Mediating role of accelerated aging in the association between depression and mortality risk: findings from NHANES

IF 3.4 3区 医学 Q2 GERIATRICS & GERONTOLOGY Aging Clinical and Experimental Research Pub Date : 2024-10-05 DOI:10.1007/s40520-024-02854-z
Cheng Xu, Jia-ni Wang, Zhen Song, Han-yu Deng, Chong-chao Li
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Abstract

Objective

To investigate the association between depression, accelerated biological aging, and mortality risk, and to assess whether accelerated aging mediates the relationship between major depression and mortality risk.

Methods

A prospective cohort of 12,761 participants aged 20 years or older from the 2005–2010 cycle of the National Health and Nutrition Examination Survey (NHANES) was analyzed. Depression was assessed using the Patient Health Questionnaire-9 (PHQ-9), with scores of ≥ 10 indicating major depression. Accelerated biological aging was measured using phenotypic age acceleration (PhenoAgeAccel). Multivariable linear regression models and subgroup analyses were used to examine the association between depression and accelerated aging, while weighted multivariable Cox proportional hazards regression models and subgroup analyses assessed the impact of major depression on mortality risk. Mediation analysis was performed to assess whether PhenoAgeAccel mediated the relationship between major depression and mortality outcomes.

Results

Among the 12,761 adults, the weighted mean age was 46.6 years, with 48.8% being male, and 6.9% experiencing major depression. The results showed a positive association between major depression and PhenoAgeAccel (β: 0.61, 95% CI: 0.06–1.16). Over a median follow-up duration of 11.3 years (interquartile range: 9.9–13.1), major depression was associated with increased all-cause mortality (HR: 1.35, 95% CI: 1.13–1.62) and cardiovascular mortality (HR: 1.73, 95% CI: 1.18–2.54). However, the relationship with cancer mortality was not statistically significant after full adjustment for confounding factors. The mediation analysis further revealed that PhenoAgeAccel accounted for 10.32% and 5.12% of the associations between major depression and all-cause mortality, and cardiovascular mortality, respectively.

Conclusion

Depression is associated with accelerated aging and contributes to increased all-cause and cardiovascular mortality. Accelerated aging partially mediates the association between major depression and mortality risk. Our findings highlight the urgent need to incorporate mental health care into public health strategies to delay population aging and reduce mortality risk.

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加速衰老在抑郁与死亡风险之间的关联中的中介作用:NHANES 的研究结果。
摘要研究抑郁症、加速生物衰老与死亡风险之间的关系,并评估加速衰老是否会介导重度抑郁症与死亡风险之间的关系:方法:分析了美国国家健康与营养调查(NHANES)2005-2010 年周期中 12,761 名 20 岁及以上参与者的前瞻性队列。抑郁采用患者健康问卷-9(PHQ-9)进行评估,得分≥10分表示重度抑郁。生物衰老加速度采用表型年龄加速度(PhenoAgeAccel)进行测量。多变量线性回归模型和亚组分析用于研究抑郁症与加速衰老之间的关系,而加权多变量考克斯比例危险回归模型和亚组分析则用于评估重度抑郁症对死亡风险的影响。还进行了中介分析,以评估 PhenoAgeAccel 是否对重度抑郁症和死亡结果之间的关系起中介作用:在 12,761 名成年人中,加权平均年龄为 46.6 岁,48.8% 为男性,6.9% 患有重度抑郁症。结果显示,重度抑郁症与 PhenoAgeAccel 呈正相关(β:0.61,95% CI:0.06-1.16)。中位随访时间为 11.3 年(四分位间范围:9.9-13.1),重度抑郁症与全因死亡率(HR:1.35,95% CI:1.13-1.62)和心血管死亡率(HR:1.73,95% CI:1.18-2.54)的增加有关。然而,在对混杂因素进行全面调整后,与癌症死亡率的关系在统计学上并不显著。中介分析进一步显示,在重度抑郁症与全因死亡率和心血管死亡率之间的关系中,PhenoAgeAccel分别占10.32%和5.12%:抑郁症与加速衰老有关,并导致全因死亡率和心血管死亡率上升。加速衰老在一定程度上介导了重度抑郁症与死亡风险之间的关联。我们的研究结果突出表明,迫切需要将心理保健纳入公共卫生战略,以延缓人口老龄化并降低死亡风险。
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来源期刊
CiteScore
7.90
自引率
5.00%
发文量
283
审稿时长
1 months
期刊介绍: Aging clinical and experimental research offers a multidisciplinary forum on the progressing field of gerontology and geriatrics. The areas covered by the journal include: biogerontology, neurosciences, epidemiology, clinical gerontology and geriatric assessment, social, economical and behavioral gerontology. “Aging clinical and experimental research” appears bimonthly and publishes review articles, original papers and case reports.
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