Selby Warwick, Pavli Paul, Crotty Brendan, Florin Tim, Radford-Smith Graham, Gibson Peter, Mitchell Brent, Connell William, Read Robert, Merrett Michael, Ee Hooi, Hetzel David
Royal Prince Alfred Hospital, Sydney, Australia.
Gastroenterology. 2007 Jun;132(7):2313-9. doi: 10.1053/j.gastro.2007.03.031. Epub 2007 Mar 21.
BACKGROUND & AIMS: Mycobacterium avium subspecies paratuberculosis has been proposed as a cause of Crohn's disease. We report a prospective, parallel, placebo-controlled, double-blind, randomized trial of 2 years of clarithromycin, rifabutin, and clofazimine in active Crohn's disease, with a further year of follow-up.
Two hundred thirteen patients were randomized to clarithromycin 750 mg/day, rifabutin 450 mg/day, clofazimine 50 mg/day or placebo, in addition to a 16-week tapering course of prednisolone. Those in remission (Crohn's Disease Activity Index <or=150) at week 16 continued their study medications in the maintenance phase of the trial. Primary end points were the proportion of patients experiencing at least 1 relapse at 12, 24, and 36 months.
At week 16, there were significantly more subjects in remission in the antibiotic arm (66%) than the placebo arm (50%; P=.02). Of 122 subjects entering the maintenance phase, 39% taking antibiotics experienced at least 1 relapse between weeks 16 and 52, compared with 56% taking placebo (P=.054). At week 104, the figures were 26% and 43%, respectively (P=.14). During the following year, 59% of the antibiotic group and 50% of the placebo group relapsed (P=.54).
Using combination antibiotic therapy with clarithromycin, rifabutin, and clofazimine for up to 2 years, we did not find evidence of a sustained benefit. This finding does not support a significant role for Mycobacterium avium subspecies paratuberculosis in the pathogenesis of Crohn's disease in the majority of patients. Short-term improvement was seen when this combination was added to corticosteroids, most likely because of nonspecific antibacterial effects.
鸟分枝杆菌副结核亚种被认为是克罗恩病的病因之一。我们报告了一项前瞻性、平行、安慰剂对照、双盲、随机试验,该试验对213例活动性克罗恩病患者使用克拉霉素、利福布汀和氯法齐明进行为期2年的治疗,并进行了为期1年的随访。
213例患者被随机分为接受每日750毫克克拉霉素、每日450毫克利福布汀、每日50毫克氯法齐明或安慰剂治疗,此外还接受了为期16周的泼尼松龙递减疗程治疗。在第16周时病情缓解(克罗恩病活动指数≤150)的患者在试验的维持阶段继续服用其研究药物。主要终点是在12个月、24个月和36个月时至少经历1次复发的患者比例。
在第16周时,抗生素治疗组病情缓解的受试者(66%)显著多于安慰剂组(50%;P = 0.02)。在进入维持阶段的122例受试者中,服用抗生素的受试者中有39%在第16周至52周期间至少经历1次复发,而服用安慰剂的受试者这一比例为56%(P = 0.054)。在第104周时,这两个数字分别为26%和43%(P = 0.14)。在接下来的一年中,抗生素组59%的患者和安慰剂组50%的患者复发(P = 0.54)。
使用克拉霉素、利福布汀和氯法齐明联合抗生素治疗长达2年,我们未发现持续获益的证据。这一发现不支持鸟分枝杆菌副结核亚种在大多数克罗恩病患者发病机制中起重要作用的观点。当这种联合治疗与皮质类固醇联合使用时,可观察到短期改善,这很可能是由于非特异性抗菌作用。