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Genetic association of the rs17782313 polymorphism with antipsychotic-induced weight gain

RATIONALE: Weight gain is a frequent side effect of treatment with SGAs (second-generation antipsychotics) and a leading cause for nonadherence. Several candidate genes have been identified that could influence the amount of AIWG (antipsychotic-induced weight gain). The polymorphism rs17782313 near...

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Autores principales: Schreyer, Korbinian Felix, Leucht, Stefan, Heres, Stephan, Steimer, Werner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10006246/
https://www.ncbi.nlm.nih.gov/pubmed/36757449
http://dx.doi.org/10.1007/s00213-023-06331-9
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author Schreyer, Korbinian Felix
Leucht, Stefan
Heres, Stephan
Steimer, Werner
author_facet Schreyer, Korbinian Felix
Leucht, Stefan
Heres, Stephan
Steimer, Werner
author_sort Schreyer, Korbinian Felix
collection PubMed
description RATIONALE: Weight gain is a frequent side effect of treatment with SGAs (second-generation antipsychotics) and a leading cause for nonadherence. Several candidate genes have been identified that could influence the amount of AIWG (antipsychotic-induced weight gain). The polymorphism rs17782313 near the MC4R (human melanocortin 4 receptor gene) was strongly associated with obesity in a large scale GWAS (genome wide association study), yet previous studies investigating its impact on AIWG did not lead to a definite conclusion regarding its effect. In particular, they were all relatively short and had a naturalistic design. OBJECTIVE: We therefore examined the influence of the rs17782313 polymorphism on SGA-related weight gain. METHODS: Participants of a multicenter randomized, controlled, double-blind study comparing two treatment strategies in individuals with schizophrenia or schizoaffective disorder were genotyped using a rapid-cycle polymerase chain reaction. Up to 252 individuals completed the first 2 weeks (phase I), 212 the entire 8 weeks (hence ‘completers’). Patients received either amisulpride or olanzapine or both consecutively. Thirty-seven had their first episode. Weight gain occurring in different genotypes was statistically compared and confounding factors were adjusted by stepwise multiple linear regression. A correction for multiple testing was included. RESULTS: Within 212 ‘completers’, carriers of the C allele had a higher absolute weight gain than those homozygous for the T allele (2.6 kg vs. 1.2 kg), though this observation was not significant (P = 0.063). In the amisulpride subpopulation, this association appeared stronger and reached significance (2.5 kg vs. 0.7 kg, P = 0.043), though failed to remain significant after correction for multiple testing. A stepwise multiple linear regression showed a significant association in both the whole study population (P < 0.001) and the amisulpride subpopulation (P < 0.001). CONCLUSION: Our results indicate that the rs17782313 polymorphism might influence antipsychotic-induced weight gain and therefore confirm some of the earlier conclusions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00213-023-06331-9.
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spelling pubmed-100062462023-03-12 Genetic association of the rs17782313 polymorphism with antipsychotic-induced weight gain Schreyer, Korbinian Felix Leucht, Stefan Heres, Stephan Steimer, Werner Psychopharmacology (Berl) Original Investigation RATIONALE: Weight gain is a frequent side effect of treatment with SGAs (second-generation antipsychotics) and a leading cause for nonadherence. Several candidate genes have been identified that could influence the amount of AIWG (antipsychotic-induced weight gain). The polymorphism rs17782313 near the MC4R (human melanocortin 4 receptor gene) was strongly associated with obesity in a large scale GWAS (genome wide association study), yet previous studies investigating its impact on AIWG did not lead to a definite conclusion regarding its effect. In particular, they were all relatively short and had a naturalistic design. OBJECTIVE: We therefore examined the influence of the rs17782313 polymorphism on SGA-related weight gain. METHODS: Participants of a multicenter randomized, controlled, double-blind study comparing two treatment strategies in individuals with schizophrenia or schizoaffective disorder were genotyped using a rapid-cycle polymerase chain reaction. Up to 252 individuals completed the first 2 weeks (phase I), 212 the entire 8 weeks (hence ‘completers’). Patients received either amisulpride or olanzapine or both consecutively. Thirty-seven had their first episode. Weight gain occurring in different genotypes was statistically compared and confounding factors were adjusted by stepwise multiple linear regression. A correction for multiple testing was included. RESULTS: Within 212 ‘completers’, carriers of the C allele had a higher absolute weight gain than those homozygous for the T allele (2.6 kg vs. 1.2 kg), though this observation was not significant (P = 0.063). In the amisulpride subpopulation, this association appeared stronger and reached significance (2.5 kg vs. 0.7 kg, P = 0.043), though failed to remain significant after correction for multiple testing. A stepwise multiple linear regression showed a significant association in both the whole study population (P < 0.001) and the amisulpride subpopulation (P < 0.001). CONCLUSION: Our results indicate that the rs17782313 polymorphism might influence antipsychotic-induced weight gain and therefore confirm some of the earlier conclusions. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00213-023-06331-9. Springer Berlin Heidelberg 2023-02-09 2023 /pmc/articles/PMC10006246/ /pubmed/36757449 http://dx.doi.org/10.1007/s00213-023-06331-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Investigation
Schreyer, Korbinian Felix
Leucht, Stefan
Heres, Stephan
Steimer, Werner
Genetic association of the rs17782313 polymorphism with antipsychotic-induced weight gain
title Genetic association of the rs17782313 polymorphism with antipsychotic-induced weight gain
title_full Genetic association of the rs17782313 polymorphism with antipsychotic-induced weight gain
title_fullStr Genetic association of the rs17782313 polymorphism with antipsychotic-induced weight gain
title_full_unstemmed Genetic association of the rs17782313 polymorphism with antipsychotic-induced weight gain
title_short Genetic association of the rs17782313 polymorphism with antipsychotic-induced weight gain
title_sort genetic association of the rs17782313 polymorphism with antipsychotic-induced weight gain
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10006246/
https://www.ncbi.nlm.nih.gov/pubmed/36757449
http://dx.doi.org/10.1007/s00213-023-06331-9
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