Touchscreen cognitive testing: Cross-species translation and co-clinical trials in neurodegenerative and neuropsychiatric disease

•Most pre-clinical findings in neuroscience fail to translate to the clinic.•Cross-species differences in cognitive testing contribute to translational failure.•Touchscreen can be used to facilitate similar cognitive tests across species.•Touchscreens facilitate efficiency and efficacy of the co-cli...

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Published inNeurobiology of learning and memory Vol. 182; p. 107443
Main Authors Palmer, Daniel, Dumont, Julie R., Dexter, Tyler D., Prado, Marco A.M., Finger, Elizabeth, Bussey, Timothy J., Saksida, Lisa M.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.07.2021
Subjects
Animals
Co-clinical trials
Computer Terminals
Computers, Handheld
Haplorhini
Humans
Mental Disorders - physiopathology
Mice
Neurodegenerative disease
Neurodegenerative Diseases - physiopathology
Neuropsychological Tests
Reproducibility of Results
Touch
Touchscreen cognition
Translational neuroscience
Translational Research, Biomedical
Touchscreen cognition
Co-clinical trials
Neurodegenerative disease
Translational neuroscience
Online AccessGet full text
ISSN1074-7427
1095-9564
1095-9564
DOI10.1016/j.nlm.2021.107443

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Abstract •Most pre-clinical findings in neuroscience fail to translate to the clinic.•Cross-species differences in cognitive testing contribute to translational failure.•Touchscreen can be used to facilitate similar cognitive tests across species.•Touchscreens facilitate efficiency and efficacy of the co-clinical trial framework. Translating results from pre-clinical animal studies to successful human clinical trials in neurodegenerative and neuropsychiatric disease presents a significant challenge. While this issue is clearly multifaceted, the lack of reproducibility and poor translational validity of many paradigms used to assess cognition in animal models are central contributors to this challenge. Computer-automated cognitive test batteries have the potential to substantially improve translation between pre-clinical studies and clinical trials by increasing both reproducibility and translational validity. Given the structured nature of data output, computer-automated tests also lend themselves to increased data sharing and other open science good practices. Over the past two decades, computer automated, touchscreen-based cognitive testing methods have been developed for non-human primate and rodent models. These automated methods lend themselves to increased standardization, hence reproducibility, and have become increasingly important for the elucidation of the neurobiological basis of cognition in animal models. More recently, there have been increased efforts to use these methods to enhance translational validity by developing task batteries that are nearly identical across different species via forward (i.e., translating animal tasks to humans) and reverse (i.e., translating human tasks to animals) translation. An additional benefit of the touchscreen approach is that a cross-species cognitive test battery makes it possible to implement co-clinical trials—an approach developed initially in cancer research—for novel treatments for neurodegenerative disorders. Co-clinical trials bring together pre-clinical and early clinical studies, which facilitates testing of novel treatments in mouse models with underlying genetic or other changes, and can help to stratify patients on the basis of genetic, molecular, or cognitive criteria. This approach can help to determine which patients should be enrolled in specific clinical trials and can facilitate repositioning and/or repurposing of previously approved drugs. This has the potential to mitigate the resources required to study treatment responses in large numbers of human patients.
AbstractList Translating results from pre-clinical animal studies to successful human clinical trials in neurodegenerative and neuropsychiatric disease presents a significant challenge. While this issue is clearly multifaceted, the lack of reproducibility and poor translational validity of many paradigms used to assess cognition in animal models are central contributors to this challenge. Computer-automated cognitive test batteries have the potential to substantially improve translation between pre-clinical studies and clinical trials by increasing both reproducibility and translational validity. Given the structured nature of data output, computer-automated tests also lend themselves to increased data sharing and other open science good practices. Over the past two decades, computer automated, touchscreen-based cognitive testing methods have been developed for non-human primate and rodent models. These automated methods lend themselves to increased standardization, hence reproducibility, and have become increasingly important for the elucidation of the neurobiological basis of cognition in animal models. More recently, there have been increased efforts to use these methods to enhance translational validity by developing task batteries that are nearly identical across different species via forward (i.e., translating animal tasks to humans) and reverse (i.e., translating human tasks to animals) translation. An additional benefit of the touchscreen approach is that a cross-species cognitive test battery makes it possible to implement co-clinical trials-an approach developed initially in cancer research-for novel treatments for neurodegenerative disorders. Co-clinical trials bring together pre-clinical and early clinical studies, which facilitates testing of novel treatments in mouse models with underlying genetic or other changes, and can help to stratify patients on the basis of genetic, molecular, or cognitive criteria. This approach can help to determine which patients should be enrolled in specific clinical trials and can facilitate repositioning and/or repurposing of previously approved drugs. This has the potential to mitigate the resources required to study treatment responses in large numbers of human patients.Translating results from pre-clinical animal studies to successful human clinical trials in neurodegenerative and neuropsychiatric disease presents a significant challenge. While this issue is clearly multifaceted, the lack of reproducibility and poor translational validity of many paradigms used to assess cognition in animal models are central contributors to this challenge. Computer-automated cognitive test batteries have the potential to substantially improve translation between pre-clinical studies and clinical trials by increasing both reproducibility and translational validity. Given the structured nature of data output, computer-automated tests also lend themselves to increased data sharing and other open science good practices. Over the past two decades, computer automated, touchscreen-based cognitive testing methods have been developed for non-human primate and rodent models. These automated methods lend themselves to increased standardization, hence reproducibility, and have become increasingly important for the elucidation of the neurobiological basis of cognition in animal models. More recently, there have been increased efforts to use these methods to enhance translational validity by developing task batteries that are nearly identical across different species via forward (i.e., translating animal tasks to humans) and reverse (i.e., translating human tasks to animals) translation. An additional benefit of the touchscreen approach is that a cross-species cognitive test battery makes it possible to implement co-clinical trials-an approach developed initially in cancer research-for novel treatments for neurodegenerative disorders. Co-clinical trials bring together pre-clinical and early clinical studies, which facilitates testing of novel treatments in mouse models with underlying genetic or other changes, and can help to stratify patients on the basis of genetic, molecular, or cognitive criteria. This approach can help to determine which patients should be enrolled in specific clinical trials and can facilitate repositioning and/or repurposing of previously approved drugs. This has the potential to mitigate the resources required to study treatment responses in large numbers of human patients.
•Most pre-clinical findings in neuroscience fail to translate to the clinic.•Cross-species differences in cognitive testing contribute to translational failure.•Touchscreen can be used to facilitate similar cognitive tests across species.•Touchscreens facilitate efficiency and efficacy of the co-clinical trial framework. Translating results from pre-clinical animal studies to successful human clinical trials in neurodegenerative and neuropsychiatric disease presents a significant challenge. While this issue is clearly multifaceted, the lack of reproducibility and poor translational validity of many paradigms used to assess cognition in animal models are central contributors to this challenge. Computer-automated cognitive test batteries have the potential to substantially improve translation between pre-clinical studies and clinical trials by increasing both reproducibility and translational validity. Given the structured nature of data output, computer-automated tests also lend themselves to increased data sharing and other open science good practices. Over the past two decades, computer automated, touchscreen-based cognitive testing methods have been developed for non-human primate and rodent models. These automated methods lend themselves to increased standardization, hence reproducibility, and have become increasingly important for the elucidation of the neurobiological basis of cognition in animal models. More recently, there have been increased efforts to use these methods to enhance translational validity by developing task batteries that are nearly identical across different species via forward (i.e., translating animal tasks to humans) and reverse (i.e., translating human tasks to animals) translation. An additional benefit of the touchscreen approach is that a cross-species cognitive test battery makes it possible to implement co-clinical trials—an approach developed initially in cancer research—for novel treatments for neurodegenerative disorders. Co-clinical trials bring together pre-clinical and early clinical studies, which facilitates testing of novel treatments in mouse models with underlying genetic or other changes, and can help to stratify patients on the basis of genetic, molecular, or cognitive criteria. This approach can help to determine which patients should be enrolled in specific clinical trials and can facilitate repositioning and/or repurposing of previously approved drugs. This has the potential to mitigate the resources required to study treatment responses in large numbers of human patients.
Translating results from pre-clinical animal studies to successful human clinical trials in neurodegenerative and neuropsychiatric disease presents a significant challenge. While this issue is clearly multifaceted, the lack of reproducibility and poor translational validity of many paradigms used to assess cognition in animal models are central contributors to this challenge. Computer-automated cognitive test batteries have the potential to substantially improve translation between pre-clinical studies and clinical trials by increasing both reproducibility and translational validity. Given the structured nature of data output, computer-automated tests also lend themselves to increased data sharing and other open science good practices. Over the past two decades, computer automated, touchscreen-based cognitive testing methods have been developed for non-human primate and rodent models. These automated methods lend themselves to increased standardization, hence reproducibility, and have become increasingly important for the elucidation of the neurobiological basis of cognition in animal models. More recently, there have been increased efforts to use these methods to enhance translational validity by developing task batteries that are nearly identical across different species via forward (i.e., translating animal tasks to humans) and reverse (i.e., translating human tasks to animals) translation. An additional benefit of the touchscreen approach is that a cross-species cognitive test battery makes it possible to implement co-clinical trials-an approach developed initially in cancer research-for novel treatments for neurodegenerative disorders. Co-clinical trials bring together pre-clinical and early clinical studies, which facilitates testing of novel treatments in mouse models with underlying genetic or other changes, and can help to stratify patients on the basis of genetic, molecular, or cognitive criteria. This approach can help to determine which patients should be enrolled in specific clinical trials and can facilitate repositioning and/or repurposing of previously approved drugs. This has the potential to mitigate the resources required to study treatment responses in large numbers of human patients.
ArticleNumber 107443
Author Dexter, Tyler D.
Finger, Elizabeth
Bussey, Timothy J.
Dumont, Julie R.
Saksida, Lisa M.
Palmer, Daniel
Prado, Marco A.M.
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  givenname: Julie R.
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  fullname: Dumont, Julie R.
  organization: Robarts Research Institute, The University of Western Ontario, Ontario, Canada
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  surname: Dexter
  fullname: Dexter, Tyler D.
  organization: Department of Physiology and Pharmacology, The University of Western Ontario, Ontario, Canada
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  givenname: Marco A.M.
  orcidid: 0000-0002-3028-5778
  surname: Prado
  fullname: Prado, Marco A.M.
  organization: Robarts Research Institute, The University of Western Ontario, Ontario, Canada
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  givenname: Elizabeth
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  fullname: Bussey, Timothy J.
  organization: Robarts Research Institute, The University of Western Ontario, Ontario, Canada
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  givenname: Lisa M.
  orcidid: 0000-0002-8416-8171
  surname: Saksida
  fullname: Saksida, Lisa M.
  organization: Robarts Research Institute, The University of Western Ontario, Ontario, Canada
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ISSN 1074-7427
1095-9564
IngestDate Sun Sep 28 10:18:10 EDT 2025
Wed Feb 19 02:27:37 EST 2025
Sat Oct 25 05:25:25 EDT 2025
Thu Apr 24 23:04:34 EDT 2025
Fri Feb 23 02:44:44 EST 2024
IsPeerReviewed true
IsScholarly true
Keywords Touchscreen cognition
Co-clinical trials
Neurodegenerative disease
Translational neuroscience
Language English
License Copyright © 2021 Elsevier Inc. All rights reserved.
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PublicationTitle Neurobiology of learning and memory
PublicationTitleAlternate Neurobiol Learn Mem
PublicationYear 2021
Publisher Elsevier Inc
Publisher_xml – name: Elsevier Inc
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Snippet •Most pre-clinical findings in neuroscience fail to translate to the clinic.•Cross-species differences in cognitive testing contribute to translational...
Translating results from pre-clinical animal studies to successful human clinical trials in neurodegenerative and neuropsychiatric disease presents a...
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StartPage 107443
SubjectTerms Animals
Co-clinical trials
Computer Terminals
Computers, Handheld
Haplorhini
Humans
Mental Disorders - physiopathology
Mice
Neurodegenerative disease
Neurodegenerative Diseases - physiopathology
Neuropsychological Tests
Reproducibility of Results
Touch
Touchscreen cognition
Translational neuroscience
Translational Research, Biomedical
Title Touchscreen cognitive testing: Cross-species translation and co-clinical trials in neurodegenerative and neuropsychiatric disease
URI https://dx.doi.org/10.1016/j.nlm.2021.107443
https://www.ncbi.nlm.nih.gov/pubmed/33895351
https://www.proquest.com/docview/2518724139
Volume 182
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