Koro Carol E, Fedder Donald O, L'Italien Gilbert J, Weiss Sheila, Magder Laurence S, Kreyenbuhl Julie, Revicki Dennis, Buchanan Robert W
School of Pharmacy, University of Maryland, 506 W Fayette St, Suite 201, Baltimore, MD 21201, USA.
Arch Gen Psychiatry. 2002 Nov;59(11):1021-6. doi: 10.1001/archpsyc.59.11.1021.
The newer antipsychotic agents exhibit a superior safety profile compared with conventional antipsychotic agents in terms of extrapyramidal symptoms. Previous studies have suggested an association between olanzapine treatment and hyperlipidemia. We evaluated this association using a large health care database.
The study was derived from the England and Wales-based General Practice Research Database, composed of 3.5 million subjects followed up between June 1, 1987, and September 24, 2000. A total of 18 309 individuals diagnosed as having schizophrenia were identified. A 6:1 matched nested case-control design was used. Conditional logistic regression was used to derive adjusted odds ratios (ORs), controlling for sex, age, and other medications and disease conditions influencing lipid levels. Antipsychotic drug exposure was defined as the receipt of at least 1 prescription for an antipsychotic medication within the 3 months before the date of diagnosis of hyperlipidemia.
There were 1268 incident cases of hyperlipidemia in the cohort, matched to 7598 control subjects. Olanzapine use was associated with nearly a 5-fold increase in the odds of developing hyperlipidemia compared with no antipsychotic exposure (OR, 4.65; 95% confidence interval [CI], 2.44-8.85) (P<.001) and more than a 3-fold increase compared with those receiving conventional agents (OR, 3.36; 95% CI, 1.77-6.39) (P<.001). Risperidone was not associated with increased odds of hyperlipidemia compared with no antipsychotic exposure (OR, 1.12; 95% CI, 0.60-2.11) (P =.72) or conventional antipsychotic exposure (OR, 0.81; 95% CI, 0.44-1.52) (P =.52).
We observed a strong association between olanzapine exposure and hyperlipidemia in schizophrenic patients. The possible metabolic consequences of olanzapine use should be given serious consideration by treating physicians.
与传统抗精神病药物相比,新型抗精神病药物在外锥体外系症状方面具有更好的安全性。先前的研究表明奥氮平治疗与高脂血症之间存在关联。我们使用一个大型医疗保健数据库对这种关联进行了评估。
该研究源自基于英格兰和威尔士的全科医疗研究数据库,由1987年6月1日至2000年9月24日期间随访的350万受试者组成。共识别出18309名被诊断为精神分裂症的个体。采用6:1匹配的巢式病例对照设计。使用条件逻辑回归得出调整后的比值比(OR),并对性别、年龄以及其他影响血脂水平的药物和疾病状况进行控制。抗精神病药物暴露定义为在高脂血症诊断日期前3个月内接受至少1张抗精神病药物处方。
队列中有1268例高脂血症新发病例,与7598名对照受试者匹配。与未暴露于抗精神病药物相比,使用奥氮平发生高脂血症的几率增加近5倍(OR,4.65;95%置信区间[CI],2.44 - 8.85)(P <.001),与接受传统药物治疗的患者相比增加超过3倍(OR,3.36;95% CI,1.77 - 6.39)(P <.001)。与未暴露于抗精神病药物相比,利培酮与高脂血症几率增加无关(OR,1.12;95% CI,0.60 - 2.11)(P =.72),与暴露于传统抗精神病药物相比也无关(OR,0.81;95% CI,0.44 - 1.52)(P =.52)。
我们观察到精神分裂症患者中奥氮平暴露与高脂血症之间存在密切关联。治疗医生应认真考虑使用奥氮平可能产生的代谢后果。