Tzvetanova E
Enzyme. 1978;23(4):238-45. doi: 10.1159/000458585.
Creatine kinase isoenzymes in sera and muscle biopsies obtained from 50 controls, 72 patients with progressive muscular dystrophy (PMD), 68 patients with other neuromuscular disorders, 17 carriers of Duchenne-type PMD and 15 patients with myocardial infarction were studied. MB isoenzyme was detected in the sera of 58 patients with PMD and 56 out of 61 muscle biopsies. The MB activity varied between 4 and 400 IU/1 or 3.4--22% of total activity. The MB activity was demonstrated in a considerably smaller number of cases with polymyositis, dystrophic myotonia and Kugelberg-Welander disease. The MB isoenzyme in sera of PMD persisted for many years. It is admitted that the MB isoenzyme in the serum of patients with PMD originates chiefly from skeletal muscle.
对从50名对照者、72名进行性肌营养不良(PMD)患者、68名其他神经肌肉疾病患者、17名杜兴型PMD携带者以及15名心肌梗死患者身上获取的血清和肌肉活检样本中的肌酸激酶同工酶进行了研究。在58名PMD患者的血清以及61份肌肉活检样本中的56份中检测到了MB同工酶。MB活性在4至400 IU/1之间,或占总活性的3.4%至22%。在多肌炎、营养不良性肌强直和库格尔贝格 - 韦兰德病患者中,显示出MB活性的病例数量要少得多。PMD患者血清中的MB同工酶持续存在多年。人们认为,PMD患者血清中的MB同工酶主要源自骨骼肌。