Georgia Prevention Institute, Department of Population Health Sciences, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Department of Pediatrics, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.
Am J Hypertens. 2018 May 7;31(6):735-741. doi: 10.1093/ajh/hpy049.
Matrix Gla protein (MGP) is a vascular calcification inhibitor dependent upon vitamin K for activation. Evidence suggests that elevated plasma inactive MGP levels (desphospho-uncarboxylated MGP, dp-ucMGP; indicating poorer vascular vitamin K status) are associated with greater cardiovascular disease (CVD) risk. Despite African Americans experiencing highest rates of kidney failure and CVD events, relationships between dp-ucMGP and CVD risk markers have not been examined in this population. We investigated vascular vitamin K status (via plasma dp-ucMGP) between African American hemodialysis (HD) patients and healthy controls, and the associations of dp-ucMGP with arterial stiffness and endothelial function in HD patients only.
In 37 African American HD patients and 37 age- and race-matched controls, plasma dp-ucMGP was measured by enzyme immunoassay as a marker of vascular vitamin K status. Carotid-femoral pulse wave velocity (PWV; arterial stiffness measurement) and brachial artery flow-mediated dilation (FMD; endothelial function measurement) were assessed by applanation tonometry and ultrasound, respectively, in HD patients only.
Mean dp-ucMGP levels were 5.6 times higher in HD patients vs. controls (2,139 ± 1,102 vs. 382 ± 181 pmol/l, P < 0.01). Multiple linear regression, adjusting for age, sex, dialysis vintage, diabetes mellitus, CVD history, body mass index, and blood pressure, revealed that dp-ucMGP was independently related to PWV (standardized β = 0.49) and FMD (standardized β = -0.53) (both P < 0.01).
Our data suggest that the higher plasma dp-ucMGP concentrations found in African American HD patients may be associated with greater arterial stiffness and endothelial dysfunction.
基质 Gla 蛋白(MGP)是一种血管钙化抑制剂,其活性依赖于维生素 K。有证据表明,血浆中无活性 MGP 水平升高(脱磷酸非羧化 MGP,dp-ucMGP;表明血管维生素 K 状态较差)与心血管疾病(CVD)风险增加相关。尽管非裔美国人患肾衰竭和 CVD 事件的比率最高,但 dp-ucMGP 与 CVD 风险标志物之间的关系尚未在该人群中进行研究。我们研究了非裔美国血液透析(HD)患者和健康对照组之间的血管维生素 K 状态(通过血浆 dp-ucMGP 测量),以及仅在 HD 患者中 dp-ucMGP 与动脉僵硬和内皮功能的相关性。
在 37 名非裔美国 HD 患者和 37 名年龄和种族匹配的对照组中,通过酶免疫测定法测量血浆 dp-ucMGP 作为血管维生素 K 状态的标志物。仅在 HD 患者中,通过平板张力测量法评估颈动脉-股动脉脉搏波速度(PWV;动脉僵硬测量)和肱动脉血流介导的扩张(FMD;内皮功能测量)。
HD 患者的平均 dp-ucMGP 水平比对照组高 5.6 倍(2139 ± 1102 比 382 ± 181 pmol/l,P < 0.01)。多元线性回归,调整年龄、性别、透析龄、糖尿病、CVD 病史、体重指数和血压,显示 dp-ucMGP 与 PWV(标准化β=0.49)和 FMD(标准化β=-0.53)独立相关(均 P < 0.01)。
我们的数据表明,非裔美国 HD 患者血浆中 dp-ucMGP 浓度升高可能与动脉僵硬和内皮功能障碍有关。