Phosphodiesterase-5 Inhibitors and Dementia Risk: A Real-World Study.

IF 3.2 3区 医学 Q2 CLINICAL NEUROLOGY
Naomi Gronich, Nili Stein, Walid Saliba
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Abstract

Introduction: Biological and scarce epidemiological evidence suggested that phosphodiesterase-5 inhibitors (PDE5i) might reduce dementia risk. We aimed to examine the association between PDE5i and dementia using real-world data.

Methods: Two retrospective cohorts within the database of Clalit, the largest healthcare provider in Israel (2005-2023), were studied. The first cohort included new daily users, older than 50 years of age, of low-dose tadalafil, prescribed for benign prostatic hypertrophy (BPH), propensity-score matched to new-users of alpha-1 blockers, and analyzed using 2-year lag time. The second cohort included patients with erectile dysfunction, with/without any PDE5i treatment, using time-dependent analysis. Individuals in the cohorts were followed through May 2023 for the occurrence of dementia.

Results: The first cohort included 5,204 tadalafil initiators propensity-score matched to 18,565 alpha-1 blockers initiators. There was no association between tadalafil use and dementia risk, HR = 0.99 (95% CI: 0.88-1.12), p = 0.927. Similar results were obtained in a competing risk analysis, and in a sensitivity analysis in which we restricted the cohort to patients older than 60 years at cohort entry. The second cohort of 133,336 patients with erectile dysfunction included new users and nonusers of any PDE5i. In a mean follow-up of 7.9 years, 8,631 patients were newly diagnosed with dementia. In a time-dependent multivariable analysis, PDE5i use was not associated with reduced dementia risk, HR = 0.95 (95% CI: 0.86-1.04). Results were not changed in sensitivity analyses (patients older than 60 years or stratification by PDE5i type).

Conclusion: This study suggests that the use of PDE5 inhibitors is not associated with decreased risk of dementia.

磷酸二酯酶-5 抑制剂与痴呆症风险:一项真实世界研究。
生物学和少量流行病学证据表明,磷酸二酯酶-5 抑制剂 (PDE5i) 可降低痴呆症风险。我们旨在利用真实世界的数据研究 PDE5i 与痴呆症之间的关系。我们对以色列最大的医疗保健提供商 Clalit 数据库中的两个回顾性队列(2005-2023 年)进行了研究。第一个队列包括年龄在 50 岁以上、每天服用小剂量他达拉非的新用户,处方药为良性前列腺肥大 (BPH),倾向分数与α-1 受体阻滞剂新用户相匹配,并使用 2 年滞后时间进行分析。第二个队列包括接受/未接受任何 PDE5i 治疗的勃起功能障碍患者,采用时间依赖性分析。对队列中的个体进行了跟踪研究,直至 2023 年 5 月,以了解痴呆症的发生情况。第一个队列包括5204名他达拉非患者和18565名α-1受体阻滞剂患者。使用他达拉非与痴呆症风险之间没有关联,HR=0.99 95%CI (0.88, 1.12),P=0.927。在竞争风险分析和敏感性分析中也得到了类似的结果,在敏感性分析中,我们将队列限制为进入队列时年龄超过 60 岁的患者。第二个队列中有 133,336 名勃起功能障碍患者,其中包括任何一种 PDE5i 的新使用者和非使用者。在一项时间依赖性多变量分析中,使用 PDE5i 与痴呆症风险降低无关,HR=0.95(95%CI,0.86-1.04)。敏感性分析(60岁以上患者或按PDE5i类型分层)的结果没有变化。本研究表明,使用 PDE5 抑制剂与痴呆风险的降低无关。
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来源期刊
Neuroepidemiology
Neuroepidemiology 医学-公共卫生、环境卫生与职业卫生
CiteScore
9.90
自引率
1.80%
发文量
49
审稿时长
6-12 weeks
期刊介绍: ''Neuroepidemiology'' is the only internationally recognised peer-reviewed periodical devoted to descriptive, analytical and experimental studies in the epidemiology of neurologic disease. The scope of the journal expands the boundaries of traditional clinical neurology by providing new insights regarding the etiology, determinants, distribution, management and prevention of diseases of the nervous system.
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