Threshold analysis of selected dose-response data for endocrine active chemicals

被引:11
作者
Blair, RM
Fang, H
Gaylor, D
Sheehan, DM
机构
[1] US FDA, Natl Ctr Toxicol Res, Div Genet & Reprod Toxicol, Jefferson, AR 72079 USA
[2] US FDA, Natl Ctr Toxicol Res, Off Director, Jefferson, AR 72079 USA
关键词
dose-response; endocrine disrupter; endogenous dose; Michaelis-Menten; non-hormone controlled background; risk assessment; threshold;
D O I
10.1034/j.1600-0463.2001.090303.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Using a biologically relevant mathematical model, the Michaelis-Menten equation, we examined published data from endocrine active chemicals for evidence of no-threshold dose-response curves. Data were fit to a modified Michaelis-Menten equation which accounted for total background response. Subsequently, the data sets were analyzed using non-linear regression in order to estimate the four parameters of interest (non-hormone controlled background (B-nh), maximum response (R-max) endogenous hormone level (D-0), and the dose at which a half-maximal response was observed (ED50)) and to determine the fit to the fully modified Michaelis-Menten equation. Subsequently, response data were adjusted to account for B-nh and then normalized to R-max while dose data were adjusted to account for D-0 and then normalized to the ED50. This data set was combined into a single, composite data set and fit to the fully modified Michaelis-Menten equation. We examined 31 data sets (24 endpoints) from studies on 9 different chemical/hormone treatments. Twenty-six of the data sets fit the modified Michaelis-Menten equation with high multiple correlation coefficients (r>0.90). The normalized data demonstrated a good fit to the modified Michaelis-Menten equation. These results indicate that a variety of biological responses fit the modified Michaelis-Menten equation, which does not have a threshold dose term.
引用
收藏
页码:198 / 208
页数:11
相关论文
共 45 条
[1]   Quantitative mechanistically based dose-response modeling with endocrine-active compounds [J].
Andersen, ME ;
Conolly, RB ;
Faustman, EM ;
Kavlock, RJ ;
Portier, CJ ;
Sheehan, DM ;
Wier, PJ ;
Ziese, L .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1999, 107 :631-638
[2]  
[Anonymous], ISSUES REV TERATOLOG
[3]  
Barlow S, 1999, TERATOLOGY, V60, P365, DOI 10.1002/(SICI)1096-9926(199912)60:6<365::AID-TERA9>3.0.CO
[4]  
2-6
[5]   REFERENCE DOSE (RFD) - DESCRIPTION AND USE IN HEALTH RISK ASSESSMENTS [J].
BARNES, DG ;
DOURSON, M .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1988, 8 (04) :471-486
[7]  
Bucher JR, 1998, TOXICOL SCI, V42, P1
[8]   DEVELOPMENTAL EFFECTS OF ENDOCRINE-DISRUPTING CHEMICALS IN WILDLIFE AND HUMANS [J].
COLBORN, T ;
SAAL, FSV ;
SOTO, AM .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1993, 101 (05) :378-384
[9]   Temperature-dependent sex determination: The interplay of steroid hormones and temperature [J].
Crews, D .
ZOOLOGICAL SCIENCE, 1996, 13 (01) :1-13
[10]  
CRUMP KS, 1976, CANCER RES, V36, P2973