<i>In Silico</i> Pharmacogenomic Assessment of Glucagon-like Peptide-1 (GLP1) Agonists and the Genetic Addiction Risk Score (GARS) Related Pathways: Implications for Suicidal Ideation and Substance Use Disorder

Our findings suggest that associated polymorphisms seem to have overlapping effects with addictive behaviors of Reward Deficiency Syndrome (RDS) and dopamine regulation. Consequently, GLP1R agonists may represent a double-edged sword, potentially triggering both antiaddictive effects and SI by exacerbating depressive phenotypes. Thus, we encourage the scientific community to perform further empirical clinical studies to confirm this proposed pathway.

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Publication Details

Journal
Current Neuropharmacology
Published
2025-01-27
DOI
https://doi.org/10.2174/011570159x349579241231080602
Citations
7
Primary Topic
Diabetes Treatment and Management
Type
article
Field-Weighted Citation Impact
9.06
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article

In Silico Pharmacogenomic Assessment of Glucagon-like Peptide-1 (GLP1) Agonists and the Genetic Addiction Risk Score (GARS) Related Pathways: Implications for Suicidal Ideation and Substance Use Disorder

Jocelyn Ashford, Panayotis K. Thanos, Rossano Kepler Alvim Fiorelli, Paul R. Carney et al.
7 citations
Current Neuropharmacology
Diabetes Treatment and Management
9.06
article

In Silico Pharmacogenomic Assessment of Glucagon-like Peptide-1 (GLP1) Agonists and the Genetic Addiction Risk Score (GARS) Related Pathways: Implications for Suicidal Ideation and Substance Use Disorder

Jocelyn Ashford, Panayotis K. Thanos, Rossano Kepler Alvim Fiorelli, Paul R. Carney, Edward J. Modestino, Eliot L. Gardner, Colin Hanna, Alireza Sharafshah, David Baron, Jag Khalsa, Jean Lud Cadet, Rajendra D. Badgaiyan, Rene Cortese, Abdalla Bowirrat, Igor Elman, Albert Pinhasov, Brian Fuehrlein, Catherine A. Dennen, Sergio L. Schmidt, Kenneth Blum, Mark S. Gold, Kai-Uwe Lewandrowski, Gene Jack Wang, Aryeh R Pollack, Eric R. Braverman
article en
7 citations

Abstract

Our findings suggest that associated polymorphisms seem to have overlapping effects with addictive behaviors of Reward Deficiency Syndrome (RDS) and dopamine regulation. Consequently, GLP1R agonists may represent a double-edged sword, potentially triggering both antiaddictive effects and SI by exacerbating depressive phenotypes. Thus, we encourage the scientific community to perform further empirical clinical studies to confirm this proposed pathway.

Current NeuropharmacologyVol. 23(8)
Texas Tech University (US), Cambridge Health Alliance (US), National Institutes of Health (US), National Institute on Drug Abuse (US), Harvard University (US), George Washington University (US), Guilan University of Medical Sciences (IR), Washington University in St. Louis (US), VA Palo Alto Health Care System (US), Thomas Jefferson University Hospital (US), University of Missouri Health System (US), Yale University (US), Northeast Health (US), National Institute on Alcohol Abuse and Alcoholism (US), Desert Institute For Spine Care (US), NeuroGenetic Pharmaceuticals (United States) (US), Jacobs Institute (US), Cognitive Research (United States) (US), Fundación Universitaria Sanitas (CO), Curry College (US), Ariel University (IL), University at Buffalo, State University of New York (US), University of Missouri (US), Universidade Federal do Estado do Rio de Janeiro (BR), Jefferson College (US), Texas Tech University Health Sciences Center (US), Western University of Health Sciences (US)
Good health and well-being
Openalex Percentile: Top 2%
Diabetes Treatment and Management
9.06
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