Bedi G K, Kaur I, Behera D
Department of Dermatology, Venereology and Leprology, PGIMER, Chandigarh, India.
J Dermatol. 1999 Jul;26(7):423-7. doi: 10.1111/j.1346-8138.1999.tb02020.x.
Methotrexate is known to induce pulmonary fibrosis. The present study was undertaken to assess pulmonary toxicity, if any, in psoriasis patients on methotrexate therapy and correlate the dose and duration of the treatment with any changes in pulmonary function. Ten patients who had taken methotrexate for one year and ten patients receiving methotrexate were included in the present study. Detailed lung function studies including arterial blood gas analysis were carried out. In both groups, the only pulmonary function abnormalities detected were FEF200-1200, FEF25-75%, residual volume (RV), and RV/TLC%, which showed a decline after six months of treatment. However, this was not significant. No changes were detected in the arterial blood gas values following methotrexate therapy. Therefore, the present study did not find any significant deterioration of lung functions in psoriasis patients on methotrexate therapy.
已知甲氨蝶呤会诱发肺纤维化。本研究旨在评估接受甲氨蝶呤治疗的银屑病患者是否存在肺毒性,并将治疗剂量和疗程与肺功能的任何变化相关联。本研究纳入了10名服用甲氨蝶呤一年的患者和10名正在接受甲氨蝶呤治疗的患者。进行了包括动脉血气分析在内的详细肺功能研究。在两组中,检测到的唯一肺功能异常是用力呼气流量200-1200、用力呼气流量25-75%、残气量(RV)和RV/TLC%,这些指标在治疗六个月后出现下降。然而,这并不显著。甲氨蝶呤治疗后动脉血气值未发现变化。因此,本研究未发现接受甲氨蝶呤治疗的银屑病患者肺功能有任何显著恶化。