Airways Disease Section, National Heart and Lung Institute, Imperial College London, Dovehouse Street, London SW3 6LY, England.
Chest. 2010 Jun;137(6):1338-44. doi: 10.1378/chest.09-2363. Epub 2010 Mar 18.
Inhaled corticosteroids (ICS) have proved disappointing at reducing airway inflammation in COPD. However, previous studies indicate that low doses of theophylline enhance the activity of a key corticosteroid-associated corepressor protein, histone deacetylase (HDAC)2, which is reduced in COPD. This may account, at least in part, for the relative corticosteroid resistance. Thus, combination therapy with an ICS and low-dose theophylline may be of benefit in the treatment of COPD.
To test the hypothesis that ICS and theophylline have a greater therapeutic effect than theophylline alone, 30 patients with COPD were treated with placebo theophylline capsules and either inhaled fluticasone propionate (FP) (500 microg bid) or inhaled placebo for 4 weeks in a double-dummy, randomized, double-blind, parallel study. After a 2-week washout, patients were given active theophylline capsules (plasma level of 8.8-12.4 mg/L).
In an across-arm comparison, combination treatment with FP and theophylline did not reduce total sputum neutrophils but significantly reduced total sputum eosinophils (P < .05). Additional across-arm comparisons suggest a further reduction in percentage sputum neutrophils and sputum chemokine (C-X-C motif) ligand 8/IL-8 (P < .05). Furthermore, within-arm observational data also demonstrated increases in forced midexpiratory flow rate and FEV(1)% predicted (P < .05) following combination treatment only. In an open-label study, low-dose theophylline when added to inhaled FP increased total HDAC activity in peripheral blood monocytes ninefold (P < .01) compared with FP alone from the same patients with COPD.
Combination therapy with an inhaled corticosteroid and low-dose theophylline may attenuate airway inflammation in patients with COPD.
clinicaltrials.gov; Identifier NCT00241631.
吸入皮质类固醇(ICS)已被证明在减少 COPD 气道炎症方面效果不佳。然而,先前的研究表明,低剂量茶碱可增强关键皮质类固醇相关核心抑制蛋白组蛋白去乙酰化酶(HDAC)2 的活性,而 COPD 患者的 HDAC2 活性降低。这至少可以部分解释皮质类固醇相对抵抗的原因。因此,ICS 与低剂量茶碱联合治疗可能对 COPD 的治疗有益。
为了验证ICS 和茶碱联合治疗比单独茶碱治疗具有更大疗效的假设,30 名 COPD 患者接受了安慰剂茶碱胶囊和吸入丙酸氟替卡松(FP)(500 μg bid)或吸入安慰剂治疗,为期 4 周,采用双盲、随机、平行研究。在 2 周洗脱期后,患者给予活性茶碱胶囊(血浆水平为 8.8-12.4 mg/L)。
在跨臂比较中,FP 和茶碱联合治疗并未减少总痰中性粒细胞,但显著减少了总痰嗜酸性粒细胞(P <.05)。进一步的跨臂比较表明,痰中性粒细胞百分比和痰趋化因子(C-X-C 基序)配体 8/IL-8 也有进一步减少(P <.05)。此外,仅在联合治疗时,臂内观察数据也显示用力呼气中期流速和 FEV1%预计值增加(P <.05)。在一项开放标签研究中,与 COPD 患者单独接受 FP 治疗相比,低剂量茶碱联合吸入 FP 可使外周血单核细胞中的总 HDAC 活性增加 9 倍(P <.01)。
ICS 与低剂量茶碱联合治疗可能会减轻 COPD 患者的气道炎症。
clinicaltrials.gov;标识符 NCT00241631。