Kaarina Korhonen, Lasse Tarkiainen, Taina Leinonen, Elina Einiö, Pekka Martikainen
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A history of depression was ascertained from the national hospital register in the period 15-30 years prior to dementia follow-up. We used conventional and sibling fixed-effects Cox regression models to analyse the association between a history of depression, sociodemographic factors and dementia.</p><p><strong>Results: </strong>A history of depression was related to an adjusted hazard ratio of 1.27 (95% CI 1.23-1.31) for dementia in the conventional Cox model and of 1.55 (95% CI 1.09-2.20) in the sibling fixed-effects model. Depression was related to an elevated dementia risk similarly across all levels of education (test for interaction, <i>P</i> = 0.84), but the association was weaker for the widowed than for the married (<i>P</i> = 0.003), and stronger for men than women (<i>P</i> = 0.006). The excess risk among men attenuated following covariate adjustment (<i>P</i> = 0.10).</p><p><strong>Discussion: </strong>This study shows that a history of depression is consistently associated with later-life dementia risk. 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引用次数: 4
摘要
背景:抑郁症与痴呆风险增加有关,但从长期来看,这种关联的性质仍未得到解决,社会人口因素的作用主要未被探索。目的:评估临床抑郁史是否与老年痴呆相关,控制观察到的社会人口学因素和兄弟姐妹共有的未观察到的因素,并检验性别、教育水平和婚姻状况是否改变了这种关联。方法:我们对2001年至2018年期间年龄在65岁及以上的1 616321人进行了一项全国队列研究,使用行政医疗数据。在痴呆症随访前的15-30年间,从国家医院登记中确定了抑郁症病史。我们使用传统的和兄弟姐妹固定效应的Cox回归模型来分析抑郁史、社会人口因素和痴呆之间的关系。结果:在传统Cox模型中,抑郁史与痴呆的校正风险比为1.27 (95% CI 1.23-1.31),在兄弟姐妹固定效应模型中为1.55 (95% CI 1.09-2.20)。在所有教育水平中,抑郁与痴呆风险升高的关系相似(相互作用测试,P = 0.84),但丧偶者的相关性弱于已婚者(P = 0.003),而男性的相关性强于女性(P = 0.006)。协变量调整后,男性的过度风险降低(P = 0.10)。讨论:这项研究表明,抑郁史与晚年痴呆风险始终相关。研究结果支持了抑郁是痴呆的病因危险因素的假设。
Association between a history of clinical depression and dementia, and the role of sociodemographic factors: population-based cohort study.
Background: Depression is associated with an increased dementia risk, but the nature of the association in the long-term remains unresolved, and the role of sociodemographic factors mainly unexplored.
Aims: To assess whether a history of clinical depression is associated with dementia in later life, controlling for observed sociodemographic factors and unobserved factors shared by siblings, and to test whether gender, educational level and marital status modify the association.
Method: We conducted a national cohort study of 1 616 321 individuals aged 65 years or older between 2001 and 2018 using administrative healthcare data. A history of depression was ascertained from the national hospital register in the period 15-30 years prior to dementia follow-up. We used conventional and sibling fixed-effects Cox regression models to analyse the association between a history of depression, sociodemographic factors and dementia.
Results: A history of depression was related to an adjusted hazard ratio of 1.27 (95% CI 1.23-1.31) for dementia in the conventional Cox model and of 1.55 (95% CI 1.09-2.20) in the sibling fixed-effects model. Depression was related to an elevated dementia risk similarly across all levels of education (test for interaction, P = 0.84), but the association was weaker for the widowed than for the married (P = 0.003), and stronger for men than women (P = 0.006). The excess risk among men attenuated following covariate adjustment (P = 0.10).
Discussion: This study shows that a history of depression is consistently associated with later-life dementia risk. The results support the hypothesis that depression is an aetiological risk factor for dementia.