• 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

相似文献

1
Stability and change in reported age of onset of depression, back pain, and smoking over 29 years in a prospective cohort study.一项前瞻性队列研究中29年间抑郁症、背痛和吸烟报告发病年龄的稳定性与变化
J Psychiatr Res. 2017 May;88:105-112. doi: 10.1016/j.jpsychires.2017.01.005. Epub 2017 Jan 10.
2
Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.在流行地区,服用抗叶酸抗疟药物的人群中,叶酸补充剂与疟疾易感性和严重程度的关系。
Cochrane Database Syst Rev. 2022 Feb 1;2(2022):CD014217. doi: 10.1002/14651858.CD014217.
3
Epidemiology of back pain in older adults: prevalence and risk factors for back pain onset.老年人背痛的流行病学:背痛发病的患病率和危险因素。
Rheumatology (Oxford). 2011 Sep;50(9):1645-53. doi: 10.1093/rheumatology/ker175. Epub 2011 May 23.
4
Previous Mental Disorders and Subsequent Onset of Chronic Back or Neck Pain: Findings From 19 Countries.先前的精神障碍与随后的慢性腰背或颈部疼痛发作:来自 19 个国家的调查结果。
J Pain. 2018 Jan;19(1):99-110. doi: 10.1016/j.jpain.2017.08.011. Epub 2017 Oct 12.
5
Influence of smoking on the health status of spinal patients: the National Spine Network database.吸烟对脊柱疾病患者健康状况的影响:国家脊柱网络数据库
Spine (Phila Pa 1976). 2002 Feb 1;27(3):313-9. doi: 10.1097/00007632-200202010-00022.
6
Early age of onset of mood, anxiety and alcohol use disorders is associated with sociodemographic characteristics and health outcomes in adults: results from a cross-sectional national survey.心境、焦虑和酒精使用障碍发病年龄早与成年人的社会人口特征和健康结果相关:来自全国横断面调查的结果。
Soc Psychiatry Psychiatr Epidemiol. 2021 Oct;56(10):1835-1846. doi: 10.1007/s00127-021-02070-4. Epub 2021 Mar 31.
7
Modifiable risk factors for chronic back pain: insights using the co-twin control design.慢性背痛的可改变风险因素:采用双胞胎对照设计的见解
Spine J. 2017 Jan;17(1):4-14. doi: 10.1016/j.spinee.2016.07.533. Epub 2016 Oct 26.
8
The Age of Onset of Anxiety Disorders.焦虑症的发病年龄。
Can J Psychiatry. 2017 Apr;62(4):237-246. doi: 10.1177/0706743716640757. Epub 2016 Jul 9.
9
Prescription opioids for back pain and use of medications for erectile dysfunction.治疗背痛的处方类阿片药物和用于勃起功能障碍的药物的使用。
Spine (Phila Pa 1976). 2013 May 15;38(11):909-15. doi: 10.1097/BRS.0b013e3182830482.
10
Why does age of onset predict clinical severity in schizophrenia? A multiplex extended pedigree study.为什么发病年龄可以预测精神分裂症的临床严重程度?一项多重扩展家系研究。
Am J Med Genet B Neuropsychiatr Genet. 2020 Oct;183(7):403-411. doi: 10.1002/ajmg.b.32814. Epub 2020 Aug 19.

引用本文的文献

1
Does the millennial generation of women experience more mental illness than their mothers?千禧一代女性的精神疾病患病率是否高于她们的母亲?
BMC Psychiatry. 2021 Jul 17;21(1):359. doi: 10.1186/s12888-021-03361-5.
2
Prognosis and improved outcomes in major depression: a review.重度抑郁症的预后和改善结果:综述。
Transl Psychiatry. 2019 Apr 3;9(1):127. doi: 10.1038/s41398-019-0460-3.
3
Abnormalities in Inflammatory Cytokines Confer Susceptible to Chronic Neuropathic Pain-related Anhedonia in a Rat Model of Spared Nerve Injury.在保留神经损伤大鼠模型中,炎性细胞因子异常致使对慢性神经性疼痛相关快感缺失易感。
Clin Psychopharmacol Neurosci. 2019 May 31;17(2):189-199. doi: 10.9758/cpn.2019.17.2.189.

本文引用的文献

1
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.通过发病年龄分层进行的全基因组关联研究:精神基因组学联盟重度抑郁症工作组
Biol Psychiatry. 2017 Feb 15;81(4):325-335. doi: 10.1016/j.biopsych.2016.05.010. Epub 2016 May 24.
2
The specificity of the familial aggregation of early-onset bipolar disorder: A controlled 10-year follow-up study of offspring of parents with mood disorders.早发性双相情感障碍家族聚集性的特异性:一项对患有情绪障碍父母的后代进行的为期10年的对照随访研究。
J Affect Disord. 2016 Jan 15;190:26-33. doi: 10.1016/j.jad.2015.10.005. Epub 2015 Oct 23.
3
Age of smoking milestones: longitudinal inconsistencies and recanting.吸烟里程碑年龄:纵向不一致与反悔。
J Adolesc Health. 2015 Apr;56(4):382-8. doi: 10.1016/j.jadohealth.2014.12.005. Epub 2015 Feb 3.
4
Self-Reported Age of Onset and Telescoping for Cigarettes, Alcohol, and Marijuana Across Eight Years of the National Longitudinal Survey of Youth.在全国青少年纵向调查的八年中,关于香烟、酒精和大麻的自我报告发病年龄及时间压缩情况。
J Child Adolesc Subst Abuse. 2012 Sep 1;21(4):333-348. doi: 10.1080/1067828X.2012.710026. Epub 2012 Sep 12.
5
Age of onset: can we rely on essential tremor patients to report this? Data from a prospective, longitudinal study.发病年龄:我们能否依赖特发性震颤患者报告这一点?一项前瞻性纵向研究的数据。
Neuroepidemiology. 2013;40(2):93-8. doi: 10.1159/000341903. Epub 2012 Oct 24.
6
Dissecting the genetic heterogeneity of depression through age at onset.通过发病年龄解析抑郁症的遗传异质性。
Am J Med Genet B Neuropsychiatr Genet. 2012 Oct;159B(7):859-68. doi: 10.1002/ajmg.b.32093. Epub 2012 Aug 22.
7
The Stability of Self-Reported Marijuana Use Across Eight Years of the National Longitudinal Survey of Youth.《青少年全国纵向调查八年期间自我报告的大麻使用情况的稳定性》
J Child Adolesc Subst Abuse. 2011 Nov 1;20(5):407-420. doi: 10.1080/1067828x.2011.614873.
8
Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder.全基因组调查提示拷贝数变异(CNVs)在早发性双相情感障碍的发病机制中发挥作用。
Mol Psychiatry. 2012 Apr;17(4):421-32. doi: 10.1038/mp.2011.8. Epub 2011 Mar 1.
9
Cumulative prevalence of psychiatric disorders by young adulthood: a prospective cohort analysis from the Great Smoky Mountains Study.青少年期精神障碍的累积患病率:来自大烟山研究的前瞻性队列分析。
J Am Acad Child Adolesc Psychiatry. 2011 Mar;50(3):252-61. doi: 10.1016/j.jaac.2010.12.014. Epub 2011 Jan 26.
10
Development of lifetime comorbidity in the World Health Organization world mental health surveys.世界卫生组织世界精神卫生调查中终生共病的发展情况。
Arch Gen Psychiatry. 2011 Jan;68(1):90-100. doi: 10.1001/archgenpsychiatry.2010.180.

一项前瞻性队列研究中29年间抑郁症、背痛和吸烟报告发病年龄的稳定性与变化

Stability and change in reported age of onset of depression, back pain, and smoking over 29 years in a prospective cohort study.

作者信息

Paksarian Diana, Cui Lihong, Angst Jules, Ajdacic-Gross Vladeta, Rössler Wulf, Merikangas Kathleen R

机构信息

Genetic Epidemiology Research Branch, Intramural Research Program, National Institute of Mental Health, Bethesda, MD, USA.

Genetic Epidemiology Research Branch, Intramural Research Program, National Institute of Mental Health, Bethesda, MD, USA.

出版信息

J Psychiatr Res. 2017 May;88:105-112. doi: 10.1016/j.jpsychires.2017.01.005. Epub 2017 Jan 10.

DOI:10.1016/j.jpsychires.2017.01.005
PMID:28113111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5382717/
Abstract

Accurate age of onset (AOO) measurement is vital to etiologic and preventive research. While AOO reports are known to be subject to recall error, few population-based studies have been used to investigate agreement in AOO reports over more than a decade. We examined AOO reports for depression, back/neck pain, and daily smoking, in a population-based cohort spanning 29 years. A stratified sample of participants from Zurich, Switzerland (n = 591) completed a psychiatric and physical health interview 7 times between 1979, at ages 20 (males) and 21 (females), and 2008. We used one-way ANOVA to estimate intraclass correlations (ICCs) and weighted mixed models to estimate mean change over time and test for interactions with sex and clinical characteristics. Stratum-specific ICCs among those with 2 + reports were 0.19 and 0.29 for depression, 0.46 and 0.35 for back pain, and 0.66 and 0.75 for smoking. The average yearly increases in AOO report from the wave of first 12-month diagnosis or reported smoking, estimated in mixed models, were 0.57 years (95% confidence interval: 0.35, 0.79) for depression, 0.44 (95%CI: 0.28, 0.59) years for back pain, and 0.08 (95%CI: 0.03, 0.14) years for smoking. Initial impairment and frequency of treatment were associated with differences in average yearly change for depression. There is substantial variability in AOO reports over time and systematic increase with age. The degree of increase may differ by outcome, and for some outcomes, by participant clinical characteristics. Future studies should identify predictors of AOO report stability to ultimately benefit etiologic and preventive research.

摘要

准确测量发病年龄(AOO)对于病因学和预防研究至关重要。虽然已知AOO报告存在回忆误差,但很少有基于人群的研究用于调查十多年来AOO报告的一致性。我们在一个为期29年的基于人群的队列中检查了抑郁症、背部/颈部疼痛和每日吸烟的AOO报告。来自瑞士苏黎世的分层样本参与者(n = 591)在1979年(男性20岁,女性21岁)至2008年期间完成了7次精神和身体健康访谈。我们使用单因素方差分析来估计组内相关系数(ICC),并使用加权混合模型来估计随时间的平均变化,并检验与性别和临床特征的相互作用。在有2次及以上报告的人群中,抑郁症的分层特异性ICC分别为0.19和0.29,背痛为0.46和0.35,吸烟为0.66和0.75。在混合模型中估计,从首次12个月诊断或报告吸烟的时间点起,AOO报告的平均每年增加量,抑郁症为0.57年(95%置信区间:0.35,0.79),背痛为0.44(95%CI:0.28,0.59)年,吸烟为0.08(95%CI:0.03,0.14)年。初始损伤和治疗频率与抑郁症平均每年变化的差异有关。AOO报告随时间存在很大变异性,且随年龄系统性增加。增加程度可能因结局而异,对于某些结局,还因参与者临床特征而异。未来研究应确定AOO报告稳定性的预测因素,以最终造福病因学和预防研究。