Effect of second-generation antipsychotics on cognition: current issues and future challenges

被引:73
|
作者
Hill, S. Kristian [1 ]
Bishop, Jeffrey R. [1 ]
Palumbo, Donna [2 ,3 ]
Sweeney, John A. [1 ]
机构
[1] Univ Illinois, Ctr Cognit Med MC 913, Chicago, IL 60612 USA
[2] Univ Rochester, Med Ctr, Rochester, NY USA
[3] Pfizer Global Res & Dev, Rochester, NY USA
关键词
antipsychotic medication; biomarker; cognition; neuropsychology; schizophrenia; NAIVE 1ST-EPISODE SCHIZOPHRENIA; DOUBLE-BLIND TREATMENT; QUALITY-OF-LIFE; PREFRONTAL CORTEX; WORKING-MEMORY; FOLLOW-UP; NEUROPSYCHOLOGICAL DYSFUNCTION; NEUROCOGNITIVE DEFICITS; ATYPICAL ANTIPSYCHOTICS; DIFFERENTIAL DEFICIT;
D O I
10.1586/ERN.09.143
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Generalized cognitive impairments are stable deficits linked to schizophrenia and key factors associated with functional disability in the disorder. Preclinical data suggest that second-generation antipsychotics could potentially reduce cognitive impairments; however, recent large clinical trials indicate only modest cognitive benefits relative to first-generation antipsychotics. This might reflect a limited drug effect in humans, a differential drug effect due to brain alterations associated with schizophrenia, or limited sensitivity of the neuropsychological tests for evaluating cognitive outcomes. New adjunctive procognitive drugs may be needed to achieve robust cognitive and functional improvement. Drug discovery may benefit from greater utilization of translational neurocognitive biomarkers to bridge preclinical and clinical proof-of-concept studies, to optimize assay sensitivity, enhance cost efficiency, and speed progress in drug development.
引用
收藏
页码:43 / 57
页数:15
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