• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

晚年忧郁症:迟发性与早发性在临床表现、病程及痴呆风险方面的差异

Melancholia in later life: late and early onset differences in presentation, course, and dementia risk.

作者信息

Sachs-Ericsson Natalie, Moxley Jerad H, Corsentino Elizabeth, Rushing Nicole Collins, Sheffler Julia, Selby Edward A, Gotlib Ian, Steffens David C

机构信息

Department of Psychology, Florida State University, Tallahassee, FL, USA.

出版信息

Int J Geriatr Psychiatry. 2014 Sep;29(9):943-51. doi: 10.1002/gps.4083. Epub 2014 Feb 12.

DOI:10.1002/gps.4083
PMID:24677247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11886663/
Abstract

OBJECTIVES

Depression is a risk factor for cognitive decline and dementia. This risk may vary with age of onset and depression subtype. Late onset depression (LOD, 60 years and older) is associated with more cognitive decline, whereas early onset depression (EOD, before 60 years) is associated with more residual depressive symptoms. Potential differences may reflect divergent etiologies. These onset differences, however, have not been examined in the melancholic subtype of depression in older adults.

METHODS

Data were obtained from the Neurocognitive Outcomes of Depression in the Elderly study. Participants (N = 284, 73% EOD-melancholic (EOD-M) and 27% LOD-melancholic (LOD-M)) were followed up over 3 years. Factor analyses examined differences in baseline depressive symptoms. Hierarchical linear growth curve models examined changes in depressive symptoms (Montgomery-Asberg Depression Rating Scale) and cognition (mini mental state examination). An annual clinical review panel assigned diagnoses of dementia.

RESULTS

The LOD-M participants had more vegetative symptoms at baseline. LOD-M exhibited greater cognitive decline but fewer residual depressive symptoms than EOD-M. Among participants who remained in the study for at least 1 year, in uncontrolled analyses, a greater percentage of LOD-M compared with EOD-M developed dementia (23.0% vs. 7.8%). Whereas in logistic analyses, controlling for baseline demographics, age at onset remained a predictor of dementia, the odds ratio suggested that the effect was relatively small.

CONCLUSIONS

The EOD-M and LOD-M participants have a different presentation and course. LOD-M may represent a syndrome of neuropsychiatric deterioration with expression of both depressive symptoms and cognitive decline.

摘要

目的

抑郁症是认知功能下降和痴呆的一个风险因素。这种风险可能因发病年龄和抑郁亚型而异。晚发性抑郁症(LOD,60岁及以上)与更多的认知功能下降相关,而早发性抑郁症(EOD,60岁之前)与更多的残留抑郁症状相关。潜在差异可能反映了不同的病因。然而,这些发病差异尚未在老年抑郁症的 melancholic 亚型中进行研究。

方法

数据来自老年抑郁症的神经认知结局研究。对参与者(N = 284,73% 为早发性 melancholic 抑郁症(EOD-M),27% 为晚发性 melancholic 抑郁症(LOD-M))进行了3年的随访。因子分析检查了基线抑郁症状的差异。分层线性生长曲线模型检查了抑郁症状(蒙哥马利-阿斯伯格抑郁量表)和认知(简易精神状态检查)的变化。一个年度临床审查小组对痴呆进行诊断。

结果

LOD-M 参与者在基线时有更多的躯体症状。与 EOD-M 相比,LOD-M 表现出更大的认知功能下降,但残留抑郁症状更少。在至少参加研究1年的参与者中,在未进行控制的分析中,与 EOD-M 相比,LOD-M 发展为痴呆的比例更高(23.0% 对 7.8%)。而在逻辑分析中,在控制了基线人口统计学因素后,发病年龄仍然是痴呆的一个预测因素,优势比表明这种影响相对较小。

结论

EOD-M 和 LOD-M 参与者有不同的表现和病程。LOD-M 可能代表一种神经精神恶化综合征,既有抑郁症状的表现,又有认知功能下降。

相似文献

1
Melancholia in later life: late and early onset differences in presentation, course, and dementia risk.晚年忧郁症:迟发性与早发性在临床表现、病程及痴呆风险方面的差异
Int J Geriatr Psychiatry. 2014 Sep;29(9):943-51. doi: 10.1002/gps.4083. Epub 2014 Feb 12.
2
A longitudinal study of differences in late- and early-onset geriatric depression: depressive symptoms and psychosocial, cognitive, and neurological functioning.老年期抑郁晚发与早发患者的差异的纵向研究:抑郁症状及心理社会、认知和神经功能。
Aging Ment Health. 2013;17(1):1-11. doi: 10.1080/13607863.2012.717253. Epub 2012 Aug 30.
3
Comparison of cognitive function between early- and late-onset late-life depression in remission.比较早发性和晚发性缓解期老年期抑郁症患者的认知功能。
Psychiatry Res. 2020 Aug;290:113051. doi: 10.1016/j.psychres.2020.113051. Epub 2020 May 21.
4
Influence of gender and age on cognitive inhibition in late-onset depression: a case-control study.性别和年龄对晚发性抑郁症认知抑制的影响:病例对照研究。
Int J Geriatr Psychiatry. 2013 Nov;28(11):1125-30. doi: 10.1002/gps.3929. Epub 2013 Jan 10.
5
Depressive symptoms and cognitive decline in nondemented elderly women: a prospective study.非痴呆老年女性的抑郁症状与认知衰退:一项前瞻性研究。
Arch Gen Psychiatry. 1999 May;56(5):425-30. doi: 10.1001/archpsyc.56.5.425.
6
Cognitive and metabolic signatures of early and late-onset depression: A comparative study.早发性和晚发性抑郁症的认知与代谢特征:一项比较研究。
J Affect Disord. 2025 Jun 15;379:10-18. doi: 10.1016/j.jad.2025.02.081. Epub 2025 Feb 27.
7
Demographics, Symptoms, Psychotropic Use, and Caregiver Distress in Patients With Early vs Late Onset Dementia.早发性与晚发性痴呆患者的人口统计学、症状、精神药物使用和照料者困扰。
Am J Geriatr Psychiatry. 2024 Aug;32(8):944-954. doi: 10.1016/j.jagp.2024.03.009. Epub 2024 Mar 22.
8
Association of life events and psychosocial factors with early but not late onset depression in the elderly: implications for possible differences in aetiology.生活事件和心理社会因素与老年人早发性而非晚发性抑郁症的关联:对病因学可能差异的启示
Int J Geriatr Psychiatry. 2003 Jun;18(6):473-8. doi: 10.1002/gps.856.
9
Late-life depression and increased risk of dementia: a longitudinal cohort study.老年期抑郁症与痴呆风险增加:一项纵向队列研究。
Transl Psychiatry. 2021 Mar 2;11(1):147. doi: 10.1038/s41398-021-01269-y.
10
Association of age at depression onset with cognitive functioning in individuals with late-life depression and executive dysfunction.老年期抑郁症和执行功能障碍患者中抑郁症发病年龄与认知功能的关联。
Am J Geriatr Psychiatry. 2014 Dec;22(12):1633-41. doi: 10.1016/j.jagp.2014.02.006. Epub 2014 Feb 26.

引用本文的文献

1
Advances and Challenges in Depression Marker Research.抑郁症标志物研究的进展与挑战
Neuropsychiatr Dis Treat. 2025 Jul 31;21:1549-1567. doi: 10.2147/NDT.S527897. eCollection 2025.
2
Psilocybin for dementia prevention? The potential role of psilocybin to alter mechanisms associated with major depression and neurodegenerative diseases.色胺酮预防痴呆?色胺酮改变与重度抑郁症和神经退行性疾病相关机制的潜在作用。
Pharmacol Ther. 2024 Jun;258:108641. doi: 10.1016/j.pharmthera.2024.108641. Epub 2024 Apr 6.
3
The sociodemographic characteristics and clinical features of the late-life depression patients: results from the Beijing Anding Hospital mental health big data platform.老年期抑郁症患者的社会人口学特征和临床特征:来自北京安定医院精神卫生大数据平台的结果。
BMC Psychiatry. 2022 Nov 2;22(1):677. doi: 10.1186/s12888-022-04339-7.
4
Towards an understanding of the pathological basis of senile depression and incident dementia: Implications for treatment.探讨老年抑郁症和偶发性痴呆的病理基础:对治疗的启示。
Psychiatry Clin Neurosci. 2022 Dec;76(12):620-632. doi: 10.1111/pcn.13485. Epub 2022 Oct 22.
5
Neuropsychiatric Symptoms in Mild Cognitive Impairment and Dementia Due to AD: Relation With Disease Stage and Cognitive Deficits.阿尔茨海默病所致轻度认知障碍和痴呆中的神经精神症状:与疾病阶段和认知缺陷的关系。
Front Psychiatry. 2021 Aug 17;12:707580. doi: 10.3389/fpsyt.2021.707580. eCollection 2021.
6
Prognosis of Early-Onset Late-Onset Mild Cognitive Impairment: Comparison of Conversion Rates and Its Predictors.早发型与晚发型轻度认知障碍的预后:转化率及其预测因素的比较
Geriatrics (Basel). 2016 Apr 25;1(2):11. doi: 10.3390/geriatrics1020011.
7
Changes in the Hippocampal Volume and Shape in Early-Onset Mild Cognitive Impairment.早发性轻度认知障碍患者海马体积与形态的变化
Psychiatry Investig. 2018 May;15(5):531-537. doi: 10.30773/pi.2018.02.12. Epub 2018 Apr 27.
8
Cerebral blood flow changes in remitted early- and late-onset depression patients.缓解期早发和晚发抑郁症患者的脑血流变化
Oncotarget. 2017 Jul 12;8(44):76214-76222. doi: 10.18632/oncotarget.19185. eCollection 2017 Sep 29.
9
Longitudinal Cognitive Outcomes of Clinical Phenotypes of Late-Life Depression.老年期抑郁症临床表型的纵向认知结局。
Am J Geriatr Psychiatry. 2017 Oct;25(10):1123-1134. doi: 10.1016/j.jagp.2017.03.016. Epub 2017 Mar 28.
10
Disrupted Interhemispheric Synchrony in Default Mode Network Underlying the Impairment of Cognitive Flexibility in Late-Onset Depression.默认模式网络中半球间同步中断是晚发性抑郁症认知灵活性受损的潜在原因。
Front Aging Neurosci. 2016 Sep 27;8:230. doi: 10.3389/fnagi.2016.00230. eCollection 2016.

本文引用的文献

1
Involvement of brain-derived neurotrophic factor in late-life depression.脑源性神经营养因子与老年期抑郁症的关系
Am J Geriatr Psychiatry. 2013 May;21(5):433-49. doi: 10.1016/j.jagp.2012.10.026. Epub 2013 Mar 19.
2
The age-by-disease interaction hypothesis of late-life depression.老年期抑郁症的年龄与疾病相互作用假说。
Am J Geriatr Psychiatry. 2013 May;21(5):418-32. doi: 10.1016/j.jagp.2013.01.053. Epub 2013 Feb 6.
3
Evidence for a differential role of HPA-axis function, inflammation and metabolic syndrome in melancholic versus atypical depression.HPA 轴功能、炎症和代谢综合征在单相抑郁和双相抑郁中的作用差异。
Mol Psychiatry. 2013 Jun;18(6):692-9. doi: 10.1038/mp.2012.144. Epub 2012 Oct 23.
4
A longitudinal study of differences in late- and early-onset geriatric depression: depressive symptoms and psychosocial, cognitive, and neurological functioning.老年期抑郁晚发与早发患者的差异的纵向研究:抑郁症状及心理社会、认知和神经功能。
Aging Ment Health. 2013;17(1):1-11. doi: 10.1080/13607863.2012.717253. Epub 2012 Aug 30.
5
Late-life depression as a risk factor for mild cognitive impairment or Alzheimer's disease in 30 US Alzheimer's disease centers.30 个美国阿尔茨海默病中心的研究表明:晚年抑郁症是轻度认知障碍或阿尔茨海默病的一个风险因素。
J Alzheimers Dis. 2012;31(2):265-75. doi: 10.3233/JAD-2012-111922.
6
Depressed older patients with the atypical features of interpersonal rejection sensitivity and reversed-vegetative symptoms are similar to younger atypical patients.具有人际拒绝敏感和逆转植物性症状等非典型特征的抑郁老年患者与年轻非典型患者相似。
Am J Geriatr Psychiatry. 2012 Jul;20(7):622-34. doi: 10.1097/JGP.0b013e31822cccff.
7
Meta-review of depressive subtyping models.抑郁亚型模型的元综述。
J Affect Disord. 2012 Jul;139(2):126-40. doi: 10.1016/j.jad.2011.07.015. Epub 2011 Sep 1.
8
Age at onset and vascular pathology in late-life depression.老年期抑郁症发病年龄与血管病理学。
Am J Geriatr Psychiatry. 2012 Jun;20(6):524-32. doi: 10.1097/JGP.0b013e318227f85c.
9
Late-life depression and Alzheimer's disease: the glutamatergic system inside of this mirror relationship.晚年抑郁症与阿尔茨海默病:这种镜像关系中的谷氨酸能系统。
Brain Res Rev. 2011 Jun 24;67(1-2):344-55. doi: 10.1016/j.brainresrev.2011.04.003. Epub 2011 Apr 28.
10
Depression and risk of developing dementia.抑郁与痴呆症发病风险。
Nat Rev Neurol. 2011 May 3;7(6):323-31. doi: 10.1038/nrneurol.2011.60.