From the Washington University School of Medicine.
Division of Infectious Diseases, Department of Medicine.
J Clin Psychopharmacol. 2022;42(1):7-16. doi: 10.1097/JCP.0000000000001513.
PURPOSE/BACKGROUND: Antipsychotic drugs are well established to alter circulating prolactin levels by blocking dopamine D2 receptors in the pituitary. Prolactin activates many genes important in the development of breast cancer. Prior studies have found an association with antipsychotic use and risk of breast cancer.
METHODS/PROCEDURES: The IBM MarketScan Commercial and Medicaid Databases were used to establish a large, observational cohort of women taking antipsychotics drugs compared with anticonvulsants or lithium. A new user design was used that required 12 months of insurance enrollment before the first antipsychotic or anticonvulsant/lithium prescription. Invasive breast cancer was identified using diagnostic codes. Multivariable Cox proportional hazards models were used to evaluate the risk of breast cancer with antipsychotic drug exposure controlling for age and other risk factors.
FINDINGS/RESULTS: A total of 914 cases (0.16%) of invasive breast cancer were identified among 540,737 women. Exposure to all antipsychotics was independently associated with a 35% increased risk of breast cancer (aHR [adjusted hazard ratio], 1.35; 95% confidence interval, 1.14-1.61). Category 1 drugs (high prolactin) were associated with a 62% increased risk (aHR, 1.62; 95% CI, 1.30-2.03), category 2 drugs a 54% increased risk (aHR, 1.54; 95% CI, 1.19-1.99), and category 3 drugs were not associated with breast cancer risk.
IMPLICATIONS/CONCLUSIONS: In the largest study of antipsychotics taken by US women, a higher risk between antipsychotic drug use and increased risk for breast cancer was observed, with a differential higher association with antipsychotic categories that elevate prolactin. Our study confirms other recent observational studies of increased breast cancer risk with antipsychotics that elevate prolactin.
目的/背景:抗精神病药物通过阻断垂体中的多巴胺 D2 受体,很好地改变了循环催乳素水平。催乳素激活了许多在乳腺癌发展中重要的基因。先前的研究发现抗精神病药物的使用与乳腺癌风险之间存在关联。
方法/程序:使用 IBM MarketScan 商业和医疗补助数据库建立了一个大型的、观察性的女性队列,这些女性服用抗精神病药物与抗惊厥药或锂进行比较。使用新用户设计,要求在首次服用抗精神病药物或抗惊厥药/锂之前,有 12 个月的保险参保记录。使用诊断代码确定浸润性乳腺癌。使用多变量 Cox 比例风险模型评估抗精神病药物暴露与年龄和其他风险因素一起控制时乳腺癌的风险。
结果/发现:在 540737 名女性中,共发现 914 例(0.16%)浸润性乳腺癌病例。所有抗精神病药物的暴露与乳腺癌风险增加 35%独立相关(调整后的危害比[aHR],1.35;95%置信区间[CI],1.14-1.61)。1 类药物(催乳素水平高)与乳腺癌风险增加 62%相关(aHR,1.62;95%CI,1.30-2.03),2 类药物风险增加 54%(aHR,1.54;95%CI,1.19-1.99),而 3 类药物与乳腺癌风险无关。
在这项针对美国女性服用的最大的抗精神病药物研究中,观察到抗精神病药物的使用与乳腺癌风险之间存在更高的风险,与催乳素升高的抗精神病药物类别之间存在更高的关联。我们的研究证实了其他最近的关于催乳素升高的抗精神病药物增加乳腺癌风险的观察性研究。