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本文引用的文献

1
Amyloid-Beta Solubility in the Treatment of Alzheimer's Disease.β淀粉样蛋白的溶解性在阿尔茨海默病治疗中的作用
N Engl J Med. 2018 Jan 25;378(4):391-392. doi: 10.1056/NEJMe1714638.
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Trial of Solanezumab for Mild Dementia Due to Alzheimer's Disease.用于阿尔茨海默病所致轻度痴呆的 Solanezumab 试验。
N Engl J Med. 2018 Jan 25;378(4):321-330. doi: 10.1056/NEJMoa1705971.
3
Practice guideline update summary: Mild cognitive impairment: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology.实践指南更新概要:轻度认知障碍:美国神经病学学会指南制定、传播和实施小组委员会的报告。
Neurology. 2018 Jan 16;90(3):126-135. doi: 10.1212/WNL.0000000000004826. Epub 2017 Dec 27.
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Continuing Progress in Alzheimer's Disease Trials: Cause for Optimism.阿尔茨海默病试验的持续进展:乐观的理由。
J Prev Alzheimers Dis. 2017;4(4):211-212. doi: 10.14283/jpad.2017.34.
5
Consensus guidelines for lumbar puncture in patients with neurological diseases.神经疾病患者腰椎穿刺的共识指南。
Alzheimers Dement (Amst). 2017 May 18;8:111-126. doi: 10.1016/j.dadm.2017.04.007. eCollection 2017.
6
Comparison of CSF markers and semi-quantitative amyloid PET in Alzheimer's disease diagnosis and in cognitive impairment prognosis using the ADNI-2 database.利用ADNI-2数据库比较脑脊液标志物和半定量淀粉样蛋白PET在阿尔茨海默病诊断及认知障碍预后中的应用
Alzheimers Res Ther. 2017 Apr 26;9(1):32. doi: 10.1186/s13195-017-0260-z.
7
Recommendations for cerebrospinal fluid Alzheimer's disease biomarkers in the diagnostic evaluation of mild cognitive impairment.阿尔茨海默病脑脊液生物标志物在轻度认知障碍诊断评估中的推荐意见。
Alzheimers Dement. 2017 Mar;13(3):285-295. doi: 10.1016/j.jalz.2016.09.009. Epub 2016 Oct 27.
8
CSF and blood biomarkers for the diagnosis of Alzheimer's disease: a systematic review and meta-analysis.脑脊液和血液生物标志物在阿尔茨海默病诊断中的应用:系统评价和荟萃分析。
Lancet Neurol. 2016 Jun;15(7):673-684. doi: 10.1016/S1474-4422(16)00070-3. Epub 2016 Apr 8.
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The Italian Dementia National Plan. Commentary.意大利国家痴呆症计划。评论
Ann Ist Super Sanita. 2015;51(4):261-4. doi: 10.4415/ANN_15_04_02.
10
Detailed comparison of amyloid PET and CSF biomarkers for identifying early Alzheimer disease.用于识别早期阿尔茨海默病的淀粉样蛋白PET和脑脊液生物标志物的详细比较。
Neurology. 2015 Oct 6;85(14):1240-9. doi: 10.1212/WNL.0000000000001991. Epub 2015 Sep 9.

评估六个欧洲国家医疗保健系统基础设施对阿尔茨海默病治疗的准备情况。

Assessing the Preparedness of the Health Care System Infrastructure in Six European Countries for an Alzheimer's Treatment.

作者信息

Hlavka Jakub P, Mattke Soeren, Liu Jodi L

出版信息

Rand Health Q. 2019 May 16;8(3):2. eCollection 2019 May.

PMID:31205802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6557037/
Abstract

No disease-modifying therapy is currently available for Alzheimer's disease, but therapies are in development, and one may become available in the near future. Based on results from early-stage clinical trials, therapeutic development has focused on the hypothesis that Alzheimer's dementia must be prevented rather than cured, because candidate treatments have not been able to reverse the course of dementia. Thus, current trials target patients with early-stage Alzheimer's disease. Were a therapy to become available, patients could undergo first screening for signs of early-stage memory loss or mild cognitive impairment (MCI), testing for the Alzheimer's disease pathology, and then treatment with the aim of halting or slowing progression to Alzheimer's dementia. An important health systems challenge will arise if this new treatment paradigm bears out in late-stage clinical trials. In the 28 European Union countries, we estimate that approximately 20 million individuals over age 55 have MCI, although most people have not been tested for disease pathology. Thus, when a therapy first becomes available, there would be a substantial number of existing (or prevalent) MCI patients who would require screening, diagnosis, and then treatment as quickly as possible to prevent the progression to full-blown Alzheimer's dementia. This research analyzes the preparedness of the health care systems in six European countries-France, Germany, Italy, Spain, Sweden, and the United Kingdom-to ensure timely diagnosis and treatment of patients if a disease-modifying therapy for Alzheimer's becomes available.

摘要

目前尚无针对阿尔茨海默病的疾病修饰疗法,但相关疗法正在研发中,且可能在不久的将来问世。基于早期临床试验结果,治疗研发聚焦于这样一种假设,即阿尔茨海默病性痴呆必须预防而非治愈,因为候选治疗方法无法逆转痴呆病程。因此,当前的试验针对早期阿尔茨海默病患者。如果有了一种疗法,患者可首先接受早期记忆丧失或轻度认知障碍(MCI)迹象的筛查,进行阿尔茨海默病病理学检测,然后接受治疗,目标是阻止或延缓向阿尔茨海默病性痴呆的进展。如果这种新的治疗模式在后期临床试验中得到验证,将会出现一个重要的卫生系统挑战。在欧盟28个国家,我们估计约有2000万55岁以上的人患有MCI,不过大多数人尚未接受疾病病理学检测。因此,当一种疗法首次可用时,将会有大量现有的(或普遍存在的)MCI患者需要尽快进行筛查、诊断,然后接受治疗,以防止发展为全面的阿尔茨海默病性痴呆。本研究分析了六个欧洲国家——法国、德国、意大利、西班牙、瑞典和英国——的医疗保健系统的准备情况,以便在有针对阿尔茨海默病的疾病修饰疗法可用时确保及时诊断和治疗患者。