Price E J, Rigby S P, Clancy U, Venables P J
Department of Rheumatology, Charing Cross Hospital and Kennedy Institute of Rheumatology, London, England, UK.
J Rheumatol. 1998 May;25(5):896-9.
To establish whether there is a place for low dose azathioprine (AZA) as a disease modifying agent in patients with uncomplicated primary Sjögren's syndrome (SS).
Twenty-five patients with primary SS were entered into a double blind, placebo controlled trial of AZA (1 mg/kg/day) for a period of 6 months.
Six patients, all receiving active drug, withdrew because of side effects. There was no significant change in disease activity variables when measured clinically, serologically, or histologically.
This trial suggests that low dose AZA does not have a role as a disease modifying agent in SS.
确定低剂量硫唑嘌呤(AZA)作为一种病情改善药物在无并发症的原发性干燥综合征(SS)患者中是否有应用价值。
25例原发性SS患者进入一项AZA(1毫克/千克/天)的双盲、安慰剂对照试验,为期6个月。
6例患者均接受活性药物治疗,因副作用退出试验。在临床、血清学或组织学测量时,疾病活动变量无显著变化。
该试验表明低剂量AZA在SS中不具有病情改善药物的作用。