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Is mizoribine a new therapeutic agent for Sjogren's syndrome?

机译:咪唑立滨是否是干燥综合征的新型治疗剂?

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In a multicenter, open-label study conducted in Japan between July 2004 and May 2005, Nakayamada et al. tested the safety and efficacy of mizoribine for the treatment of primary Sjogren's syndrome (pSS). Mizoribine 50 mg was administered three times a day for 16 weeks to 59 patients with pSS, 7 of whom withdrew because of adverse drug reactions; however, no serious adverse events were noted. In the 48 patients who completed the study, an increase from baseline in median salivary secretion volume, evaluated using the Saxon test, was apparent at week 8 and was significant at week 16 (P <0.05). At 16 weeks, significant improvements from baseline were also seen in patients' assessments of dry mouth and dry eyes, physicians' assessment of oral sicca symptoms, labioangular sicca symptoms and physicians' overall assessment, all measured using a 10 cm visual analog scale. The findings suggest that mizoribine could be an effective treatment for pSS.
机译:中山田等人在2004年7月至2005年5月间在日本进行的一项多中心,开放标签的研究中。测试了咪唑立滨治疗原发性干燥综合征(pSS)的安全性和有效性。 59例pSS患者每天3次服用咪唑立滨50 mg,共16周,其中7例因药物不良反应而退出治疗。但是,没有发现严重的不良事件。在完成研究的48位患者中,使用Saxon测试评估的唾液中位分泌量中位数比基线增加,在第8周时明显,在第16周时显着(P <0.05)。在第16周时,患者的口干和眼干评估,医师的口腔干燥症状,口唇部干燥症状和医师的总体评估也均比基线有了显着改善,所有评估均使用10 cm视觉模拟量表进行。研究结果表明,咪唑立滨可能是治疗pSS的有效方法。

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