IRCCS S. Orsola-Malpighi, Hypertension and Cardiovascular Risk Factors Research Unit, Department of Medical and Surgical Science, University of Bologna, Italy (C.B., D.A., A.F.G.C.).
Department of Pediatrics, University of Valencia, Spain (E.L.).
Hypertension. 2022 Sep;79(9):1927-1936. doi: 10.1161/HYPERTENSIONAHA.122.17956. Epub 2022 Jun 6.
Uric acid is the final product of purine metabolism, and its increased serum levels have been directly involved in the pathogenesis and natural history of hypertension. The relationship between elevated uric acid and hypertension has been proven in both animals and humans, and its relevance is already evident in childhood and adolescent population. The mechanism responsible for blood pressure increase in hyperuricemic subjects is implicating both oxidative stress and intracellular urate activity with a primary involvement of XOR (xanthine-oxidoreductase activity). An increase in the relative risk of hypertension has been confirmed by genetic data and by large meta-analyses of epidemiological data. The effects of urate-lowering treatment on blood pressure control in patients with elevated serum uric acid has been investigated in a small number of reliable studies with a large heterogeneity of patient populations and study designs. However, 2 large meta-analyses suggest a significant effect of urate-lowering treatment on blood pressure, thus confirming the significant relationship between high serum urate and blood pressure. The future research should be focused on a more appropriate identification of patients with cardiovascular hyperuricemia by considering the correct cardiovascular threshold of serum urate, the time-course of uricemia fluctuations, and the identification of reliable markers of urate overproduction that could significantly clarify the clinical and therapeutic implications of the interaction between serum uric acid and hypertension.
尿酸是嘌呤代谢的终产物,其血清水平升高与高血压的发病机制和自然史直接相关。在动物和人类中都已经证明了尿酸升高与高血压之间的关系,其相关性在儿童和青少年人群中已经很明显。在高尿酸血症患者中,导致血压升高的机制涉及氧化应激和细胞内尿酸活性,XOR(黄嘌呤氧化还原酶活性)是主要的参与因素。遗传数据和大规模流行病学数据分析都证实了尿酸升高与高血压的相对风险增加有关。少数可靠研究调查了降低尿酸治疗对血清尿酸升高患者血压控制的影响,但这些研究的患者人群和研究设计存在很大的异质性。然而,两项大型荟萃分析表明,降低尿酸治疗对血压有显著影响,因此证实了高血清尿酸与血压之间的显著关系。未来的研究应集中在通过考虑正确的血清尿酸心血管阈值、尿酸波动的时间过程以及识别可靠的尿酸生成标志物,更恰当地确定心血管高尿酸血症患者,这可能会显著阐明血清尿酸与高血压之间相互作用的临床和治疗意义。