MATERNAL EXPOSURE TO N-NITROSATABLE DRUGS AS A RISK FACTOR FOR CHILDHOOD BRAIN-TUMORS

被引:24
作者
CAROZZA, SE
OLSHAN, AF
FAUSTMAN, EM
GULA, MJ
KOLONEL, LN
AUSTIN, DF
WEST, ED
WEISS, NS
SWANSON, GM
LYON, JL
HEDLEYWHYTE, T
GILLES, FH
ASCHENBRENER, C
LEVITON, A
机构
[1] UNIV WASHINGTON,DEPT ENVIRONM HLTH,SEATTLE,WA 98195
[2] UNIV PITTSBURGH,DEPT BIOSTAT,PITTSBURGH,PA 15261
[3] CANC RES CTR HAWAII,PROGRAM EPIDEMIOL,HONOLULU,HI
[4] CALIF DEPT HLTH SERV,CANC EPIDEMIOL UNIT,EMERYVILLE,CA
[5] NO CALIFORNIA CANC REGISTRY,ALAMEDA,CA
[6] UNIV WASHINGTON,DEPT EPIDEMIOL,SEATTLE,WA 98195
[7] FRED HUTCHINSON CANC RES CTR,SEATTLE,WA 98104
[8] MICHIGAN STATE UNIV,CTR COMPREHENS BREAST CANC,E LANSING,MI
[9] UNIV UTAH,DEPT FAMILY & COMMUNITY MED,SALT LAKE CITY,UT
[10] MASSACHUSETTS GEN HOSP,DEPT NEUROPATHOL,BOSTON,MA
[11] CHILDRENS HOSP LOS ANGELES,LOS ANGELES,CA 90027
[12] UNIV SO CALIF,LOS ANGELES,CA
[13] UNIV NEBRASKA,MED CTR,OMAHA,NE
[14] CHILDRENS HOSP,BOSTON,MA
[15] HARVARD UNIV,SCH MED,BOSTON,MA
关键词
D O I
10.1093/ije/24.2.308
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background. Animal models suggest that compounds containing a nitrosyl group (N-nitroso compounds (NNO)) can act as potent transplacental carcinogens. Many common drug formulations have the potential to undergo nitrosation in vivo. The association between maternal use of nitrosatable drugs during pregnancy and development of brain tumours in the offspring was examined in a SEER-based case-control study. Methods. Maternal exposure to nitrosatable drugs during pregnancy was compared among 361 childhood brain tumour cases and 1083 matched controls recruited through random-digit dialling. Results. There was no increase in risk observed for childhood brain tumours overall (OR = 1.15; 95% CI : 0.69-1.94) or for astrocytomas individually (OR = 1.16; 95% CI : 0.50-2.69). A slight elevation in risk was noted for medulloblastomas (OR = 1.47; 95% CI : 0.28-7.62) and 'other' tumours (OR = 1.27; 95% CI : 0.56-2.86), however, both estimates were based on small numbers. Conclusions. Our findings suggest that no increased risk of childhood brain tumours was associated with maternal exposure to nitrosatable drugs. The study results should be Viewed with caution given the imprecision of the point estimates as well as the lack of data on specific timing and dosage of exposure and degree of nitrosatability of drugs taken.
引用
收藏
页码:308 / 312
页数:5
相关论文
共 25 条
[1]   MUTAGENICITY OF AMINE DRUGS AND THEIR PRODUCTS OF NITROSATION [J].
ANDREWS, AW ;
LIJINSKY, W ;
SNYDER, SW .
MUTATION RESEARCH, 1984, 135 (02) :105-108
[2]  
BRAMBILLA G, 1985, J TOXICOL ENV HEALTH, V15, P1
[3]   GENOTOXIC EFFECTS OF DRUG NITRITE INTERACTION PRODUCTS - EVIDENCE FOR THE NEED OF RISK ASSESSMENT [J].
BRAMBILLA, G .
PHARMACOLOGICAL RESEARCH COMMUNICATIONS, 1985, 17 (04) :307-321
[4]  
Breslow N, 1980, STATISTICAL METHODS, V32
[5]   RELATION BETWEEN MATERNAL DIET AND SUBSEQUENT PRIMITIVE NEUROECTODERMAL BRAIN-TUMORS IN YOUNG-CHILDREN [J].
BUNIN, GR ;
KUIJTEN, RR ;
BUCKLEY, JD ;
RORKE, LB ;
MEADOWS, AT .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (08) :536-541
[6]  
COULSTON F, 1978, POTENTIAL CARCINOGEN
[7]   CHILDHOOD BRAIN-TUMOR RISK IN RELATION TO BIRTH CHARACTERISTICS [J].
EMERSON, JC ;
MALONE, KE ;
DALING, JR ;
STARZYK, P .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1991, 44 (11) :1159-1166
[8]   RISK-FACTORS FOR BRAIN-TUMORS IN CHILDREN [J].
GOLD, E ;
GORDIS, L ;
TONASCIA, J ;
SZKLO, M .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1979, 109 (03) :309-319
[9]   PARENTAL SMOKING AND RISK OF CHILDHOOD BRAIN-TUMORS [J].
GOLD, EB ;
LEVITON, A ;
LOPEZ, R ;
GILLES, FH ;
HEDLEYWHYTE, ET ;
KOLONEL, LN ;
LYON, JL ;
SWANSON, GM ;
WEISS, NS ;
WEST, D ;
ASCHENBRENER, C ;
AUSTIN, DF .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1993, 137 (06) :620-628
[10]  
HOTCHKISS JH, 1989, CANCER SURV, V8, P295