Schacter L P, DelVillano B C, Gordon E M, Klein B L
Am J Hematol. 1985 Jun;19(2):137-44. doi: 10.1002/ajh.2830190205.
Patients with sickle cell anemia vary in the severity of their symptoms but the basis of this variability is unknown. We have tested the hypothesis that this variability is related to differences in the activity of the antioxidant superoxide dismutase (SOD). The amount of superoxide dismutase I (SOD) enzyme activity in red cells of patients with different degrees of symptom severity and healthy black and white controls was measured and correlated with symptom severity in SCA patients. Blacks with normal (AA) hemoglobin had significantly (p less than .001) more SOD activity (1.82 U/mg Hb) than white controls (1.44 U/mg Hb). Patients with moderate or severe symptoms had less SOD activity (1.16 and 0.95 U/mg Hb, respectively) than control blacks or SCA patients with mild symptoms (1.62 U/mg Hb). The correlation of SOD activity and symptom severity was not a function of age or sex and was unrelated to reticulocyte count or fetal hemoglobin level.
镰状细胞贫血患者症状的严重程度各不相同,但这种变异性的基础尚不清楚。我们检验了这样一个假设,即这种变异性与抗氧化超氧化物歧化酶(SOD)活性的差异有关。我们测量了不同症状严重程度的患者以及健康黑人和白人对照者红细胞中超氧化物歧化酶I(SOD)的酶活性,并将其与镰状细胞贫血患者的症状严重程度进行关联。具有正常(AA)血红蛋白的黑人的SOD活性(1.82 U/mg Hb)显著高于白人对照者(1.44 U/mg Hb)(p<0.001)。中度或重度症状患者的SOD活性(分别为1.16和0.95 U/mg Hb)低于对照黑人或轻度症状的镰状细胞贫血患者(1.62 U/mg Hb)。SOD活性与症状严重程度的相关性不是年龄或性别的函数,且与网织红细胞计数或胎儿血红蛋白水平无关。