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DOI 10.1001/archpsyc.64.6.633

Медицинская библиотека · Archives of general psychiatry · 2007

Neurocognitive effects of antipsychotic medications in patients with chronic schizophrenia in the CATIE Trial.

Keefe Richard S E, Bilder Robert M, Davis Sonia M, Harvey Philip D, Palmer Barton W, Gold James M, Meltzer Herbert Y, Green Michael F, Capuano George, Stroup T Scott, McEvoy Joseph P, Swartz Marvin S, Rosenheck Robert A, Perkins Diana O, Davis Clarence E, Hsiao John K, Lieberman Jeffrey A, CATIE Investigators, Neurocognitive Working Group

Сравнительное исследованиеСтатьяМногоцентровое исследованиеРандомизированное исследованиеПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

CONTEXT: Neurocognitive impairment in schizophrenia is severe and is an important predictor of functional outcome. The relative effect of the second-generation (atypical) antipsychotic drugs and older agents on neurocognition has not been comprehensively determined.

OBJECTIVE

To compare the neurocognitive effects of several second-generation antipsychotics and a first-generation antipsychotic, perphenazine.

DESIGN

Randomized, double-blind study of patients with schizophrenia assigned to receive treatment with olanzapine, perphenazine, quetiapine fumarate, or risperidone for up to 18 months as reported previously by Lieberman et al. Ziprasidone hydrochloride was included after its approval by the Food and Drug Administration.

SETTING

Fifty-seven sites participated, including academic sites and treatment mental health facilities representative of the community.

PATIENTS: From a cohort of 1460 patients in the treatment study, 817 completed neurocognitive testing immediately prior to randomization and then after 2 months of treatment.

MAIN OUTCOME MEASURES: The primary outcome was change in a neurocognitive composite score after 2 months of treatment. Secondary outcomes included neurocognitive composite score change at 6 months and 18 months after continued treatment and changes in neurocognitive domains.

RESULTS

At 2 months, treatment resulted in small neurocognitive improvements of z = 0.13 for olanzapine (P<.002), 0.25 for perphenazine (P<.001), 0.18 for quetiapine (P<.001), 0.26 for risperidone (P<.001), and 0.12 for ziprasidone (P<.06), with no significant differences between groups. Results at 6 months were similar. After 18 months of treatment, neurocognitive improvement was greater in the perphenazine group than in the olanzapine and risperidone groups. Neurocognitive improvement predicted longer time to treatment discontinuation, independently from symptom improvement, in patients treated with quetiapine or ziprasidone.

CONCLUSIONS

After 2 months of antipsychotic treatment, all groups had a small but significant improvement in neurocognition. There were no differences between any pair of agents, including the typical drug perphenazine. These results differ from the majority of previous studies, and the possible reasons are discussed.

Для цитирования: Keefe Richard S E, Bilder Robert M, Davis Sonia M, Harvey Philip D, Palmer Barton W, Gold James M, Meltzer Herbert Y, Green Michael F, Capuano George, Stroup T Scott, McEvoy Joseph P, Swartz Marvin S, Rosenheck Robert A, Perkins Diana O, Davis Clarence E, Hsiao John K, Lieberman Jeffrey A, CATIE Investigators, Neurocognitive Working Group. Neurocognitive effects of antipsychotic medications in patients with chronic schizophrenia in the CATIE Trial.. Archives of general psychiatry. 2007. DOI: 10.1001/archpsyc.64.6.633.

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