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血液黏稠对大脑有害吗?:卡菲利前瞻性研究中的止血和炎症系统与痴呆。

Is sticky blood bad for the brain?: Hemostatic and inflammatory systems and dementia in the Caerphilly Prospective Study.

机构信息

Department of Epidemiology, Statistics and Public Health, Centre for Health Sciences Research, Heath Park, Cardiff CF14 4XN, Wales, England.

出版信息

Arterioscler Thromb Vasc Biol. 2010 Mar;30(3):599-604. doi: 10.1161/ATVBAHA.109.197368. Epub 2009 Dec 3.

Abstract

OBJECTIVE

Hemostasis and inflammation have been implicated in dementia. This study investigates the role of specific hemostatic and inflammatory pathways with incident vascular and nonvascular dementia.

METHODS AND RESULTS

This was a prospective study of a population sample of men aged 65 to 84 years, with baseline assessment of hemostatic and inflammatory factors and cognition measured 17 years later. The sample included 865 men (59 had dementia and 112 had cognitive impairment, not dementia), free of vascular disease at baseline and for whom hemostatic and inflammatory marker data were available and cognitive status was known. A total of 15 hemostatic and 6 inflammatory markers were assessed. Factor analysis was used to identify hemostatic subsystems. The National Institute of Neurological Disorders and Stroke-Association Internationale pour la Recherche et l'Enseignement en Neurologie criteria were used to identify vascular dementia. By using standardized (z) scores for hemostatic and inflammatory markers, and after adjustment for age and risk factors, vascular dementia was associated with fibrinogen (hazard ratio [HR], 1.68; 95% confidence interval [CI], 1.02-2.76), factor VIII (HR, 1.79; 95% CI, 1.09-3.00), and plasminogen activator inhibitor 1 (HR, 3.13; 95% CI, 1.73-5.70). For vascular dementia, the HR risk from high levels of all three hemostatic variables (fibrinogen, factor VIII, and plasminogen activator inhibitor 1) was 2.97 (P<0.001). Inflammatory factors were not associated with vascular dementia.

CONCLUSIONS

The associations of these hemostatic markers with vascular dementia may implicate clot formation as the primary mechanism and are consistent with a microinfarct model of vascular dementia.

摘要

目的

止血和炎症与痴呆有关。本研究调查了特定止血和炎症途径在血管性和非血管性痴呆发病中的作用。

方法和结果

这是一项针对 65 至 84 岁人群的前瞻性研究,基线评估止血和炎症因子,17 年后测量认知功能。该样本包括 865 名男性(59 名患有痴呆症,112 名患有认知障碍但非痴呆症),基线时无血管疾病,且有止血和炎症标志物数据,认知状态已知。共评估了 15 种止血和 6 种炎症标志物。使用因子分析来识别止血子系统。使用国家神经疾病和中风协会-国际神经病学研究与教育协会标准来识别血管性痴呆。通过使用止血和炎症标志物的标准化(z)评分,并在调整年龄和危险因素后,血管性痴呆与纤维蛋白原(危险比 [HR],1.68;95%置信区间 [CI],1.02-2.76)、因子 VIII(HR,1.79;95% CI,1.09-3.00)和纤溶酶原激活物抑制剂 1(HR,3.13;95% CI,1.73-5.70)相关。对于血管性痴呆,这三种止血变量(纤维蛋白原、因子 VIII 和纤溶酶原激活物抑制剂 1)高水平的 HR 风险为 2.97(P<0.001)。炎症因子与血管性痴呆无关。

结论

这些止血标志物与血管性痴呆的相关性可能表明血栓形成是主要机制,与血管性痴呆的微梗死模型一致。

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