Duan Yinghui, Grady James J, Albertsen Peter C, Helen Wu Z
Department of Community Medicine and Health Care, University of Connecticut Health Center, Farmington, CT, USA.
Connecticut Institute for Clinical and Translational Science (CICATS), Farmington, CT, USA.
Pharmacoepidemiol Drug Saf. 2018 Mar;27(3):340-348. doi: 10.1002/pds.4361. Epub 2018 Jan 9.
Clinicians use tamsulosin, an α1-adrenoceptor antagonist, to manage symptomatic benign prostatic hyperplasia (BPH). Because α1-adrenoceptors are also present in the brain, the potential exists for adverse effects on cognitive functions. We explored the association between tamsulosin use and dementia risk.
We used Medicare data (2006-2012) to conduct a cohort study among patients aged ≥65 years and diagnosed with BPH. Men taking tamsulosin (n = 253 136) were matched at a 1:1 ratio using propensity-scores to each of 6 comparison cohorts: patients who used no BPH-medication (n = 180 926), and patients who used the following alternative-BPH-medications: doxazosin (n = 28 581), terazosin (n = 23 858), alfuzosin (n = 17 934), dutasteride (n = 34 027), and finasteride (n = 38 767). Assessment began following the first fill of BPH-medication to identify incident dementia by ICD-9 diagnosis codes. We estimated hazard ratios (HR) and 95% confidence intervals (CI) for dementia using Cox proportional hazard regression for each of the 6 propensity-score-matched cohort-pairs.
The median follow-up period for all cohorts was 19.8 months. After propensity-score matching, the tamsulosin cohort had an incidence of dementia of 31.3/1000 person-years compared with only 25.9/1000 person-years in the no-BPH-medication cohort. The risk of dementia was significantly higher in the tamsulosin cohort, when compared with the no-BPH-medication cohort (HR [95% CI]: 1.17 [1.14, 1.21]) and each of the alternative-BPH-medication cohorts: doxazosin (1.20 [1.12, 1.28]), terazosin (1.11 [1.04, 1.19]), alfuzosin (1.12 [1.03, 1.22]), dutasteride (1.26 [1.19, 1.34]), and finasteride (1.13 [1.07, 1.19]). The significance of these findings persisted in sensitivity analyses.
Tamsulosin may increase the risk of dementia in older men with BPH.
临床医生使用α1肾上腺素能受体拮抗剂坦索罗辛来治疗有症状的良性前列腺增生(BPH)。由于α1肾上腺素能受体也存在于大脑中,因此存在对认知功能产生不良反应的可能性。我们探讨了使用坦索罗辛与痴呆风险之间的关联。
我们利用医疗保险数据(2006 - 2012年)对年龄≥65岁且被诊断为BPH的患者进行了一项队列研究。使用倾向评分将服用坦索罗辛的男性(n = 253136)以1:1的比例与6个对照队列中的每一个进行匹配:未使用BPH药物的患者(n = 180926),以及使用以下替代BPH药物的患者:多沙唑嗪(n = 28581)、特拉唑嗪(n = 23858)、阿夫唑嗪(n = 17934)、度他雄胺(n = 34027)和非那雄胺(n = 38767)。在首次开具BPH药物后开始评估,通过ICD - 9诊断代码识别新发痴呆。我们使用Cox比例风险回归对6个倾向评分匹配的队列对中的每一个估计痴呆的风险比(HR)和95%置信区间(CI)。
所有队列的中位随访期为19.8个月。倾向评分匹配后,坦索罗辛队列的痴呆发病率为31.3/1000人年,而未使用BPH药物的队列仅为25.9/1000人年。与未使用BPH药物的队列相比,坦索罗辛队列的痴呆风险显著更高(HR [95% CI]:1.17 [1.14, 1.21]),并且与每一个替代BPH药物队列相比也是如此:多沙唑嗪(1.20 [1.12, 1.28])、特拉唑嗪(1.11 [1.04, 1.19])、阿夫唑嗪(1.12 [1.03, 1.22])、度他雄胺(1.26 [1.19, 1.34])和非那雄胺(1.13 [1.07, 1.19])。这些发现的显著性在敏感性分析中持续存在。
坦索罗辛可能会增加老年BPH男性患痴呆的风险。