Department of Psychiatry and Behavioral Sciences, Johns Hopkins Bayview Medical Center, Baltimore, MD, USA.
Int J Geriatr Psychiatry. 2012 Dec;27(12):1248-57. doi: 10.1002/gps.3769. Epub 2012 Feb 29.
The use of psychotropic medications in Alzheimer's disease (AD) has been associated with both deleterious and potentially beneficial outcomes. We examined the longitudinal association of psychotropic medication use with cognitive, functional, and neuropsychiatric symptom (NPS) trajectories among community-ascertained incident AD cases from the Cache County Dementia Progression Study.
A total of 230 participants were followed for a mean of 3.7 years. Persistency index (PI) was calculated for all antidepressants, selective serotonin reuptake inhibitors (SSRIs), antipsychotics (atypical and typical), and benzodiazepines as the proportion of observed time of medication exposure. Mixed-effects models were used to examine the association between PI for each medication class and Mini-Mental State Exam (MMSE), Clinical Dementia Rating Sum of Boxes (CDR-Sum), and Neuropsychiatric Inventory - Total (NPI-Total) trajectories, controlling for appropriate demographic and clinical covariates.
At baseline, psychotropic medication use was associated with greater severity of dementia and poorer medical status. Higher PI for all medication classes was associated with a more rapid decline in MMSE. For antidepressant, SSRI, benzodiazepine, and typical antipsychotic use, a higher PI was associated with a more rapid increase in CDR-Sum. For SSRIs, antipsychotics, and typical antipsychotics, a higher PI was associated with more rapid increase in NPI-Total.
Psychotropic medication use was associated with more rapid cognitive and functional decline in AD, and not with improved NPS. Clinicians may tend to prescribe psychotropic medications to AD patients at risk of poorer outcomes, but one cannot rule out the possibility of poorer outcomes being caused by psychotropic medications.
在阿尔茨海默病(AD)中使用精神药物与有害和潜在有益的结果都有关联。我们通过从 Cache 县痴呆进展研究的社区确诊 AD 病例中,检查精神药物使用与认知、功能和神经精神症状(NPS)轨迹的纵向关联,来探讨这一问题。
共有 230 名参与者平均随访 3.7 年。抗抑郁药、选择性 5-羟色胺再摄取抑制剂(SSRIs)、抗精神病药(典型和非典型)和苯二氮䓬类药物的持久性指数(PI),是通过观察到的药物暴露时间的比例计算得出的。混合效应模型用于检查每种药物类别与简易精神状态检查(MMSE)、临床痴呆评定量表总和(CDR-Sum)和神经精神问卷-总(NPI-Total)轨迹之间的关联,同时控制适当的人口统计学和临床协变量。
在基线时,精神药物的使用与痴呆症的严重程度更高和较差的医疗状况有关。所有药物类别的 PI 越高,MMSE 下降的速度就越快。对于抗抑郁药、SSRIs、苯二氮䓬类药物和典型抗精神病药,PI 越高,CDR-Sum 的增加速度就越快。对于 SSRIs、抗精神病药和典型抗精神病药,PI 越高,NPI-Total 的增加速度就越快。
精神药物的使用与 AD 患者认知和功能的快速下降有关,而与 NPS 的改善无关。临床医生可能倾向于给有较差预后风险的 AD 患者开精神药物,但也不能排除精神药物导致较差预后的可能性。