Somer H, Dubowitz V, Donner M
J Neurol Sci. 1976 Oct;29(2-4):129-36. doi: 10.1016/0022-510x(76)90165-9.
Determination of the creatine kinase isoenzyme pattern in 62 biopsy samples obtained from patients with neuromuscular disease revealed changes mainly in Duchenne muscular dystrophy. The BB isoenzyme was detected in 10 out of 17 cases with Duchenne muscular dystrophy and the relative amount of MB+BB isoenzyme was significantly increased in this group (P less than 0.005). In serum the MB isoenzyme was detected in all 28 cases with progressive muscular dystrophy and frequently also in other neuromuscular diseases. Among 152 control samples the MB isoenzyme was detected only in 2 cases. It is suggested that the finding of MB isoenzyme in the serum with normal or only slightly elevated total CK activity may be a further proof of neuromuscular disorder, but the finding is not specific for any particular disease.
对62例神经肌肉疾病患者的活检样本进行肌酸激酶同工酶谱分析,结果显示主要在杜兴氏肌营养不良症中出现了变化。在17例杜兴氏肌营养不良症患者中,有10例检测到了BB同工酶,且该组中MB + BB同工酶的相对含量显著增加(P小于0.005)。在血清中,28例进行性肌营养不良症患者均检测到了MB同工酶,其他神经肌肉疾病患者中也经常检测到。在152份对照样本中,仅2例检测到了MB同工酶。有人提出,在总CK活性正常或仅略有升高的血清中发现MB同工酶可能是神经肌肉疾病的进一步证据,但这一发现并非任何特定疾病所特有。