Späth M, Welzel D, Färber L
Friedrich-Baur-Institut, University of Munich, MünchenGermany.
Scand J Rheumatol Suppl. 2000;113:72-7.
The serotonin system presumably is involved in the pathogenesis of chronic fatigue syndrome (CFS). Results from a few studies led to the hypothesis of a "postsynaptic hyperresponsiveness" in CFS. Therefore we intended to evaluate the efficacy of 5-HT3 receptor antagonists in the treatment of CFS.
2 patient groups (10 patients each; CFS according to the CDC classification criteria) received either oral tropisetron (5 mg once daily) or oral ondansetron (2 x 8 mg daily), open-labelled. Treatment duration was 15 days. Treatment response was evaluated by visual analog scales (VAS) for fatigue and capability.
19 patients finished their respective study. In the tropisetron group 6/9 (VAS fatigue) and 7/9 (VAS capability) patients documented benefit, 8/10 rsp. 8/10 patients in the ondansetron group. The score changes (VAS before and after treatment) in case of response were more pronounced in the tropisetron group. The frequency of concomitant symptoms did not differ significantly in the treatment groups. The overall analysis of both studies showed a remarkable improvement (> or = 35%) of approximately one third of the patients in both VAS. Treatment was well tolerated.
Our preliminary results encourage to perform placebo-controlled, double-blind studies to further evaluate the efficacy of 5-HT3 receptor antagonists in the treatment of CFS.
血清素系统可能参与慢性疲劳综合征(CFS)的发病机制。一些研究结果提出了CFS中“突触后高反应性”的假说。因此,我们旨在评估5-HT3受体拮抗剂治疗CFS的疗效。
2组患者(每组10例;根据美国疾病控制与预防中心分类标准诊断为CFS),分别接受口服托烷司琼(5mg,每日1次)或口服昂丹司琼(2×8mg,每日1次),采用开放标签。治疗持续15天。通过视觉模拟量表(VAS)评估疲劳和能力方面的治疗反应。
19例患者完成各自的研究。托烷司琼组中,6/9(VAS疲劳)和7/9(VAS能力)的患者记录有获益,昂丹司琼组分别为8/10和8/10例患者。有反应的患者中,托烷司琼组治疗前后的评分变化(VAS)更为明显。治疗组中伴随症状的发生率无显著差异。两项研究的总体分析显示,在两个VAS量表中约三分之一的患者有显著改善(≥35%)。治疗耐受性良好。
我们的初步结果鼓励开展安慰剂对照的双盲研究,以进一步评估5-HT3受体拮抗剂治疗CFS的疗效。