Ohta M, Itagaki Y, Itoh N, Hayashi K, Nishitani H, Ohta K
Clinical Research Center, Utano National Hospital, Kyoto, Japan.
Clin Chem. 1991 Jan;37(1):36-9.
We measured with a radioimmunoassay the concentrations of carbonic anhydrase III (CA-III, EC 4.2.1.1) in sera from 68 patients with muscular dystrophy, 10 carriers of Duchenne muscular dystrophy (DMD), and 63 patients with other neurological disorders. The values obtained were compared with those for creatine kinase (CK, EC 2.7.3.2). Serum CA-III was strikingly increased in patients with DMD (mean, 274.4 micrograms/L) and congenital (Fukuyama-type) (182.8 micrograms/L) and limb-girdle (203.7 micrograms/L) dystrophies and positively correlated with the activities of CK in patients with DMD. CA-III concentration decreased with the subjects' age and the severity of the disease, similar to the tendency observed between age or severity and the concentration of CK. We found moderately increased CA-III in patients with polymyositis, myotonic dystrophy, amyotrophic lateral sclerosis, spinal progressive muscular atrophy, or Kugelberg-Welander disease and in carriers of DMD.
我们采用放射免疫分析法测定了68例肌营养不良患者、10例杜氏肌营养不良(DMD)携带者以及63例其他神经系统疾病患者血清中碳酸酐酶III(CA-III,EC 4.2.1.1)的浓度。将所得值与肌酸激酶(CK,EC 2.7.3.2)的值进行比较。DMD患者(平均274.4微克/升)、先天性(福山型)(182.8微克/升)和肢带型(203.7微克/升)肌营养不良患者血清CA-III显著升高,且与DMD患者的CK活性呈正相关。CA-III浓度随受试者年龄和疾病严重程度降低,这与年龄或严重程度与CK浓度之间观察到的趋势相似。我们发现多发性肌炎、强直性肌营养不良、肌萎缩侧索硬化症、脊髓性进行性肌萎缩或库格尔贝格-韦兰德病患者以及DMD携带者的CA-III中度升高。