Literature DB >> 21105275

Predictive value of early changes in triglycerides and weight for longer-term changes in metabolic measures during olanzapine, ziprasidone or aripiprazole treatment for schizophrenia and schizoaffective disorder post hoc analyses of 3 randomized, controlled clinical trials.

Vicki P Hoffmann1, Michael Case, Virginia L Stauffer, Jennie G Jacobson, Robert R Conley.   

Abstract

The objective of this study was to determine if early changes in triglycerides and weight may be useful in predicting longer-term changes in weight and other metabolic parameters. Data were from three 24- to 28-week randomized, controlled studies comparing olanzapine to ziprasidone or aripiprazole for treatment of schizophrenia. Analyses were restricted to completers with fasting laboratory data at all protocol specified time points. Analyses were primarily descriptive and included mean changes and categorical outcomes. In all treatment groups, participants who did not experience a 20 mg/dL or greater increase in triglycerides at early time points were unlikely to experience a change of 50 mg/dL or more in triglycerides after 6 months. Negative predictive values were 83% to 95%. However, early change in triglycerides was not useful for predicting later change in glucose, cholesterol, or weight. Similarly, early weight change gave robust negative predictive values for longer-term weight change (≥10 kg), but not for change in glucose or cholesterol. Lack of early elevation in triglyceride concentrations was predictive of later lack of substantial increase in triglycerides in olanzapine-, ziprasidone-, and aripiprazole-treated participants. Lack of early elevation in weight was predictive of later lack of substantial increase in weight in all 3 treatment groups. Early monitoring of triglyceride concentrations and weight may help clinicians assess risk that individuals will experience significant increase in triglycerides or weight gain, allowing assessments of potential risks and benefits earlier in treatment. Clinical monitoring is advised throughout treatment for all patients.

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Year:  2010        PMID: 21105275     DOI: 10.1097/jcp.0b013e3181faf670

Source DB:  PubMed          Journal:  J Clin Psychopharmacol        ISSN: 0271-0749            Impact factor:   3.153


  4 in total

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Authors:  A A Verhaegen; L F Van Gaal
Journal:  J Endocrinol Invest       Date:  2017-06-28       Impact factor: 4.256

2.  White matter changes associated with antipsychotic treatment in first-episode psychosis.

Authors:  Philip R Szeszko; Delbert G Robinson; Toshikazu Ikuta; Bart D Peters; Juan A Gallego; John Kane; Anil K Malhotra
Journal:  Neuropsychopharmacology       Date:  2013-10-16       Impact factor: 7.853

3.  Long-Term Evolution of Metabolic Status in Patients with Schizophrenia Stably Maintained on Second-Generation Antipsychotics.

Authors:  Seong Hoon Jeong; Nam Young Lee; Se Hyun Kim; In Won Chung; Tak Youn; Ung Gu Kang; Yong Min Ahn; Han Young You; Yong Sik Kim
Journal:  Psychiatry Investig       Date:  2018-06-21       Impact factor: 2.505

4.  Previous exposure to antipsychotic drug treatment is an effective predictor of metabolic disturbances experienced with current antipsychotic drug treatments.

Authors:  Ye Yang; Peng Xie; Yujun Long; Jing Huang; Jingmei Xiao; Jingping Zhao; Weihua Yue; Renrong Wu
Journal:  BMC Psychiatry       Date:  2022-03-21       Impact factor: 3.630

  4 in total

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