Conway Richard, Low Candice, Coughlan Robert J, O'Donnell Martin J, Carey John J
Department of Rheumatology, Galway University Hospitals, Galway, Republic of Ireland National University of Ireland Galway, Galway, Republic of Ireland
Department of Rheumatology, Connolly Hospital Blanchardstown, Dublin, Republic of Ireland.
BMJ. 2015 Mar 13;350:h1269. doi: 10.1136/bmj.h1269.
To evaluate the relative risk of pulmonary disease among patients with psoriasis, psoriatic arthritis, and inflammatory bowel disease treated with methotrexate.
PubMed, Cochrane central register of controlled trials, and Embase to 9 January 2014.
Double blind randomised controlled trials of methotrexate versus placebo or active comparator agents in adults with psoriatic arthritis, psoriasis, or inflammatory bowel disease. Studies with fewer than 50 participants or of less than 12 weeks' duration were excluded.
Two investigators independently searched both databases. All authors reviewed selected studies. We compared relative risk differences using the Mantel-Haenszel random effects method to assess total respiratory adverse events, infectious respiratory adverse events, non-infectious respiratory adverse events, interstitial lung disease, and death.
Seven studies met our inclusion criteria, six with placebo as the comparator. Heterogeneity across the studies was not significant (I(2)=0%), allowing combination of trial results. 504 respiratory adverse events were documented in 1630 participants. Methotrexate was not associated with an increased risk of adverse respiratory events (relative risk 1.03, 95% confidence interval 0.90 to 1.17), respiratory infections (1.02, 0.88 to 1.19), or non-infectious respiratory events (1.07, 0.58 to 1.96). No pulmonary deaths occurred.
Findings suggested that there was no increased risk of lung disease in methotrexate treated patients with non-malignant inflammatory diseases. Given the limitations of the study, however, we cannot exclude a small but clinically important risk.
评估接受甲氨蝶呤治疗的银屑病、银屑病关节炎和炎症性肠病患者发生肺部疾病的相对风险。
截至2014年1月9日的PubMed、Cochrane对照试验中央注册库和Embase。
甲氨蝶呤与安慰剂或活性对照药物用于成人银屑病关节炎、银屑病或炎症性肠病的双盲随机对照试验。排除参与者少于50例或持续时间少于12周的研究。
两名研究者独立检索两个数据库。所有作者对入选研究进行了评估。我们使用Mantel-Haenszel随机效应方法比较相对风险差异,以评估总的呼吸道不良事件、感染性呼吸道不良事件、非感染性呼吸道不良事件、间质性肺病和死亡情况。
七项研究符合我们的纳入标准,六项以安慰剂作为对照。各研究间的异质性不显著(I²=0%),因此可以合并试验结果。1630名参与者中记录到504例呼吸道不良事件。甲氨蝶呤与呼吸道不良事件风险增加无关(相对风险1.03,95%置信区间0.90至1.17)、呼吸道感染(1.02,0.88至1.19)或非感染性呼吸道事件(1.07,0.58至1.96)。未发生肺部死亡。
研究结果表明,接受甲氨蝶呤治疗的非恶性炎症性疾病患者发生肺部疾病的风险没有增加。然而,鉴于该研究的局限性,我们不能排除存在虽小但具有临床意义的风险。