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Antipsychotic induced weight gain: genetics, epigenetics, and biomarkers reviewed
Tahireh A Shams1, Daniel J Müller
1Pharmacogenetics Research Clinic, Centre for Addiction and Mental Health, 250 College Street, Toronto, ON, M5T 1R8, Canada.
Abstract:
Antipsychotic-induced weight gain (AIWG) is a prevalent side effect of antipsychotic treatment, particularly with second generation antipsychotics, such as clozapine and olanzapine. At this point, there is virtually nothing that can be done to predict who will be affected by AIWG. However, hope for the future of prediction lies with genetic risk factors. Many genes have been studied for their association with AIWG with a variety of promising findings. This review will focus on genetic findings in the last year and will discuss the first epigenetic and biomarker findings as well. Although there are significant findings in many other genes, the most consistently replicated findings are in the melanocortin 4 receptor (MC4R), the serotonin 2C receptor (HTR2C), the leptin, the neuropeptide Y (NPY) and the cannabinoid receptor 1 (CNR1) genes. The study of genetic risk variants poses great promise in creating predictive tools for side effects such as AIWG.
Insights
Genetic factors may predict antipsychotic-induced weight gain (AIWG). Recent studies highlight genes like MC4R and HTR2C, offering hope for personalized treatment and predicting AIWG risks.
Area of Science:
- Pharmacogenetics
- Neuroscience
- Metabolic Disorders
Background:
- Antipsychotic-induced weight gain (AIWG) is a common, significant side effect of antipsychotic medications, particularly second-generation agents.
- Current methods for predicting AIWG are limited, impacting patient treatment adherence and outcomes.
- Identifying predictive markers is crucial for personalized psychiatric care.
Purpose of the Study:
- To review recent genetic, epigenetic, and biomarker findings associated with AIWG.
- To highlight consistently replicated genetic associations for AIWG prediction.
- To explore the potential of genetic risk variants in developing predictive tools for AIWG.
Main Methods:
- Literature review focusing on genetic, epigenetic, and biomarker research in AIWG over the past year.
- Analysis of consistently replicated gene associations.
- Synthesis of findings related to predictive modeling for AIWG.
Main Results:
- Several genes show associations with AIWG, with melanocortin 4 receptor (MC4R), serotonin 2C receptor (HTR2C), leptin, neuropeptide Y (NPY), and cannabinoid receptor 1 (CNR1) demonstrating consistent replication.
- Emerging epigenetic and biomarker findings are also contributing to understanding AIWG.
- Genetic risk variants show promise as predictive markers for AIWG.
Conclusions:
- Genetic factors represent a promising avenue for predicting AIWG.
- Continued research into genetic and other biomarkers may lead to tools for personalized antipsychotic therapy.
- Future predictive models incorporating genetic risk variants could mitigate AIWG adverse effects.
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