The methylenetetrahydrofolate reductase C677T gene polymorphism decreases the risk of childhood acute lymphocytic leukaemia

被引:125
作者
Franco, RF [1 ]
Simöes, BP
Tone, LG
Gabellini, SM
Zago, MA
Falcao, RP
机构
[1] Univ Sao Paulo, Sch Med Ribeirao Preto, Dept Clin Med, Haematol Lab, BR-14048900 Ribeirao Preto, SP, Brazil
[2] Univ Sao Paulo, Ctr Cell Based Therapy, Ribeirao Preto, SP, Brazil
[3] Univ Sao Paulo, Dept Paediat, BR-05508 Sao Paulo, Brazil
关键词
acute lymphocytic leukaemia; MTHFR; polymorphisms; risk factor; folate metabolism;
D O I
10.1046/j.1365-2141.2001.03140.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We have determined the prevalence of methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C in 71 children (less than or equal to 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 AIL 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.
引用
收藏
页码:616 / 618
页数:3
相关论文
共 12 条
  • [1] Effect of metylenetetrahydrofolate reductase 677 C-T, 1298 A-C, and 1317 T-C on factor V 1691 mutation in Turkish deep vein thrombosis patients
    Akar, N
    Akar, E
    Akçay, R
    Avcu, F
    Yalcin, A
    Cin, S
    [J]. THROMBOSIS RESEARCH, 2000, 97 (03) : 163 - 167
  • [2] Cancer prevention and diet: Help from single nucleotide polymorphisms
    Ames, BN
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) : 12216 - 12218
  • [3] Chen J, 1996, CANCER RES, V56, P4862
  • [4] Analysis of the 677 C→T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groups
    Franco, RF
    Araújo, AG
    Guerreiro, JF
    Elion, J
    Zago, MA
    [J]. THROMBOSIS AND HAEMOSTASIS, 1998, 79 (01) : 119 - 121
  • [5] A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease
    Franco, RF
    Morelli, V
    Lourenço, D
    Maffei, FH
    Tavella, MH
    Piccinato, CE
    Thomazini, IA
    Zago, MA
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1999, 105 (02) : 556 - 559
  • [6] A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE
    FROSST, P
    BLOM, HJ
    MILOS, R
    GOYETTE, P
    SHEPPARD, CA
    MATTHEWS, RG
    BOERS, GJH
    DENHEIJER, M
    KLUIJTMANS, LAJ
    VANDENHEUVEL, LP
    ROZEN, R
    [J]. NATURE GENETICS, 1995, 10 (01) : 111 - 113
  • [7] Ma J, 1997, CANCER RES, V57, P1098
  • [8] A SIMPLE SALTING OUT PROCEDURE FOR EXTRACTING DNA FROM HUMAN NUCLEATED CELLS
    MILLER, SA
    DYKES, DD
    POLESKY, HF
    [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (03) : 1215 - 1215
  • [9] CD10 and CD19 fluorescence intensity of B-cell precursors in normal and leukemic bone marrow.: Clinical characterization of CD10+strong and CD10+weak common acute lymphoblastic leukemia
    Rego, EM
    Tone, LG
    Garcia, AB
    Falcao, RP
    [J]. LEUKEMIA RESEARCH, 1999, 23 (05) : 441 - 450
  • [10] ROZEN R, 1997, THROMB DIATH HAEMO, V78, P297