A Diagnostic Approach for Rodent Progressive Cardiomyopathy and Like Lesions in Toxicology Studies up to 28 Days in the Sprague Dawley Rat (Part 1 of 2)

Author:

Hailey James R.1,Maleeff Beverly E.2,Thomas Heath C.3,Pearse Gail4,Klapwijk Jan C.4,Cristofori Patrizia G.4,Berridge Brian2,Kimbrough Carie L.5,Parker George A.6,Morton Daniel7,Elmore Susan8,Hardisty Jerry F.9,Dybdal Noel O.10,Rehagen David A.11,Fikes James D.12,Lamb Martin12,Biddle Kathleen7,Buetow Bernard S.13,Carreira Vinicius14,Nyska Abraham15,Tripathi Niraj K.16,Workman Heather C.17,Bienvenu Jean-Guy18,Brees Ingrid19,Turk James R.20,Adler Rick R.2

Affiliation:

1. Covance Laboratories, Inc., Chantilly, Virginia, USA

2. GlaxoSmithKline, King of Prussia, Pennsylvania, USA

3. Experimental Pathology Laboratories, Collegeville, Pennsylvania, USA

4. GlaxoSmithKline, Ware, Hertfordshire, United Kingdom

5. PAREXEL International, Durham, North Carolina, USA

6. Charles River Laboratories, Durham, North Carolina, USA

7. Pfizer, Groton, Connecticut, USA

8. National Institute of Environmental Sciences, Research Triangle Park, North Carolina, USA

9. Experimental Pathology Laboratories, Research Triangle Park, North Carolina, USA

10. Genentech, Inc., South San Francisco, California, USA

11. MPI Research, Inc., Mattawan, Michigan, USA

12. Biogen Idec, Cambridge, Massachusetts, USA

13. Pfizer, San Diego, California, USA

14. Vet Path Services, Inc., Mason, Ohio, USA

15. Sackler School of Medicine, Tel Aviv University, Timrat, Israel

16. Covance Laboratories, Inc., Madison, Wisconsin, USA

17. Covance Laboratories, Inc., Greenfield, Indiana, USA

18. Charles Rivers Laboratories, Montreal, Quebec, Canada

19. Novartis Pharma AG, Basel, Switzerland

20. Amgen, Thousand Oaks, California, USA

Abstract

Spontaneous rodent progressive cardiomyopathy (PCM) in the Sprague Dawley rat may confound identification and/or interpretation of potential test article (TA)-related cardiotoxicity. Pathologists apply diagnostic term(s) and thresholds for diagnosing and assigning severity grades for PCM and/or PCM-like (PCM/like) lesions consistently within a study, which is necessary to identify and interpret TA-related findings. Due to differences in training and/or experiences, diagnostic terms and thresholds may vary between pathologists. Harmonized terminology and thresholds across studies will generate better historical control data, will likely enhance interpretation of study data, and may further enhance our understanding of the spontaneous change. An assessment of the diagnostic approaches of a group of 37 pathologists identified an approach that is relatively easily applied; and if adopted, it could enhance diagnostic consistency across studies. This approach uses the single “slash” term “necrosis/inflammatory cell infiltrate (NICI)” as the diagnosis for the spectrum of lesions seen in younger rats, uses no threshold for diagnosis (e.g., diagnose all lesions clearly identifiable as PCM/like), and uses aggregate lesion size of approximately ≥45% of the field of view (FOV) using a 10×/22 eyepiece and the 40× objective or approximately ≥100% of the FOV using the 60× objective as the criterion separating minimal from mild severities.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

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1. Preclinical Safety Evaluation of the Human-Identical Milk Oligosaccharide Lacto-N-Triose II;International Journal of Toxicology;2023-09-28

2. Assigning Adversity to Toxicologic Outcomes;Haschek and Rousseaux's Handbook of Toxicologic Pathology, Volume 2 : Safety Assessment Environmental Toxicologic Pathology;2023

3. Endocrine-Disrupting Effects of Bisphenol A on the Cardiovascular System: A Review;Journal of Xenobiotics;2022-07-13

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5. Using Artificial Intelligence to Detect, Classify, and Objectively Score Severity of Rodent Cardiomyopathy;Toxicologic Pathology;2020-12-08

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