Psychiatric Center Copenhagen, Rigshospitalet, University Hospital of Copenhagen, Denmark.
Int Clin Psychopharmacol. 2011 Nov;26(6):316-22. doi: 10.1097/YIC.0b013e32834ace0f.
Studies on humans show that depressive disorder is associated with an increased risk of developing cognitive dysfunction, and animal studies suggest that antidepressants may have neuroprotective abilities. On the basis of these observations, it was hypothesized that treatment with antidepressants may decrease the risk of developing dementia in patients with depression. We investigated whether continued treatment with antidepressants is associated with a decreased rate of dementia in a population of patients discharged from psychiatric healthcare service with a diagnosis of depression. We used register data on all prescribed antidepressants in all patients discharged from psychiatric healthcare service with a diagnosis of depression and with subsequent diagnoses of dementia in Denmark from 1995 to 2005. A total of 37 658 patients with a diagnosis of depression at their first psychiatric contact and who were exposed to antidepressants after discharge were included in the study. A total of 2007 patients (5.3%) were subsequently diagnosed with dementia of any kind. The rate of dementia decreased during periods of two or more prescriptions of older antidepressants compared with the period of only one prescription of older antidepressants [relative risk (RR)=0.83 (95% confidence interval (CI)=0.70-0.98)]. This finding was replicated with Alzheimer's disease as the outcome [RR=0.66 (95% CI=0.47-0.94)] but not with dementia of other kinds as the outcome [RR=0.88 (95% CI=0.73-1.06)]. In contrast, during periods of continued use of selective serotonin reuptake inhibitors or newer nonselective serotonin reuptake inhibitors, the rate of dementia was not decreased, regardless of the subtype of dementia. It was concluded that continued long-term treatment with older antidepressants is associated with a reduced rate of dementia in patients treated in psychiatric healthcare settings, whereas continued treatment with other kinds of antidepressants is not. Methodological reasons for these findings cannot be excluded because of the nonrandomized nature of data.
研究表明,抑郁症与认知功能障碍的风险增加有关,动物研究表明抗抑郁药可能具有神经保护作用。基于这些观察结果,有人假设抗抑郁药治疗可能会降低抑郁症患者发生痴呆的风险。我们研究了在丹麦,从 1995 年至 2005 年期间,从精神保健服务出院的被诊断患有抑郁症的患者中,继续使用抗抑郁药是否与痴呆的发生率降低有关。我们使用了丹麦所有精神保健服务出院的被诊断患有抑郁症且随后被诊断患有痴呆的所有患者的抗抑郁药处方登记数据。共有 37658 名首次精神科就诊时被诊断患有抑郁症且出院后使用抗抑郁药的患者纳入研究。共有 2007 名患者(5.3%)随后被诊断为任何类型的痴呆。与仅使用一种旧的抗抑郁药相比,使用两种或更多种旧的抗抑郁药的时期痴呆发生率降低[相对风险(RR)=0.83(95%置信区间(CI)=0.70-0.98)]。这一发现与阿尔茨海默病的结果一致[RR=0.66(95%CI=0.47-0.94)],但与其他类型的痴呆的结果不一致[RR=0.88(95%CI=0.73-1.06)]。相比之下,在继续使用选择性 5-羟色胺再摄取抑制剂或新型非选择性 5-羟色胺再摄取抑制剂期间,无论痴呆的亚型如何,痴呆的发生率均未降低。研究结论为,在精神保健环境中接受治疗的患者中,长期持续使用旧的抗抑郁药与痴呆发生率降低有关,而继续使用其他类型的抗抑郁药则没有。由于数据的非随机性,不能排除这些发现的方法学原因。