精神疾病共发生与痴呆之间的强烈关联:对14年临床数据仓库的贝叶斯方法。

IF 4.9 0 PSYCHIATRY
Edouard Baudouin,Emmanuelle Duron,Marie Verdoux,Matthieu Gasnier,Yann Pelloux,Hugo Bottemanne,Emmanuelle Corruble,Romain Colle
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引用次数: 0

摘要

背景:精神疾病本身就与痴呆风险增加有关。然而,共同发生的精神疾病和痴呆几率之间的关系尚不清楚。本研究旨在评估患有几种精神疾病的个体患痴呆(所有类型)的几率,并确定相关的共发生模式。方法数据取自法国Bicêtre医院2009年8月29日至2023年10月29日精神科临床数据仓库。年龄在45岁及以上的患者被诊断患有至少一种精神障碍——抑郁症、焦虑症、精神病性障碍、物质使用障碍、人格障碍或双相情感障碍。建立了亚组来评估与痴呆相关的精神病学共同发生的特定模式。在本病例对照研究中,使用贝叶斯模型,包括分层模型和调整年龄、性别和心血管危险因素的logistic回归,来估计痴呆的后验概率和or。结果3688例受试者中,痴呆组(653例(17.7%))和非痴呆组(3035例(82.3%))的平均年龄(SD)分别为68.7岁(12.1岁)和58.2岁(10.5岁)。与患有一种精神疾病的患者(2608例(70.7%))相比,痴呆症的调整OR(95%可信区间)从2.3(1.7-3)例伴有两种合并症的患者(789例(21.4%))增加到11.1(5.5 -22.2)例伴有四种合并症的患者(65例(1.8%))。同时出现情绪和焦虑障碍的患者患痴呆的平均后验概率为48%(34.1-62.2)至89.6%(76.8-98.6)。结论随着精神疾病合并症数量的增加,痴呆的发生率显著增加,其中情绪障碍和焦虑障碍合并症的后验概率最高。应该为这些患者制定有针对性的筛查策略,特别关注患有一种以上精神疾病的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Strong association between psychiatric disorders co-occurrence and dementia: a Bayesian approach on a 14-year clinical data warehouse.
BACKGROUND Psychiatric disorders alone are associated with an increased risk of developing dementia. However, the relationship between co-occurring psychiatric disorders and dementia odds remains unclear. This study aimed to assess the odds of dementia (all types) among individuals with several psychiatric disorders and identify relevant co-occurrence patterns. METHODS Data were extracted from the clinical data warehouse of the psychiatry department of Bicêtre Hospital, France, between 29 August 2009 and 29 October 2023. Patients aged 45 years and older diagnosed with at least one psychiatric disorder-depressive disorders, anxiety disorders, psychotic disorders, substance use disorders, personality disorders or bipolar disorders-were included. Subgroups were created to evaluate specific patterns of psychiatric co-occurrence associated with dementia. In this case-control study, Bayesian models, including hierarchical models and logistic regression adjusted for age, sex and cardiovascular risk factors, were used to estimate posterior probabilities and ORs for dementia. RESULTS Among 3688 subjects, the mean (SD) age at inclusion was 68.7 (12.1) in the dementia group (653 (17.7%) subjects) and 58.2 (10.5) in the non-dementia group (3035 (82.3%) individuals). Compared with those with one psychiatric disorder (2608 (70.7%) patients), the adjusted OR (95% credible interval) for dementia increased from 2.3 (1.7-3) with two comorbidities (789 (21.4%) patients) to 11.1 (5.4-22.2) with four comorbidities (65 (1.8%) subjects). Patients with co-occurrence of mood and anxiety disorders had a mean posterior probability from 48% (34.1-62.2) up to 89.6% (76.8-98.6) of dementia. CONCLUSIONS Dementia odds significantly increase with the number of psychiatric comorbidities, with mood and anxiety disorder co-occurrence showing the highest posterior probabilities. Targeted screening strategies should be developed for these patients, with a special focus on patients developing more than one psychiatric disorder.
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