Obeid Rima, Geisel Juergen, Nix Wilfred A
Department of Clinical Chemistry and Laboratory Medicine, Saarland University Hospital, Building 57, 66424 Homburg/Saar, Germany.
Department of Neurology, Mains University Hospital, Langenbeckstr 1, 55131 Mainz, Germany.
Diagnostics (Basel). 2019 Mar 6;9(1):28. doi: 10.3390/diagnostics9010028.
Vascular diseases are multifactorial and several risk factors may have synergetic effect on the global vascular risk. Among patients with diabetes, we investigated whether vitamin B6 species differ according to global cardiovascular risk.
The present observational study included 122 patients with type 2 diabetes (mean (SD) age = 69.9 (9.1) years; 50% men). Concentrations of vitamin B6 vitamers were measured. Classical blood biomarkers and risk factors were used to compute a multivariate risk score.
Plasma concentrations of 4-pyridoxic acid were higher in patients with high risk versus those with low risk scores (48.2 (63.7) vs. 31.9 (15.0) nmol/L; = 0.031). Plasma pyridoxine was significantly lowered in patients at high risk (2.8 (28.4) vs. 38.1 (127.8) nmol/L; = 0.003). PAr index (4-pyridoxic acid/pyridoxal + pyridoxal 5'-phosphate) (1.05 (0.07) vs. 0.84 (0.06); = 0.017) and the ratio of 4-pyridoxic acid/pyridoxine (7.0 (4.8) vs. 3.9 (3.2); < 0.001) were higher in patients at high risk. After adjustment for cystatin C and C-reactive protein, only pyridoxine and 4-pyridoxic acid/pyridoxine ratio remained significantly different according to vascular risk scores. 4-Pyridoxic acid/pyridoxine ratio was the best marker to discriminate between patients according to their risk scores-area under the curve (AUC) (95% confidence intervals (CI)) = 0.72 (0.62⁻0.81). 4-Pyridoxic acid/pyridoxine ratio was directly related to plasma levels of soluble vascular cell adhesion molecule 1.
Vitamin B6 metabolism was shifted in patients with multiple vascular risk factors. The catabolism to 4-pyridoxic acid was enhanced, whereas the catabolism to pyridoxine was lowered. High 4-Pyridoxic acid/pyridoxine ratio is independently associated with global cardiovascular risk.
血管疾病是多因素导致的,多种风险因素可能对整体血管风险产生协同作用。在糖尿病患者中,我们研究了维生素B6各成分是否因整体心血管风险而异。
本观察性研究纳入了122例2型糖尿病患者(平均(标准差)年龄 = 69.9(9.1)岁;50%为男性)。测量了维生素B6各形式的浓度。使用经典血液生物标志物和风险因素计算多变量风险评分。
高风险患者的4-吡哆酸血浆浓度高于低风险评分患者(48.2(63.7)对31.9(15.0)nmol/L;P = 0.031)。高风险患者的血浆吡哆醇显著降低(2.8(28.4)对38.1(127.8)nmol/L;P = 0.003)。高风险患者的PAr指数(4-吡哆酸/吡哆醛 + 吡哆醛5'-磷酸)(1.05(0.07)对0.84(0.06);P = 0.017)以及4-吡哆酸/吡哆醇的比值(7.0(4.8)对3.9(3.2);P < 0.001)更高。在调整胱抑素C和C反应蛋白后,根据血管风险评分,只有吡哆醇和4-吡哆酸/吡哆醇比值仍存在显著差异。4-吡哆酸/吡哆醇比值是根据风险评分区分患者的最佳标志物 - 曲线下面积(AUC)(95%置信区间(CI)) = 0.72(0.62⁻0.81)。4-吡哆酸/吡哆醇比值与可溶性血管细胞粘附分子1的血浆水平直接相关。
具有多种血管风险因素的患者维生素B6代谢发生改变。向4-吡哆酸的分解代谢增强,而向吡哆醇的分解代谢降低。高4-吡哆酸/吡哆醇比值与整体心血管风险独立相关。