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Ther Adv Infect Dis. 2023 May 22;10:20499361231174289. doi: 10.1177/20499361231174289. eCollection 2023 Jan-Dec.
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Theranostics. 2023 Jan 1;13(2):543-559. doi: 10.7150/thno.77088. eCollection 2023.
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Clinical features predicting COVID-19 mortality risk.预测新型冠状病毒肺炎死亡风险的临床特征。
Eur J Transl Myol. 2022 Apr 12;32(2):10268. doi: 10.4081/ejtm.2022.10268.
3
2022 Alzheimer's disease facts and figures.2022 年阿尔茨海默病事实和数据。
Alzheimers Dement. 2022 Apr;18(4):700-789. doi: 10.1002/alz.12638. Epub 2022 Mar 14.
4
Factors associated with hospital admission and severe outcomes for older patients with COVID-19.与 COVID-19 老年患者住院和严重结局相关的因素。
J Am Geriatr Soc. 2022 Jul;70(7):1906-1917. doi: 10.1111/jgs.17718. Epub 2022 Feb 25.
5
Long COVID, neuropsychiatric disorders, psychotropics, present and future.长期新冠、神经精神障碍、精神药物,现状与未来。
Acta Neuropsychiatr. 2022 Jun;34(3):109-126. doi: 10.1017/neu.2022.6. Epub 2022 Mar 3.
6
Comorbidity Trajectories Associated With Alzheimer's Disease: A Matched Case-Control Study in a United States Claims Database.与阿尔茨海默病相关的共病轨迹:一项在美国理赔数据库中的匹配病例对照研究。
Front Neurosci. 2021 Oct 8;15:749305. doi: 10.3389/fnins.2021.749305. eCollection 2021.
7
COVID-19 Case Fatality and Alzheimer's Disease.COVID-19 病死率与阿尔茨海默病
J Alzheimers Dis. 2021;84(4):1447-1452. doi: 10.3233/JAD-215161.
8
SARS-CoV-2 Susceptibility and COVID-19 Mortality Among Older Adults With Cognitive Impairment: Cross-Sectional Analysis From Hospital Records in a Diverse US Metropolitan Area.认知障碍老年人中SARS-CoV-2易感性和COVID-19死亡率:来自美国一个多元化大都市地区医院记录的横断面分析
Front Neurol. 2021 Jul 22;12:692662. doi: 10.3389/fneur.2021.692662. eCollection 2021.
9
Clinical Characterization and Prediction of Clinical Severity of SARS-CoV-2 Infection Among US Adults Using Data From the US National COVID Cohort Collaborative.利用美国国家 COVID 队列协作的数据,对美国成年人中 SARS-CoV-2 感染的临床特征和临床严重程度进行临床描述和预测。
JAMA Netw Open. 2021 Jul 1;4(7):e2116901. doi: 10.1001/jamanetworkopen.2021.16901.
10
Drugs that offer the potential to reduce hospitalization and mortality from SARS-CoV-2 infection: The possible role of the sigma-1 receptor and autophagy.能够降低 SARS-CoV-2 感染住院率和死亡率的药物:sigma-1 受体和自噬的可能作用。
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在新冠肺炎感染期间,多奈哌齐对阿尔茨海默病患者的生存益处得以保留,但未增强。

Donepezil-associated survival benefits among Alzheimer's disease patients are retained but not enhanced during COVID-19 infections.

作者信息

Edmiston Elizabeth A, Bej Taissa A, Wilson Brigid, Jump Robin L P, Phillips Joy A

机构信息

Interprofessional Improvement Research, Education and Clinical Center, VA Northeast Ohio Healthcare System, Cleveland, OH, USA.

Geriatric Research Education and Clinical Center (GRECC), VA Northeast Ohio Healthcare System, Cleveland, OH, USA.

出版信息

Ther Adv Infect Dis. 2023 May 22;10:20499361231174289. doi: 10.1177/20499361231174289. eCollection 2023 Jan-Dec.

DOI:10.1177/20499361231174289
PMID:37234745
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10203853/
Abstract

BACKGROUND AND AIM

Donepezil is a front-line treatment for Alzheimer's disease. Donepezil treatment is associated with decreased risk of all-cause mortality. Specific protection is observed in pneumonia and cardiovascular disease. We hypothesized that donepezil treatment would improve mortality among Alzheimer's patients following infection with COVID-19. The objective of this study is to assess the influence of ongoing donepezil treatment on survival in Alzheimer's disease patients after polymerase chain reaction (PCR)-confirmed COVID-19 infection.

METHODS

This is a retrospective cohort study. We conducted a national survey of Veterans with Alzheimer's disease to assess the influence of ongoing donepezil treatment on survival in Alzheimer's disease patients after PCR-confirmed COVID-19 infection. We assessed all-cause 30-day mortality stratified by COVID-19 infection and donepezil use, estimating odds ratios using multivariate logistic regression.

RESULTS

Among people with Alzheimer's disease and COVID-19, all-cause 30-day mortality was 29% (47/163) for people taking donepezil compared with 38% (159/419) for those who were not. Among people with Alzheimer's disease without COVID-19, all-cause 30-day mortality was 5% (189/4189) for people taking donepezil compared with 7% (712/10,241) for those who were not. Adjusting for covariates, the decrease in mortality associated with donepezil did not differ between people with and without COVID-19 (interaction  = 0.710).

CONCLUSION

The known survival benefits of donepezil were retained but not found to be specific to COVID-19 among people with Alzheimer's disease.

摘要

背景与目的

多奈哌齐是治疗阿尔茨海默病的一线药物。多奈哌齐治疗与全因死亡率降低相关。在肺炎和心血管疾病方面观察到了特异性保护作用。我们假设多奈哌齐治疗可降低阿尔茨海默病患者感染新型冠状病毒肺炎(COVID-19)后的死亡率。本研究的目的是评估在聚合酶链反应(PCR)确诊COVID-19感染后,持续使用多奈哌齐治疗对阿尔茨海默病患者生存的影响。

方法

这是一项回顾性队列研究。我们对患有阿尔茨海默病的退伍军人进行了全国性调查,以评估在PCR确诊COVID-19感染后,持续使用多奈哌齐治疗对阿尔茨海默病患者生存的影响。我们评估了按COVID-19感染情况和多奈哌齐使用情况分层的全因30天死亡率,使用多变量逻辑回归估计比值比。

结果

在患有阿尔茨海默病和COVID-19的人群中,服用多奈哌齐的患者全因30天死亡率为29%(47/163),未服用者为38%(159/419)。在未感染COVID-19的阿尔茨海默病患者中,服用多奈哌齐的患者全因30天死亡率为5%(189/4189),未服用者为7%(712/10241)。校正协变量后,服用多奈哌齐相关的死亡率降低在感染COVID-19和未感染COVID-19的人群中无差异(交互作用=0.710)。

结论

多奈哌齐已知的生存益处依然存在,但在患有阿尔茨海默病的人群中未发现其对COVID-19具有特异性。