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澳大利亚原住民的痴呆症发病率、基因型与认知衰退风险因素:一项纵向队列研究。

Dementia Incidence, Genotype, and Risk Factors for Cognitive Decline in Aboriginal Australians: A Longitudinal Cohort Study.

作者信息

Lavrencic Louise M, Delbaere Kim, Broe Gerald A, Daylight Gail, Draper Brian, Cumming Robert G, Garvey Gail, Allan Wendy, Hill Thi Yen, Lasschuit Danielle, Schofield Peter R, Radford Kylie

机构信息

From Neuroscience Research Australia (L.M.L., K.D., G.A.B., G.D., W.A., T.Y.H., D.L., P.R.S., K.R.), Randwick; University of New South Wales (L.M.L., K.D., G.A.B., B.D., P.R.S., K.R.); Ageing Futures Institute (L.M.L., K.D., G.A.B., K.R.), University of New South Wales, Sydney; Prince of Wales Hospital (B.D., T.Y.H., D.L.), Randwick; School of Public Health (R.G.C.), University of Sydney, Camperdown, NSW; and Menzies School of Health Research (G.G.), Brisbane, QLD, Australia.

出版信息

Neurology. 2022 Mar 15;98(11):e1124-e1136. doi: 10.1212/WNL.0000000000013295. Epub 2022 Feb 9.

Abstract

BACKGROUND AND OBJECTIVES

Aboriginal Australians are disproportionately affected by dementia, with incidence in remote populations approximately double that of non-Indigenous populations. This study aimed to identify dementia incidence and risk factors in Aboriginal Australians residing in urban areas, which are currently unknown.

METHODS

A population-based cohort of Aboriginal Australians ≥60 years of age was assessed at baseline and 6-year follow-up. Life-course risk factors (baseline) were examined for incident dementia or mild cognitive impairment (MCI) through logistic regression analyses; adjustments were made for age. genotyping was available for 86 people.

RESULTS

Data were included from 155 participants 60 to 86 years of age (mean 65.70 years, SD 5.65 years; 59 male). There were 16 incident dementia cases (age-standardized rate 35.97/1,000 person-years, 95% confidence interval [CI] 18.34-53.60) and 36 combined incident MCI and dementia cases. Older age (odds ratio [OR] 2.29, 95% CI 1.42-3.70), male sex (OR 4.14, 95% CI 1.60-10.77), unskilled work history (OR 5.09, 95% CI 1.95-13.26), polypharmacy (OR 3.11, 95% CI 1.17-8.28), and past smoking (OR 0.24, 95% CI 0.08-0.75) were associated with incident MCI/dementia in the final model. ε4 allele frequency was 24%; heterozygous or homozygous ε4 was associated with incident MCI/dementia (bivariate OR 3.96, 95% CI 1.25-12.50).

DISCUSSION

These findings provide evidence for higher dementia incidence in Aboriginal Australians from urban areas, where the majority of Aboriginal people reside. This study also sheds light on sociodemographic, health, and genetic factors associated with incident MCI/dementia at older ages in this population, which is critical for targeted prevention strategies.

摘要

背景与目的

澳大利亚原住民受痴呆症影响的比例过高,偏远地区的发病率约为非原住民的两倍。本研究旨在确定居住在城市地区的澳大利亚原住民的痴呆症发病率及风险因素,目前这些情况尚不清楚。

方法

对一个以≥60岁的澳大利亚原住民为基础的队列进行了基线评估和6年随访。通过逻辑回归分析检查了痴呆症或轻度认知障碍(MCI)的发病风险因素(基线);对年龄进行了调整。86人可进行基因分型。

结果

纳入了155名60至86岁的参与者的数据(平均65.70岁,标准差5.65岁;59名男性)。有16例痴呆症发病病例(年龄标准化发病率为35.97/1000人年,95%置信区间[CI]为18.34 - 53.60)以及36例MCI和痴呆症合并发病病例。在最终模型中,年龄较大(比值比[OR]为2.29,95% CI为1.42 - 3.70)、男性(OR为4.14,95% CI为1.60 - 10.77)、无技能工作经历(OR为5.09,95% CI为1.95 - 13.26)、多种药物治疗(OR为3.11,95% CI为1.17 - 8.28)以及既往吸烟(OR为0.24,95% CI为0.08 - 0.75)与MCI/痴呆症发病相关。ε4等位基因频率为24%;杂合或纯合ε4与MCI/痴呆症发病相关(二元OR为3.96,95% CI为1.25 - 12.50)。

讨论

这些发现为居住在城市地区(大多数原住民居住于此)的澳大利亚原住民中痴呆症发病率较高提供了证据。本研究还揭示了该人群中与老年MCI/痴呆症发病相关的社会人口学、健康和遗传因素,这对于制定有针对性的预防策略至关重要。

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