医学
非布索坦
痛风
低尿酸血症
内科学
尿酸
尿酸
不利影响
安慰剂
高尿酸血症
临床试验
黄嘌呤氧化酶
观察研究
重症监护医学
病理
替代医学
生物化学
化学
酶
作者
María Vanessa Pérez-Gómez,Lorenz-Alexander Bartsch,Esmeralda Castillo-Rodríguez,Raúl Fernández-Prado,Mehmet Kanbay,Alberto Ortíz
标识
DOI:10.1016/j.amjmed.2018.12.010
摘要
In observational studies, high serum urate levels are associated with adverse outcomes, including mortality. However, the hypothesis that urate-lowering may improve nongout outcomes has not been confirmed by placebo-controlled clinical trials. On the contrary, 7 recent placebo-controlled trials of urate-lowering drugs with different mechanisms of action (uricosuric: lesinurad; xanthine oxidase inhibition: febuxostat; uricase: pegloticase) have observed higher mortality or trends to higher mortality in gout patients, with the largest decreases in serum urate. Because all urate-lowering mechanisms were implicated, this raises safety concerns about urate-lowering itself. Far from unexpected, the higher mortality associated with more intense urate-lowering is in line with the U-shaped association of urate with mortality in some observational studies. Urate accounts for most of the antioxidant capacity of plasma, and strategies to increase urate are undergoing clinical trials in neurological disease. Post hoc analysis of recent trials should explore whether the magnitude of urate-lowering is associated with adverse outcomes, and safety trials are needed before guidelines recommend lowering serum urate below certain thresholds.
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