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Atypical Antipsychotics and the Human Skeletal Muscle Lipidome

Atypical antipsychotics (AAPs) are a class of medications associated with significant metabolic side effects, including insulin resistance. The aim of this study was to analyze the skeletal muscle lipidome of patients on AAPs, compared to mood stabilizers, to further understand the molecular changes...

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Autores principales: Burghardt, Kyle J., Ward, Kristen M., Sanders, Elani J., Howlett, Bradley H., Seyoum, Berhane, Yi, Zhengping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316471/
https://www.ncbi.nlm.nih.gov/pubmed/30322152
http://dx.doi.org/10.3390/metabo8040064
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author Burghardt, Kyle J.
Ward, Kristen M.
Sanders, Elani J.
Howlett, Bradley H.
Seyoum, Berhane
Yi, Zhengping
author_facet Burghardt, Kyle J.
Ward, Kristen M.
Sanders, Elani J.
Howlett, Bradley H.
Seyoum, Berhane
Yi, Zhengping
author_sort Burghardt, Kyle J.
collection PubMed
description Atypical antipsychotics (AAPs) are a class of medications associated with significant metabolic side effects, including insulin resistance. The aim of this study was to analyze the skeletal muscle lipidome of patients on AAPs, compared to mood stabilizers, to further understand the molecular changes underlying AAP treatment and side effects. Bipolar patients on AAPs or mood stabilizers underwent a fasting muscle biopsy and assessment of insulin sensitivity. A lipidomic analysis of total fatty acids (TFAs), phosphatidylcholines (PCs) and ceramides (CERs) was performed on the muscle biopsies, then lipid species were compared between treatment groups, and correlation analyses were performed with insulin sensitivity. TFAs and PCs were decreased and CERs were increased in the AAP group relative to those in the mood stabilizer group (FDR q-value <0.05). A larger number of TFAs and PCs were positively correlated with insulin sensitivity in the AAP group compared to those in the mood stabilizer group. In contrast, a larger number of CERs were negatively correlated with insulin sensitivity in the AAP group compared to that in the mood stabilizer group. The findings here suggest that AAPs are associated with changes in the lipid profiles of human skeletal muscle when compared to mood stabilizers and that these changes correlate with insulin sensitivity.
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spelling pubmed-63164712019-01-10 Atypical Antipsychotics and the Human Skeletal Muscle Lipidome Burghardt, Kyle J. Ward, Kristen M. Sanders, Elani J. Howlett, Bradley H. Seyoum, Berhane Yi, Zhengping Metabolites Article Atypical antipsychotics (AAPs) are a class of medications associated with significant metabolic side effects, including insulin resistance. The aim of this study was to analyze the skeletal muscle lipidome of patients on AAPs, compared to mood stabilizers, to further understand the molecular changes underlying AAP treatment and side effects. Bipolar patients on AAPs or mood stabilizers underwent a fasting muscle biopsy and assessment of insulin sensitivity. A lipidomic analysis of total fatty acids (TFAs), phosphatidylcholines (PCs) and ceramides (CERs) was performed on the muscle biopsies, then lipid species were compared between treatment groups, and correlation analyses were performed with insulin sensitivity. TFAs and PCs were decreased and CERs were increased in the AAP group relative to those in the mood stabilizer group (FDR q-value <0.05). A larger number of TFAs and PCs were positively correlated with insulin sensitivity in the AAP group compared to those in the mood stabilizer group. In contrast, a larger number of CERs were negatively correlated with insulin sensitivity in the AAP group compared to that in the mood stabilizer group. The findings here suggest that AAPs are associated with changes in the lipid profiles of human skeletal muscle when compared to mood stabilizers and that these changes correlate with insulin sensitivity. MDPI 2018-10-13 /pmc/articles/PMC6316471/ /pubmed/30322152 http://dx.doi.org/10.3390/metabo8040064 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Burghardt, Kyle J.
Ward, Kristen M.
Sanders, Elani J.
Howlett, Bradley H.
Seyoum, Berhane
Yi, Zhengping
Atypical Antipsychotics and the Human Skeletal Muscle Lipidome
title Atypical Antipsychotics and the Human Skeletal Muscle Lipidome
title_full Atypical Antipsychotics and the Human Skeletal Muscle Lipidome
title_fullStr Atypical Antipsychotics and the Human Skeletal Muscle Lipidome
title_full_unstemmed Atypical Antipsychotics and the Human Skeletal Muscle Lipidome
title_short Atypical Antipsychotics and the Human Skeletal Muscle Lipidome
title_sort atypical antipsychotics and the human skeletal muscle lipidome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6316471/
https://www.ncbi.nlm.nih.gov/pubmed/30322152
http://dx.doi.org/10.3390/metabo8040064
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