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阿尔茨海默病与唐氏综合征患者预期寿命的关联。

Association of Alzheimer Disease With Life Expectancy in People With Down Syndrome.

机构信息

Sant Pau Memory Unit, Department of Neurology, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain.

Center of Biomedical Investigation Network for Neurodegenerative Diseases, Madrid, Spain.

出版信息

JAMA Netw Open. 2022 May 2;5(5):e2212910. doi: 10.1001/jamanetworkopen.2022.12910.

Abstract

IMPORTANCE

People with Down syndrome have a high risk of developing Alzheimer disease dementia. However, penetrance and age at onset are considered variable, and the association of this disease with life expectancy remains unclear because of underreporting in death certificates.

OBJECTIVE

To assess whether the variability in symptom onset of Alzheimer disease in Down syndrome is similar to autosomal dominant Alzheimer disease and to assess its association with mortality.

DESIGN, SETTING, AND PARTICIPANTS: This study combines a meta-analysis with the assessment of mortality data from US death certificates (n = 77 347 case records with a International Classification of Diseases code for Down syndrome between 1968 to 2019; 37 900 [49%] female) and from a longitudinal cohort study (n = 889 individuals; 46% female; 3.2 [2.1] years of follow-up) from the Down Alzheimer Barcelona Neuroimaging Initiative (DABNI).

MAIN OUTCOMES AND MEASURES

A meta-analysis was conducted to investigate the age at onset, age at death, and duration of Alzheimer disease dementia in Down syndrome. PubMed/Medline, Embase, Web of Science, and CINAHL were searched for research reports, and OpenGray was used for gray literature. Studies with data about the age at onset or diagnosis, age at death, and disease duration were included. Pooled estimates with corresponding 95% CIs were calculated using random-effects meta-analysis. The variability in disease onset was compared with that of autosomal dominant Alzheimer disease. Based on these estimates, a hypothetical distribution of age at death was constructed, assuming fully penetrant Alzheimer disease. These results were compared with real-world mortality data.

RESULTS

In this meta-analysis, the estimate of age at onset was 53.8 years (95% CI, 53.1-54.5 years; n = 2695); the estimate of age at death, 58.4 years (95% CI, 57.2-59.7 years; n = 324); and the estimate of disease duration, 4.6 years (95% CI, 3.7-5.5 years; n = 226). Coefficients of variation and 95% prediction intervals of age at onset were comparable with those reported in autosomal dominant Alzheimer disease. US mortality data revealed an increase in life expectancy in Down syndrome (median [IQR], 1 [0.3-16] years in 1968 to 57 [49-61] years in 2019), but with clear ceiling effects in the highest percentiles of age at death in the last decades (90th percentile: 1990, age 63 years; 2019, age 65 years). The mortality data matched the limits projected by a distribution assuming fully penetrant Alzheimer disease in up to 80% of deaths (corresponding to the highest percentiles). This contrasts with dementia mentioned in 30% of death certificates but is in agreement with the mortality data in DABNI (78.9%). Important racial disparities persisted in 2019, being more pronounced in the lower percentiles (10th percentile: Black individuals, 1 year; White individuals, 30 years) than in the higher percentiles (90th percentile: Black individuals, 64 years; White individuals, 66 years).

CONCLUSIONS AND RELEVANCE

These findings suggest that the mortality data and the consistent age at onset were compatible with fully penetrant Alzheimer disease. Lifespan in persons with Down syndrome will not increase until disease-modifying treatments for Alzheimer disease are available.

摘要

重要性

唐氏综合征患者患阿尔茨海默病痴呆的风险很高。然而,鉴于该病与预期寿命的关联因死亡证明中漏报而尚不明确,因此认为该病的外显率和发病年龄存在差异。

目的

评估唐氏综合征中阿尔茨海默病的发病变异性是否与常染色体显性阿尔茨海默病相似,并评估其与死亡率的关系。

设计、设置和参与者:本研究结合荟萃分析和美国死亡证明的死亡率数据评估(1968 年至 2019 年期间国际疾病分类第 7 版唐氏综合征编码的 77347 例病例记录;37900[49%]名女性)和来自唐氏阿尔茨海默病巴塞罗那神经影像学倡议(DABNI)的纵向队列研究(889 名个体;46%为女性;3.2[2.1]年随访)。

主要结局和测量

进行荟萃分析以调查唐氏综合征中阿尔茨海默病的发病年龄、死亡年龄和疾病持续时间。通过 PubMed/Medline、Embase、Web of Science 和 CINAHL 搜索研究报告,并使用 OpenGray 搜索灰色文献。纳入了包含发病年龄或诊断年龄、死亡年龄和疾病持续时间数据的研究。使用随机效应荟萃分析计算汇总估计值及其相应的 95%置信区间。比较了疾病发病的变异性与常染色体显性阿尔茨海默病的变异性。基于这些估计值,假设完全外显的阿尔茨海默病,构建了一个假设的死亡年龄分布。将这些结果与实际的死亡率数据进行比较。

结果

在这项荟萃分析中,发病年龄的估计值为 53.8 岁(95%置信区间,53.1-54.5 岁;n=2695);死亡年龄的估计值为 58.4 岁(95%置信区间,57.2-59.7 岁;n=324);疾病持续时间的估计值为 4.6 年(95%置信区间,3.7-5.5 年;n=226)。发病年龄的变异系数和 95%预测区间与常染色体显性阿尔茨海默病报道的相似。美国死亡率数据显示唐氏综合征患者的预期寿命有所增加(中位数[IQR],1968 年为 1[0.3-16]岁,2019 年为 57[49-61]岁),但在过去几十年的最高死亡年龄百分位中存在明显的上限效应(第 90 百分位:1990 年,年龄 63 岁;2019 年,年龄 65 岁)。死亡率数据与假设完全外显的阿尔茨海默病的分布所预测的极限相匹配(最高百分位)。这与 30%的死亡证明中提到的痴呆症形成对比,但与 DABNI 的死亡率数据一致(78.9%)。2019 年仍存在严重的种族差异,在较低的百分位(第 10 百分位:黑人,1 年;白人,30 年)比在较高的百分位(第 90 百分位:黑人,64 年;白人,66 年)更为明显。

结论和相关性

这些发现表明,死亡率数据和一致的发病年龄与完全外显的阿尔茨海默病一致。在阿尔茨海默病的疾病修饰治疗可用之前,唐氏综合征患者的预期寿命不会增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3818/9127560/6eea7e7c65a3/jamanetwopen-e2212910-g001.jpg

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