Gordon M M, Porter D R, Capell H A
Centre for Rheumatic Diseases, Glasgow Royal Infirmary, Glasgow.
Ann Rheum Dis. 1999 May;58(5):288-90. doi: 10.1136/ard.58.5.288.
Sulphasalazine (SSZ) has been reported to cause drug induced systemic lupus erythematosus (SLE), but diagnosis of this complication in the context of rheumatoid arthritis (RA) is difficult.
To determine prospectively: (1) if patients become seropositive for antinuclear antibodies (ANA) during prolonged treatment with SSZ without clinical evidence of SLE; (2) if ANA positive patients develop more adverse reactions than ANA negative patients; (3) if drug induced SLE was identified in this cohort.
200 patients enrolled in a randomised prospective trial of SSZ and auranofin (AUR) were followed up for five years. Baseline and annual ANA results were collected along with information on drug toxicity and reasons for discontinuation of treatment.
Over five years 24 patients stopped taking SSZ and 49 AUR because of side effects. Of the features common to SLE, rash developed in nine SSZ patients and 11 AUR treated patients and mouth ulcers in three and four patients respectively. Six SSZ treated patients and three treated with AUR developed leucopenia, which promptly resolved with drug withdrawal. No adverse event was ascribed to drug induced SLE. Of the 72 SSZ treated patients who were ANA negative or weakly positive at outset, 14 (19%) became strongly ANA positive compared with 11 (14%) of 80 AUR patients. Patients ANA positive at baseline or who became ANA positive were not more likely to develop drug toxicity or to withdraw from treatment than those ANA negative throughout.
ANA positivity is common in patients with RA, but the presence or development of ANA did not increase the likelihood of withdrawing from treatment. No case of drug induced SLE was seen over five years in this study.
据报道,柳氮磺胺吡啶(SSZ)可引起药物性系统性红斑狼疮(SLE),但在类风湿关节炎(RA)背景下诊断这种并发症很困难。
前瞻性地确定:(1)在长期接受SSZ治疗且无SLE临床证据的患者中,抗核抗体(ANA)是否会转为阳性;(2)ANA阳性患者是否比ANA阴性患者出现更多不良反应;(3)该队列中是否能识别出药物性SLE。
对200名参加SSZ和金诺芬(AUR)随机前瞻性试验的患者进行了五年随访。收集基线和年度ANA结果以及药物毒性信息和停药原因。
在五年期间,24名患者因副作用停止服用SSZ,49名患者停止服用AUR。在SLE常见的特征中,9名服用SSZ的患者和11名接受AUR治疗的患者出现皮疹,分别有3名和4名患者出现口腔溃疡。6名接受SSZ治疗的患者和3名接受AUR治疗的患者出现白细胞减少,停药后迅速缓解。没有不良事件归因于药物性SLE。在72名最初ANA阴性或弱阳性的接受SSZ治疗的患者中,14名(19%)ANA转为强阳性,而80名接受AUR治疗的患者中有11名(14%)。基线时ANA阳性或ANA转为阳性的患者与始终ANA阴性的患者相比,发生药物毒性或停药的可能性并不更高。
ANA阳性在RA患者中很常见,但ANA的存在或出现并没有增加停药的可能性。在本研究的五年中未发现药物性SLE病例。