Human variability in mercury toxicokinetics and steady state biomarker ratios

被引:33
作者
Bartell, SM [1 ]
Ponce, RA
Sanga, RN
Faustman, EM
机构
[1] Univ Washington, Dept Environm Hlth, Seattle, WA 98105 USA
[2] Univ Washington, Inst Risk Anal & Risk Commun, Seattle, WA 98105 USA
关键词
biokinetic; methylmercury; exposure; risk; uncertainty;
D O I
10.1006/enrs.2000.4104
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Regulatory guidelines regarding methylmercury exposure depend on dose-response models relating observed mercury concentrations in maternal blood, cord blood, and maternal hair to developmental neurobehavioral endpoints. Generalized estimates of the maternal blood-to-hair, blood-to-intake, or hair-to-intake ratios are necessary for linking exposure to biomarker-based dose-response models. Most assessments have used point estimates for these ratios; however, significant interindividual and interstudy variability has been reported. For example, a maternal ratio of 250 ppm in hair per mgiL in blood is commonly used in models, but a 1990 WHO review reports mean ratios ranging from 140 to 370 ppm per mg/L. To account for interindividual and interstudy variation in applying these ratios to risk and safety assessment, some researchers have proposed representing the ratios with probability distributions and conducting probabilistic assessments. Such assessments would allow regulators to consider the range and likelihood of mercury exposures in a population, rather than limiting the evaluation to an estimate of the average exposure or a single conservative exposure estimate. However, no consensus exists on the most appropriate distributions for representing these parameters. We discuss published reviews of blood-to-hair and blood-to-intake steady state ratios for mercury and suggest statistical approaches for combining existing datasets to form generalized probability distributions for mercury distribution ratios. Although generalized distributions may not be applicable to all populations, they allow a more informative assessment than point estimates where individual biokinetic information is un-available. Whereas development and use of these distributions will improve existing exposure and risk models, additional efforts in data generation and model development are required. (C) 2000 Academic Press.
引用
收藏
页码:127 / 132
页数:6
相关论文
共 26 条
[1]   VARIATION OF BIOLOGICAL HALF-LIFE OF METHYLMERCURY IN MAN [J].
ALSHAHRISTANI, H ;
SHIHAB, KM .
ARCHIVES OF ENVIRONMENTAL HEALTH, 1974, 28 (06) :342-344
[2]  
[Anonymous], 1997, MERC STUD REP C
[3]  
BALLATORI N, 1984, BIOCHEM PHARMACOL, V33, P1087, DOI 10.1016/0006-2952(84)90518-5
[4]   BILIARY TRANSPORT OF GLUTATHIONE AND METHYLMERCURY [J].
BALLATORI, N ;
CLARKSON, TW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1983, 244 (04) :G435-G441
[5]   LIMITATIONS OF THE VARIOUS METHODS FOR COLLECTING DIETARY-INTAKE DATA [J].
BINGHAM, SA .
ANNALS OF NUTRITION AND METABOLISM, 1991, 35 (03) :117-127
[6]   STUDIES ON HUMANS EXPOSED TO METHYL MERCURY THROUGH FISH CONSUMPTION [J].
BIRKE, G ;
SJOSTRAND, B ;
SKERFVING, S ;
WESTERMARK, T ;
JOHNELS, AG ;
PLANTIN, LO .
ARCHIVES OF ENVIRONMENTAL HEALTH, 1972, 25 (02) :77-+
[8]  
Boischio AAP, 1996, NEUROTOXICOLOGY, V17, P169
[9]  
CLARKSON TW, 1981, MEASUREMENT RISKS, P111
[10]   DOSE-RESPONSE ANALYSIS OF INFANTS PRENATALLY EXPOSED TO METHYL MERCURY - AN APPLICATION OF A SINGLE COMPARTMENT MODEL TO SINGLE-STRAND HAIR ANALYSIS [J].
COX, C ;
CLARKSON, TW ;
MARSH, DO ;
AMINZAKI, L ;
TIKRITI, S ;
MYERS, GG .
ENVIRONMENTAL RESEARCH, 1989, 49 (02) :318-332