Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Department of Radiology, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
Am J Clin Nutr. 2019 Oct 1;110(4):883-890. doi: 10.1093/ajcn/nqz147.
Vitamin K occurs in the diet as phylloquinone and menaquinones. Observational studies have shown that both phylloquinone and menaquinone intake might reduce cardiovascular disease (CVD) risk. However, the effect of vitamin K on vascular calcification is unknown.
The aim of this study was to assess if menaquinone supplementation, compared to placebo, decreases vascular calcification in people with type 2 diabetes and known CVD.
In this double-blind, randomized, placebo-controlled trial, we randomly assigned men and women with type 2 diabetes and CVD to 360 µg/d menaquinone-7 (MK-7) or placebo for 6 mo. Femoral arterial calcification at baseline and 6 mo was measured with 18sodium fluoride positron emission tomography (18F-NaF PET) scans as target-to-background ratios (TBRs), a promising technique to detect active calcification. Calcification mass on conventional computed tomography (CT) scan was measured as secondary outcome. Dephosphorylated-uncarboxylated matrix Gla protein (dp-ucMGP) concentrations were measured to assess compliance. Linear regression analyses were performed with either TBR or CT calcification at follow-up as the dependent variable, and treatment and baseline TBR or CT calcification as independent variables.
We randomly assigned 35 patients to the MK-7 group (33 completed follow-up) and 33 to the placebo group (27 completed follow-up). After the 6-mo intervention, TBR tended to increase in the MK-7 group compared with placebo (0.25; 95% CI: -0.02, 0.51; P = 0.06), although this was not significant. Log-transformed CT calcification mass did not increase in the intervention group compared with placebo (0.50; 95% CI: -0.23, 1.36; P = 0.18). MK-7 supplementation significantly reduced dp-ucMGP compared with placebo (-205.6 pmol/L; 95% CI: -255.8, -155.3 pmol/L). No adverse events were reported.
MK-7 supplementation tended to increase active calcification measured with 18F-NaF PET activity compared with placebo, but no effect was found on conventional CT. Additional research investigating the interpretation of 18F-NaF PET activity is necessary. This trial was registered at clinicaltrials.gov as NCT02839044.
维生素 K 以叶绿醌和甲萘醌的形式存在于饮食中。观察性研究表明,叶绿醌和甲萘醌的摄入都可能降低心血管疾病 (CVD) 的风险。然而,维生素 K 对血管钙化的影响尚不清楚。
本研究旨在评估与安慰剂相比,补充甲萘醌是否会降低 2 型糖尿病和已知 CVD 患者的血管钙化。
在这项双盲、随机、安慰剂对照试验中,我们将 2 型糖尿病和 CVD 患者随机分配至每天 360μg 甲萘醌-7 (MK-7) 或安慰剂组,干预 6 个月。基线和 6 个月时采用 18 氟-氟化钠正电子发射断层扫描 (18F-NaF PET) 扫描测量股动脉钙化,以靶区-背景比 (TBR) 作为目标检测活跃钙化的有前途的技术。常规计算机断层扫描 (CT) 扫描测量钙化质量作为次要终点。测量去磷酸化未羧化基质 Gla 蛋白 (dp-ucMGP) 浓度以评估依从性。采用线性回归分析,以随访时 TBR 或 CT 钙化作为因变量,以治疗和基线 TBR 或 CT 钙化作为自变量。
我们将 35 名患者随机分配至 MK-7 组 (33 名完成随访) 和安慰剂组 (27 名完成随访)。干预 6 个月后,与安慰剂相比,MK-7 组 TBR 呈上升趋势(0.25;95%CI:-0.02,0.51;P=0.06),但差异无统计学意义。干预组 CT 钙化质量的对数值未较安慰剂组增加(0.50;95%CI:-0.23,1.36;P=0.18)。与安慰剂相比,MK-7 补充剂可显著降低 dp-ucMGP(205.6 pmol/L;95%CI:-255.8,-155.3 pmol/L)。未报告不良事件。
与安慰剂相比,MK-7 补充剂可使 18F-NaF PET 活性测量的活性钙化增加,但对常规 CT 无影响。需要进一步研究以解释 18F-NaF PET 活性。本试验在 clinicaltrials.gov 上注册为 NCT02839044。