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与向神经认知障碍和死亡过渡相关的社会经济不平等。

Socioeconomic inequalities linked to the transitioning to neurocognitive disorders and mortality.

机构信息

Department of Epidemiology and Public Health, University College London, 1-19 Torrington Place, London, WC1E 7HB, UK.

Department of Behavioural Science and Health, Institute of Epidemiology and Public Health, University College London, 1-19 Torrington Place, London, WC1E 7HB, UK.

出版信息

Sci Rep. 2024 Nov 1;14(1):24690. doi: 10.1038/s41598-024-74125-w.

Abstract

Research on socioeconomic position (SEP) and mild neurocognitive impairment, considered a transient state between normal cognitive function and dementia is limited. The purpose of this study was to determine the role of SEP in transitioning between different cognitive states and mortality risk. Using nationally representative English data and utilising a multistate model association between SEP and the risk of transitioning from no cognitive impairment (NOCI) to Cognitive impairment no dementia (CIND), dementia and death were investigated. The potential reverse transition from CIND to NOCI was also explored. The probabilities of transitioning between cognitive states and time spent in each state differed significantly between those with lower and higher levels of SEP. Higher wealth was associated with a reverse transition from CIND to NOCI [HR = 1.56, CI (1.42,1.72)]. Socioeconomic advantage might protect against the progression to the early stages of neurocognitive disorders (CIND) and facilitate the potential reversion from mild cognitive impairment to a healthy cognitive state in later life. Lower levels of education affect the risk of mortality after the onset of dementia.

摘要

社会经济地位(SEP)与轻度认知障碍的研究有限,后者被认为是正常认知功能与痴呆之间的短暂状态。本研究旨在确定 SEP 在不同认知状态之间转变和死亡风险中的作用。本研究使用具有全国代表性的英文数据,利用多状态模型,研究了 SEP 与从不认知障碍(NOCI)向认知障碍但非痴呆(CIND)、痴呆和死亡的风险之间的关联。还探讨了从 CIND 向 NOCI 的潜在反向转变。在认知状态之间转变的概率和在每个状态中花费的时间在 SEP 水平较低和较高的人群之间存在显著差异。较高的财富与从 CIND 向 NOCI 的反向转变相关[HR=1.56,CI(1.42,1.72)]。社会经济优势可能有助于预防向神经认知障碍(CIND)的早期阶段进展,并促进从中度认知障碍向晚年健康认知状态的潜在恢复。较低的教育水平会影响痴呆发生后的死亡率风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e694/11530460/cf980c4427f6/41598_2024_74125_Fig1_HTML.jpg

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