Intertwined depressive and cognitive trajectories and the risk of dementia and death in older adults: a competing risk analysis

IF 5.3 3区 医学 Q1 PSYCHIATRY General Psychiatry Pub Date : 2024-04-01 DOI:10.1136/gpsych-2023-101156
Ziyang Ren, Lirong Nie, Yushan Du, Jufen Liu
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Abstract

Background Depressive symptoms and cognitive impairment often interact, rendering their associations controversial. To date, their joint trajectories and associations with dementia and death remain underexplored. Aims To explore the interactions between depressive symptoms and cognitive function, their developmental trajectories and the associations with all-cause dementia, Alzheimer’s disease (AD) and all-cause death in older adults. Methods Data were from the Health and Retirement Study. Depressive symptoms and cognitive function were measured using the 8-item Centre for Epidemiologic Studies Depression Scale and the Telephone Interview of Cognitive Status, respectively. All-cause dementia and AD were defined by self-reported or proxy-reported physician diagnoses. All-cause death was determined by interviews. The restricted cubic spline, group-based trajectory modelling and subdistribution hazard regression were used. Results Significant interactions between depressive symptoms and cognitive function in 2010 in their association with new-onset all-cause dementia and AD from 2010 to 2020 were found, especially in women (p for interaction <0.05). Independent trajectory analysis showed that emerging or high (vs no) depressive trajectories and poor or rapidly decreased cognitive trajectories (vs very good) from 1996 to 2010 were at significantly higher risk of subsequent all-cause dementia, AD and all-cause death. 15 joint trajectories of depressive symptoms and cognitive function from 1996 to 2010 were determined, where rapidly decreased cognitive function was more common in those with no depressive symptoms. Compared with older adults with the trajectory of no depressive symptoms and very good cognitive function, those with the trajectory of no depressive symptoms but rapidly decreased cognitive function were much more likely to develop new-onset all-cause dementia and death, with subdistribution hazard ratios (95% confidence intervals) of 4.47 (2.99 to 6.67) and 1.84 (1.43 to 2.36), especially in women. Conclusions To effectively mitigate the risk of dementia and death, it is crucial to acknowledge the importance of preventing cognitive decline in older adults without depressive symptoms, particularly in women. Data are available upon reasonable request.
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相互交织的抑郁和认知轨迹与老年人患痴呆症和死亡的风险:竞争风险分析
背景 抑郁症状和认知障碍常常相互影响,因此它们之间的关联颇具争议。迄今为止,它们的共同轨迹以及与痴呆症和死亡的关系仍未得到充分探讨。目的 探讨抑郁症状与认知功能之间的相互作用、其发展轨迹以及与老年人全因痴呆症、阿尔茨海默病(AD)和全因死亡的关联。方法 数据来自健康与退休研究。抑郁症状和认知功能分别使用 8 项流行病学研究中心抑郁量表和认知状况电话访谈进行测量。全因痴呆症和注意力缺失症是根据自我报告或代理报告的医生诊断确定的。全因死亡由访谈确定。研究中使用了限制性三次样条曲线、基于群体的轨迹模型和子分布危险回归。结果 2010 年的抑郁症状和认知功能与 2010 年至 2020 年新发全因痴呆症和注意力缺失症之间存在显著的交互作用,尤其是在女性中(交互作用的 p <0.05)。独立轨迹分析表明,1996 年至 2010 年期间出现抑郁轨迹或抑郁程度高(vs 无)、认知轨迹差或认知功能迅速下降(vs 非常好)的人,随后罹患全因痴呆症、注意力缺失症和全因死亡的风险明显更高。研究人员确定了 1996 年至 2010 年期间抑郁症状和认知功能的 15 个共同轨迹,其中认知功能迅速下降在无抑郁症状的人群中更为常见。与没有抑郁症状且认知功能非常好的老年人相比,没有抑郁症状但认知功能迅速下降的老年人更容易患上新发全因痴呆症和死亡,其次分布危险比(95% 置信区间)分别为 4.47(2.99 至 6.67)和 1.84(1.43 至 2.36),尤其是女性。结论 为有效降低痴呆症和死亡风险,必须认识到预防无抑郁症状的老年人(尤其是女性)认知能力下降的重要性。如有合理要求,可提供相关数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
General Psychiatry
General Psychiatry 医学-精神病学
CiteScore
21.90
自引率
2.50%
发文量
848
期刊介绍: General Psychiatry (GPSYCH), an open-access journal established in 1959, has been a pioneer in disseminating leading psychiatry research. Addressing a global audience of psychiatrists and mental health professionals, the journal covers diverse topics and publishes original research, systematic reviews, meta-analyses, forums on topical issues, case reports, research methods in psychiatry, and a distinctive section on 'Biostatistics in Psychiatry'. The scope includes original articles on basic research, clinical research, community-based studies, and ecological studies, encompassing a broad spectrum of psychiatric interests.
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