Mia Maria Günak, Jo Billings, Emily Carratu, Natalie L Marchant, Graziella Favarato, Vasiliki Orgeta
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We used random- and fixed-effects meta-analyses to pool estimates across studies.</p><p><strong>Results: </strong>PTSD was associated with a significant risk for all-cause dementia: pooled hazard ratio HR = 1.61 (95% CI 1.43-1.81, I2= 85.8%, P < 0.001; n = 1 693 678; 8 studies). Pooled HR was 1.61 (95% CI 1.46-1.78; I2= 80.9%, P < 0.001; n = 905 896; 5 studies) in veterans, and 2.11 (95% CI 1.03-4.33, I2= 91.2%, P < 0.001; n = 787 782; 3 studies) in the general population. The association between PTSD and dementia remained significant after excluding studies with high risk of bias (HR = 1.55, 95% CI 1.39-1.73, I2= 83.9%, P < 0.001; n = 1 684 928; 7 studies). Most studies included were retrospective and there was evidence of high heterogeneity.</p><p><strong>Conclusions: </strong>This is the first meta-analysis quantifying the association of PTSD and risk of dementia showing that PTSD is a strong and potentially modifiable risk factor for all-cause dementia. Future studies investigating potential causal mechanisms, and the protective value of treating PTSD are needed.</p>","PeriodicalId":520791,"journal":{"name":"The British journal of psychiatry : the journal of mental science","volume":" ","pages":"600-608"},"PeriodicalIF":0.0000,"publicationDate":"2020-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1192/bjp.2020.150","citationCount":"51","resultStr":"{\"title\":\"Post-traumatic stress disorder as a risk factor for dementia: systematic review and meta-analysis.\",\"authors\":\"Mia Maria Günak, Jo Billings, Emily Carratu, Natalie L Marchant, Graziella Favarato, Vasiliki Orgeta\",\"doi\":\"10.1192/bjp.2020.150\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Post-traumatic stress disorder (PTSD) has been identified as a potential risk factor for developing dementia. 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引用次数: 51
摘要
背景:创伤后应激障碍(PTSD)已被确定为发展为痴呆的潜在危险因素。然而,目前还没有量化这种风险的荟萃分析。目的:系统地回顾和量化人群中与PTSD相关的未来痴呆的风险。普洛斯彼罗注册号CRD42019130392。方法:我们检索了截至2019年10月25日的9个电子数据库,以评估PTSD和痴呆风险的纵向研究。我们使用随机效应和固定效应的荟萃分析来汇总所有研究的估计。结果:PTSD与全因痴呆的显著风险相关:合并风险比HR = 1.61 (95% CI 1.43-1.81, I2= 85.8%, P < 0.001;N = 1 693 678;8研究)。合并风险比为1.61 (95% CI 1.46-1.78;I2= 80.9%, p < 0.001;N = 905 896;5项研究),2.11项(95% CI 1.03-4.33, I2= 91.2%, P < 0.001;N = 787 782;(3项研究)。排除高偏倚风险研究后,PTSD与痴呆之间的相关性仍然显著(HR = 1.55, 95% CI 1.39 ~ 1.73, I2= 83.9%, P < 0.001;N = 1 684 928;7研究)。大多数纳入的研究是回顾性的,有证据表明异质性很高。结论:这是第一个量化PTSD与痴呆风险关联的荟萃分析,表明PTSD是全因痴呆的一个强大且潜在可改变的危险因素。未来的研究需要调查潜在的因果机制,以及治疗PTSD的保护价值。
Post-traumatic stress disorder as a risk factor for dementia: systematic review and meta-analysis.
Background: Post-traumatic stress disorder (PTSD) has been identified as a potential risk factor for developing dementia. There are currently, however, no meta-analyses quantifying this risk.
Aims: To systematically review and quantify the risk of future dementia associated with PTSD across populations. PROSPERO registration number CRD42019130392.
Method: We searched nine electronic databases up to 25 October 2019 for longitudinal studies assessing PTSD and risk of dementia. We used random- and fixed-effects meta-analyses to pool estimates across studies.
Results: PTSD was associated with a significant risk for all-cause dementia: pooled hazard ratio HR = 1.61 (95% CI 1.43-1.81, I2= 85.8%, P < 0.001; n = 1 693 678; 8 studies). Pooled HR was 1.61 (95% CI 1.46-1.78; I2= 80.9%, P < 0.001; n = 905 896; 5 studies) in veterans, and 2.11 (95% CI 1.03-4.33, I2= 91.2%, P < 0.001; n = 787 782; 3 studies) in the general population. The association between PTSD and dementia remained significant after excluding studies with high risk of bias (HR = 1.55, 95% CI 1.39-1.73, I2= 83.9%, P < 0.001; n = 1 684 928; 7 studies). Most studies included were retrospective and there was evidence of high heterogeneity.
Conclusions: This is the first meta-analysis quantifying the association of PTSD and risk of dementia showing that PTSD is a strong and potentially modifiable risk factor for all-cause dementia. Future studies investigating potential causal mechanisms, and the protective value of treating PTSD are needed.