Foley Debra L, Morley Katherine I
Applied Genetics and Biostatistics, Orygen Youth Health Research Centre, the University of Melbourne, Parkville, Victoria, Australia.
Arch Gen Psychiatry. 2011 Jun;68(6):609-16. doi: 10.1001/archgenpsychiatry.2011.2. Epub 2011 Feb 7.
The increased mortality associated with schizophrenia is largely due to cardiovascular disease. Treatment with antipsychotics is associated with weight gain and changes in other cardiovascular risk factors. Early identification of modifiable cardiovascular risk factors is a clinical imperative but prospective longitudinal studies of the early cardiometabolic adverse effects of antipsychotic drug treatment other than weight gain have not been previously reviewed.
To assess the methods and reporting of cardiometabolic outcome studies of the first treated episode of psychosis, review key findings, and suggest directions for future research.
PsycINFO, MEDLINE, and Scopus from January 1990 to June 2010.
Subjects were experiencing their first treated episode of psychosis. Subjects were antipsychotic naive or had been exposed to antipsychotics for a short known period at the beginning of the study. Cardiometabolic indices were assessed. Studies used a longitudinal design.
Sixty-four articles were identified describing 53 independent studies; 25 studies met inclusion criteria and were retained for detailed review.
Consolidated Standards of Reporting Trials and Strengthening the Reporting of Observational Studies in Epidemiology checklists were used to assess the methods and reporting of studies. A qualitative review of findings was conducted.
Two key hypotheses were identified based on this review: (1) in general, there is no difference in cardiovascular risk assessed by weight or metabolic indices between individuals with an untreated first episode of psychosis and healthy controls and (2) cardiovascular risk increases after first exposure to any antipsychotic drug. A rank order of drugs can be derived but there is no evidence of significant class differences. Recommended directions for future research include assessing the effect on cardiometabolic outcomes of medication adherence and dosage effects, determining the therapeutic window for antipsychotic use in adults and youth, and testing for moderation of outcomes by demographic factors, including sex and age, and clinical and genetic factors.
精神分裂症相关死亡率增加主要归因于心血管疾病。抗精神病药物治疗与体重增加及其他心血管危险因素变化相关。早期识别可改变的心血管危险因素是临床的当务之急,但此前尚未对除体重增加外抗精神病药物治疗早期心脏代谢不良反应的前瞻性纵向研究进行综述。
评估首次治疗精神病发作的心脏代谢结局研究的方法和报告情况,综述关键发现,并为未来研究提出方向。
1990年1月至2010年6月的PsycINFO、MEDLINE和Scopus数据库。
受试者为首次接受治疗的精神病发作患者。受试者未使用过抗精神病药物或在研究开始时已知短时间接触过抗精神病药物。评估心脏代谢指标。研究采用纵向设计。
识别出64篇文章描述了53项独立研究;25项研究符合纳入标准并保留用于详细综述。
使用《报告试验的统一标准》和《加强流行病学观察性研究报告》清单评估研究方法和报告情况。对研究结果进行定性综述。
基于本次综述确定了两个关键假设:(1)一般而言,未治疗的首次精神病发作个体与健康对照者在通过体重或代谢指标评估的心血管风险方面无差异;(2)首次接触任何抗精神病药物后心血管风险增加。可得出药物的排序,但没有证据表明存在显著的类别差异。未来研究的推荐方向包括评估药物依从性和剂量效应对心脏代谢结局的影响,确定成人和青少年使用抗精神病药物的治疗窗,以及测试人口统计学因素(包括性别和年龄)、临床和遗传因素对结局的调节作用。