Department of Psychiatry and Behavioral Sciences, Duke University Medical Center, Durham, NC, USA.
Schizophr Bull. 2013 Mar;39(2):417-35. doi: 10.1093/schbul/sbr153. Epub 2011 Nov 22.
In light of the number of studies conducted to examine the treatment of cognitive impairment associated with schizophrenia (CIAS), we critically reviewed recent CIAS trials. Trials were identified through searches of the website "www.clinicaltrials.gov" using the terms "schizophrenia AND cognition," "schizophrenia AND neurocognition," "schizophrenia AND neurocognitive tests," "schizophrenia AND MATRICS," "schizophrenia AND MCCB," "schizophrenia AND BACS," "schizophrenia AND COGSTATE," and "schizophrenia AND CANTAB" and "first-episode schizophrenia AND cognition." The cutoff date was 20 April 2011. Included trials were conducted in people with schizophrenia, the effects on cognition were either a primary or secondary outcome, and the effect of a pharmacologically active substance was examined. Drug challenge, pharmacokinetic, pharmacodynamic, or prodrome of psychosis studies were excluded. We identified 118 trials, with 62% using an add-on parallel group design. The large majority of completed trials were underpowered to detect moderate effect sizes, had ≤8 weeks duration, and were performed in samples of participants with chronic stable schizophrenia. The ongoing add-on trials are longer, have larger sample sizes (with a number of them being adequately powered to detect moderate effect sizes), and are more likely to use a widely accepted standardized cognitive battery (eg, the MATRICS Consensus Cognitive Battery) and MATRICS guidelines. Ongoing studies performed in subjects with recent onset schizophrenia may help elucidate which subjects are most likely to show an effect in cognition. New insights into the demands of CIAS trial design and methodology may help increase the probability of identifying treatments with beneficial effect on cognitive impairment in schizophrenia.
鉴于有大量研究探讨精神分裂症相关认知障碍(CIAS)的治疗方法,我们对最近的 CIAS 试验进行了批判性评估。通过在“www.clinicaltrials.gov”网站上使用“schizophrenia AND cognition”、“schizophrenia AND neurocognition”、“schizophrenia AND neurocognitive tests”、“schizophrenia AND MATRICS”、“schizophrenia AND MCCB”、“schizophrenia AND BACS”、“schizophrenia AND COGSTATE”和“schizophrenia AND CANTAB”以及“first-episode schizophrenia AND cognition”等术语进行搜索,确定了试验。截止日期为 2011 年 4 月 20 日。纳入的试验是在精神分裂症患者中进行的,认知的影响是主要或次要结局,并且研究了药理活性物质的效果。排除了药物挑战、药代动力学、药效动力学或精神病前驱期研究。我们确定了 118 项试验,其中 62%采用附加平行组设计。已完成的绝大多数试验都没有足够的能力来检测中等效应大小,持续时间≤8 周,并且是在慢性稳定精神分裂症患者样本中进行的。正在进行的附加试验时间更长,样本量更大(其中一些试验有足够的能力来检测中等效应大小),并且更有可能使用广泛接受的标准化认知电池(例如,MATRICS 共识认知电池)和 MATRICS 指南。在发病初期的精神分裂症患者中进行的正在进行的研究可能有助于阐明哪些患者最有可能在认知方面显示出效果。对 CIAS 试验设计和方法学的新见解可能有助于增加确定对精神分裂症认知障碍具有有益效果的治疗方法的可能性。