DOSE-RESPONSE MODELS FOR DEVELOPMENTAL MALFORMATIONS

被引:10
作者
GAYLOR, DW
CHEN, JJ
机构
[1] National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, Arkansas
关键词
D O I
10.1002/tera.1420470406
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
An empirical dose-response model can generally be found for bioassay data, which provides a mathematical relationship between the incidence of a developmental malformation and dose of a toxicant in the experimental dose range. If biological principles and data can be used in the formulation of the dose-response model, the estimation of the incidence of malformations outside of the experimental dose range may be improved. In this paper, exponential growth of morphological structures in rodents during gestation is assumed. Further, it is assumed that some structural malformations are the result of reduced or delayed growth and the incidence of structurally normal fetuses is proportional to fetal weight raised to a power. When the exponential growth rate constant is reduced by dose raised to a power, a Weibull dose-response function is obtained. When the exponential growth rate constant is modeled by a polynomial function of dose, a polynomial-exponential dose-response model is obtained. The Weibull and the polynomial-exponential model, restricted to degrees from one up to the number of dosed groups, were fit to a database of bioassay data assembled from Teratology Vol. 1 (1968) to Vol. 42 (1990). In general the two models gave similar results and often gave exactly the same fit. The linear term appeared in the polynomial-exponential model in about one-fourth of the cases and was not related to the background incidence.
引用
收藏
页码:291 / 297
页数:7
相关论文
共 31 条
[1]   DIAZEPAM-INDUCED CLEFT-PALATE IN THE MOUSE - THE ROLE OF ENDOGENOUS MATERNAL CORTICOSTERONE [J].
BARLOW, SM ;
KNIGHT, AF ;
SULLIVAN, FM .
TERATOLOGY, 1980, 21 (02) :149-155
[2]   QUANTITATIVE RISK ASSESSMENT FOR TERATOLOGICAL EFFECTS [J].
CHEN, JJ ;
KODELL, RL .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1989, 84 (408) :966-971
[3]   A NEW METHOD FOR DETERMINING ALLOWABLE DAILY INTAKES [J].
CRUMP, KS .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1984, 4 (05) :854-871
[4]   TERATOGENIC EFFECTS OF CYPROTERONE-ACETATE AND MEDROY-PROGESTERONE TREATMENT DURING THE PRE-IMPLANTATION AND POSTIMPLANTATION PERIOD OF MOUSE EMBRYOS .1. [J].
EIBS, HG ;
SPIELMANN, H ;
HAGELE, M .
TERATOLOGY, 1982, 25 (01) :27-36
[5]   CYCLOPHOSPHAMIDE TERATOGENESIS - EVIDENCE FOR COMPENSATORY RESPONSES TO INDUCED CELLULAR TOXICITY [J].
FRANCIS, BM ;
ROGERS, JM ;
SULIK, KK ;
ALLES, AJ ;
ELSTEIN, KH ;
ZUCKER, RM ;
MASSARO, EJ ;
ROSEN, MB ;
CHERNOFF, N .
TERATOLOGY, 1990, 42 (05) :473-482
[6]   EMBRYOTOXIC EFFECTS OF METHYLMERCURIC CHLORIDE ADMINISTERED TO MICE AND RATS DURING ORGANOGENESIS [J].
FUYUTA, M ;
FUJIMOTO, T ;
HIRATA, S .
TERATOLOGY, 1978, 18 (03) :353-+
[7]   PROCESS OF BUILDING BIOLOGICALLY BASED DOSE-RESPONSE MODELS FOR DEVELOPMENTAL DEFECTS [J].
GAYLOR, DW ;
RAZZAGHI, M .
TERATOLOGY, 1992, 46 (06) :573-581
[8]  
HACKMAN RM, 1972, TERATOLOGY, V8, P313
[10]   ANALYSIS OF DICHOTOMOUS RESPONSE DATA FROM CERTAIN TOXICOLOGICAL EXPERIMENTS [J].
HASEMAN, JK ;
KUPPER, LL .
BIOMETRICS, 1979, 35 (01) :281-293