Benzene exposure, assessed by urinary trans,trans-muconic acid, in urban children with elevated blood lead levels

被引:39
作者
Weaver, VM
Davoli, CT
Heller, PJ
Fitzwilliam, A
Peters, HL
Sunyer, J
Murphy, SE
Goldstein, GW
Groopman, JD
机构
[1] JOHNS HOPKINS UNIV, SCH MED, BALTIMORE, MD 21205 USA
[2] KENNEDY KRIEGER INST, BALTIMORE, MD 21205 USA
[3] JOHNS HOPKINS UNIV, SCH HYG & PUBL HLTH, DEPT EPIDEMIOL, BALTIMORE, MD 21205 USA
[4] AMER HLTH FDN, VALHALLA, NY 10595 USA
[5] IMIM, DEPT EPIDEMIOL & PUBL HLTH, BARCELONA, SPAIN
关键词
biological monitoring; biomarkers; cotinine; environmental benzene exposure; trans; trans-muconic acid; urban pollution;
D O I
10.2307/3432891
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A pilot study was performed to evaluate the feasibility of using trans,trans-muconic acid (MA) as a biomarker of environmental benzene exposure. A secondary aim was to provide data on the extent of exposure to selected toxicants in a unique population consisting of inner-city children who were already overexposed to one urban hazard, lead. Potential sources of benzene were assessed by a questionnaire. Exposure biomarkers including urinary MA and continine and blood lead. Mean MA was 176.6 +/- 341.7 ng/mg creatinine in the 79 children who participated. A wide range of values was found with as many as 10.1%, depending on the comparison study, above the highest levels reported in adults not exposed by occupation. Mean MA was increased in children evaluated in the afternoon compared to morning, those at or above the median for time spent playing near the street, and those studied in the first half of the investigation. MA levels were not associated with blood lead or, consistently, with either questionnaire environmental tobacco smoke (ETS) data or cotinine. As expected, the mean blood lead level was elevated (23.6 mu g/dl). Mean continine was also increased at 79.2 ng/mg creatinine. We conclude that the use of MA as a biomarker for environmental benzene exposure is feasible since it was detectable in 72% of subjects with a wide range of values present. In future studies, correlation of MA with personal air sampling in environmental exposure will be essential to fully interpret the significance of these findings. In addition, these inner-city children comprise a high risk group for exposure to environmental toxicants including ETS, lead, and probably benzene, based on questionnaire sources and its presence in ETS.
引用
收藏
页码:318 / 323
页数:6
相关论文
共 23 条
[1]   EVALUATION OF ASSAYS FOR THE IDENTIFICATION AND QUANTITATION OF MUCONIC ACID, A BENZENE METABOLITE IN HUMAN URINE [J].
BARTCZAK, A ;
KLINE, SA ;
YU, R ;
WEISEL, CP ;
GOLDSTEIN, BD ;
WITZ, G ;
BECHTOLD, WE .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1994, 42 (03) :245-258
[2]  
BECHTOLD WE, 1991, AM IND HYG ASSOC J, V52, P473, DOI 10.1202/0002-8894(1991)052<0473:MADIUA>2.0.CO
[3]  
2
[4]   BIOLOGICAL MONITORING OF EXPOSURE TO BENZENE - A COMPARISON BETWEEN S-PHENYLMERCAPTURIC ACID, TRANS,TRANS-MUCONIC ACID, AND PHENOL [J].
BOOGAARD, PJ ;
VANSITTERT, NJ .
OCCUPATIONAL AND ENVIRONMENTAL MEDICINE, 1995, 52 (09) :611-620
[5]  
*CDC, 1991, PREV LEAD POIS YOUNG
[6]   TRANS, TRANS-MUCONIC ACID, A RELIABLE BIOLOGICAL INDICATOR FOR THE DETECTION OF INDIVIDUAL BENZENE EXPOSURE DOWN TO THE PPM LEVEL [J].
DUCOS, P ;
GAUDIN, R ;
BEL, J ;
MAIRE, C ;
FRANCIN, JM ;
ROBERT, A ;
WILD, P .
INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH, 1992, 64 (05) :309-313
[7]   IMPROVEMENT IN HPLC ANALYSIS OF URINARY TRANS,TRANS-MUCONIC ACID, A PROMISING SUBSTITUTE FOR PHENOL IN THE ASSESSMENT OF BENZENE EXPOSURE [J].
DUCOS, P ;
GAUDIN, R ;
ROBERT, A ;
FRANCIN, JM ;
MAIRE, C .
INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH, 1990, 62 (07) :529-534
[8]   CHILDHOOD ASTHMA AND PASSIVE SMOKING - URINARY COTININE AS A BIOMARKER OF EXPOSURE [J].
EHRLICH, R ;
KATTAN, M ;
GODBOLD, J ;
SALTZBERG, DS ;
GRIMM, KT ;
LANDRIGAN, PJ ;
LILIENFELD, DE .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 145 (03) :594-599
[9]   VALIDATION OF SELF-REPORTED SMOKING-BEHAVIOR - BIOCHEMICAL ANALYSES OF COTININE AND THIOCYANATE [J].
HALEY, NJ ;
AXELRAD, CM ;
TILTON, KA .
AMERICAN JOURNAL OF PUBLIC HEALTH, 1983, 73 (10) :1204-1207
[10]   PERSPECTIVES ON RISK ASSESSMENT IMPACT OF RECENT REPORTS ON BENZENE [J].
JOHNSON, ES ;
LUCIER, G .
AMERICAN JOURNAL OF INDUSTRIAL MEDICINE, 1992, 21 (05) :749-757