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Translational issues in precision medicine in neuropathic pain
Anthony H Dickenson1, Ryan Patel1
1Department of Neuroscience, Physiology and Pharmacology, University College London, London, UK.
Summary
Neuropathic pain treatments often fail due to the translational gap. This review examines preclinical rodent data to better align animal models with clinical observations for improved drug development in neuropathic pain.
Area of Science:
- Neuroscience
- Pharmacology
- Translational Medicine
Background:
- Neuropathic pain is a challenging condition with limited effective treatments.
- The traditional bench-to-bedside research model faces a significant translational gap.
- Bridging this gap may involve back-translating clinical observations to preclinical models.
Purpose of the Study:
- To review historical rodent data to re-evaluate drug effects on sensory neuronal endpoints.
- To align preclinical findings with clinical observations in neuropathic pain.
- To guide future clinical studies by informing preclinical research strategies.
Main Methods:
- Retrospective analysis of historical rodent datasets.
- Examination of drug effects on sensory neuronal endpoints in animal models.
- Comparison of preclinical data with clinical observations.
Main Results:
- Quantitative sensory testing in patients can improve treatment selection and outcomes.
- Preclinical phenotyping using quantitative sensory testing is not yet mainstream.
- Reconsidering rodent data may reveal better alignment with clinical observations for drug efficacy.
Conclusions:
- Aligning preclinical research with clinical observations is crucial for effective neuropathic pain drug development.
- Back-translation from clinical findings to animal models can help bridge the translational gap.
- Future studies should integrate quantitative sensory testing in preclinical models to enhance clinical translation.
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