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Randomized Controlled Trial
. 2014 May;39(6):1324-31.
doi: 10.1038/npp.2013.288. Epub 2013 Oct 16.

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

Affiliations
Randomized Controlled Trial

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

Philip R Szeszko et al. Neuropsychopharmacology. 2014 May.

Abstract

Second-generation antipsychotics are utilized extensively in the treatment of psychotic disorders and other psychiatric conditions, but the effects of these medications on human brain white matter are not well understood. We thus investigated the effects of second-generation antipsychotics on white matter integrity using tract-based spatial statistics in patients experiencing a first episode of psychosis with little or no prior antipsychotic exposure, and how potential changes were associated with metabolic side effects. Thirty-five (26 men/9 women) patients experiencing a first episode of psychosis received diffusion tensor imaging (DTI) exams, clinical assessments, and provided fasting blood samples at the onset of antipsychotic treatment, and then again after 12 weeks of treatment with either risperidone or aripiprazole in a double-blind randomized clinical trial. In addition, 35 (26 men/9 women) healthy volunteers received DTI exams at a baseline time point and then after 12 weeks. Patients demonstrated significant (p<0.05; family-wise error corrected) fractional anisotropy reductions within the parietal and occipital white matter following antipsychotic treatment. Greater overall fractional anisotropy reduction was significantly correlated with greater increases in low-density lipoprotein. There were no significant fractional anisotropy increases among patients following treatment. Moreover, healthy volunteers did not demonstrate either significant increases or decreases in fractional anisotropy across a comparable 12-week interval. The use of antipsychotics may be associated with a subtle loss of white matter integrity that is related to greater side effects, thus raising potentially important considerations regarding risk/benefit in their usage. Limitations of the current study, however, include a prior history of substance use among patients and our inability to exclude the possibility of disease progression.

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Figures

Figure 1
Figure 1
Significant fractional anisotropy reductions (in blue) Following 12 weeks of antipsychotic treatment in patients overlaid onto the TBSS skeleton. Note: for better visualization, significant clusters are ‘thickened' (in red) using the ‘TBSS_fill' script.'
Figure 2
Figure 2
Individual changes in average fractional anisotropy across seven regions in patients (a) surviving family-wise error correction in TBSS from baseline to follow-up and corresponding changes within the average of these regions in healthy volunteers (b). Note: red line indicates mean change in both groups.
Figure 3
Figure 3
Scatterplot of changes in average fractional anisotropy and low-density lipoprotein in patients following 12 weeks of antipsychotic treatment.

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