Literature DB >> 10560587

Interpreting the toxicologic significance of alterations in anogenital distance: potential for confounding effects of progeny body weights.

R H Gallavan1, J F Holson, D G Stump, J F Knapp, V L Reynolds.   

Abstract

Anogenital distance (AGD) is an endpoint that was recently added to the U.S. EPA testing guidelines for reproductive toxicity studies. This endpoint is sensitive to hormonal effects of test chemicals. It is possible that apparent alterations in AGD might occur after treatment with agents that affect overall pup body size. In such cases, hormonal activity might be associated incorrectly with the test treatment. The analyses in this report evaluated statistical correlations between pup body weight and AGD in control litters. AGDs were measured on postnatal day 1 in 1501 pups derived from 113 untreated female Sprague-Dawley rats in two independent two-generation reproductive toxicity studies. Significant correlations were detected between AGD and body weight and between AGD and the cube root of body weight. In males, AGD increased 0.26 mm for each 1 g increase in body weight. In females, AGD increased 0.13 mm per 1 g increase in body weight. Although there were essentially no differences between the regression models developed to predict AGD in either males or females using body weight as a covariate and those based on the cube root of body weight, such similarities in predictivity might not occur in larger animals with broader weight ranges than those encountered in this analysis. Normalization of AGD by dividing by body weight significantly overcompensated for differences in body size. Normalizing with the cube root of body weight resulted in an AGD/cube root of body weight ratio that was constant across the range of body weights observed in this study. In conclusion, as a preferred method to account for body size effects on AGD, analysis of covariance is recommended. If a normalization is done directly, the ratio of AGD to the cube root of body weight is the more appropriate metric.

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Year:  1999        PMID: 10560587     DOI: 10.1016/s0890-6238(99)00036-2

Source DB:  PubMed          Journal:  Reprod Toxicol        ISSN: 0890-6238            Impact factor:   3.143


  37 in total

1.  Prenatal PCBs disrupt early neuroendocrine development of the rat hypothalamus.

Authors:  Sarah M Dickerson; Stephanie L Cunningham; Andrea C Gore
Journal:  Toxicol Appl Pharmacol       Date:  2011-01-26       Impact factor: 4.219

2.  Prenatal Exposure to Persistent Organic Pollutants and Anogenital Distance in Children at 18 Months.

Authors:  Miguel García-Villarino; Isolina Riaño-Galán; Ana Cristina Rodriguez-Dehli; Esther Vizcaíno; Joan O Grimalt; Adonina Tardón; Ana Fernández-Somoano
Journal:  Horm Res Paediatr       Date:  2018-09-13       Impact factor: 2.852

3.  In utero exposure to the antiandrogen 1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene (DDE) in relation to anogenital distance in male newborns from Chiapas, México.

Authors:  Matthew P Longnecker; Beth C Gladen; Lea A Cupul-Uicab; S Patricia Romano-Riquer; Jean-Phillipe Weber; Robert E Chapin; Mauricio Hernández-Avila
Journal:  Am J Epidemiol       Date:  2007-01-31       Impact factor: 4.897

4.  Exposure to an environmentally relevant phthalate mixture during prostate development induces microRNA upregulation and transcriptome modulation in rats.

Authors:  Wellerson R Scarano; Amina Bedrat; Luiz G Alonso-Costa; Ariana M Aquino; Bruno Fantinatti; Luis A Justulin; Luis F Barbisan; Paula P Freire; Jodi A Flaws; Lemos Bernardo
Journal:  Toxicol Sci       Date:  2019-06-14       Impact factor: 4.849

5.  Anogenital Distance and Perineal Measurements of the Pelvic Organ Prolapse (POP) Quantification System.

Authors:  María Luisa Sánchez-Ferrer; María Teresa Prieto-Sánchez; Carlos Moya-Jiménez; Jaime Mendiola; Carmen María García-Hernández; Ana Carmona-Barnosi; Anibal Nieto; Alberto M Torres-Cantero
Journal:  J Vis Exp       Date:  2018-09-20       Impact factor: 1.355

6.  Perinatal androgens organize sex differences in mast cells and attenuate anaphylaxis severity into adulthood.

Authors:  Emily Mackey; Kyan M Thelen; Vedrana Bali; Mahsa Fardisi; Madalyn Trowbridge; Cynthia L Jordan; Adam J Moeser
Journal:  Proc Natl Acad Sci U S A       Date:  2020-09-11       Impact factor: 11.205

7.  Exposure to an Environmentally Relevant Phthalate Mixture Causes Transgenerational Effects on Female Reproduction in Mice.

Authors:  Changqing Zhou; Liying Gao; Jodi A Flaws
Journal:  Endocrinology       Date:  2017-06-01       Impact factor: 4.736

8.  Prenatal exposure to an environmentally relevant phthalate mixture accelerates biomarkers of reproductive aging in a multiple and transgenerational manner in female mice.

Authors:  Emily Brehm; Changqing Zhou; Liying Gao; Jodi A Flaws
Journal:  Reprod Toxicol       Date:  2020-10-28       Impact factor: 3.143

9.  Non-monotonic dose effects of in utero exposure to di(2-ethylhexyl) phthalate (DEHP) on testicular and serum testosterone and anogenital distance in male mouse fetuses.

Authors:  Rylee Phuong Do; Richard W Stahlhut; Davide Ponzi; Frederick S Vom Saal; Julia A Taylor
Journal:  Reprod Toxicol       Date:  2012-10-03       Impact factor: 3.143

10.  Anogenital distance from birth to 2 years: a population study.

Authors:  Ajay Thankamony; Ken K Ong; David B Dunger; Carlo L Acerini; Ieuan A Hughes
Journal:  Environ Health Perspect       Date:  2009-07-13       Impact factor: 9.031

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