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Unresolved Issues for Utilization of Atypical Antipsychotics in Schizophrenia: Antipsychotic Polypharmacy and Metabolic Syndrome

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2017 Oct 24
PMID 29057817
Citations 33
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Abstract

Atypical antipsychotics (AAP) are the prevailing form of schizophrenia treatment today due to their low side effects and superior efficacy. Nevertheless, some issues still need to be addressed. First, there are still a large number of patients with treatment-resistant schizophrenia (TRS), which has led to a growing trend to resort to AAP polypharmacy with few side effects. Most clinical treatment guidelines recommend clozapine monotherapy in TRS, but around one third of schizophrenic patients fail to respond to clozapine. For these patients, with clozapine-resistant schizophrenia AAP polypharmacy is a common strategy with a continually growing evidence base. Second, AAP generally have great risks for developing metabolic syndrome, such as weight gain, abnormality in glucose, and lipid metabolism. These metabolic side effects have become huge stumbling blocks in today's schizophrenia treatment that aims to improve patients' quality of life as well as symptoms. The exact reasons why this particular syndrome occurs in patients treated with AAP is as yet unclear though factors such as interaction of AAP with neurotransmitter receptors, genetic pholymorphisms, type of AAPs, length of AAP use, and life style of schizophrenic patients that may contribute to its development. The present article aimed to review the evidence underlying these key issues and provide the most reasonable interpretations to expand the overall scope of antipsychotics usage.

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References
1.
Torniainen M, Mittendorfer-Rutz E, Tanskanen A, Bjorkenstam C, Suvisaari J, Alexanderson K . Antipsychotic treatment and mortality in schizophrenia. Schizophr Bull. 2014; 41(3):656-63. PMC: 4393693. DOI: 10.1093/schbul/sbu164. View

2.
Casey D . Dyslipidemia and atypical antipsychotic drugs. J Clin Psychiatry. 2004; 65 Suppl 18:27-35. View

3.
Fleischhacker W, Heikkinen M, Olie J, Landsberg W, Dewaele P, McQuade R . Effects of adjunctive treatment with aripiprazole on body weight and clinical efficacy in schizophrenia patients treated with clozapine: a randomized, double-blind, placebo-controlled trial. Int J Neuropsychopharmacol. 2010; 13(8):1115-25. DOI: 10.1017/S1461145710000490. View

4.
Taniguchi A, Nakai Y, Fukushima M, Kawamura H, Imura H, Nagata I . Pathogenic factors responsible for glucose intolerance in patients with NIDDM. Diabetes. 1992; 41(12):1540-6. DOI: 10.2337/diab.41.12.1540. View

5.
Potkin S, Thyrum P, Alva G, Bera R, Yeh C, Arvanitis L . The safety and pharmacokinetics of quetiapine when coadministered with haloperidol, risperidone, or thioridazine. J Clin Psychopharmacol. 2002; 22(2):121-30. DOI: 10.1097/00004714-200204000-00004. View