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      Animal to human translation: a systematic scoping review of reported concordance rates

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          Abstract

          Background

          Drug development is currently hampered by high attrition rates; many developed treatments fail during clinical testing. Part of the attrition may be due to low animal-to-human translational success rates; so-called “translational failure”. As far as we know, no systematic overview of published translational success rates exists.

          Systematic scoping review

          The following research question was examined: “What is the observed range of the animal-to-human translational success (and failure) rates within the currently available empirical evidence?”. We searched PubMed and Embase on 16 October 2017. We included reviews and all other types of “umbrella”-studies of meta-data quantitatively comparing the translational results of studies including at least two species with one being human. We supplemented our database searches with additional strategies. All abstracts and full-text papers were screened by two independent reviewers. Our scoping review comprises 121 references, with various units of measurement: compound or intervention (k = 104), study/experiment (k = 10), and symptom or event (k = 7). Diagnostic statistics corresponded with binary and continuous definitions of successful translation. Binary definitions comprise percentages below twofold error, percentages accurately predicted, and predictive values. Quantitative definitions comprise correlation/regression (r 2) and meta-analyses (percentage overlap of 95% confidence intervals). Translational success rates ranged from 0 to 100%.

          Conclusion

          The wide range of translational success rates observed in our study might indicate that translational success is unpredictable; i.e. it might be unclear upfront if the results of primary animal studies will contribute to translational knowledge. However, the risk of bias of the included studies was high, and much of the included evidence is old, while newer models have become available. Therefore, the reliability of the cumulative evidence from current papers on this topic is insufficient. Further in-depth “umbrella”-studies of translational success rates are still warranted. These are needed to evaluate the probabilistic evidence for predictivity of animal studies for the human situation more reliably, and to determine which factors affect this process.

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          Most cited references59

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          Modeling transformations of neurodevelopmental sequences across mammalian species.

          A general model of neural development is derived to fit 18 mammalian species, including humans, macaques, several rodent species, and six metatherian (marsupial) mammals. The goal of this work is to describe heterochronic changes in brain evolution within its basic developmental allometry, and provide an empirical basis to recognize equivalent maturational states across animals. The empirical data generating the model comprises 271 developmental events, including measures of initial neurogenesis, axon extension, establishment, and refinement of connectivity, as well as later events such as myelin formation, growth of brain volume, and early behavioral milestones, to the third year of human postnatal life. The progress of neural events across species is sufficiently predictable that a single model can be used to predict the timing of all events in all species, with a correlation of modeled values to empirical data of 0.9929. Each species' rate of progress through the event scale, described by a regression equation predicting duration of development in days, is highly correlated with adult brain size. Neural heterochrony can be seen in selective delay of retinogenesis in the cat, associated with greater numbers of rods in its retina, and delay of corticogenesis in all species but rodents and the rabbit, associated with relatively larger cortices in species with delay. Unexpectedly, precocial mammals (those unusually mature at birth) delay the onset of first neurogenesis but then progress rapidly through remaining developmental events.
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            Are animal models predictive for humans?

            It is one of the central aims of the philosophy of science to elucidate the meanings of scientific terms and also to think critically about their application. The focus of this essay is the scientific term predict and whether there is credible evidence that animal models, especially in toxicology and pathophysiology, can be used to predict human outcomes. Whether animals can be used to predict human response to drugs and other chemicals is apparently a contentious issue. However, when one empirically analyzes animal models using scientific tools they fall far short of being able to predict human responses. This is not surprising considering what we have learned from fields such evolutionary and developmental biology, gene regulation and expression, epigenetics, complexity theory, and comparative genomics.
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              PREPARE: guidelines for planning animal research and testing

              There is widespread concern about the quality, reproducibility and translatability of studies involving research animals. Although there are a number of reporting guidelines available, there is very little overarching guidance on how to plan animal experiments, despite the fact that this is the logical place to start ensuring quality. In this paper we present the PREPARE guidelines: Planning Research and Experimental Procedures on Animals: Recommendations for Excellence. PREPARE covers the three broad areas which determine the quality of the preparation for animal studies: formulation, dialogue between scientists and the animal facility, and quality control of the various components in the study. Some topics overlap and the PREPARE checklist should be adapted to suit specific needs, for example in field research. Advice on use of the checklist is available on the Norecopa website, with links to guidelines for animal research and testing, at https://norecopa.no/PREPARE.
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                Author and article information

                Contributors
                0031-6-83375595 , Leenaars.Cathalijn@mh-hannover.de
                c.j.kouwenaar@students.uu.nl
                F.R.Stafleu@uu.nl
                bleich.andre@mh-hannover.de
                Merel.Ritskes-Hoitinga@radboudumc.nl
                Rob.deVries@radboudumc.nl
                F.L.B.Meijboom@uu.nl
                Journal
                J Transl Med
                J Transl Med
                Journal of Translational Medicine
                BioMed Central (London )
                1479-5876
                15 July 2019
                15 July 2019
                2019
                : 17
                : 223
                Affiliations
                [1 ]ISNI 0000000120346234, GRID grid.5477.1, Department of Animals in Science and Society, Faculty of Veterinary Sciences, , Utrecht University, ; Utrecht, The Netherlands
                [2 ]ISNI 0000 0000 9529 9877, GRID grid.10423.34, Institute for Laboratory Animal Science, , Hannover Medical School, ; Hannover, Germany
                [3 ]ISNI 0000 0004 0444 9382, GRID grid.10417.33, SYRCLE, Department for Health Evidence (section HTA), Radboud Institute for Health Sciences, , Radboud University Medical Center, ; Nijmegen, The Netherlands
                Author information
                http://orcid.org/0000-0002-8212-7632
                Article
                1976
                10.1186/s12967-019-1976-2
                6631915
                31307492
                a768aece-b78e-4928-b9e3-6504827cf792
                © The Author(s) 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 8 May 2019
                : 8 July 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001826, ZonMW;
                Award ID: 40-42600-98-417
                Award Recipient :
                Funded by: NWO
                Award ID: 313-99-310
                Award Recipient :
                Funded by: the Federal State of Lower Saxony
                Award ID: R2N
                Award Recipient :
                Categories
                Review
                Custom metadata
                © The Author(s) 2019

                Medicine
                translation,prediction,systematic review
                Medicine
                translation, prediction, systematic review

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