Effect of different sampling designs on outcome of endocrine disrupter studies

被引:30
作者
Elswick, BA [1 ]
Welsch, F [1 ]
Janszen, DB [1 ]
机构
[1] Chem Ind Inst Toxicol, Res Triangle Pk, NC 27709 USA
关键词
sampling design; intralitter variability; endocrine disrupter; ventral prostate; bisphenol A; di-n-butyl phthalate; statistical modeling; false positive; false negative;
D O I
10.1016/S0890-6238(00)00092-7
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this article, we demonstrate how sampling strategy can influence the outcome of endocrine disrupter studies. In a study of the weak xenoestrogen bisphenol A (BPA), possible treatment-related effects on ventral prostate (VP) fresh weight were found in rat offspring at 6 months of age when only one or two male pups were randomly selected from each litter. In subsequent BPA and di-n-butyl phthalate studies, large intralitter variability of this specific end point was apparent when the VP weights from entire litter complements were examined. We modeled the effects of sampling 1, 2, or 3 pups from each litter using the full-litter complement data. When one pup was randomly selected, a substantial percentage of incorrect conclusions about the presence or absence of treatment effects occurred. These statistical modeling analyses raise significant concern about the selection of one pup per litter for highly variable end points. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:359 / 367
页数:9
相关论文
共 28 条
[1]   Lack of effects for low dose levels of bisphenol A and diethylstilbestrol on the prostate gland of CF1 mice exposed in utero [J].
Ashby, J ;
Tinwell, H ;
Haseman, J .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1999, 30 (02) :156-166
[2]   Reproducibility of endocrine disruption data [J].
Ashby, J ;
Elliott, BM .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1997, 26 (01) :94-95
[3]   Normal sexual development of rats exposed to butyl benzyl phthalate from conception to weaning [J].
Ashby, J ;
Tinwell, H ;
Lefevre, PA ;
Odum, J ;
Paton, D ;
Millward, SW ;
Tittensor, S ;
Brooks, AN .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1997, 26 (01) :102-118
[4]  
BOSLAND MC, 1992, MONOGRAPHS PATHOLOGY, V1, P443
[5]   Normal reproductive organ development in CF-1 mice following prenatal exposure to bisphenol A [J].
Cagen, SZ ;
Waechter, JM ;
Dimond, SS ;
Breslin, WJ ;
Butala, JH ;
Jekat, FW ;
Joiner, RL ;
Shiotsuka, RN ;
Veenstra, GE ;
Harris, LR .
TOXICOLOGICAL SCIENCES, 1999, 50 (01) :36-44
[6]   A toxicologically based weight-of-evidence methodology for the relative ranking of chemicals of endocrine disruption potential [J].
Calabrese, EJ ;
Baldwin, LA ;
Kostecki, PT ;
Potter, TL .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1997, 26 (01) :36-40
[7]   The effects of environmental hormones on reproduction [J].
Danzo, BJ .
CELLULAR AND MOLECULAR LIFE SCIENCES, 1998, 54 (11) :1249-1264
[8]  
ELSWICK BA, 2000, TOXICOLOGIST, V54, P256
[9]   Endocrine disruptor risk characterization: An EPA perspective [J].
FennerCrisp, PA .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1997, 26 (01) :70-73
[10]  
GORSKI RA, 1986, ENVIRON HEALTH PERSP, V70, P163