Astbury C, Hill J, Bird H A
Clinical Pharmacology Unit, Royal Bath Hospital, Harrogate.
Ann Rheum Dis. 1988 Apr;47(4):323-7. doi: 10.1136/ard.47.4.323.
The antirheumatoid activity of sulphasalazine and sulphapyridine may result from their antibacterial properties. The second line activity of sulphamethoxazole, in the form of cotrimoxazole (CTZ), has been investigated by treatment of 13 patients with RA for 24 weeks with CTZ (480 mg three times a day). The drug was found to be poorly tolerated, only five of the thirteen patients recruited completing the study. High circulating concentrations of sulphamethoxazole were found, with mean (SD) steady state serum concentrations reaching 54.02 (23.38) micrograms/ml. A significant reduction in serum IgM from 280 to 130 IU/l was observed, but otherwise disease activity remained unchanged or deteriorated throughout the course of the study. In contrast, patients with RA treated with sulphapyridine (1.25 g a day) showed improvement in disease activity. The results argue against an antibacterial mechanism of action for sulphasalazine and sulphapyridine in rheumatoid arthritis, unless this occurs at a site inaccessible to sulphamethoxazole.
柳氮磺吡啶和磺胺吡啶的抗类风湿活性可能源于它们的抗菌特性。以复方新诺明(CTZ)形式存在的磺胺甲恶唑的二线活性,已通过对13例类风湿关节炎患者使用CTZ(每日三次,每次480毫克)进行24周治疗进行了研究。发现该药物耐受性差,招募的13例患者中只有5例完成了研究。发现磺胺甲恶唑的循环浓度很高,平均(标准差)稳态血清浓度达到54.02(23.38)微克/毫升。观察到血清IgM从280 IU/l显著降低至130 IU/l,但在整个研究过程中,疾病活动度保持不变或恶化。相比之下,接受磺胺吡啶(每日1.25克)治疗的类风湿关节炎患者疾病活动度有所改善。这些结果表明,柳氮磺吡啶和磺胺吡啶在类风湿关节炎中的作用机制并非抗菌机制,除非这种作用发生在磺胺甲恶唑无法到达的部位。