Cholinesterase inhibitors are associated with reduced mortality in patients with Alzheimer's disease and previous myocardial infarction.

IF 5.3 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Bahira Shahim, Hong Xu, Kristina Haugaa, Henrik Zetterberg, Juliane Jurga, Dorota Religa, Maria Eriksdotter
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引用次数: 0

Abstract

Background: Cholinesterase inhibitors (ChEIs) are the first-line symptomatic pharmacologic treatment for patients with mild-to-moderate Alzheimer's disease (AD). Although the target organ for this group of drugs is the brain, inhibition of the enzyme may affect cardiac function through vagotonic and anti-inflammatory effects.

Objective: To assess the impact of ChEIs on outcomes in patients with AD who have experienced myocardial infarction (MI) prior to the AD diagnosis.

Methods: Patients who had experienced MI before they were diagnosed with AD or Alzheimer's mixed dementia between 2008 and 2018 were identified from the Swedish Dementia Registry (SveDem, www.svedem.se), which was linked to the National Patient Registry to obtain data on MI and mortality. Cox proportional hazards regression model among a propensity score-matched dataset was performed to assess the association between ChEI treatment and clinical outcomes.

Results: Of 3198 patients with previous MI and a diagnosis of AD or mixed dementia, 1705 (53%) were on treatment with ChEIs. Patients treated with ChEIs were more likely to be younger and have a better overall cardiovascular (CV) risk profile. The incidence rate of all-cause death (per 1000 patient-years) in the propensity-matched cohort of 1016 ChEI users and 1016 non-users was 168.6 in patients on treatment with ChEIs compared with 190.7 in patients not on treatment with ChEIs. In this propensity-matched cohort, treatment with ChEIs was associated with a significantly lower risk of all-cause death (adjusted hazard ratio 0.81, 95% confidence interval 0.71-0.92) and a greater reduction with higher doses of ChEIs. While in the unadjusted analysis, ChEIs were associated with a lower risk of both CV and non-CV death, only the association with non-CV death remained significant after accounting for baseline differences.

Conclusion: Treatment with ChEIs was associated with a significantly reduced risk of all-cause death, driven by lower rates of non-CV death in a nationwide cohort of patients with previous MI and a diagnosis of AD or mixed dementia. These associations were greater with higher ChEI doses.

Condensed abstract: We assessed the association between cholinesterase inhibitors (ChEIs) and clinical outcomes in a nationwide cohort of patients with previous myocardial infarction (MI) and a diagnosis of Alzheimer's disease (AD) or mixed dementi. In propensity-matched analysis, treatment with ChEIs was associated with a 19% reduction in all-cause death driven by non-cardiovascular death. The reduction in all-cause death was greater with the higher doses of ChEIs.

胆碱酯酶抑制剂可降低阿尔茨海默病患者和既往心肌梗死患者的死亡率。
背景:胆碱酯酶抑制剂(ChEIs)是轻度至中度阿尔茨海默病(AD)患者的一线对症药物治疗。虽然这类药物的靶器官是大脑,但抑制胆碱酯酶可能会通过迷走神经和抗炎作用影响心脏功能:目的:评估胆碱酯酶抑制剂对确诊前曾发生心肌梗死(MI)的 AD 患者预后的影响:从瑞典痴呆症登记处(SveDem,www.svedem.se)中找出在2008年至2018年期间被诊断为AD或阿尔茨海默氏症混合痴呆症之前经历过心肌梗死的患者,该登记处与国家患者登记处相连,以获得心肌梗死和死亡率的数据。在倾向得分匹配数据集中建立了Cox比例危险回归模型,以评估ChEI治疗与临床结局之间的关联:结果:在3198名既往有心肌梗死并被诊断为AD或混合性痴呆的患者中,有1705人(53%)接受了ChEIs治疗。接受胆碱酯酶抑制剂治疗的患者更年轻,整体心血管(CV)风险状况更好。在 1016 名 ChEI 使用者和 1016 名非使用者的倾向匹配队列中,接受 ChEI 治疗的患者全因死亡发生率(每 1000 患者年)为 168.6,而未接受 ChEI 治疗的患者为 190.7。在这一倾向匹配队列中,使用 ChEIs 治疗可显著降低全因死亡风险(调整后危险比为 0.81,95% 置信区间为 0.71-0.92),使用较大剂量的 ChEIs 治疗可显著降低全因死亡风险。在未经调整的分析中,氯乙酸类药物与较低的冠心病和非冠心病死亡风险相关,但在考虑基线差异后,只有与非冠心病死亡的相关性仍然显著:在一个全国性队列中,既往有心肌梗死、诊断为注意力缺失症或混合性痴呆的患者接受 ChEIs 治疗后,全因死亡风险显著降低,这与非 CV 死亡风险降低有关。浓缩摘要:我们评估了全国范围内既往有心肌梗死(MI)且诊断为阿尔茨海默病(AD)或混合性痴呆患者队列中胆碱酯酶抑制剂(ChEIs)与临床结局之间的关联。在倾向匹配分析中,接受 ChEIs 治疗后,非心血管疾病导致的全因死亡减少了 19%。剂量越大的 ChEIs 对全因死亡的降低作用越大。
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来源期刊
European Heart Journal - Cardiovascular Pharmacotherapy
European Heart Journal - Cardiovascular Pharmacotherapy Medicine-Cardiology and Cardiovascular Medicine
CiteScore
10.10
自引率
14.10%
发文量
65
期刊介绍: The European Heart Journal - Cardiovascular Pharmacotherapy (EHJ-CVP) is an international, peer-reviewed journal published in English, specifically dedicated to clinical cardiovascular pharmacology. EHJ-CVP publishes original articles focusing on clinical research involving both new and established drugs and methods, along with meta-analyses and topical reviews. The journal's primary aim is to enhance the pharmacological treatment of patients with cardiovascular disease by interpreting and integrating new scientific developments in this field. While the emphasis is on clinical topics, EHJ-CVP also considers basic research articles from fields such as physiology and molecular biology that contribute to the understanding of cardiovascular drug therapy. These may include articles related to new drug development and evaluation, the physiological and pharmacological basis of drug action, metabolism, drug interactions, and side effects.
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