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Atypical Antipsychotics and Metabolic Syndrome: From Molecular Mechanisms to Clinical Differences
Atypical antipsychotics (AAPs) are commonly prescribed medications to treat schizophrenia, bipolar disorders and other psychotic disorders. However, they might cause metabolic syndrome (MetS) in terms of weight gain, dyslipidemia, type 2 diabetes (T2D), and high blood pressure, which are responsible...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001502/ https://www.ncbi.nlm.nih.gov/pubmed/33800403 http://dx.doi.org/10.3390/ph14030238 |
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author | Carli, Marco Kolachalam, Shivakumar Longoni, Biancamaria Pintaudi, Anna Baldini, Marco Aringhieri, Stefano Fasciani, Irene Annibale, Paolo Maggio, Roberto Scarselli, Marco |
author_facet | Carli, Marco Kolachalam, Shivakumar Longoni, Biancamaria Pintaudi, Anna Baldini, Marco Aringhieri, Stefano Fasciani, Irene Annibale, Paolo Maggio, Roberto Scarselli, Marco |
author_sort | Carli, Marco |
collection | PubMed |
description | Atypical antipsychotics (AAPs) are commonly prescribed medications to treat schizophrenia, bipolar disorders and other psychotic disorders. However, they might cause metabolic syndrome (MetS) in terms of weight gain, dyslipidemia, type 2 diabetes (T2D), and high blood pressure, which are responsible for reduced life expectancy and poor adherence. Importantly, there is clear evidence that early metabolic disturbances can precede weight gain, even if the latter still remains the hallmark of AAPs use. In fact, AAPs interfere profoundly with glucose and lipid homeostasis acting mostly on hypothalamus, liver, pancreatic β-cells, adipose tissue, and skeletal muscle. Their actions on hypothalamic centers via dopamine, serotonin, acetylcholine, and histamine receptors affect neuropeptides and 5′AMP-activated protein kinase (AMPK) activity, thus producing a supraphysiological sympathetic outflow augmenting levels of glucagon and hepatic glucose production. In addition, altered insulin secretion, dyslipidemia, fat deposition in the liver and adipose tissues, and insulin resistance become aggravating factors for MetS. In clinical practice, among AAPs, olanzapine and clozapine are associated with the highest risk of MetS, whereas quetiapine, risperidone, asenapine and amisulpride cause moderate alterations. The new AAPs such as ziprasidone, lurasidone and the partial agonist aripiprazole seem more tolerable on the metabolic profile. However, these aspects must be considered together with the differences among AAPs in terms of their efficacy, where clozapine still remains the most effective. Intriguingly, there seems to be a correlation between AAP’s higher clinical efficacy and increase risk of metabolic alterations. Finally, a multidisciplinary approach combining psychoeducation and therapeutic drug monitoring (TDM) is proposed as a first-line strategy to avoid the MetS. In addition, pharmacological treatments are discussed as well. |
format | Online Article Text |
id | pubmed-8001502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80015022021-03-28 Atypical Antipsychotics and Metabolic Syndrome: From Molecular Mechanisms to Clinical Differences Carli, Marco Kolachalam, Shivakumar Longoni, Biancamaria Pintaudi, Anna Baldini, Marco Aringhieri, Stefano Fasciani, Irene Annibale, Paolo Maggio, Roberto Scarselli, Marco Pharmaceuticals (Basel) Review Atypical antipsychotics (AAPs) are commonly prescribed medications to treat schizophrenia, bipolar disorders and other psychotic disorders. However, they might cause metabolic syndrome (MetS) in terms of weight gain, dyslipidemia, type 2 diabetes (T2D), and high blood pressure, which are responsible for reduced life expectancy and poor adherence. Importantly, there is clear evidence that early metabolic disturbances can precede weight gain, even if the latter still remains the hallmark of AAPs use. In fact, AAPs interfere profoundly with glucose and lipid homeostasis acting mostly on hypothalamus, liver, pancreatic β-cells, adipose tissue, and skeletal muscle. Their actions on hypothalamic centers via dopamine, serotonin, acetylcholine, and histamine receptors affect neuropeptides and 5′AMP-activated protein kinase (AMPK) activity, thus producing a supraphysiological sympathetic outflow augmenting levels of glucagon and hepatic glucose production. In addition, altered insulin secretion, dyslipidemia, fat deposition in the liver and adipose tissues, and insulin resistance become aggravating factors for MetS. In clinical practice, among AAPs, olanzapine and clozapine are associated with the highest risk of MetS, whereas quetiapine, risperidone, asenapine and amisulpride cause moderate alterations. The new AAPs such as ziprasidone, lurasidone and the partial agonist aripiprazole seem more tolerable on the metabolic profile. However, these aspects must be considered together with the differences among AAPs in terms of their efficacy, where clozapine still remains the most effective. Intriguingly, there seems to be a correlation between AAP’s higher clinical efficacy and increase risk of metabolic alterations. Finally, a multidisciplinary approach combining psychoeducation and therapeutic drug monitoring (TDM) is proposed as a first-line strategy to avoid the MetS. In addition, pharmacological treatments are discussed as well. MDPI 2021-03-08 /pmc/articles/PMC8001502/ /pubmed/33800403 http://dx.doi.org/10.3390/ph14030238 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Review Carli, Marco Kolachalam, Shivakumar Longoni, Biancamaria Pintaudi, Anna Baldini, Marco Aringhieri, Stefano Fasciani, Irene Annibale, Paolo Maggio, Roberto Scarselli, Marco Atypical Antipsychotics and Metabolic Syndrome: From Molecular Mechanisms to Clinical Differences |
title | Atypical Antipsychotics and Metabolic Syndrome: From Molecular Mechanisms to Clinical Differences |
title_full | Atypical Antipsychotics and Metabolic Syndrome: From Molecular Mechanisms to Clinical Differences |
title_fullStr | Atypical Antipsychotics and Metabolic Syndrome: From Molecular Mechanisms to Clinical Differences |
title_full_unstemmed | Atypical Antipsychotics and Metabolic Syndrome: From Molecular Mechanisms to Clinical Differences |
title_short | Atypical Antipsychotics and Metabolic Syndrome: From Molecular Mechanisms to Clinical Differences |
title_sort | atypical antipsychotics and metabolic syndrome: from molecular mechanisms to clinical differences |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8001502/ https://www.ncbi.nlm.nih.gov/pubmed/33800403 http://dx.doi.org/10.3390/ph14030238 |
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