Hypertension in Africa Research Team (HART) and.
MRC Research Unit for Hypertension and Cardiovascular Disease, North-West University, Potchefstroom, South Africa.
J Hypertens. 2019 Jun;37(6):1157-1166. doi: 10.1097/HJH.0000000000002040.
Early-life exposures to cardiovascular risk factors may manifest as early vascular ageing, a phenomenon to which black populations are more prone. The metabolome provides insight into the current state and regulation of physiological processes and was used to investigate the early molecular determinants of arterial stiffness.
Black (N = 80) and white (N = 80) men and women (aged 20-30 years, clinic blood pressure <140 and 90 mmHg) across the arterial stiffness spectrum were included. Carotid-femoral pulse wave velocity, central SBP (cSBP) and central pulse pressure (cPP) were measured. NMR spectroscopy, liquid chromatography tandem mass spectrometry and gas chromatography-time of flight-mass spectrometry methods produced metabolomic data.
Differences (d ≥ 0.3) in 34 metabolites between black and white groups were found (adjusted for multiple comparisons). Only cSBP were higher in the black group (P = 0.003). Lower dietary protein intake (P < 0.001), but higher urinary nonessential amino acid levels were found in the black group (q ≤ 0.05). In multivariable-adjusted regression models cSBP and cPP inversely correlated with various nonessential amino acids, but only in black adults. These include associations of cSBP with 4-hydroxyproline (β = -0.24; P = 0.042), alanine: (β = -0.29; P = 0.015), glutamine (β = -0.25; P = 0.028), glycine (β = -0.26; P = 0.027), histidine (β = -0.30; P = 0.009), serine (β = -0.29; P = 0.012), and associations of cPP with alanine (β = -0.31; P = 0.005) and serine (β = -0.26; P = 0.019).
These amino acids play pivotal roles in collagen metabolism, glucose metabolism and oxidative stress and this ethnic-specific finding suggests that biosynthesis of nonessential amino acids may be upregulated to protect the vasculature against the onset of early vascular deterioration.
心血管危险因素的早期暴露可能表现为血管早期老化,黑人更易发生这种现象。代谢组学可深入了解生理过程的现状和调控机制,被用于研究动脉僵硬的早期分子决定因素。
纳入了动脉僵硬谱内的黑人(N=80)和白人(N=80)男性和女性(年龄 20-30 岁,诊室血压<140 和 90mmHg)。测量了颈股脉搏波速度、中心收缩压(cSBP)和中心脉压(cPP)。NMR 光谱、液相色谱串联质谱和气相色谱飞行时间质谱方法产生了代谢组学数据。
发现黑人组与白人组之间有 34 种代谢物存在差异(经多重比较调整)。黑人组的 cSBP 更高(P=0.003)。黑人组的饮食蛋白质摄入量较低(P<0.001),但尿中非必需氨基酸水平较高(q≤0.05)。在多变量调整回归模型中,cSBP 和 cPP 与各种非必需氨基酸呈负相关,但仅在黑人成年人中如此。这包括 cSBP 与 4-羟脯氨酸(β=-0.24;P=0.042)、丙氨酸(β=-0.29;P=0.015)、谷氨酰胺(β=-0.25;P=0.028)、甘氨酸(β=-0.26;P=0.027)、组氨酸(β=-0.30;P=0.009)、丝氨酸(β=-0.29;P=0.012)之间的相关性,以及 cPP 与丙氨酸(β=-0.31;P=0.005)和丝氨酸(β=-0.26;P=0.019)之间的相关性。
这些氨基酸在胶原代谢、糖代谢和氧化应激中发挥关键作用,这种种族特异性发现表明非必需氨基酸的生物合成可能上调,以保护血管免受早期血管恶化的发生。