Kay Khaing MMed, Xenia Dolja-Gore PhD, Balakrishnan R. Nair MD, Julie Byles PhD, John Attia PhD
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The Fine–Gray subdistribution hazard model was computed to assess dementia risk, while adjusting for the competing risk of death.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Chronic anxiety and new onset anxiety at follow-up were associated with all-cause dementia risk (HR 2.80, 95% CI 1.35–5.72 and HR 3.20, 95% CI 1.40–7.45 respectively) with an average time to dementia diagnosis of 10 years (SD = 1.7) whereas resolved anxiety was not. In subgroup analyses, these results were driven particularly by chronic and new anxiety among participants below the age of 70 years (HR 4.58, 95% CI 01.12–18.81 and HR 7.21, 95%CI 1.86–28.02 respectively). Sensitivity analyses imputing missing data and addressing reverse causation gave very similar results.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Chronic and new anxiety were associated with increased risk of all-cause dementia, and this association was significant in those 70 years and younger. 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引用次数: 0
摘要
背景:焦虑是一种常见病,但长期焦虑对痴呆症的影响尚未得到探讨。本研究旨在评估慢性焦虑、缓解焦虑和新发焦虑与全因痴呆风险之间的纵向关系:方法:从猎人社区研究中招募了 2132 名参与者,平均年龄为 76 岁。焦虑采用凯斯勒心理压力量表(K10)进行测量。痴呆症根据《国际疾病分类-10》代码进行定义。计算Fine-Gray子分布危险模型以评估痴呆症风险,同时对死亡的竞争风险进行调整:结果:长期焦虑和随访时新发焦虑与全因痴呆风险相关(HR 分别为 2.80,95% CI 1.35-5.72 和 HR 3.20,95% CI 1.40-7.45),平均痴呆诊断时间为 10 年(SD = 1.7),而缓解焦虑与全因痴呆风险无关。在亚组分析中,70 岁以下参与者中的慢性焦虑和新焦虑对上述结果的影响尤为明显(HR 分别为 4.58,95% CI 01.12-18.81 和 HR 7.21,95% CI 1.86-28.02)。对缺失数据和反向因果关系的敏感性分析结果非常相似:结论:长期焦虑和新焦虑与全因痴呆风险的增加有关,这种关联在 70 岁及以下人群中非常显著。然而,在随访过程中焦虑症得到缓解后,患痴呆症的风险就会降低,这与未接触焦虑症人群的情况相似。这些结果表明,及时控制焦虑可能是降低痴呆症风险的可行策略。
The effect of anxiety on all-cause dementia: A longitudinal analysis from the Hunter Community Study
Background
Anxiety is common, however, the effect of chronicity of anxiety on dementia has not been explored. This study aims to assess the longitudinal relationship between chronic versus resolved versus new onset anxiety, and all-cause dementia risk.
Methods
A total of 2132 participants with mean age 76 years from the Hunter Community Study were recruited. Anxiety was measured using Kessler Psychological Distress Scale (K10). Dementia was defined as per International Classification of Disease—10 codes. The Fine–Gray subdistribution hazard model was computed to assess dementia risk, while adjusting for the competing risk of death.
Results
Chronic anxiety and new onset anxiety at follow-up were associated with all-cause dementia risk (HR 2.80, 95% CI 1.35–5.72 and HR 3.20, 95% CI 1.40–7.45 respectively) with an average time to dementia diagnosis of 10 years (SD = 1.7) whereas resolved anxiety was not. In subgroup analyses, these results were driven particularly by chronic and new anxiety among participants below the age of 70 years (HR 4.58, 95% CI 01.12–18.81 and HR 7.21, 95%CI 1.86–28.02 respectively). Sensitivity analyses imputing missing data and addressing reverse causation gave very similar results.
Conclusion
Chronic and new anxiety were associated with increased risk of all-cause dementia, and this association was significant in those 70 years and younger. However, the resolved anxiety at follow-up reduced the risk, similar to that of the non-exposed group. These results suggest that timely management of anxiety may be a viable strategy in reducing the risk of dementia.
期刊介绍:
Journal of the American Geriatrics Society (JAGS) is the go-to journal for clinical aging research. We provide a diverse, interprofessional community of healthcare professionals with the latest insights on geriatrics education, clinical practice, and public policy—all supporting the high-quality, person-centered care essential to our well-being as we age. Since the publication of our first edition in 1953, JAGS has remained one of the oldest and most impactful journals dedicated exclusively to gerontology and geriatrics.