Helal Mohamed Mohsen, Almosilhy Nereen A, Hamam Nada G, Abdelbaset Mohamed Ahmed Adel, Shelbaya Ali Nagy, Musse Halima Abdirashid Y, Prasad Aishwarya
Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Medical Research Group of Egypt, Negida Academy, Arlington, Massachusetts, USA.
Drugs Aging. 2025 Jul 29. doi: 10.1007/s40266-025-01233-1.
Sacubitril/valsartan, an angiotensin receptor neprilysin inhibitor (ARNI), has become a cornerstone therapy for heart failure (HF) since its approval over a decade ago. However, concerns have emerged about potential cognitive risks, as neprilysin inhibition may contribute to the accumulation of amyloid-beta (Aβ) in the brain-a hallmark of Alzheimer's disease, the most common form of dementia.
Given the already elevated risk of dementia in patients with HF and the widespread use of sacubitril/valsartan, this meta-analysis aimed to evaluate whether its use is associated with an increased risk of all-cause dementia in HF populations.
A systematic literature search was conducted on 23 March 2025, to identify eligible studies comparing the risk of dementia in patients receiving sacubitril/valsartan versus those receiving placebo, no treatment, or other HF medications. Risk ratios (RRs) and 95% confidence intervals (CIs) were pooled using a random-effects model.
Six studies, comprising 101,074 participants and published between 2017 and 2024, were included in the meta-analysis. Treatment with sacubitril/valsartan was associated with a significant 15% reduction in the risk of all-cause dementia (RR = 0.85; 95% CI: 0.74-0.98; p = 0.02). Leave-one-out sensitivity and subgroup analyses confirmed the robustness of the findings.
This meta-analysis suggests that sacubitril/valsartan is associated with a reduced risk of dementia in patients with HF, helping to alleviate previous concerns about potential cognitive adverse effects. These findings support the continued use of sacubitril/valsartan as a foundational therapy in this high-risk population.
沙库巴曲缬沙坦,一种血管紧张素受体脑啡肽酶抑制剂(ARNI),自十多年前获批以来已成为心力衰竭(HF)的基石疗法。然而,由于脑啡肽酶抑制可能导致大脑中β淀粉样蛋白(Aβ)的积累——这是最常见的痴呆形式阿尔茨海默病的一个标志,人们对其潜在的认知风险产生了担忧。
鉴于心力衰竭患者患痴呆症的风险本就较高,且沙库巴曲缬沙坦应用广泛,本荟萃分析旨在评估其使用是否与心力衰竭人群全因性痴呆风险增加相关。
于2025年3月23日进行了系统的文献检索,以确定比较接受沙库巴曲缬沙坦治疗的患者与接受安慰剂、未治疗或其他心力衰竭药物治疗的患者患痴呆症风险的合格研究。使用随机效应模型汇总风险比(RRs)和95%置信区间(CIs)。
荟萃分析纳入了6项研究,共101,074名参与者,发表于2017年至2024年之间。沙库巴曲缬沙坦治疗与全因性痴呆风险显著降低15%相关(RR = 0.85;95% CI:0.74 - 0.98;p = 0.02)。逐一剔除敏感性分析和亚组分析证实了研究结果的稳健性。
本荟萃分析表明,沙库巴曲缬沙坦与降低心力衰竭患者患痴呆症的风险相关,有助于减轻先前对潜在认知不良反应的担忧。这些发现支持在这一高危人群中继续使用沙库巴曲缬沙坦作为基础治疗方法。