Literature DB >> 21240150

Metabolic syndrome with different antipsychotics: a multicentre cross-sectional study.

Cem Cerit1, Meltem Vural, S Ükriye Bos Gelmez, Eylem Ozten, Ahmet Tamer Aker, Mustafa Yıldız.   

Abstract

OBJECTIVE: High prevalence of metabolic syndrome (MS) and related metabolic disturbances in patients with schizophrenia and bipolar affective disorder have been in main focus of interest in recent years since the introduction of second-generation antipsychotics. This study aims to examine these questions: 1) Is there a relation between antipsychotic treatment and MS prevalence? 2) Which antipsychotic users have higher MS prevalence? 3) Do patients on antipsychotic polytherapy have higher rates of MS than patients on antipsychotic monotherapy? 4) Which metabolic parameters are considerably disturbed on which antipsychotic users?
METHODS: 242 Patients with schizophrenia, schizoaffective disorder and bipolar disorder without any other psychiatric comorbidity according to DSM-IV and using the same antipsychotic(s) and/or mood stabilizers at least for the last 6 months included to the final assessment.
RESULTS: The sample was divided into 7 drug groups. The MS prevalence was highest in the combined antipsychotic (AA) group (48.1%) according to ATP III criteria. According to IDF criteria clozapine (C) group had the highest MS prevalence (74%).
CONCLUSIONS: When metabolic parameters evaluated overall, metabolic risk with antipsychotics is found to be highest in clozapine group, followed by combined AP group. Olanzapine and risperidone have intermediate risk while zuclopentixole has lowest.

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Year:  2010        PMID: 21240150

Source DB:  PubMed          Journal:  Psychopharmacol Bull        ISSN: 0048-5764


  7 in total

1.  Dietary intake and plasma metabolomic analysis of polyunsaturated fatty acids in bipolar subjects reveal dysregulation of linoleic acid metabolism.

Authors:  Simon J Evans; Rachel N Ringrose; Gloria J Harrington; Peter Mancuso; Charles F Burant; Melvin G McInnis
Journal:  J Psychiatr Res       Date:  2014-06-12       Impact factor: 4.791

2.  A Randomized Controlled Trial to Compare the Efficacy, Safety and Tolerability of Asenapine versus Olanzapine in Management of Schizophrenia.

Authors:  Arpita Maitra; Swati Bhattacharyya; Sabyasachi Mukhopadhyay; Asim Kumar Mallick; Supreeti Biswas; Om Prakash Singh
Journal:  Clin Psychopharmacol Neurosci       Date:  2020-11-30       Impact factor: 2.582

3.  High H1-affinity antidepressants and risk of metabolic syndrome in bipolar disorder.

Authors:  Virginio Salvi; Francesco Barone-Adesi; Virginia D'Ambrosio; Umberto Albert; Giuseppe Maina
Journal:  Psychopharmacology (Berl)       Date:  2015-09-26       Impact factor: 4.530

4.  Metabolic syndrome and adverse clinical outcomes in patients with bipolar disorder.

Authors:  Ya-Mei Bai; Cheng-Ta Li; Shih-Jen Tsai; Pei-Chi Tu; Mu-Hong Chen; Tung-Ping Su
Journal:  BMC Psychiatry       Date:  2016-12-15       Impact factor: 3.630

5.  Switching to paliperidone extended release in patients with schizophrenia dissatisfied with previous olanzapine treatment: Post hoc analysis of an open-label, prospective study.

Authors:  Tian Mei Si; Shang Li Cai; Jian Min Zhuo; Li Li Zhang
Journal:  Medicine (Baltimore)       Date:  2019-01       Impact factor: 1.817

Review 6.  Metabolic syndrome in schizophrenia.

Authors:  Nidhi Malhotra; Sandeep Grover; Subho Chakrabarti; Parmanand Kulhara
Journal:  Indian J Psychol Med       Date:  2013-07

7.  Antipsychotic Medications and Risk of Acute Coronary Syndrome in Schizophrenia: A Nested Case-Control Study.

Authors:  Hsing-Cheng Liu; Shu-Yu Yang; Ya-Tang Liao; Chiao-Chicy Chen; Chian-Jue Kuo
Journal:  PLoS One       Date:  2016-09-22       Impact factor: 3.240

  7 in total

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