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社会经济地位与痴呆和阿尔茨海默病发病风险的相关性受白细胞端粒长度的影响:一项基于人群的队列研究。

The associations of socioeconomic status with incident dementia and Alzheimer's disease are modified by leucocyte telomere length: a population-based cohort study.

机构信息

Healthy High Density Cities Lab, HKUrbanLab, The University of Hong Kong, Knowles Building, Pokfulam Road, Hong Kong Special Administrative Region, China.

Department of Urban Planning and Design, The University of Hong Kong, Knowles Building, Pokfulam Road, Hong Kong Special Administrative Region, China.

出版信息

Sci Rep. 2023 Apr 15;13(1):6163. doi: 10.1038/s41598-023-32974-x.

Abstract

Socio-economic status (SES) and biological aging are risk factors for dementia, including Alzheimer's disease, however, it is less clear if the associations with SES vary sufficiently across different biological age strata. We used data from 331,066 UK Biobank participants aged 38-73 with mean follow-up of 12 years to examine if associations between SES (assessed by educational attainment, employment status and household income) and dementia and Alzheimer's disease are modified by biological age (assessed by leucocyte telomere length: LTL). Diagnosis of events was ascertained through hospital admissions data. Cox regressions were used to estimate hazard ratios [HRs]. A consistent dose-response relationship was found, with participants in low SES and shorter LTL strata (double-exposed group) reporting 3.28 (95% confidence interval [CI] 2.57-4.20) and 3.44 (95% CI 2.35-5.04) times higher risks of incident dementia and Alzheimer's disease respectively, compared to those of high SES and longer LTL (least-exposed group). Of interest is a synergistic interaction between SES and LTL to increase risk of dementia (RERI 0.57, 95% CI 0.07-1.06) and Alzheimer's disease (RERI 0.79, 95% CI 0.02-1.56). Our findings that SES and biological age (LTL) are synergistic risk factors of dementia and Alzheimer's disease may suggest the need to target interventions among vulnerable sub-groups.

摘要

社会经济地位(SES)和生物年龄是痴呆症的风险因素,包括阿尔茨海默病,但 SES 与不同生物年龄层次之间的关联是否存在足够差异尚不清楚。我们使用了来自英国生物银行的 331066 名年龄在 38-73 岁的参与者的数据,这些参与者的平均随访时间为 12 年,以研究 SES(通过受教育程度、就业状况和家庭收入来评估)和痴呆症与阿尔茨海默病之间的关联是否会因生物年龄(通过白细胞端粒长度来评估:LTL)而改变。通过住院记录数据来确定事件的诊断。使用 Cox 回归来估计风险比(HR)。研究发现,SES 和 LTL 均较低的参与者(双重暴露组)的痴呆症和阿尔茨海默病的发病风险分别比 SES 和 LTL 均较高的参与者(最低暴露组)高 3.28(95%置信区间 [CI] 2.57-4.20)和 3.44(95% CI 2.35-5.04)倍。有趣的是,SES 和 LTL 之间存在协同交互作用,增加了痴呆症的发病风险(RERI 0.57,95% CI 0.07-1.06)和阿尔茨海默病的发病风险(RERI 0.79,95% CI 0.02-1.56)。我们的研究结果表明,SES 和生物年龄(LTL)是痴呆症和阿尔茨海默病的协同风险因素,这可能表明需要针对脆弱亚群进行干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a633/10105714/35758be0d88c/41598_2023_32974_Fig1_HTML.jpg

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