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A precision medicine approach to pharmacological adjuncts to extinction: a call to broaden research
Gabrielle King1, Kathryn D Baker2, Madelyne A Bisby2
1School of Psychology, The University of New South Wales, Sydney, Australia. g.king@unsw.edu.au.
Abstract:
There is a pressing need to improve treatments for anxiety. Although exposure-based therapy is currently the gold-standard treatment, many people either do not respond to this therapy or experience a relapse of symptoms after treatment has ceased. In recent years, there have been many novel pharmacological agents identified in preclinical research that have potential as adjuncts for exposure therapy, yet very few of these are regularly integrated into clinical practice. Unfortunately, the robust effects observed in the laboratory animal often do not translate to a clinical population. In this review, we discuss how age, sex, genetics, stress, medications, diet, alcohol, and the microbiome can vary across a clinical population and yet are rarely considered in drug development. While not an exhaustive list, we have focused on these factors because they have been shown to influence an individual's vulnerability to anxiety and alter the neurotransmitter systems often targeted by pharmacological adjuncts to therapy. We argue that for potential adjuncts to be successfully translated from the lab to the clinic empirical research must be broadened to consider how individual difference factors will influence drug efficacy.
Insights
New anxiety treatments are needed as exposure therapy isn't always effective. Researchers suggest considering individual differences in drug development to improve the success of new anxiety medications.
Area of Science:
- Neuroscience
- Pharmacology
- Clinical Psychology
Background:
- Exposure therapy is the standard anxiety treatment, but many patients do not respond or relapse.
- Novel pharmacological agents show promise as adjuncts to exposure therapy in preclinical research.
- Translating preclinical findings to clinical practice remains a significant challenge.
Purpose of the Study:
- To review factors influencing the efficacy of pharmacological adjuncts for anxiety.
- To highlight the gap between preclinical findings and clinical application of anxiety treatments.
- To advocate for broader consideration of individual differences in drug development for anxiety.
Main Methods:
- Literature review of factors affecting anxiety vulnerability and drug response.
- Analysis of how individual differences impact neurotransmitter systems targeted by anxiety medications.
- Discussion of translational challenges in psychopharmacology.
Main Results:
- Preclinical drug effects often fail to translate to human clinical populations.
- Factors such as age, sex, genetics, stress, diet, and microbiome significantly influence anxiety and drug efficacy.
- Current drug development rarely accounts for these individual variations.
Conclusions:
- Individual differences are critical for understanding and improving anxiety treatment outcomes.
- Future research must incorporate these factors to enhance the translation of promising anxiety medications.
- A personalized approach to drug development is essential for effective anxiety pharmacotherapy.
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