通过生物标志物评估日本慢性心力衰竭患者接受血管紧张素受体-奈普利素抑制剂治疗的认知功能

Circulation reports Pub Date : 2025-05-24 eCollection Date: 2025-07-10 DOI:10.1253/circrep.CR-24-0175
Masaya Kogure, Fukiko Kitani-Morii, Tomoya Kitani, Masatsugu Oishi, Hirokazu Shiraishi, Harutsugu Tatebe, Satoaki Matoba, Takahiko Tokuda, Takashi Kasai
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引用次数: 0

摘要

背景:血管紧张素受体-嗜碱溶素抑制剂(ARNIs)可改善慢性心力衰竭(CHF)患者的预后。然而,neprilysin是大脑中主要的淀粉样蛋白β (a β)降解酶,尽管先前的研究表明ARNI的使用不会引起CHF患者的神经认知功能障碍,但日本患者的数据有限。方法和结果:这项单中心、前瞻性、观察性研究纳入了15例CHF患者:6例接受ARNI治疗(ARNI), 9例未接受ARNI治疗(非ARNI)。在基线和1年随访时评估认知评估和血液生物标志物。来自帕金森病和阿尔茨海默病维度神经影像学倡议队列的参与者,包括7名大脑Aβ沉积(Aβ阳性)和7名无沉积(Aβ阴性)的患者,用于比较。尽管样本量小,但在a β阴性组和a β阳性组之间,日本版蒙特利尔认知评估评分和苏氨酸181水平的tau磷酸化水平存在显著差异。相比之下,在基线或随访1年后,非ARNI组和ARNI组在认知功能或血液生物标志物方面没有发现显著差异。结论:在这项中试研究中,日本CHF患者使用ARNI与认知功能障碍或与认知功能障碍相关的血液生物标志物升高无关。由于样本量和随访时间有限,需要在更大规模的长期试验中进一步验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of Cognitive Function via Biomarkers in Japanese Patients With Chronic Heart Failure Treated With Angiotensin-Receptor-Neprilysin Inhibitor.

Background: Angiotensin-receptor-neprilysin inhibitors (ARNIs) improve outcomes in patients with chronic heart failure (CHF). However, neprilysin is a major amyloid beta (Aβ)-degrading enzyme in the brain and although previous studies suggest that ARNI use does not induce neurocognitive dysfunction in CHF patients, data in Japanese patients are limited.

Methods and results: This single-center, prospective, observational study enrolled 15 CHF patients: 6 who were being treated with ARNI (ARNI) and 9 who were not (non-ARNI). Cognitive assessments and blood biomarkers were evaluated at baseline and 1-year follow-up. Participants from the Parkinson's and Alzheimer's Disease Dimensional Neuroimaging Initiative cohort, comprising 7 patients with cerebral Aβ deposition (Aβ-positive) and 7 patients without deposition (Aβ-negative), were used for comparison. Despite the small sample size, significant differences in the Japanese version of Montreal Cognitive Assessment score and tau phosphorylated at threonine 181 level were observed between the Aβ-negative and Aβ-positive groups. In contrast, no significant difference in cognitive function or blood biomarkers were found between the non-ARNI and ARNI groups at baseline or after 1 year of follow-up.

Conclusions: In this pilot-scale study, ARNI use was not associated with cognitive impairment or elevated blood biomarkers related to cognitive dysfunction in Japanese patients with CHF. Due to the limited sample size and follow-up, further validation in larger, long-term trials is warranted.

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