Characterizing dose-response I: Critical assessment of the benchmark dose concept

被引:41
作者
Murrell, JA [1 ]
Portier, CJ
Morris, RW
机构
[1] Analyt Sci Inc, Durham, NC USA
[2] NIEHS, Lab Computat Biol & Risk Anal, Res Triangle Pk, NC 27709 USA
关键词
benchmark dose; dose-response; risk-assessment; NOAEL; noncancer endpoints;
D O I
10.1111/j.1539-6924.1998.tb00911.x
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
We present a critical assessment of the benchmark dose (BMD) method introduced by Crump((1)) as an alternative method for setting a characteristic dose level for toxicant risk assessment. The no-observed-adverse-effect-level (NOAEL) method has been criticized because it does not use all of the data and because the characteristic dose level obtained depends on the dose levels and the statistical precision (sample sizes) of the study design. Defining the BMD in terms of a confidence bound on a point estimate results in a characteristic dose that also varies with the statistical precision and still depends on the study dose levels.((2)), Indiscriminate choice of benchmark response level may result in a BMD that reflects little about the dose-response behavior available from using all of the data. Another concern is that the definition of the BMD for the quantal response case is different for the continuous response case. Specifically, defining the BMD for continuous data using a ratio of increased effect divided by the background response results in an arbitrary dependence on the natural background for the endpoint being studied, making comparison among endpoints less meaningful and standards more arbitrary. We define a modified benchmark dose as a point estimate using the ratio of increased effect divided by the full adverse response range which enables consistent placement of the benchmark response level and provides a BMD with a more consistent relationship to the dose-response curve shape.
引用
收藏
页码:13 / 26
页数:14
相关论文
共 42 条
[1]   PHARMACOKINETICS AND BIOLOGICAL-ACTIVITY OF 2,3,7,8-TETRACHLORODIBENZO-PARA-DIOXIN .1. DOSE-DEPENDENT TISSUE DISTRIBUTION AND INDUCTION OF HEPATIC ETHOXYRESORUFIN O-DEETHYLASE IN RATS FOLLOWING A SINGLE INJECTION [J].
ABRAHAM, K ;
KROWKE, R ;
NEUBERT, D .
ARCHIVES OF TOXICOLOGY, 1988, 62 (05) :359-368
[2]   DOSE-RESPONSE ASSESSMENT FOR DEVELOPMENTAL TOXICITY .3. STATISTICAL-MODELS [J].
ALLEN, BC ;
KAVLOCK, RJ ;
KIMMEL, CA ;
FAUSTMAN, EM .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1994, 23 (04) :496-509
[3]   DOSE-RESPONSE ASSESSMENT FOR DEVELOPMENTAL TOXICITY .2. COMPARISON OF GENERIC BENCHMARK DOSE ESTIMATES WITH NO OBSERVED ADVERSE EFFECT LEVELS [J].
ALLEN, BC ;
KAVLOCK, RJ ;
KIMMEL, CA ;
FAUSTMAN, EM .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1994, 23 (04) :487-495
[4]   CALCULATION OF BENCHMARK DOSES FROM TERATOLOGY DATA [J].
AUTON, TR .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1994, 19 (02) :152-167
[5]   BENCHMARK DOSE WORKSHOP - CRITERIA FOR USE OF A BENCHMARK DOSE TO ESTIMATE A REFERENCE DOSE [J].
BARNES, DG ;
DASTON, GP ;
EVANS, JS ;
JARABEK, AM ;
KAVLOCK, RJ ;
KIMMEL, CA ;
PARK, C ;
SPITZER, HL .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1995, 21 (02) :296-306
[6]   CALCULATION OF BENCHMARK DOSES FROM CONTINUOUS DATA [J].
CRUMP, KS .
RISK ANALYSIS, 1995, 15 (01) :79-89
[7]   A NEW METHOD FOR DETERMINING ALLOWABLE DAILY INTAKES [J].
CRUMP, KS .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1984, 4 (05) :854-871
[8]   IMMUNOSUPPRESSIVE ACTIVITIES OF POLYCHLORINATED DIBENZOFURAN CONGENERS - QUANTITATIVE STRUCTURE ACTIVITY RELATIONSHIPS AND INTERACTIVE EFFECTS [J].
DAVIS, D ;
SAFE, S .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1988, 94 (01) :141-149
[9]   ANTIESTROGENIC ACTION OF 2,3,7,8-TETRACHLORODIBENZO-P-DIOXIN - TISSUE-SPECIFIC REGULATION OF ESTROGEN-RECEPTOR IN CD1 MICE [J].
DEVITO, MJ ;
THOMAS, T ;
MARTIN, E ;
UMBREIT, TH ;
GALLO, MA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1992, 113 (02) :284-292
[10]   DOSE-RESPONSE ASSESSMENT FOR DEVELOPMENTAL TOXICITY .1. CHARACTERIZATION OF DATABASE AND DETERMINATION OF NO OBSERVED ADVERSE EFFECT LEVELS [J].
FAUSTMAN, EM ;
ALLEN, BC ;
KAVLOCK, RJ ;
KIMMEL, CA .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1994, 23 (04) :478-486