI 0.2-0.9) and for homozygotes it was 0.3 (95%CI 0.09-0.8). MTHFR A1298C yielded an overall OR for ALL of 1.3 (95% CI: 0.7-2.6); for heterozygotes it was 1.3 (95% CI: 0.7-7.6) and for homozygotes it was 2.8 (95% CI 0.5-15.6). In conclusion, MTHFR C677T was linked to a significant 2.4-fold decreased risk of developing childhood ALL, whereas MTHFR A1298C did not significantly affect the risk of ALL in our population.
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Jing Ma, Meir J. Stampfer, Edward L. Giovannucci et al. · PubMed · 1997 · 794 citations
Christine F. Skibola, Martyn T. Smith, Eleanor Kane et al. · Proceedings of the National Academy of Sciences · 1999 · 530 citations · Full text
A methylenetetrahydrofolate reductase polymorphism and the risk of colorectal cancer.
J. Chen, Edward L. Giovannucci, Karl T. Kelsey et al. · PubMed · 1996 · 520 citations