Cargando…
Lurasidone for the treatment of bipolar depression: an evidence-based review
Bipolar disorder (BD) is a debilitating and difficult-to-treat psychiatric disease that presents a serious burden to patients’ lives as well as health care systems around the world. The essential diagnostic criterion for BD is episodes of mania or hypomania; however, the patients report that the maj...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4547662/ https://www.ncbi.nlm.nih.gov/pubmed/26316760 http://dx.doi.org/10.2147/NDT.S50961 |
_version_ | 1782387092546912256 |
---|---|
author | Franklin, Rachel Zorowitz, Sam Corse, Andrew K Widge, Alik S Deckersbach, Thilo |
author_facet | Franklin, Rachel Zorowitz, Sam Corse, Andrew K Widge, Alik S Deckersbach, Thilo |
author_sort | Franklin, Rachel |
collection | PubMed |
description | Bipolar disorder (BD) is a debilitating and difficult-to-treat psychiatric disease that presents a serious burden to patients’ lives as well as health care systems around the world. The essential diagnostic criterion for BD is episodes of mania or hypomania; however, the patients report that the majority of their time is spent in a depressive phase. Current treatment options for this component of BD have yet to achieve satisfactory remission rates. Lurasidone is a drug in the benzisothiazole class approved by the US Food and Drug Administration in June 2013 for the acute treatment of bipolar depression. Its pharmacological profile features high-affinity antagonism at D(2), 5-HT(2A), and 5-HT(7) receptors; moderate-affinity antagonism at α(2C)-adrenergic receptors; low- to very low-affinity antagonism at α(1A)-adrenergic, α(2A)-adrenergic, H(1), M(1), and 5-HT(2C) receptors; and high-affinity partial agonism at 5-HT(1A). Preliminary findings from two recent double-blinded clinical trials suggest that lurasidone is efficacious in treating bipolar I depression, with clinical effects manifesting as early as the first 2–3 weeks of treatment (as measured by the Montgomery–Åsberg Depression Rating Scale and Clinical Global Impressions Scale for use in bipolar illness). Its therapeutic benefit appears to be comparable to the current US Food and Drug Administration-indicated treatments: quetiapine and olanzapine–fluoxetine, according to a measure of effect size known as number needed to treat. These studies reported relatively limited extrapyramidal and metabolic side effects as a result of treatment with lurasidone, with the most common side effect being nausea. Safety data drawn from these studies, as well as a more extensive body of schizophrenia research, indicate that in comparison with other atypical antipsychotics, treatment with lurasidone is less likely to result in metabolic side effects such as weight gain or disturbances of serum glucose or lipid levels. Lurasidone holds clinical potential as a novel, efficacious pharmacological treatment for bipolar depression. However, current data on its use for the treatment of BD are limited, and more extensive research, both longer in duration as well as independently conducted, is needed. |
format | Online Article Text |
id | pubmed-4547662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45476622015-08-27 Lurasidone for the treatment of bipolar depression: an evidence-based review Franklin, Rachel Zorowitz, Sam Corse, Andrew K Widge, Alik S Deckersbach, Thilo Neuropsychiatr Dis Treat Review Bipolar disorder (BD) is a debilitating and difficult-to-treat psychiatric disease that presents a serious burden to patients’ lives as well as health care systems around the world. The essential diagnostic criterion for BD is episodes of mania or hypomania; however, the patients report that the majority of their time is spent in a depressive phase. Current treatment options for this component of BD have yet to achieve satisfactory remission rates. Lurasidone is a drug in the benzisothiazole class approved by the US Food and Drug Administration in June 2013 for the acute treatment of bipolar depression. Its pharmacological profile features high-affinity antagonism at D(2), 5-HT(2A), and 5-HT(7) receptors; moderate-affinity antagonism at α(2C)-adrenergic receptors; low- to very low-affinity antagonism at α(1A)-adrenergic, α(2A)-adrenergic, H(1), M(1), and 5-HT(2C) receptors; and high-affinity partial agonism at 5-HT(1A). Preliminary findings from two recent double-blinded clinical trials suggest that lurasidone is efficacious in treating bipolar I depression, with clinical effects manifesting as early as the first 2–3 weeks of treatment (as measured by the Montgomery–Åsberg Depression Rating Scale and Clinical Global Impressions Scale for use in bipolar illness). Its therapeutic benefit appears to be comparable to the current US Food and Drug Administration-indicated treatments: quetiapine and olanzapine–fluoxetine, according to a measure of effect size known as number needed to treat. These studies reported relatively limited extrapyramidal and metabolic side effects as a result of treatment with lurasidone, with the most common side effect being nausea. Safety data drawn from these studies, as well as a more extensive body of schizophrenia research, indicate that in comparison with other atypical antipsychotics, treatment with lurasidone is less likely to result in metabolic side effects such as weight gain or disturbances of serum glucose or lipid levels. Lurasidone holds clinical potential as a novel, efficacious pharmacological treatment for bipolar depression. However, current data on its use for the treatment of BD are limited, and more extensive research, both longer in duration as well as independently conducted, is needed. Dove Medical Press 2015-08-19 /pmc/articles/PMC4547662/ /pubmed/26316760 http://dx.doi.org/10.2147/NDT.S50961 Text en © 2015 Franklin et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Franklin, Rachel Zorowitz, Sam Corse, Andrew K Widge, Alik S Deckersbach, Thilo Lurasidone for the treatment of bipolar depression: an evidence-based review |
title | Lurasidone for the treatment of bipolar depression: an evidence-based review |
title_full | Lurasidone for the treatment of bipolar depression: an evidence-based review |
title_fullStr | Lurasidone for the treatment of bipolar depression: an evidence-based review |
title_full_unstemmed | Lurasidone for the treatment of bipolar depression: an evidence-based review |
title_short | Lurasidone for the treatment of bipolar depression: an evidence-based review |
title_sort | lurasidone for the treatment of bipolar depression: an evidence-based review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4547662/ https://www.ncbi.nlm.nih.gov/pubmed/26316760 http://dx.doi.org/10.2147/NDT.S50961 |
work_keys_str_mv | AT franklinrachel lurasidoneforthetreatmentofbipolardepressionanevidencebasedreview AT zorowitzsam lurasidoneforthetreatmentofbipolardepressionanevidencebasedreview AT corseandrewk lurasidoneforthetreatmentofbipolardepressionanevidencebasedreview AT widgealiks lurasidoneforthetreatmentofbipolardepressionanevidencebasedreview AT deckersbachthilo lurasidoneforthetreatmentofbipolardepressionanevidencebasedreview |