Livingston G, Walker A E, Katona C L E, Cooper C
Department of Mental Health Sciences, University College London, Holborn Union Building, Archway Campus, Highgate Hill, London N19 5LW, UK.
J Neurol Neurosurg Psychiatry. 2007 Jan;78(1):25-9. doi: 10.1136/jnnp.2006.094342. Epub 2006 Jun 26.
To investigate in a longitudinal cohort of people with Alzheimer's disease whether taking antipsychotics is associated with more rapid cognitive deterioration.
From a sample of 224 people with Alzheimer's disease recruited as epidemiologically representative, those taking antipsychotic drugs for more than 6 months were compared with those who were not, in terms of change in three measures of cognition. The effects of potential mediators and confounders (demographic factors, neuropsychiatric symptoms, cognitive severity and cholinesterase inhibitors) were also examined.
No significant difference was observed in cognitive decline between those taking antipsychotics (atypical or any) and others on any measure of cognition. The only predictor of more cognitive decline was greater baseline cognitive severity (B = 3.3, 95% confidence interval 0.6 to 6.1, t = 2.4, p<0.05). Although mortality was higher in those treated with antipsychotics, this reflected their greater age and severity of dementia. The results were the same when the whole cohort was included rather than the select group with potential to change who had been taking antipsychotics continuously.
In this, the first cohort study investigating the effects of atypical antipsychotics on cognitive outcome in Alzheimer's disease, those taking antipsychotics were no more likely to decline cognitively over 6 months. Although clinicians should remain cautious when prescribing antipsychotic drugs to people with Alzheimer's disease, any increase in cognitive deterioration is not of the magnitude previously reported. There is a need for cohort studies that follow up patients from first prescription in clinical practice for a period of months rather than weeks to determine "real-life" risks and benefits.
在一个阿尔茨海默病患者的纵向队列中研究服用抗精神病药物是否与认知功能更快衰退相关。
从招募的224名具有流行病学代表性的阿尔茨海默病患者样本中,将服用抗精神病药物超过6个月的患者与未服用者在三项认知指标的变化方面进行比较。还检查了潜在中介因素和混杂因素(人口统计学因素、神经精神症状、认知严重程度和胆碱酯酶抑制剂)的影响。
在任何认知指标上,服用抗精神病药物(非典型或任何类型)的患者与其他患者在认知衰退方面均未观察到显著差异。认知衰退更明显的唯一预测因素是更高的基线认知严重程度(B = 3.3,95%置信区间0.6至6.1,t = 2.4,p<0.05)。尽管服用抗精神病药物的患者死亡率较高,但这反映了他们更大的年龄和更严重的痴呆程度。当纳入整个队列而非仅纳入持续服用抗精神病药物且有潜在变化可能的特定组时,结果相同。
在这项首次调查非典型抗精神病药物对阿尔茨海默病认知结局影响的队列研究中,服用抗精神病药物的患者在6个月内认知衰退的可能性并不更高。尽管临床医生在给阿尔茨海默病患者开抗精神病药物时应保持谨慎,但认知恶化的增加幅度并非先前报道的那样。需要进行队列研究,在临床实践中从首次开处方开始对患者进行数月而非数周的随访,以确定“实际生活”中的风险和益处。