TY - JOUR
T1 - Head-to-head comparisons of metabolic side effects of second generation antipsychotics in the treatment of schizophrenia
T2 - A systematic review and meta-analysis
AU - Rummel-Kluge, Christine
AU - Komossa, Katja
AU - Schwarz, Sandra
AU - Hunger, Heike
AU - Schmid, Franziska
AU - Lobos, Claudia Asenjo
AU - Kissling, Werner
AU - Davis, John M.
AU - Leucht, Stefan
N1 - Funding Information:
Financial support was provided by a grant from the Technische Universität München (HWP II) (CR), the German Federal Ministry of Education and Research, no FKZ: 01KG 0606, GZ: GFKG01100506 (SL); and a grant from the National Institute of Mental Health, Advanced Center for Intervention and Services Research Center (MH-68580), Grant No. 1 P01MH68580-01 CFDA #93.242, the Maryland Psychiatric Research Center (JD). The funding source had no involvement in study design, collection, analysis and interpretation of data, writing the report and in the decision to submit the paper for publication.
PY - 2010/11
Y1 - 2010/11
N2 - Objective: The metabolic side effects of second-generation antipsychotics (SGA) are serious and have not been compared head to head in a meta-analysis. We conducted a meta-analysis of studies comparing the metabolic side effects of the following SGAs head-to-head: amisulpride, aripiprazole, clozapine, olanzapine, quetiapine, risperidone, sertindole, ziprasidone, zotepine. Method: We searched the register of the Cochrane schizophrenia group (last search May 2007), supplemented by MEDLINE and EMBASE (last search January 2009) for randomized, blinded studies comparing the above mentioned SGA in the treatment of schizophrenia or related disorders. At least three reviewers extracted the data independently. The primary outcome was weight change. We also assessed changes of cholesterol and glucose. The results were combined in a meta-analysis. Results: We included 48 studies with 105 relevant arms. Olanzapine produced more weight gain than all other second-generation antipsychotics except for clozapine where no difference was found. Clozapine produced more weight gain than risperidone, risperidone more than amisulpride, and sertindole more than risperidone. Olanzapine produced more cholesterol increase than aripiprazole, risperidone and ziprasidone. (No differences with amisulpride, clozapine and quetiapine were found). Quetiapine produced more cholesterol increase than risperidone and ziprasidone. Olanzapine produced more increase in glucose than amisulpride, aripiprazole, quetiapine, risperidone and ziprasidone; no difference was found with clozapine. Conclusions: Some SGAs lead to substantially more metabolic side effects than other SGAs. When choosing an SGA for an individual patient these side effects with their potential cause of secondary diseases must be weighed against efficacy and characteristics of the individual patient.
AB - Objective: The metabolic side effects of second-generation antipsychotics (SGA) are serious and have not been compared head to head in a meta-analysis. We conducted a meta-analysis of studies comparing the metabolic side effects of the following SGAs head-to-head: amisulpride, aripiprazole, clozapine, olanzapine, quetiapine, risperidone, sertindole, ziprasidone, zotepine. Method: We searched the register of the Cochrane schizophrenia group (last search May 2007), supplemented by MEDLINE and EMBASE (last search January 2009) for randomized, blinded studies comparing the above mentioned SGA in the treatment of schizophrenia or related disorders. At least three reviewers extracted the data independently. The primary outcome was weight change. We also assessed changes of cholesterol and glucose. The results were combined in a meta-analysis. Results: We included 48 studies with 105 relevant arms. Olanzapine produced more weight gain than all other second-generation antipsychotics except for clozapine where no difference was found. Clozapine produced more weight gain than risperidone, risperidone more than amisulpride, and sertindole more than risperidone. Olanzapine produced more cholesterol increase than aripiprazole, risperidone and ziprasidone. (No differences with amisulpride, clozapine and quetiapine were found). Quetiapine produced more cholesterol increase than risperidone and ziprasidone. Olanzapine produced more increase in glucose than amisulpride, aripiprazole, quetiapine, risperidone and ziprasidone; no difference was found with clozapine. Conclusions: Some SGAs lead to substantially more metabolic side effects than other SGAs. When choosing an SGA for an individual patient these side effects with their potential cause of secondary diseases must be weighed against efficacy and characteristics of the individual patient.
KW - Cholesterol
KW - Glucose
KW - Individual treatment
KW - Weight
UR - http://www.scopus.com/inward/record.url?scp=77957923642&partnerID=8YFLogxK
U2 - 10.1016/j.schres.2010.07.012
DO - 10.1016/j.schres.2010.07.012
M3 - Article
C2 - 20692814
AN - SCOPUS:77957923642
SN - 0920-9964
VL - 123
SP - 225
EP - 233
JO - Schizophrenia Research
JF - Schizophrenia Research
IS - 2-3
ER -