Stip Emmanuel, Sepehry Amir Ali, Chouinard Sylvie
Centre de Recherche Fernand-Seguin, Hechelaga, Montreal, Quebec, Canada.
Clin Neuropharmacol. 2007 Jul-Aug;30(4):218-29. doi: 10.1097/WNF.0b013e318059be76.
Memory impairment is frequent in schizophrenia and remains difficult to treat. Improved memory function is associated with a better functional outcome. Some clinical trials have used add-on therapy with acetylcholinesterase inhibitors (AChEIs) to test the cognitive enhancement effect of this kind of medication, which is usually prescribed for other indications than schizophrenia.
To perform a systematic review with meta-analysis.
Studies were identified using electronic search engines, hand searches, cross-referencing of studies, and contacts with investigators. Eligible studies were those comparing cognitive performance in patients with schizophrenia before and after AChEI treatment, randomized controlled trials, and crossover and open trials of AChEI in people with schizophrenia, with trial duration of more than 2 weeks. Validated neurocognitive measures and computerized batteries were used to corroborate the effect.
Our findings reveal a small to medium improvement in short-term memory and long-term memory (LTM) performance when patients are compared with the baseline performance, but when compared with controls (placebo treatment) at the end of the trial, they performed worse on both short-term memory and on LTM. However, the effects were nonsignificant. The LTM magnitude estimate demonstrating a treatment effect between the start and end points of the trial consisted of 8 studies (before treatment, n = 209; overall attrition rate, 8%). The effect estimate was significant and close to heterogeneous. Duration of trial increases the effect estimate slightly. The analysis was broken down by AChEI: 5 studies of donepezil (effect size [ES], -0.352), 2 studies of rivastigmine (ES, 0.383), and 1 study of galantamine. There were 6 studies of AChEI added to second-generation antipsychotics (ES, 0.424) and 2 studies of first-generation antipsychotics (ES, 0.207).
Notwithstanding an extensive investigation, eligible data for the meta-analysis were nominal. To date, and overall, our quantitative systematic review provides no clear evidence on whether AChEIs should be prescribed for memory enhancement in patients with schizophrenia.
记忆障碍在精神分裂症中很常见,且仍然难以治疗。记忆功能的改善与更好的功能结局相关。一些临床试验使用乙酰胆碱酯酶抑制剂(AChEIs)附加疗法来测试这类药物的认知增强效果,这类药物通常用于治疗精神分裂症以外的其他适应症。
进行一项系统评价并荟萃分析。
通过电子搜索引擎、手工检索、研究交叉引用以及与研究者联系来识别研究。符合条件的研究包括比较精神分裂症患者在接受AChEI治疗前后的认知表现的研究、随机对照试验以及AChEI在精神分裂症患者中的交叉试验和开放试验,试验持续时间超过2周。使用经过验证的神经认知测量方法和计算机化测试组合来证实效果。
我们的研究结果显示,与基线表现相比,患者的短期记忆和长期记忆(LTM)表现有小到中等程度的改善,但在试验结束时与对照组(安慰剂治疗)相比,他们在短期记忆和LTM方面的表现都更差。然而,这些效果并不显著。显示试验起点和终点之间存在治疗效果的LTM效应量估计包括8项研究(治疗前,n = 209;总体损耗率,8%)。效应估计显著且接近异质性。试验持续时间会使效应估计略有增加。分析按AChEI进行细分:5项多奈哌齐研究(效应大小[ES],-0.352),2项卡巴拉汀研究(ES,0.383),以及1项加兰他敏研究。有6项研究将AChEI添加到第二代抗精神病药物中(ES,0.424),2项研究将AChEI添加到第一代抗精神病药物中(ES,0.207)。
尽管进行了广泛的调查,但荟萃分析的合格数据很少。总体而言,迄今为止,我们的定量系统评价没有提供明确证据表明是否应该为精神分裂症患者开具AChEIs以增强记忆。