Levine T D, Pestronk A
Department of Neurology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
Muscle Nerve. 1998 Dec;21(12):1724-8. doi: 10.1002/(sici)1097-4598(199812)21:12<1724::aid-mus15>3.0.co;2-2.
Inflammatory myopathy with cytochrome oxidase negative muscle fibers (IM/COX-) is characterized by slowly progressive weakness, most prominent in the quadriceps, muscle fibers with reduced COX staining and mitochondrial DNA mutations, and a poor response to corticosteroid treatment. We reviewed records of quantitative measurements of muscle strength in 7 IM/COX- patients to evaluate the outcomes after treatment with oral, once weekly, methotrexate for an average of 15 months. We compared the results to 6 patients with IM/COX- who received no long-term immunosuppression, and to 4 with inclusion body myositis (IBM) who received methotrexate during the same period. Methotrexate treatment of IM/ COX- was followed by improved muscle strength in 5 of 7 patients, averaging 17+/-5%. In contrast, there was no improvement in the strength of 6 untreated IM/COX- patients (-6+/-4%; P=0.003), or 4 methotrexate-treated IBM patients (1+/-2%; P=0.03). We conclude that, despite clinical similarities to inclusion body myositis, which is usually refractory to immunosuppressive therapy, strength in IM/COX- appears to improve with methotrexate treatment. Biopsy studies of inflammatory myopathies with evaluation of muscle for mitochondrial changes and vacuoles can help to direct the choice of appropriate immunomodulating treatments.
伴有细胞色素氧化酶阴性肌纤维的炎性肌病(IM/COX-)的特征为缓慢进展性肌无力,以股四头肌最为明显,存在细胞色素氧化酶染色减少的肌纤维和线粒体DNA突变,且对皮质类固醇治疗反应不佳。我们回顾了7例IM/COX-患者的肌肉力量定量测量记录,以评估口服甲氨蝶呤(每周一次,平均治疗15个月)后的治疗效果。我们将结果与6例未接受长期免疫抑制治疗的IM/COX-患者以及4例同期接受甲氨蝶呤治疗的包涵体肌炎(IBM)患者进行了比较。7例接受甲氨蝶呤治疗的IM/COX-患者中有5例肌肉力量得到改善,平均改善17±5%。相比之下,6例未接受治疗的IM/COX-患者的力量没有改善(-6±4%;P=0.003),4例接受甲氨蝶呤治疗的IBM患者的力量也没有改善(1±2%;P=0.03)。我们得出结论,尽管IM/COX-在临床上与通常对免疫抑制治疗难治的包涵体肌炎相似,但甲氨蝶呤治疗似乎能改善IM/COX-患者的力量。对炎性肌病进行活检研究并评估肌肉的线粒体变化和空泡,有助于指导选择合适的免疫调节治疗方法。