Suppr超能文献

阿尔茨海默病的疾病严重程度和死亡率:使用美国国家阿尔茨海默病协调中心统一数据集进行的分析。

Disease severity and mortality in Alzheimer's disease: an analysis using the U.S. National Alzheimer's Coordinating Center Uniform Data Set.

机构信息

F. Hoffmann-La Roche Ltd, Basel, Switzerland.

Genesis Research, Hoboken, NJ, USA.

出版信息

BMC Neurol. 2023 Aug 14;23(1):302. doi: 10.1186/s12883-023-03353-w.

Abstract

BACKGROUND

Evidence on the relative risk of death across all stages of Alzheimer's disease (AD) is lacking but greatly needed for the evaluation of new interventions. We used data from the Uniform Data Set (UDS) of the National Alzheimer's Coordinating Center (NACC) to assess the expected survival of a person progressing to a particular stage of AD and the relative risk of death for a person in a particular stage of AD compared with cognitively normal (CN) people.

METHODS

This was a retrospective observational cohort study of mortality and its determinants in participants with incident mild cognitive impairment (MCI) due to AD or AD dementia compared with CN participants. Overall survival and hazard ratios of all-cause mortality in participants ≥ 50 years of age with clinically assessed or diagnosed MCI due to AD, or mild, moderate, or severe AD dementia, confirmed by Clinical Dementia Rating scores, versus CN participants were estimated, using NACC UDS data. Participants were followed until death, censoring, or until information to determine disease stage was missing.

RESULTS

Aged between 50 and 104 years, 12,414 participants met the eligibility criteria for the study. Participants progressing to MCI due to AD or AD dementia survived a median of 3-12 years, with higher mortality observed in more severe stages. Risk of death increased with the severity of AD dementia, with the increase significantly higher at younger ages. Participants with MCI due to AD and CN participants had a similar risk of death after controlling for confounding factors.

CONCLUSIONS

Relative all-cause mortality risk increases with AD severity, more so at younger ages. Mortality does not seem to be higher for those remaining in MCI due to AD. Findings might imply potential benefit of lower mortality if preventing or delaying the progression of AD is successful, and importantly, this potential benefit might be greater in relatively younger people. Future research should replicate our study in other samples more representative of the general US population as well as other populations around the world.

摘要

背景

缺乏针对阿尔茨海默病(AD)所有阶段的死亡相对风险的证据,但这对于评估新干预措施非常重要。我们使用国家阿尔茨海默病协调中心(NACC)的统一数据集(UDS)的数据,评估进展到特定 AD 阶段的个体的预期存活时间,以及特定 AD 阶段的个体与认知正常(CN)个体相比的死亡相对风险。

方法

这是一项回顾性观察性队列研究,比较了因 AD 导致的轻度认知障碍(MCI)或 AD 痴呆的参与者与 CN 参与者的死亡率及其决定因素。使用 NACC UDS 数据,对年龄在 50 岁及以上、临床评估或诊断为 AD 所致 MCI、或轻度、中度或重度 AD 痴呆(通过临床痴呆评定量表评分证实)且符合纳入标准的参与者,评估其全因死亡率的总生存率和风险比,CN 参与者作为对照。参与者随访至死亡、删失或确定疾病阶段的信息缺失。

结果

年龄在 50 岁至 104 岁之间,有 12414 名参与者符合研究标准。进展为 AD 或 AD 痴呆所致 MCI 的参与者中位存活时间为 3-12 年,随着疾病严重程度的增加,死亡率更高。AD 痴呆的严重程度与死亡风险增加相关,在较年轻的年龄组中,这种增加更为显著。在控制混杂因素后,AD 所致 MCI 参与者和 CN 参与者的死亡风险相似。

结论

AD 严重程度与全因死亡率的相对风险增加相关,在较年轻的年龄组中更为显著。对于那些仍处于 AD 所致 MCI 的患者,死亡率似乎没有更高。如果成功预防或延缓 AD 的进展,这可能意味着死亡率降低的潜在获益,而且重要的是,这种潜在获益在相对较年轻的人群中可能更大。未来的研究应该在更具代表性的美国普通人群样本和世界各地的其他人群样本中复制我们的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0e1/10424331/6da95472d7ac/12883_2023_3353_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验