Bomalaski John S, Clark Mike A
Medical College of Pennsylvania Hospital, Drexel University College of Medicine, 3300 Henry Avenue, Philadelphia, PA 19129, USA.
Curr Rheumatol Rep. 2004 Jun;6(3):240-7. doi: 10.1007/s11926-004-0075-3.
Although allopurinol has been available for approximately 50 years, hyperuricemia and its sequelae are not only prevalent, but the incidence and costs associated with this disorder continue to increase. However, several new therapies have been developed. Recombinant urate oxidase has been useful in the treatment of tumor lysis hyperuricemia, and pegylated urate oxidase shows promise in patients with hyperuricemia and gout. Febuxostat and Y-700 are new oral xanthine oxidase inhibitors that are in human clinical trials. Tailoring of antilipid therapy in selected hyperuricemic and hyperlipidemic patients with fenofibrate may be of benefit in lowering blood cholesterol and uric acid levels. Similarly, treatment of selected hyperuricemic patients who also are hypertensive with losartan or amlodipine may be beneficial in lowering blood pressure and hyperuricemia. Despite these advances, new treatments for hyperuricemia are needed.
尽管别嘌醇已问世约50年,但高尿酸血症及其后遗症不仅普遍存在,而且与这种疾病相关的发病率和成本仍在不断增加。然而,已经开发出了几种新的治疗方法。重组尿酸氧化酶已用于治疗肿瘤溶解引起的高尿酸血症,聚乙二醇化尿酸氧化酶在高尿酸血症和痛风患者中显示出前景。非布索坦和Y-700是正在进行人体临床试验的新型口服黄嘌呤氧化酶抑制剂。在选定的高尿酸血症和高脂血症患者中使用非诺贝特进行抗脂质治疗的调整,可能有助于降低血液胆固醇和尿酸水平。同样,对选定的同时患有高血压的高尿酸血症患者使用氯沙坦或氨氯地平进行治疗,可能有助于降低血压和高尿酸血症。尽管有这些进展,但仍需要新的高尿酸血症治疗方法。