Department of Cardiovascular, Renal and Metabolic Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan.
Department of Public Health, Sapporo Medical University School of Medicine, Sapporo, Japan.
Hypertens Res. 2021 Sep;44(9):1213-1220. doi: 10.1038/s41440-021-00679-1. Epub 2021 Jun 11.
Xanthine oxidoreductase (XOR), a rate-limiting and catalyzing enzyme of uric acid formation in purine metabolism, is involved in reactive oxygen species generation. Plasma XOR activity has been shown to be a novel metabolic biomarker related to obesity, liver dysfunction, hyperuricemia, dyslipidemia, and insulin resistance. However, the association between plasma XOR activity and hypertension has not been fully elucidated. We investigated the association of hypertension with plasma XOR activity in 271 nondiabetic subjects (male/female: 119/152) who had not taken any medications in the Tanno-Sobetsu Study, a population-based cohort. Males had higher plasma XOR activity than females. Plasma XOR activity was positively correlated with mean arterial pressure (r = 0.128, P = 0.036). When the subjects were divided by the presence and absence of hypertension into an HT group (male/female: 34/40) and a non-HT group (male/female: 85/112), plasma XOR activity in the HT group was significantly higher than that in the non-HT group (median: 39 vs. 28 pmol/h/mL, P = 0.028). There was no significant difference in uric acid levels between the two groups. Multivariable logistic regression analysis showed that plasma XOR activity (odds ratio: 1.091 [95% confidence interval: 1.023-1.177] per 10 pmol/h/mL, P = 0.007) was an independent determinant of the risk for hypertension after adjustment for age, sex, current smoking and alcohol consumption, estimated glomerular filtration rate, brain natriuretic peptide, and insulin resistance index. The interaction of sex with plasma XOR activity was not significant for the risk of hypertension. In conclusion, plasma XOR activity is independently associated with hypertension in nondiabetic individuals who are not taking any medications.
黄嘌呤氧化还原酶(XOR)是嘌呤代谢中尿酸形成的限速酶和催化酶,参与活性氧的产生。已证实血浆 XOR 活性是与肥胖、肝功能障碍、高尿酸血症、血脂异常和胰岛素抵抗相关的新型代谢生物标志物。然而,血浆 XOR 活性与高血压之间的关系尚未完全阐明。我们在 Tanno-Sobetsu 研究中调查了 271 名未服用任何药物的非糖尿病受试者(男性/女性:119/152)的高血压与血浆 XOR 活性之间的关系,该研究是一项基于人群的队列研究。男性的血浆 XOR 活性高于女性。血浆 XOR 活性与平均动脉压呈正相关(r=0.128,P=0.036)。当根据是否存在高血压将受试者分为 HT 组(男性/女性:34/40)和非-HT 组(男性/女性:85/112)时,HT 组的血浆 XOR 活性显著高于非-HT 组(中位数:39 与 28 pmol/h/mL,P=0.028)。两组的尿酸水平无显著差异。多变量逻辑回归分析显示,在校正年龄、性别、当前吸烟和饮酒、估算肾小球滤过率、脑钠肽和胰岛素抵抗指数后,血浆 XOR 活性(每增加 10 pmol/h/mL,比值比:1.091 [95%置信区间:1.023-1.177],P=0.007)是高血压风险的独立决定因素。性别与血浆 XOR 活性对高血压风险的交互作用不显著。总之,在未服用任何药物的非糖尿病个体中,血浆 XOR 活性与高血压独立相关。