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Trace amine-associated receptor 1 (TAAR1) agonists for psychosis: protocol for a living systematic review and meta-analysis of human and non-human studies

Abstract:
BackgroundThere is an urgent need to develop more effective and safer antipsychotics beyond dopamine 2 receptor antagonists. An emerging and promising approach is TAAR1 agonism. Therefore, we will conduct a living systematic review and meta-analysis to synthesize and triangulate the evidence from preclinical animal experiments and clinical studies on the efficacy, safety, and underlying mechanism of action of TAAR1 agonism for psychosis.MethodsIndependent searches will be conducted in multiple electronic databases to identify clinical and animal experimental studies comparing TAAR1 agonists with licensed antipsychotics or other control conditions in individuals with psychosis or animal models for psychosis, respectively. The primary outcomes will be overall psychotic symptoms and their behavioural proxies in animals. Secondary outcomes will include side effects and neurobiological measures. Two independent reviewers will conduct study selection, data extraction using predefined forms, and risk of bias assessment using suitable tools based on the study design. Ontologies will be developed to facilitate study identification and data extraction. Data from clinical and animal studies will be synthesized separately using random-effects meta-analysis if appropriate, or synthesis without meta-analysis. Study characteristics will be investigated as potential sources of heterogeneity. Confidence in the evidence for each outcome and source of evidence will be evaluated, considering the summary of the association, potential concerns regarding internal and external validity, and reporting biases. When multiple sources of evidence are available for an outcome, an overall conclusion will be drawn in a triangulation meeting involving a multidisciplinary team of experts. We plan trimonthly updates of the review, and any modifications in the protocol will be documented. The review will be co-produced by multiple stakeholders aiming to produce impactful and relevant results and bridge the gap between preclinical and clinical research on psychosis.Protocol registrationPROSPERO-ID: CRD42023451628.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.12688/wellcomeopenres.19866.1

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Role:
Author
ORCID:
0000-0001-8264-2039
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Institution:
University of Oxford
Role:
Author
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Role:
Author
ORCID:
0000-0002-6196-3308
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0002-8717-0832
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Role:
Author
ORCID:
0000-0003-3295-256X


Publisher:
Taylor and Francis
Journal:
Wellcome Open Research More from this journal
Volume:
8
Pages:
365
Publication date:
2023-08-25
DOI:
ISSN:
2398-502X
Pmid:
38634067


Language:
English
Keywords:
Source identifiers:
1926378
Deposit date:
2024-07-20
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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