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Metabolic and clinical effect of alpha-lipoic acid administration in schizophrenic subjects stabilized with atypical antipsychotics: A 12-week, open-label, uncontrolled study

BACKGROUND: Many of the atypical antipsychotics induce metabolic side effects, limiting their use in clinical practice. Alpha-lipoic acid (ALA) was proposed as a new approach in schizophrenia to improve metabolic effects of atypical antipsychotics. The aim of the study is to evaluate the effect of A...

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Autores principales: Iannuzzo, Fiammetta, Basile, Gianpaolo Antonio, Campolo, Domenica, Genovese, Giovanni, Pandolfo, Gianluca, Giunta, Loretta, Ruggeri, Domenica, Di Benedetto, Antonino, Bruno, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389248/
https://www.ncbi.nlm.nih.gov/pubmed/35992380
http://dx.doi.org/10.1016/j.crphar.2022.100116
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author Iannuzzo, Fiammetta
Basile, Gianpaolo Antonio
Campolo, Domenica
Genovese, Giovanni
Pandolfo, Gianluca
Giunta, Loretta
Ruggeri, Domenica
Di Benedetto, Antonino
Bruno, Antonio
author_facet Iannuzzo, Fiammetta
Basile, Gianpaolo Antonio
Campolo, Domenica
Genovese, Giovanni
Pandolfo, Gianluca
Giunta, Loretta
Ruggeri, Domenica
Di Benedetto, Antonino
Bruno, Antonio
author_sort Iannuzzo, Fiammetta
collection PubMed
description BACKGROUND: Many of the atypical antipsychotics induce metabolic side effects, limiting their use in clinical practice. Alpha-lipoic acid (ALA) was proposed as a new approach in schizophrenia to improve metabolic effects of atypical antipsychotics. The aim of the study is to evaluate the effect of ALA on metabolic and clinical parameters among schizophrenic subjects. METHODS: 15 schizophrenic subjects, in stable atypical antipsychotic monotherapy were included in the study. ALA was administrated at the oral daily dose of 600 ​mg/d in addition to antipsychotic therapy. Metabolic, clinical, and psychopathological parameters were measured at typical antipsychotics. e initial screening, and after 12 weeks. RESULTS: ALA produced a statistically significant reduction in QTc (p ​= ​0.012), blood glucose (p ​= 0.005), AST (p ​= ​0.021), γGT (p ​= ​0.035), CPK (p ​= ​0.005) and prolactinaemia (p ​= ​0.026). In contrast, there was a significant increase in HbA1c (p ​= ​0.026). No effects on body weight and blood lipid levels (triglycerides, total cholesterol, HDL, LDL) emerged. CONCLUSIONS: ALA treatment appeared to be effective for reducing diabetes risk, liver functionality parameters, hyperprolactinaemia and QTC interval. ALA appears to be safe as adjunctive components in schizophrenia.
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spelling pubmed-93892482022-08-20 Metabolic and clinical effect of alpha-lipoic acid administration in schizophrenic subjects stabilized with atypical antipsychotics: A 12-week, open-label, uncontrolled study Iannuzzo, Fiammetta Basile, Gianpaolo Antonio Campolo, Domenica Genovese, Giovanni Pandolfo, Gianluca Giunta, Loretta Ruggeri, Domenica Di Benedetto, Antonino Bruno, Antonio Curr Res Pharmacol Drug Discov Research Article BACKGROUND: Many of the atypical antipsychotics induce metabolic side effects, limiting their use in clinical practice. Alpha-lipoic acid (ALA) was proposed as a new approach in schizophrenia to improve metabolic effects of atypical antipsychotics. The aim of the study is to evaluate the effect of ALA on metabolic and clinical parameters among schizophrenic subjects. METHODS: 15 schizophrenic subjects, in stable atypical antipsychotic monotherapy were included in the study. ALA was administrated at the oral daily dose of 600 ​mg/d in addition to antipsychotic therapy. Metabolic, clinical, and psychopathological parameters were measured at typical antipsychotics. e initial screening, and after 12 weeks. RESULTS: ALA produced a statistically significant reduction in QTc (p ​= ​0.012), blood glucose (p ​= 0.005), AST (p ​= ​0.021), γGT (p ​= ​0.035), CPK (p ​= ​0.005) and prolactinaemia (p ​= ​0.026). In contrast, there was a significant increase in HbA1c (p ​= ​0.026). No effects on body weight and blood lipid levels (triglycerides, total cholesterol, HDL, LDL) emerged. CONCLUSIONS: ALA treatment appeared to be effective for reducing diabetes risk, liver functionality parameters, hyperprolactinaemia and QTC interval. ALA appears to be safe as adjunctive components in schizophrenia. Elsevier 2022-06-28 /pmc/articles/PMC9389248/ /pubmed/35992380 http://dx.doi.org/10.1016/j.crphar.2022.100116 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Iannuzzo, Fiammetta
Basile, Gianpaolo Antonio
Campolo, Domenica
Genovese, Giovanni
Pandolfo, Gianluca
Giunta, Loretta
Ruggeri, Domenica
Di Benedetto, Antonino
Bruno, Antonio
Metabolic and clinical effect of alpha-lipoic acid administration in schizophrenic subjects stabilized with atypical antipsychotics: A 12-week, open-label, uncontrolled study
title Metabolic and clinical effect of alpha-lipoic acid administration in schizophrenic subjects stabilized with atypical antipsychotics: A 12-week, open-label, uncontrolled study
title_full Metabolic and clinical effect of alpha-lipoic acid administration in schizophrenic subjects stabilized with atypical antipsychotics: A 12-week, open-label, uncontrolled study
title_fullStr Metabolic and clinical effect of alpha-lipoic acid administration in schizophrenic subjects stabilized with atypical antipsychotics: A 12-week, open-label, uncontrolled study
title_full_unstemmed Metabolic and clinical effect of alpha-lipoic acid administration in schizophrenic subjects stabilized with atypical antipsychotics: A 12-week, open-label, uncontrolled study
title_short Metabolic and clinical effect of alpha-lipoic acid administration in schizophrenic subjects stabilized with atypical antipsychotics: A 12-week, open-label, uncontrolled study
title_sort metabolic and clinical effect of alpha-lipoic acid administration in schizophrenic subjects stabilized with atypical antipsychotics: a 12-week, open-label, uncontrolled study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9389248/
https://www.ncbi.nlm.nih.gov/pubmed/35992380
http://dx.doi.org/10.1016/j.crphar.2022.100116
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