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Erschienen in: Cancer Causes & Control 8/2012

01.08.2012 | Original Paper

Folic acid supplementation, MTHFR and MTRR polymorphisms, and the risk of childhood leukemia: the ESCALE study (SFCE)

verfasst von: Alicia Amigou, Jérémie Rudant, Laurent Orsi, Stéphanie Goujon-Bellec, Guy Leverger, André Baruchel, Yves Bertrand, Brigitte Nelken, Geneviève Plat, Gérard Michel, Stéphanie Haouy, Pascal Chastagner, Stéphane Ducassou, Xavier Rialland, Denis Hémon, Jacqueline Clavel

Erschienen in: Cancer Causes & Control | Ausgabe 8/2012

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Abstract

Purpose

Fetal folate deficiency may increase the risk of subsequent childhood acute leukemia (AL), since folates are required for DNA methylation, synthesis, and repair, but the literature remains scarce. This study tested the hypothesis that maternal folic acid supplementation before or during pregnancy reduces AL risk, accounting for the SNPs rs1801133 (C677T) and rs1801131 (A1298C) in MTHFR and rs1801394 (A66G) and rs1532268 (C524T) in MTRR, assumed to modify folate metabolism.

Methods

The nationwide registry-based case–control study, ESCALE, carried out in 2003–2004, included 764 AL cases and 1,681 controls frequency matched with the cases on age and gender. Information on folic acid supplementation was obtained by standardized telephone interview. The genotypes were obtained using high-throughput platforms and imputation for untyped polymorphisms. Odds ratios (OR) were estimated using unconditional regression models adjusted for potential confounders.

Results

AL was significantly inversely associated with maternal folic acid supplementation before and during pregnancy (OR = 0.4; 95 % confidence interval: [0.3–0.6]). MTHFR and MTRR genetic polymorphisms were not associated with AL. However, AL was positively associated with homozygosity for any of the MTHFR polymorphisms and carriership of both MTRR variant alleles (OR = 1.6 [0.9–3.1]). No interaction was observed between MTHFR, MTRR, and maternal folate supplementation.

Conclusion

The study findings support the hypothesis that maternal folic acid supplementation may reduce the risk of childhood AL. The findings also suggest that the genotype homozygous for any of the MTHFR variants and carrying both MTRR variants could be a risk factor for AL.
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Literatur
1.
Zurück zum Zitat Clavel J, Goubin A, Auclerc MF et al (2004) Incidence of childhood leukaemia and non-Hodgkin’s lymphoma in France: National Registry of Childhood Leukaemia and Lymphoma, 1990–1999. Eur J Cancer Prev 13:97–103PubMedCrossRef Clavel J, Goubin A, Auclerc MF et al (2004) Incidence of childhood leukaemia and non-Hodgkin’s lymphoma in France: National Registry of Childhood Leukaemia and Lymphoma, 1990–1999. Eur J Cancer Prev 13:97–103PubMedCrossRef
2.
Zurück zum Zitat Lacour B, Guyot-Goubin A, Guissou S, Bellec S, Desandes E, Clavel J (2010) Incidence of childhood cancer in France: National Children Cancer Registries, 2000–2004. Eur J Cancer Prev 19:173–181PubMedCrossRef Lacour B, Guyot-Goubin A, Guissou S, Bellec S, Desandes E, Clavel J (2010) Incidence of childhood cancer in France: National Children Cancer Registries, 2000–2004. Eur J Cancer Prev 19:173–181PubMedCrossRef
3.
Zurück zum Zitat Anderson LM (2006) Environmental genotoxicants/carcinogens and childhood cancer: bridgeable gaps in scientific knowledge. Mutat Res-Genet Toxicol Environ Mutagen 608:136–156CrossRef Anderson LM (2006) Environmental genotoxicants/carcinogens and childhood cancer: bridgeable gaps in scientific knowledge. Mutat Res-Genet Toxicol Environ Mutagen 608:136–156CrossRef
4.
Zurück zum Zitat Buffler PA, Kwan ML, Reynolds P, Urayama KY (2005) Environmental and genetic risk factors for childhood leukemia: appraising the evidence. Cancer Invest 23:60–75PubMedCrossRef Buffler PA, Kwan ML, Reynolds P, Urayama KY (2005) Environmental and genetic risk factors for childhood leukemia: appraising the evidence. Cancer Invest 23:60–75PubMedCrossRef
5.
Zurück zum Zitat McNally RJ, Parker L (2006) Environmental factors and childhood acute leukemias and lymphomas. Leuk Lymphoma 47:583–598PubMedCrossRef McNally RJ, Parker L (2006) Environmental factors and childhood acute leukemias and lymphomas. Leuk Lymphoma 47:583–598PubMedCrossRef
6.
Zurück zum Zitat Dockerty JD, Herbison P, Skegg DC, Elwood M (2007) Vitamin and mineral supplements in pregnancy and the risk of childhood acute lymphoblastic leukaemia: a case-control study. BMC Public Health 7:136PubMedCrossRef Dockerty JD, Herbison P, Skegg DC, Elwood M (2007) Vitamin and mineral supplements in pregnancy and the risk of childhood acute lymphoblastic leukaemia: a case-control study. BMC Public Health 7:136PubMedCrossRef
7.
Zurück zum Zitat French AE, Grant R, Weitzman S et al (2003) Folic acid food fortification is associated with a decline in neuroblastoma. Clin Pharmacol Ther 74:288–294PubMedCrossRef French AE, Grant R, Weitzman S et al (2003) Folic acid food fortification is associated with a decline in neuroblastoma. Clin Pharmacol Ther 74:288–294PubMedCrossRef
8.
Zurück zum Zitat Grupp SG, Greenberg ML, Ray JG et al (2011) Pediatric cancer rates after universal folic acid flour fortification in Ontario. J Clin Pharmacol 51:60–65PubMedCrossRef Grupp SG, Greenberg ML, Ray JG et al (2011) Pediatric cancer rates after universal folic acid flour fortification in Ontario. J Clin Pharmacol 51:60–65PubMedCrossRef
9.
Zurück zum Zitat Milne E, Royle JA, Miller M et al (2010) Maternal folate and other vitamin supplementation during pregnancy and risk of acute lymphoblastic leukemia in the offspring. Int J Cancer 126:2690–2699PubMed Milne E, Royle JA, Miller M et al (2010) Maternal folate and other vitamin supplementation during pregnancy and risk of acute lymphoblastic leukemia in the offspring. Int J Cancer 126:2690–2699PubMed
10.
Zurück zum Zitat Schuz J, Weihkopf T, Kaatsch P (2007) Medication use during pregnancy and the risk of childhood cancer in the offspring. Eur J Pediatr 166:433–441PubMedCrossRef Schuz J, Weihkopf T, Kaatsch P (2007) Medication use during pregnancy and the risk of childhood cancer in the offspring. Eur J Pediatr 166:433–441PubMedCrossRef
11.
Zurück zum Zitat Shaw AK, Infante-Rivard C, Morrison HI (2004) Use of medication during pregnancy and risk of childhood leukemia (Canada). Cancer Causes Control 15:931–937PubMedCrossRef Shaw AK, Infante-Rivard C, Morrison HI (2004) Use of medication during pregnancy and risk of childhood leukemia (Canada). Cancer Causes Control 15:931–937PubMedCrossRef
12.
Zurück zum Zitat Thompson JR, Gerald PF, Willoughby ML, Armstrong BK (2001) Maternal folate supplementation in pregnancy and protection against acute lymphoblastic leukaemia in childhood: a case-control study. Lancet 358:1935–1940PubMedCrossRef Thompson JR, Gerald PF, Willoughby ML, Armstrong BK (2001) Maternal folate supplementation in pregnancy and protection against acute lymphoblastic leukaemia in childhood: a case-control study. Lancet 358:1935–1940PubMedCrossRef
13.
Zurück zum Zitat Alcasabas P, Ravindranath Y, Goyette G et al (2008) 5, 10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms and the risk of acute lymphoblastic leukemia (ALL) in Filipino children. Pediatr Blood Cancer 51:178–182PubMedCrossRef Alcasabas P, Ravindranath Y, Goyette G et al (2008) 5, 10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms and the risk of acute lymphoblastic leukemia (ALL) in Filipino children. Pediatr Blood Cancer 51:178–182PubMedCrossRef
14.
Zurück zum Zitat Balta G, Yuksek N, Ozyurek E et al (2003) Characterization of MTHFR, GSTM1, GSTT1, GSTP1, and CYP1A1 genotypes in childhood acute leukemia. Am J Hematol 73:154–160PubMedCrossRef Balta G, Yuksek N, Ozyurek E et al (2003) Characterization of MTHFR, GSTM1, GSTT1, GSTP1, and CYP1A1 genotypes in childhood acute leukemia. Am J Hematol 73:154–160PubMedCrossRef
15.
Zurück zum Zitat Chan JY, Ugrasena DG, Lum DW, Lu Y, Yeoh AE (2010) Xenobiotic and folate pathway gene polymorphisms and risk of childhood acute lymphoblastic leukaemia in Javanese children. Hematol Oncol 29:116–123 Chan JY, Ugrasena DG, Lum DW, Lu Y, Yeoh AE (2010) Xenobiotic and folate pathway gene polymorphisms and risk of childhood acute lymphoblastic leukaemia in Javanese children. Hematol Oncol 29:116–123
16.
Zurück zum Zitat Chatzidakis K, Goulas A, Athanassiadou-Piperopoulou F, Fidani L, Koliouskas D, Mirtsou V (2006) Methylenetetrahydrofolate reductase C677T polymorphism: Association with risk for childhood acute lymphoblastic leukemia and response during the initial phase of chemotherapy in Greek patients. Pediatr Blood Cancer 47:147–151PubMedCrossRef Chatzidakis K, Goulas A, Athanassiadou-Piperopoulou F, Fidani L, Koliouskas D, Mirtsou V (2006) Methylenetetrahydrofolate reductase C677T polymorphism: Association with risk for childhood acute lymphoblastic leukemia and response during the initial phase of chemotherapy in Greek patients. Pediatr Blood Cancer 47:147–151PubMedCrossRef
17.
Zurück zum Zitat de Jonge R, Tissing WJE, Hooijberg JH et al (2009) Polymorphisms in folate-related genes and risk of pediatric acute lymphoblastic leukemia. Blood 113:2284–2289PubMedCrossRef de Jonge R, Tissing WJE, Hooijberg JH et al (2009) Polymorphisms in folate-related genes and risk of pediatric acute lymphoblastic leukemia. Blood 113:2284–2289PubMedCrossRef
18.
Zurück zum Zitat Gast A, Bermejo JL, Flohr T et al (2007) Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: a case-control study. Leukemia 21:320–325PubMedCrossRef Gast A, Bermejo JL, Flohr T et al (2007) Folate metabolic gene polymorphisms and childhood acute lymphoblastic leukemia: a case-control study. Leukemia 21:320–325PubMedCrossRef
19.
Zurück zum Zitat Kamel AM, Moussa HS, Ebid GT, Bu RR, Bhatia KG (2007) Synergistic effect of methyltetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphism as risk modifiers of pediatric acute lymphoblastic leukemia. J Egypt Natl Canc Inst 19:96–105PubMed Kamel AM, Moussa HS, Ebid GT, Bu RR, Bhatia KG (2007) Synergistic effect of methyltetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphism as risk modifiers of pediatric acute lymphoblastic leukemia. J Egypt Natl Canc Inst 19:96–105PubMed
20.
Zurück zum Zitat Kim NK, Chong SY, Jang MJ et al (2006) Association of the methylenetetrahydrofolate reductase polymorphism in Korean patients with childhood acute lymphoblastic leukemia. Anticancer Res 26:2879–2881PubMed Kim NK, Chong SY, Jang MJ et al (2006) Association of the methylenetetrahydrofolate reductase polymorphism in Korean patients with childhood acute lymphoblastic leukemia. Anticancer Res 26:2879–2881PubMed
21.
Zurück zum Zitat Krajinovic M, Lamothe S, Labuda D et al (2004) Role of MTHFR genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia. Blood 103:252–257PubMedCrossRef Krajinovic M, Lamothe S, Labuda D et al (2004) Role of MTHFR genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia. Blood 103:252–257PubMedCrossRef
22.
Zurück zum Zitat Lightfoot TJ, Johnston WT, Painter D et al (2010) Genetic variation in the folate metabolic pathway and risk of childhood leukemia. Blood 115:3923–3929PubMedCrossRef Lightfoot TJ, Johnston WT, Painter D et al (2010) Genetic variation in the folate metabolic pathway and risk of childhood leukemia. Blood 115:3923–3929PubMedCrossRef
23.
Zurück zum Zitat Metayer C, Scelo G, Chokkalingam AP et al (2011) Genetic variants in the folate pathway and risk of childhood acute lymphoblastic leukemia. Cancer Causes Control 22:1243–1258PubMedCrossRef Metayer C, Scelo G, Chokkalingam AP et al (2011) Genetic variants in the folate pathway and risk of childhood acute lymphoblastic leukemia. Cancer Causes Control 22:1243–1258PubMedCrossRef
24.
Zurück zum Zitat Oliveira E, Alves S, Quental S et al (2005) The MTHFR C677T and A1298C polymorphisms and susceptibility to childhood acute lymphoblastic leukemia in Portugal. J Pediatr Hematol Oncol 27:425–429PubMedCrossRef Oliveira E, Alves S, Quental S et al (2005) The MTHFR C677T and A1298C polymorphisms and susceptibility to childhood acute lymphoblastic leukemia in Portugal. J Pediatr Hematol Oncol 27:425–429PubMedCrossRef
25.
Zurück zum Zitat Petra BG, Janez J, Vita D (2007) Gene-gene interactions in the folate metabolic pathway influence the risk for acute lymphoblastic leukemia in children. Leuk Lymphoma 48:786–792PubMedCrossRef Petra BG, Janez J, Vita D (2007) Gene-gene interactions in the folate metabolic pathway influence the risk for acute lymphoblastic leukemia in children. Leuk Lymphoma 48:786–792PubMedCrossRef
26.
Zurück zum Zitat Reddy H, Jamil K (2006) Polymorphisms in the MTHFR gene and their possible association with susceptibility to childhood acute lymphocytic leukemia in an Indian population. Leuk Lymphoma 47:1333–1339PubMedCrossRef Reddy H, Jamil K (2006) Polymorphisms in the MTHFR gene and their possible association with susceptibility to childhood acute lymphocytic leukemia in an Indian population. Leuk Lymphoma 47:1333–1339PubMedCrossRef
27.
Zurück zum Zitat Schnakenberg E, Mehles A, Cario G et al. (2005) Polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and susceptibility to pediatric acute lymphoblastic leukemia in a German study population. Bmc Med Genet 6:23 Schnakenberg E, Mehles A, Cario G et al. (2005) Polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and susceptibility to pediatric acute lymphoblastic leukemia in a German study population. Bmc Med Genet 6:23
28.
Zurück zum Zitat Thirumaran RK, Gast A, Flohr T et al. (2005) MTHFR genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukemia. Blood 106:590–591; author reply 1–2 Thirumaran RK, Gast A, Flohr T et al. (2005) MTHFR genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukemia. Blood 106:590–591; author reply 1–2
29.
Zurück zum Zitat Tong N, Fang Y, Li J et al (2010) Methylenetetrahydrofolate reductase polymorphisms, serum methylenetetrahydrofolate reductase levels, and risk of childhood acute lymphoblastic leukemia in a Chinese population. Cancer Sci 101:782–786PubMedCrossRef Tong N, Fang Y, Li J et al (2010) Methylenetetrahydrofolate reductase polymorphisms, serum methylenetetrahydrofolate reductase levels, and risk of childhood acute lymphoblastic leukemia in a Chinese population. Cancer Sci 101:782–786PubMedCrossRef
30.
Zurück zum Zitat Wiemels JL, Smith RN, Taylor GM, Eden OB, Alexander FE, Greaves MF (2001) Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and risk of molecularly defined subtypes of childhood acute leukemia. Proc Natl Acad Sci USA 98:4004–4009PubMedCrossRef Wiemels JL, Smith RN, Taylor GM, Eden OB, Alexander FE, Greaves MF (2001) Methylenetetrahydrofolate reductase (MTHFR) polymorphisms and risk of molecularly defined subtypes of childhood acute leukemia. Proc Natl Acad Sci USA 98:4004–4009PubMedCrossRef
31.
Zurück zum Zitat Yang L, Liu L, Wang JX et al (2011) Polymorphisms in folate-related genes: impact on risk of adult acute lymphoblastic leukemia rather than pediatric in Han Chinese. Leuk Lymphoma 52:1770–1776PubMedCrossRef Yang L, Liu L, Wang JX et al (2011) Polymorphisms in folate-related genes: impact on risk of adult acute lymphoblastic leukemia rather than pediatric in Han Chinese. Leuk Lymphoma 52:1770–1776PubMedCrossRef
32.
Zurück zum Zitat Yeoh AEJ, Lu Y, Chan JYS et al (2010) Genetic susceptibility to childhood acute lymphoblastic leukemia shows protection in Malay boys: results from the Malaysia–Singapore ALL Study Group. Leuk Res 34:276–283PubMedCrossRef Yeoh AEJ, Lu Y, Chan JYS et al (2010) Genetic susceptibility to childhood acute lymphoblastic leukemia shows protection in Malay boys: results from the Malaysia–Singapore ALL Study Group. Leuk Res 34:276–283PubMedCrossRef
33.
Zurück zum Zitat Zanrosso CW, Hatagima A, Emerenciano M et al (2006) The role of methylenetetrahydrofolate reductase in acute lymphoblastic leukemia in a Brazilian mixed population. Leuk Res 30:477–481PubMedCrossRef Zanrosso CW, Hatagima A, Emerenciano M et al (2006) The role of methylenetetrahydrofolate reductase in acute lymphoblastic leukemia in a Brazilian mixed population. Leuk Res 30:477–481PubMedCrossRef
34.
Zurück zum Zitat Frosst P, Blom HJ, Milos R et al (1995) A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10:111–113PubMedCrossRef Frosst P, Blom HJ, Milos R et al (1995) A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10:111–113PubMedCrossRef
35.
Zurück zum Zitat Weisberg I, Tran P, Christensen B, Sibani S, Rozen R (1998) A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 64:169–172PubMedCrossRef Weisberg I, Tran P, Christensen B, Sibani S, Rozen R (1998) A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 64:169–172PubMedCrossRef
36.
Zurück zum Zitat Weisberg IS, Jacques PF, Selhub J et al (2001) The 1298A–>C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine. Atherosclerosis 156:409–415PubMedCrossRef Weisberg IS, Jacques PF, Selhub J et al (2001) The 1298A–>C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine. Atherosclerosis 156:409–415PubMedCrossRef
37.
Zurück zum Zitat Han D, Shen C, Meng X et al (2012) Methionine synthase reductase A66G polymorphism contributes to tumor susceptibility: evidence from 35 case-control studies. Mol Biol Rep 39:805–816PubMedCrossRef Han D, Shen C, Meng X et al (2012) Methionine synthase reductase A66G polymorphism contributes to tumor susceptibility: evidence from 35 case-control studies. Mol Biol Rep 39:805–816PubMedCrossRef
38.
Zurück zum Zitat Brosselin P, Rudant J, Orsi L et al (2009) Acute childhood leukaemia and residence next to petrol stations and automotive repair garages: the ESCALE study (SFCE). Occup Environ Med 66:598–606PubMedCrossRef Brosselin P, Rudant J, Orsi L et al (2009) Acute childhood leukaemia and residence next to petrol stations and automotive repair garages: the ESCALE study (SFCE). Occup Environ Med 66:598–606PubMedCrossRef
39.
Zurück zum Zitat Rudant J, Menegaux F, Leverger G et al (2008) Childhood hematopoietic malignancies and parental use of tobacco and alcohol: the ESCALE study (SFCE). Cancer Causes Control 19:1277–1290PubMedCrossRef Rudant J, Menegaux F, Leverger G et al (2008) Childhood hematopoietic malignancies and parental use of tobacco and alcohol: the ESCALE study (SFCE). Cancer Causes Control 19:1277–1290PubMedCrossRef
40.
Zurück zum Zitat Rudant J, Menegaux F, Leverger G et al (2007) Household exposure to pesticides and risk of childhood hematopoietic malignancies: the ESCALE study (SFCE). Environ Health Perspect 115:1787–1793PubMedCrossRef Rudant J, Menegaux F, Leverger G et al (2007) Household exposure to pesticides and risk of childhood hematopoietic malignancies: the ESCALE study (SFCE). Environ Health Perspect 115:1787–1793PubMedCrossRef
41.
Zurück zum Zitat Rudant J, Orsi L, Menegaux F et al (2010) Childhood acute leukemia, early common infections, and allergy: the ESCALE study. Am J Epidemiol 172:1015–1027PubMedCrossRef Rudant J, Orsi L, Menegaux F et al (2010) Childhood acute leukemia, early common infections, and allergy: the ESCALE study. Am J Epidemiol 172:1015–1027PubMedCrossRef
42.
Zurück zum Zitat Amigou A, Sermage-Faure C, Orsi L et al (2011) Road traffic and childhood leukemia: the ESCALE study (SFCE). Environ Health Perspect 119:566–572PubMedCrossRef Amigou A, Sermage-Faure C, Orsi L et al (2011) Road traffic and childhood leukemia: the ESCALE study (SFCE). Environ Health Perspect 119:566–572PubMedCrossRef
43.
Zurück zum Zitat Desandes E, Clavel J, Berger C et al (2004) Cancer incidence among children in France, 1990–1999. Pediatr Blood Cancer 43:749–757PubMedCrossRef Desandes E, Clavel J, Berger C et al (2004) Cancer incidence among children in France, 1990–1999. Pediatr Blood Cancer 43:749–757PubMedCrossRef
44.
Zurück zum Zitat Howie BN, Donnelly P, Marchini J (2009) A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 5:e1000529 Howie BN, Donnelly P, Marchini J (2009) A flexible and accurate genotype imputation method for the next generation of genome-wide association studies. PLoS Genet 5:e1000529
45.
Zurück zum Zitat Blondel B, Norton J, du Mazaubrun C, Breart G (2001) Development of the main indicators of perinatal health in metropolitan France between 1995 and 1998. Results of the national perinatal survey. J Gynecol Obstet Biol Reprod (Paris) 30:552–564 Blondel B, Norton J, du Mazaubrun C, Breart G (2001) Development of the main indicators of perinatal health in metropolitan France between 1995 and 1998. Results of the national perinatal survey. J Gynecol Obstet Biol Reprod (Paris) 30:552–564
46.
Zurück zum Zitat Blondel B, Supernant K, Du Mazaubrun C, Breart G (2006) Trends in perinatal health in metropolitan France between 1995 and 2003: results from the National Perinatal Surveys. J Gynecol Obstet Biol Reprod (Paris) 35:373–387CrossRef Blondel B, Supernant K, Du Mazaubrun C, Breart G (2006) Trends in perinatal health in metropolitan France between 1995 and 2003: results from the National Perinatal Surveys. J Gynecol Obstet Biol Reprod (Paris) 35:373–387CrossRef
47.
Zurück zum Zitat Infante-Rivard C, Jacques L (2000) Empirical study of parental recall bias. Am J Epidemiol 152:480–486PubMedCrossRef Infante-Rivard C, Jacques L (2000) Empirical study of parental recall bias. Am J Epidemiol 152:480–486PubMedCrossRef
48.
Zurück zum Zitat Dehe S, Vodovar et al. (2000) Prévention primaire des anomalies de fermeture du tube neural par supplémentation périconceptionnelle en acide folique. Bulletin épidémiologique hebdomadaire 21:87–89 Dehe S, Vodovar et al. (2000) Prévention primaire des anomalies de fermeture du tube neural par supplémentation périconceptionnelle en acide folique. Bulletin épidémiologique hebdomadaire 21:87–89
49.
Zurück zum Zitat Marchini J, Howie B (2010) Genotype imputation for genome-wide association studies. Nat Rev Genet 11:499–511PubMedCrossRef Marchini J, Howie B (2010) Genotype imputation for genome-wide association studies. Nat Rev Genet 11:499–511PubMedCrossRef
50.
Zurück zum Zitat Nothnagel M, Ellinghaus D, Schreiber S, Krawczak M, Franke A (2009) A comprehensive evaluation of SNP genotype imputation. Hum Genet 125:163–171PubMedCrossRef Nothnagel M, Ellinghaus D, Schreiber S, Krawczak M, Franke A (2009) A comprehensive evaluation of SNP genotype imputation. Hum Genet 125:163–171PubMedCrossRef
51.
Zurück zum Zitat Friso S, Choi SW, Girelli D et al (2002) A common mutation in the 5, 10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. Proc Nat Acad Sci USA 99:5606–5611PubMedCrossRef Friso S, Choi SW, Girelli D et al (2002) A common mutation in the 5, 10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. Proc Nat Acad Sci USA 99:5606–5611PubMedCrossRef
52.
Zurück zum Zitat Olteanu H, Munson T, Banerjee R (2002) Differences in the efficiency of reductive activation of methionine synthase and exogenous electron acceptors between the common polymorphic variants of human methionine synthase reductase. Biochemistry 41:13378–13385PubMedCrossRef Olteanu H, Munson T, Banerjee R (2002) Differences in the efficiency of reductive activation of methionine synthase and exogenous electron acceptors between the common polymorphic variants of human methionine synthase reductase. Biochemistry 41:13378–13385PubMedCrossRef
53.
Zurück zum Zitat Koppen IJ, Hermans FJ, Kaspers GJ (2010) Folate related gene polymorphisms and susceptibility to develop childhood acute lymphoblastic leukaemia. Br J Haematol 148:3–14PubMedCrossRef Koppen IJ, Hermans FJ, Kaspers GJ (2010) Folate related gene polymorphisms and susceptibility to develop childhood acute lymphoblastic leukaemia. Br J Haematol 148:3–14PubMedCrossRef
54.
Zurück zum Zitat Zintzaras E, Koufakis T, Ziakas PD, Rodopoulou P, Giannouli S, Voulgarelis M (2006) A meta-analysis of genotypes and haplotypes of methylenetetrahydrofolate reductase gene polymorphisms in acute lymphoblastic leukemia. Eur J Epidemiol 21:501–510PubMedCrossRef Zintzaras E, Koufakis T, Ziakas PD, Rodopoulou P, Giannouli S, Voulgarelis M (2006) A meta-analysis of genotypes and haplotypes of methylenetetrahydrofolate reductase gene polymorphisms in acute lymphoblastic leukemia. Eur J Epidemiol 21:501–510PubMedCrossRef
55.
Zurück zum Zitat Pereira TV, Rudnicki M, Pereira AC, Pombo-De-Oliveira MS, Franco RF (2006) 5, 10-methylenetetrahydrofolate reductase polymorphisms and acute lymphoblastic leukemia risk: a meta-analysis. Cancer Epidemiol Biomark Prev 15:1956–1963CrossRef Pereira TV, Rudnicki M, Pereira AC, Pombo-De-Oliveira MS, Franco RF (2006) 5, 10-methylenetetrahydrofolate reductase polymorphisms and acute lymphoblastic leukemia risk: a meta-analysis. Cancer Epidemiol Biomark Prev 15:1956–1963CrossRef
56.
Zurück zum Zitat Vijayakrishnan J, Houlston RS (2010) Candidate gene association studies and risk of childhood acute lymphoblastic leukemia: a systematic review and meta-analysis. Haematologica 95:1405–1414PubMedCrossRef Vijayakrishnan J, Houlston RS (2010) Candidate gene association studies and risk of childhood acute lymphoblastic leukemia: a systematic review and meta-analysis. Haematologica 95:1405–1414PubMedCrossRef
57.
Zurück zum Zitat Wang J, Zhan P, Chen B, Zhou R, Yang Y, Ouyang J (2010) MTHFR C677T polymorphisms and childhood acute lymphoblastic leukemia: a meta-analysis. Leuk Res 34:1596–1600PubMedCrossRef Wang J, Zhan P, Chen B, Zhou R, Yang Y, Ouyang J (2010) MTHFR C677T polymorphisms and childhood acute lymphoblastic leukemia: a meta-analysis. Leuk Res 34:1596–1600PubMedCrossRef
58.
Zurück zum Zitat Rozen R (1997) Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR). Thromb Haemost 78:523–526PubMed Rozen R (1997) Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR). Thromb Haemost 78:523–526PubMed
59.
Zurück zum Zitat Blount BC, Mack MM, Wehr CM et al (1997) Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. Proc Nat Acad Sci USA 94:3290–3295PubMedCrossRef Blount BC, Mack MM, Wehr CM et al (1997) Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. Proc Nat Acad Sci USA 94:3290–3295PubMedCrossRef
60.
Zurück zum Zitat Kim YI (2000) Methylenetetrahydrofolate reductase polymorphisms, folate, and cancer risk: a paradigm of gene-nutrient interactions in carcinogenesis. Nutr Rev 58:205–209PubMedCrossRef Kim YI (2000) Methylenetetrahydrofolate reductase polymorphisms, folate, and cancer risk: a paradigm of gene-nutrient interactions in carcinogenesis. Nutr Rev 58:205–209PubMedCrossRef
61.
Zurück zum Zitat Milne E, de Klerk NH, van Bockxmeer F et al (2006) Is there a folate-related gene–environment interaction in the etiology of childhood acute lymphoblastic leukemia? Int J Cancer 119:229–232PubMedCrossRef Milne E, de Klerk NH, van Bockxmeer F et al (2006) Is there a folate-related gene–environment interaction in the etiology of childhood acute lymphoblastic leukemia? Int J Cancer 119:229–232PubMedCrossRef
Metadaten
Titel
Folic acid supplementation, MTHFR and MTRR polymorphisms, and the risk of childhood leukemia: the ESCALE study (SFCE)
verfasst von
Alicia Amigou
Jérémie Rudant
Laurent Orsi
Stéphanie Goujon-Bellec
Guy Leverger
André Baruchel
Yves Bertrand
Brigitte Nelken
Geneviève Plat
Gérard Michel
Stéphanie Haouy
Pascal Chastagner
Stéphane Ducassou
Xavier Rialland
Denis Hémon
Jacqueline Clavel
Publikationsdatum
01.08.2012
Verlag
Springer Netherlands
Erschienen in
Cancer Causes & Control / Ausgabe 8/2012
Print ISSN: 0957-5243
Elektronische ISSN: 1573-7225
DOI
https://doi.org/10.1007/s10552-012-0004-0

Weitere Artikel der Ausgabe 8/2012

Cancer Causes & Control 8/2012 Zur Ausgabe

CUP-Syndrom: Künstliche Intelligenz kann Primärtumor finden

30.04.2024 Künstliche Intelligenz Nachrichten

Krebserkrankungen unbekannten Ursprungs (CUP) sind eine diagnostische Herausforderung. KI-Systeme können Pathologen dabei unterstützen, zytologische Bilder zu interpretieren, um den Primärtumor zu lokalisieren.

Sind Frauen die fähigeren Ärzte?

30.04.2024 Gendermedizin Nachrichten

Patienten, die von Ärztinnen behandelt werden, dürfen offenbar auf bessere Therapieergebnisse hoffen als Patienten von Ärzten. Besonders gilt das offenbar für weibliche Kranke, wie eine Studie zeigt.

Adjuvante Immuntherapie verlängert Leben bei RCC

25.04.2024 Nierenkarzinom Nachrichten

Nun gibt es auch Resultate zum Gesamtüberleben: Eine adjuvante Pembrolizumab-Therapie konnte in einer Phase-3-Studie das Leben von Menschen mit Nierenzellkarzinom deutlich verlängern. Die Sterberate war im Vergleich zu Placebo um 38% geringer.

Alectinib verbessert krankheitsfreies Überleben bei ALK-positivem NSCLC

25.04.2024 NSCLC Nachrichten

Das Risiko für Rezidiv oder Tod von Patienten und Patientinnen mit reseziertem ALK-positivem NSCLC ist unter einer adjuvanten Therapie mit dem Tyrosinkinase-Inhibitor Alectinib signifikant geringer als unter platinbasierter Chemotherapie.

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