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轻度认知障碍、痴呆和死亡率的风险因素:悉尼记忆与衰老研究

Risk Factors for Mild Cognitive Impairment, Dementia and Mortality: The Sydney Memory and Ageing Study.

作者信息

Lipnicki Darren M, Crawford John, Kochan Nicole A, Trollor Julian N, Draper Brian, Reppermund Simone, Maston Kate, Mather Karen A, Brodaty Henry, Sachdev Perminder S

机构信息

CHeBA (Centre for Healthy Brain Ageing), School of Psychiatry, University of New South Wales, Sydney, NSW, Australia.

CHeBA (Centre for Healthy Brain Ageing), School of Psychiatry, University of New South Wales, Sydney, NSW, Australia; Neuropsychiatric Institute, Prince of Wales Hospital, Sydney, NSW, Australia.

出版信息

J Am Med Dir Assoc. 2017 May 1;18(5):388-395. doi: 10.1016/j.jamda.2016.10.014. Epub 2016 Dec 31.

Abstract

BACKGROUND

The nature and commonality of late-life risk factors for mild cognitive impairment (MCI), dementia, and mortality remain unclear. Our aim was to investigate potential risk factors, simultaneously in a single cohort including many individuals initially with normal cognition and followed for 6 years.

METHODS

We classified 873 community-dwelling individuals (70-90 years old and without dementia at baseline) from the Sydney Memory and Ageing Study as cognitively normal (CN), having MCI or dementia, or deceased 6 years after baseline. Associations with baseline demographic, lifestyle, health, and medical factors were investigated, including apolipoprotein (APOE) genotype, MCI at baseline, and reversion from MCI to CN within 2 years of baseline.

RESULTS

Eighty-three (9.5%) participants developed dementia and 114 (13%) died within 6 years; nearly 33% had MCI at baseline, of whom 28% reverted to CN within 2 years. A core set of baseline factors was associated with MCI and dementia at 6 years, including older age (per year: odds ratios and 95% confidence intervals = 1.08, 1.01-1.14 for MCI; 1.19, 1.09-1.31 for dementia), MCI at baseline (5.75, 3.49-9.49; 8.23, 3.93-17.22), poorer smelling ability (per extra test point: 0.89, 0.79-1.02; 0.80, 0.68-0.94), slower walking speed (per second: 1.12, 1.00-1.25; 1.21, 1.05-1.39), and being an APOE ε4 carrier (1.84, 1.07-3.14; 3.63, 1.68-7.82). All except APOE genotype were also associated with mortality (age: 1.11, 1.03-1.20; MCI: 3.87, 1.97-7.59; smelling ability: 0.83, 0.70-0.97; walking speed: 1.18, 1.03-1.34). Compared with stable CN participants, individuals reverting from MCI to CN after 2 years were at greater risk of future MCI (3.06, 1.63-5.72). Those who reverted exhibited some different associations between baseline risk factors and 6-year outcomes than individuals with stable MCI.

CONCLUSION

A core group of late-life risk factors indicative of physical and mental frailty are associated with each of dementia, MCI, and mortality after 6 years. Tests for slower walking speed and poorer smelling ability may help screen for cognitive decline. Individuals with normal cognition are at greater risk of future cognitive impairment if they have a history of MCI.

摘要

背景

轻度认知障碍(MCI)、痴呆和死亡率的晚年风险因素的性质和共性仍不明确。我们的目的是在一个包括许多初始认知正常并随访6年的单一队列中同时调查潜在风险因素。

方法

我们将悉尼记忆与衰老研究中的873名社区居住个体(70 - 90岁,基线时无痴呆)分类为认知正常(CN)、患有MCI或痴呆,或在基线后6年死亡。研究了与基线人口统计学、生活方式、健康和医学因素的关联,包括载脂蛋白(APOE)基因型、基线时的MCI以及基线后2年内从MCI恢复到CN的情况。

结果

83名(9.5%)参与者在6年内发展为痴呆,114名(13%)死亡;近33%在基线时患有MCI,其中28%在2年内恢复为CN。一组核心的基线因素与6年后的MCI和痴呆相关,包括年龄较大(每年:MCI的比值比和95%置信区间 = 1.08,1.01 - 1.14;痴呆的比值比和95%置信区间 = 1.19,1.09 - 1.31)、基线时的MCI(5.75,3.49 - 9.49;8.23,3.93 - 17.22)、嗅觉能力较差(每个额外测试点:0.89,0.79 - 1.02;0.80,0.68 - 0.94)、步行速度较慢(每秒:1.12,1.00 - 1.25;1.21,1.05 - 1.39)以及是APOE ε4携带者(1.84,1.07 - 3.14;3.63,1.68 - 7.82)。除APOE基因型外,所有因素也与死亡率相关(年龄:1.11,1.03 - 1.20;MCI:3.87,1.97 - 7.59;嗅觉能力:0.83,0.70 - 0.97;步行速度:1.18,1.03 - 1.34)。与稳定的CN参与者相比,2年后从MCI恢复到CN的个体未来发生MCI的风险更高(3.06,1.63 - 5.72)。恢复者在基线风险因素与6年结局之间表现出一些与稳定MCI个体不同的关联。

结论

一组表明身体和精神虚弱的晚年核心风险因素与6年后的痴呆、MCI和死亡率均相关。步行速度较慢和嗅觉能力较差的测试可能有助于筛查认知衰退。有MCI病史的认知正常个体未来发生认知障碍的风险更高。

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