Late-Onset Depression but not Early-Onset Depression may Increase the Risk of All-Cause Mortality in Older Age: 8-Year Follow-Up of the Salus in Apulia Study

医学 萧条(经济学) 晚年抑郁症 危险系数 人口 比例危险模型 队列 人口学 老年学 共病 队列研究 糖尿病 内科学 精神科 认知 置信区间 内分泌学 宏观经济学 社会学 经济 环境卫生
作者
Madia Lozupone,Fabio Castellana,Rodolfo Sardone,Giuseppe Berardino,Anita Mollica,Roberta Zupo,Giovanni De Pergola,Chiara Griseta,Roberta Stallone,Maddalena La Montagna,Vittorio Dibello,Davide Seripa,Antonio Daniele,Mario Altamura,Vincenzo Solfrizzi,Antonello Bellomo,Francesco Panza
出处
期刊:Journal of the American Medical Directors Association [Elsevier BV]
卷期号:24 (5): 679-687 被引量:5
标识
DOI:10.1016/j.jamda.2022.12.005
摘要

Individuals with late-life depression (LLD) may have shorter survival, but there is a lack of findings in population-based settings about health-related outcomes of LLD and its subtypes: early-onset depression (EOD) and late-onset depression (LOD). We aimed to evaluate the risk of all-cause mortality of individuals with LLD and its subtypes in an older population-based cohort. Moreover, we investigated whether inflammatory, cognitive, genetic features and multimorbidity could modify the effect of this association.Longitudinal population-based study with 8-year follow-up.We analyzed data on a sample of 1479 participants, all aged >65 years, in the Salus in Apulia Study.LLD was diagnosed through DSM-IV-TR criteria and LOD and EOD according to the age of onset. Multimorbidity status was defined as the copresence of 2 or more chronic diseases.The overall prevalence of LLD in this older sample from Southern Italy was 10.2%, subdivided into 3.4% EOD and 6.8% LOD. In multivariable Cox models adjusted for age, gender, education, global cognition, apolipoprotein E ε4 allele, physical frailty, interleukin-6, and multimorbidity, LLD showed a greater risk of all-cause mortality. LOD differed from EOD regarding gender, education, cognitive dysfunctions, and diabetes mellitus. There was a significantly increased risk of all-cause mortality for participants with LOD (hazard ratio:1.99; 95% CI 1.33-2.97) in the time of observation between enrollment date and death date (7.31 ± 2.17 months).In older age, individuals with LOD but not with EOD had a significantly decreased survival, probably related to increased inflammation, multimorbidity, and cognitive impairments.
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