Childhood acute leukemia, maternal beverage intake during pregnancy, and metabolic polymorphisms

被引:27
|
作者
Bonaventure, Audrey [1 ,2 ]
Rudant, Jeremie [1 ,2 ,3 ]
Goujon-Bellec, Stephanie [1 ,2 ,3 ]
Orsi, Laurent [1 ,2 ]
Leverger, Guy [4 ,5 ]
Baruchel, Andre [6 ,7 ]
Bertrand, Yves [8 ]
Nelken, Brigitte [9 ,10 ]
Pasquet, Marlene [11 ]
Michel, Gerard [12 ]
Sirvent, Nicolas [13 ]
Bordigoni, Pierre [14 ]
Ducassou, Stephane [15 ]
Rialland, Xavier [16 ,17 ]
Zelenika, Diana [18 ]
Hemon, Denis [1 ,2 ]
Clavel, Jacqueline [1 ,2 ,3 ]
机构
[1] INSERM, U1018, Ctr Res Epidemiol & Populat Hlth CESP, Environm Epidemiol Canc Grp, F-94807 Villejuif, France
[2] Univ Paris Sud, UMRS 1018, F-94807 Villejuif, France
[3] Natl Registry Childhood Hematopoiet Malignancies, RNHE, Villejuif, France
[4] Hop Armand Trousseau, AP HP, Paris, France
[5] Univ Paris 06, Paris, France
[6] Hop Robert Debre, AP HP, F-75019 Paris, France
[7] Univ Paris 07, Paris, France
[8] Inst Hematooncol Pediat, Lyon, France
[9] CHRU, Hop Jeanne de Flandre, Lille, France
[10] Univ Lille Nord France, F-59000 Lille, France
[11] Hop Enfants, Toulouse, France
[12] Hop Enfants La Timone, AP HM, Marseille, France
[13] Hop Arnaud de Villeneuve, Montpellier, France
[14] CHU Nancy, Vandoeuvre Les Nancy, France
[15] Bordeaux Univ Hosp, Childrens Hosp, Bordeaux, France
[16] CHU Nantes, Hop Mere Enfant, F-44035 Nantes 01, France
[17] CHU Angers, Angers, France
[18] Inst Ctr Natl Genotypage, Commissariat Energie Atom CEA Genom, Evry, France
关键词
Childhood leukemia; Coffee; Alcohol; Pregnancy; Gene; Interaction; GENETIC POLYMORPHISMS; ALCOHOL-CONSUMPTION; PARENTAL SMOKING; INFANT LEUKEMIA; SUSCEPTIBILITY; RISK; ENZYMES; CYP2E1; ONTOGENY; EXPOSURE;
D O I
10.1007/s10552-013-0161-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study aimed to analyze the associations between childhood acute leukemia (AL) and maternal caffeinated beverage consumption during pregnancy, and to explore interactions between caffeinated and alcoholic beverage consumption and polymorphisms of enzymes involved in caffeine and ethanol metabolisms. The data were generated by the French ESCALE study, which included 764 AL cases and 1,681 controls in 2003-2004. The case and control mothers were interviewed on their consumption habits during pregnancy using a standardized questionnaire. Genotypes of the candidate alleles (NAT2*5 rs1801280, ADH1C*2 rs698 and rs1693482, CYP2E1*5 rs2031920 and rs3813867) were obtained using high-throughput genotyping and imputation data for 493 AL cases and 549 controls with at least two grandparents born in Europe. Maternal regular coffee consumption during pregnancy was associated with childhood AL (OR = 1.2 [1.0-1.5], p = 0.02); the odds ratios increased linearly with daily intake (p for trend < 0.001; > 2 cups per day vs. no or less than 1 cup per week: AL: OR = 1.6 [1.2-2.1], lymphoblastic AL: OR = 1.5 [1.1-2.0], myeloblastic AL: OR = 2.4 [1.3-4.3]). The association was slightly more marked for children born to non-smoking mothers. Lymphoblastic AL was also associated with cola soda drinking (OR = 1.3 [1.0-1.5], p = 0.02). No significant gene-environment interactions with coffee, tea, cola soda, or alcohol drinking were observed. This study provides additional evidence that maternal coffee consumption during pregnancy may be associated with childhood AL. Coffee consumption is a prevalent habit and its potential involvement in childhood AL needs to be considered further.
引用
收藏
页码:783 / 793
页数:11
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