Atherosclerosis Research Unit, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Department of Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Clin Hemorheol Microcirc. 2021;78(4):339-353. doi: 10.3233/CH-211147.
Described to be antithrombotic and antihypertensive, nattokinase is consumed for putative cardiovascular benefit. However, no large-scale, long-term cardiovascular study has been conducted with nattokinase supplementation.
To determine the effect of nattokinase on subclinical atherosclerosis progression and atherothrombotic biomarkers.
In this double-blinded trial, 265 individuals of median age 65.3 years, without clinical evidence of cardiovascular disease (CVD) were randomized to oral nattokinase 2,000 fibrinolytic units or matching placebo. Primary outcome was rate of change in subclinical atherosclerosis measured by serial carotid ultrasound every 6 months as carotid artery intima-media thickness (CIMT) and carotid arterial stiffness (CAS). Additional outcomes determined at least every 6 months were clinical parameters including blood pressure and laboratory measures including metabolic factors, blood rheology parameters, blood coagulation and fibrinolysis factors, inflammatory markers and monocyte/macrophage cellular activation markers.
After median 3 years of randomized treatment, annualized rate of change in CIMT and CAS did not significantly differ between nattokinase supplementation and placebo. Additionally, there was no significant effect of nattokinase supplementation on blood pressure or any laboratory determination.
Results of this trial show that nattokinase supplementation has a null effect on subclinical atherosclerosis progression in healthy individuals at low risk for CVD.
纳豆激酶具有抗血栓和降血压的作用,被认为对心血管有益,因此被人们所食用。然而,目前尚未进行大规模、长期的纳豆激酶补充剂对心血管的研究。
评估纳豆激酶对亚临床动脉粥样硬化进展和动脉粥样血栓形成生物标志物的影响。
在这项双盲试验中,265 名年龄中位数为 65.3 岁的个体没有心血管疾病(CVD)的临床证据,他们被随机分配口服纳豆激酶 2000 纤维蛋白溶解单位或匹配的安慰剂。主要结局是通过每 6 个月进行一次颈动脉超声检查来测量亚临床动脉粥样硬化的变化率,即颈动脉内膜中层厚度(CIMT)和颈动脉僵硬度(CAS)。至少每 6 个月确定的其他结局包括临床参数,包括血压和实验室测量,包括代谢因素、血液流变学参数、血液凝血和纤溶因子、炎症标志物和单核细胞/巨噬细胞细胞活化标志物。
在随机治疗中位数为 3 年后,纳豆激酶补充组和安慰剂组的 CIMT 和 CAS 的年变化率没有显著差异。此外,纳豆激酶补充对血压或任何实验室检测均无显著影响。
本试验结果表明,纳豆激酶补充剂对 CVD 低危健康个体的亚临床动脉粥样硬化进展没有影响。