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Sensitivity of male reproductive endpoints in nonhuman primate toxicity studies: A statistical power analysis
Affiliation:1. Worldwide Research & Development, Pfizer Inc, Groton, CT, USA;2. Covance Laboratories GmbH, Münster, Germany;1. Department of Animal Morphology and Physiology, Sao Paulo State University-UNESP FCAV at Jaboticabal, SP, Brazil;2. Department of Physiology, Institute of Bioscience, Sao Paulo State University-UNESP, Botucatu, SP, Brazil;1. Louis Stokes Cleveland DVA Medical Center, Cleveland, OH, United States;2. Neogene Biosciences LLC, Cleveland, OH, United States;3. Case Western Reserve University, Cleveland, OH, United States;4. Division of Pulmonary, Critical Care, and Sleep Medicine, UH Case Medical Center, Cleveland, OH 44016, United States;1. Department of Anesthesiology, Kanagawa Dental University, Yokosuka City 238-8580, Japan;2. Department of Physiology, Faculty of Health Sciences, Uekusa Gakuen University, Chiba City 264-0007, Japan;3. Center for Medical Sciences, Ibaraki Prefectural University of Health Sciences, Ibaraki-ken 300-0394, Japan;1. MPI Research, Mattawan, MI, 49009, USA;2. Beckman Coulter, Southfield, MI, 48033, USA;3. TOXpertise, Princeton, NJ, 08540, USA;4. Abbott Laboratories, Columbus, OH, 43219, USA;5. Experimur, Chicago, IL, 60609, USA;1. Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands;2. Department of Medical Sciences, University of Ferrara, Ferrara, Italy;3. United Parent Project Muscular Dystrophy, The Netherlands
Abstract:To determine the sensitivity of male reproductive toxicity endpoints in NHPs we performed a power analysis of routine and triggered endpoints using control data from sexually mature Asian and Mauritian NHPs. The power to detect a 50% change from control was 13–30% for male reproductive organ weights, ∼30% for testicular volume, 6–66% for seminal analyses and 10–78% for male hormones. Overall, male reproductive endpoints have poor power (less than 80%) to detect a 50% change from control with a group size of 3 monkeys. Confidently identifying adverse male reproductive effects with these endpoints would likely require specialized study designs with larger group sizes. Triggering of non-routine endpoints in cases where there is special concern for male reproductive toxicity is unlikely to increase sensitivity to detect adverse effects.
Keywords:NHP  Male reproductive toxicity  Power analysis  Seminal analysis  Inhibin B  Testosterone  Sperm count  Sperm motility
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