School of Nursing, College of Nursing, Taipei Medical University, Taipei, Taiwan.
Department of Community Psychiatry and Addiction Psychiatry, Bali Psychiatric Center, New Taipei City, Taiwan.
Schizophr Res. 2019 Oct;212:150-156. doi: 10.1016/j.schres.2019.07.049. Epub 2019 Aug 6.
Long-term cataract risks associated with first-generation antipsychotics (FGAs) and second-generation antipsychotics (SGAs), and their associations with metabolism-related diseases are not yet elucidated.
Using Taiwan National Health Insurance data, we conducted a propensity score matched population-based cohort study consisting of 10,014 patients with newly diagnosed schizophrenia from 2005 to 2009 and followed them until the end of 2013. A Cox hazard model with metabolism-related diseases as time-dependent covariates was adapted to estimate the hazard ratio (HR) of cataracts between SGAs and FGAs groups.
During the 8-year follow-up, patients receiving SGAs were associated with a higher risk of cataract than those receiving FGAs with an adjusted HR of 1.59 (95% confidence interval [CI] = 1.06-2.36). Patients receiving high-metabolic-risk SGAs (clozapine and olanzapine) showed the highest risk of cataracts among SGAs when compared with those receiving FGAs (aHR = 2.57, 95% CI: 1.35-4.88). SGAs demonstrated a stronger contribution in the risk of cataract in patients without diabetes mellitus (DM) and hyperlipidemia than in those developed these diseases. Patients who developed DM or hyperlipidemia after receiving antipsychotics had an approximately 2.5-fold increased cataract risk over those who did not develop these diseases.
Regardless of the condition of metabolic-related diseases, SGAs were independently associated with an increased risk of cataract. DM and hyperlipidemia developed after antipsychotics contributed to the risk of cataract risk.
第一代抗精神病药(FGAs)和第二代抗精神病药(SGAs)长期白内障风险及其与代谢相关疾病的关系尚不清楚。
利用台湾全民健康保险数据库,我们开展了一项基于倾向评分匹配的人群队列研究,纳入了 2005 年至 2009 年期间新诊断为精神分裂症的 10014 例患者,随访至 2013 年底。采用伴有代谢相关疾病的时依性协变量的 Cox 风险模型来估计 SGA 和 FGA 组白内障的风险比(HR)。
在 8 年的随访期间,与 FGAs 相比,接受 SGAs 治疗的患者发生白内障的风险更高,校正 HR 为 1.59(95%置信区间 [CI]:1.06-2.36)。与 FGAs 相比,接受高代谢风险 SGA(氯氮平和奥氮平)治疗的患者发生白内障的风险最高(aHR=2.57,95%CI:1.35-4.88)。与患有糖尿病(DM)和高脂血症的患者相比,SGAs 在无 DM 和高脂血症的患者中对白内障风险的贡献更强。与未发生这些疾病的患者相比,在接受抗精神病药治疗后发生 DM 或高脂血症的患者发生白内障的风险增加了约 2.5 倍。
无论代谢相关疾病的状况如何,SGAs 与白内障风险增加独立相关。抗精神病药治疗后发生的 DM 和高脂血症也增加了白内障风险。