Wolfson Centre for Prevention of Stroke and Dementia, Wolfson Building, Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, UK; NIHR Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK; Departments of Acute General Internal Medicine and Geratology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Wolfson Centre for Prevention of Stroke and Dementia, Wolfson Building, Nuffield Department of Clinical Neurosciences, John Radcliffe Hospital, University of Oxford, Oxford, UK.
Lancet Healthy Longev. 2024 Feb;5(2):e131-e140. doi: 10.1016/S2666-7568(23)00266-0.
The increased risk of dementia after delirium and infection might be influenced by cerebral white matter disease (WMD). In patients with transient ischaemic attack (TIA) and minor stroke, we assessed associations between hospital admissions with delirium and 5-year dementia risk and between admissions with infection and dementia risk, stratified by WMD severity (moderate or severe vs absent or mild) on baseline brain imaging.
We included patients with TIA and minor stroke (National Institutes of Health Stroke Score <3) from the Oxford Vascular Study (OXVASC), a longitudinal population-based study of the incidence and outcomes of acute vascular events in a population of 94 567 individuals, with no age restrictions, attending eight general practices in Oxfordshire, UK. Hospitalisation data were obtained through linkage to the Oxford Cognitive Comorbidity, Frailty, and Ageing Research Database-Electronic Patient Records (ORCHARD-EPR). Brain imaging was done using CT and MRI, and WMD was prospectively graded according to the age-related white matter changes (ARWMC) scale and categorised into absent, mild, moderate, or severe WMD. Delirium and infection were defined by ICD-10 coding supplemented by hand-searching of hospital records. Dementia was diagnosed using clinical or cognitive assessment, medical records, and death certificates. Associations between hospitalisation with delirium and hospitalisation with infection, and post-event dementia were assessed using time-varying Cox analysis with multivariable adjustment, and all models were stratified by WMD severity.
From April 1, 2002, to March 31, 2012, 1369 individuals were prospectively recruited into the study. Of 1369 patients (655 with TIA and 714 with minor stroke, mean age 72 [SD 13] years, 674 female and 695 male, and 364 with moderate or severe WMD), 209 (15%) developed dementia. Hospitalisation during follow-up occurred in 891 (65%) patients of whom 103 (12%) had at least one delirium episode and 236 (26%) had at least one infection episode. Hospitalisation without delirium or infection did not predict subsequent dementia (HR 1·01, 95% CI 0·86-1·20). In contrast, hospitalisation with delirium predicted subsequent dementia independently of infection in patients with and without WMD (2·64, 1·47-4·74; p=0·0013 vs 3·41, 1·91-6·09; p<0·0001) especially in those with unimpaired baseline cognition (cognitive test score above cutoff; 4·01, 2·23-7·19 vs 3·94, 1·95-7·93; both p≤0·0001). However, hospitalisation with infection only predicted dementia in those with moderate or severe WMD (1·75, 1·04-2·94 vs 0·68, 0·39-1·20; p=0·023).
The increased risk of dementia after delirium is unrelated to the presence of WMD, whereas infection increases risk only in patients with WMD, suggesting differences in underlying mechanisms and in potential preventive strategies.
National Institute for Health and Care Research and Wellcome Trust.
谵妄和感染后痴呆风险增加可能与脑白质疾病(WMD)有关。在短暂性脑缺血发作(TIA)和小卒中患者中,我们评估了基线脑影像学检查中存在或不存在(轻度或无)WMD 时,因谵妄住院与 5 年痴呆风险之间的关联,以及因感染住院与痴呆风险之间的关联。
我们纳入了牛津血管研究(OXVASC)中 TIA 和小卒中(NIHSS<3)患者,这是一项针对牛津郡 94567 名个体中急性血管事件的发病率和结局的基于人群的纵向研究,没有年龄限制,在英国牛津郡的 8 个普通诊所就诊。通过与牛津认知合并症、虚弱和衰老研究数据库-电子患者记录(ORCHARD-EPR)的链接获得住院数据。使用 CT 和 MRI 进行脑成像,根据年龄相关的白质改变(ARWMC)量表对 WMD 进行前瞻性分级,并分为无、轻度、中度或重度 WMD。通过 ICD-10 编码定义谵妄和感染,并通过手动搜索医院记录进行补充。使用临床或认知评估、病历和死亡证明诊断痴呆。使用时间变化 Cox 分析和多变量调整评估因谵妄住院和因感染住院与发病后痴呆之间的关联,所有模型均按 WMD 严重程度分层。
从 2002 年 4 月 1 日至 2012 年 3 月 31 日,前瞻性招募了 1369 名患者。在 1369 名患者(655 名 TIA 和 714 名小卒中,平均年龄 72[13]岁,674 名女性和 695 名男性,364 名中度或重度 WMD)中,209 名(15%)发生痴呆。在随访期间发生住院治疗的 891 名患者中,103 名(12%)至少发生过一次谵妄发作,236 名(26%)至少发生过一次感染发作。没有谵妄或感染的住院治疗并不能预测随后的痴呆(HR 1.01,95%CI 0.86-1.20)。相反,在有和没有 WMD 的患者中,因谵妄而住院与随后发生痴呆独立相关(2.64,1.47-4.74;p=0.0013 与 3.41,1.91-6.09;p<0.0001),尤其是在基线认知能力未受损的患者中(认知测试评分高于临界值;4.01,2.23-7.19 与 3.94,1.95-7.93;均 p≤0.0001)。然而,感染仅与中重度 WMD 患者的痴呆相关(1.75,1.04-2.94 与 0.68,0.39-1.20;p=0.023)。
谵妄后痴呆风险增加与 WMD 无关,而感染仅增加 WMD 患者的风险,这表明潜在机制和潜在预防策略存在差异。
英国国民健康保险制度和惠康信托基金会。