Epiphare (French National Medicines Agency ANSM and French National Health Insurance CNAM), Saint-Denis, France.
French National Health Insurance (CNAM), Paris, France.
Sci Rep. 2023 Mar 31;13(1):5308. doi: 10.1038/s41598-023-32356-3.
Finasteride, a 5α-reductase inhibitor used in benign prostatic hyperplasia and androgenetic alopecia, has been associated with an increased suicidal risk, whereas it is unclear whether such risk is similar to that for another 5α-reductase inhibitor, dutasteride. We aimed to assess the risk of suicidal behaviours with finasteride relative to dutasteride. A nationwide cohort study was conducted using the French National Health Data System (SNDS). Men aged 50 years or older initiating finasteride 5 mg or dutasteride 0.5 mg in France between 01-01-2012 and 30-06-2016 were included and followed until outcome (suicide death identified from death certificate or self-harm hospitalisation), treatment discontinuation or switch, death, or 31-12-2016. Self-harm by violent means or resulting in admission to an intensive care unit were also examined. Cox proportional hazards models controlled for age and psychiatric and non-psychiatric conditions by inverse probability of treatment weighting (IPTW). Analyses were stratified according to psychiatric history. The study compared 69,786 finasteride new users to 217,577 dutasteride new users (median age: 72.0 years [Q1-Q3 = 64.5-80.2] vs. 71.1 [Q1-Q3 = 65.0-79.2]). During follow-up, 18 suicide deaths (0.57/1000 person-years) and 34 self-harm hospitalisations (1.08/1000) occurred among finasteride users versus 47 deaths (0.43/1000) and 87 hospitalisations (0.79/1000) among dutasteride users. Overall, finasteride was not associated with an increased risk of any suicidal outcome (IPTW-adjusted Hazard Ratio = 1.21 [95% Confidence Interval .87-1.67]), suicide death or self-harm hospitalisation. However, among individuals with a history of mood disorders, finasteride was associated with an increased risk of any suicidal outcome (25 versus 46 events; HR = 1.64 [95% CI 1.00-2.68]), suicide death (8 versus 10 events; HR = 2.71 [95% CI 1.07-6.91]), self-harm by violent means (6 versus 6 events; HR = 3.11 [95% CI 1.01-9.61]), and self-harm with admission to an intensive care unit (7 versus 5 events; HR = 3.97 [95% CI 1.26-12.5]). None of these risks was significantly increased among individuals without a psychiatric history. These findings do not support an increased risk of suicide with finasteride used in the treatment of benign prostatic hyperplasia. However, an increased risk cannot be excluded among men with a history of mood disorder, but this result based on a limited number of events should be interpreted with caution.
非那雄胺是一种用于治疗良性前列腺增生和雄激素性脱发的 5α-还原酶抑制剂,与自杀风险增加有关,而其风险是否与另一种 5α-还原酶抑制剂达特罗terone 相似尚不清楚。我们旨在评估非那雄胺相对于达特罗terone 发生自杀行为的风险。使用法国国家健康数据系统(SNDS)进行了一项全国性队列研究。2012 年 1 月 1 日至 2016 年 6 月 30 日期间,年龄在 50 岁或以上的男性在法国开始使用非那雄胺 5mg 或达特罗terone 0.5mg,随访至结局(通过死亡证明或自残住院确定的自杀死亡)、治疗停药或换药、死亡或 2016 年 12 月 31 日。还检查了通过暴力手段自残或导致入住重症监护病房的情况。通过逆概率治疗加权(Inverse Probability of Treatment Weighting,IPTW)对 Cox 比例风险模型进行了调整,以控制年龄和精神和非精神疾病状况。分析根据精神病史进行分层。该研究比较了 69786 名非那雄胺新使用者和 217577 名达特罗terone 新使用者(中位年龄:72.0 岁[四分位距(Interquartile Range,IQR)=64.5-80.2] vs. 71.1 [IQR=65.0-79.2])。在随访期间,非那雄胺使用者中有 18 例自杀死亡(0.57/1000人年)和 34 例自残住院(1.08/1000),而达特罗terone 使用者中有 47 例死亡(0.43/1000)和 87 例住院(0.79/1000)。总体而言,非那雄胺与任何自杀结局(IPTW 调整的危害比(Hazard Ratio,HR)=1.21[95%置信区间(Confidence Interval,CI).87-1.67])、自杀死亡或自残住院无关。然而,在有心境障碍病史的个体中,非那雄胺与任何自杀结局的风险增加相关(25 例与 46 例事件;HR=1.64[95%CI 1.00-2.68])、自杀死亡(8 例与 10 例事件;HR=2.71[95%CI 1.07-6.91])、暴力自残(6 例与 6 例事件;HR=3.11[95%CI 1.01-9.61])和入住重症监护病房的自残(7 例与 5 例事件;HR=3.97[95%CI 1.26-12.5])。在没有精神病史的个体中,这些风险均未显著增加。这些发现不支持非那雄胺用于治疗良性前列腺增生与自杀风险增加有关。然而,不能排除有心境障碍病史的男性自杀风险增加,但基于有限数量的事件,该结果应谨慎解释。