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血管性血友病因子和 ADAMTS13 活性与痴呆风险的关系:一项基于人群的研究。

Von Willebrand factor and ADAMTS13 activity in relation to risk of dementia: a population-based study.

机构信息

Department of Epidemiology, Erasmus Medical Centre, Rotterdam, The Netherlands.

Department of Neurology, Erasmus Medical Centre, Rotterdam, The Netherlands.

出版信息

Sci Rep. 2018 Apr 3;8(1):5474. doi: 10.1038/s41598-018-23865-7.

Abstract

Low ADAMTS13 activity is associated with an increased risk of cardiovascular disease, which is generally attributed to its proteolytic effects on Von Willebrand factor (VWF). Cardiovascular health is an important determinant of cognitive decline, but the association of either VWF or ADAMTS13 with risk of dementia is unknown. Between 1997-2002, we measured VWF antigen and ADAMTS13 activity in 6055 participants of the population-based Rotterdam Study (mean age 69.3 years, 57.2% women). At baseline, 85 participants had dementia, and during 15 years of follow-up 821 developed dementia. Higher VWF was associated with prevalence and risk of dementia, unaffected by concurrent ADAMTS13 activity, but estimates strongly attenuated over time and were no longer statistically significant at 4 years of follow-up (relative risks [95% CI] per standard deviation increase- cross-sectional: 1.37 [1.06-1.77], and longitudinal: 1.05 [0.97-1.14]). In contrast, low ADAMTS13 was associated with increased risk of dementia throughout follow-up (hazard ratio per SD decrease- 1.16 [1.06-1.28]), which alike for ischaemic stroke, was modified by the presence of diabetes (P-interaction = 0.003). In conclusion, higher VWF and low ADAMTS13 activity are associated with increased risk of dementia, but differences in time-course and lack of synergistic effects may indicate in part independent underlying mechanisms.

摘要

ADAMTS13 活性降低与心血管疾病风险增加相关,这通常归因于其对血管性血友病因子 (VWF) 的蛋白水解作用。心血管健康是认知能力下降的重要决定因素,但 VWF 或 ADAMTS13 与痴呆风险的关联尚不清楚。1997-2002 年间,我们在基于人群的鹿特丹研究中测量了 6055 名参与者的 VWF 抗原和 ADAMTS13 活性(平均年龄 69.3 岁,57.2%为女性)。在基线时,85 名参与者患有痴呆症,在 15 年的随访期间,821 名参与者发展为痴呆症。较高的 VWF 与痴呆症的患病率和风险相关,不受同时存在的 ADAMTS13 活性的影响,但随着时间的推移,估计值会强烈减弱,在 4 年的随访中不再具有统计学意义(每增加一个标准差的相对风险 [95%CI]-横断面:1.37 [1.06-1.77],纵向:1.05 [0.97-1.14])。相比之下,ADAMTS13 活性降低与整个随访期间的痴呆风险增加相关(每减少一个标准差的风险比-1.16 [1.06-1.28]),这与缺血性中风一样,受糖尿病存在的影响(P 交互作用=0.003)。总之,较高的 VWF 和 ADAMTS13 活性与痴呆风险增加相关,但时间进程的差异和缺乏协同作用可能表明部分独立的潜在机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3313/5882924/c8b5c1ec85fa/41598_2018_23865_Fig1_HTML.jpg

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