Tzortzatou-Stathopoulou F, Zannos-Mariolea L, Karayiannis P, Constantsas N, Matsaniotis N
Eur J Pediatr. 1980 Oct;135(1):37-9. doi: 10.1007/BF00445890.
The activity of glucose-6-phosphate dehydrogenase (G-6-PD) in leucocytes was studied in the following group of Greek people. Group 1: 43 male children and 16 male students with mean values of enzyme activity of 27.7 +/- 16.6 units and 24.6 +/- 5.6 units, respectively. Group 2: 15 G-6-PD deficient male children who had never experienced an acute haemolytic episode with a mean value of 10.8 +/- 4.6 units. Group 3: 19 G-6-PD deficient male children during favism and 3 months after the haemolytic crisis with mean values of 8 +/- 4 units and 9.2 +/- 1.9 units, respectively. Group 4: 19 mothers of children from group 3 who by definition were carriers of G-6-PD deficiency had a mean value of 18.2 +/- 8.2 units. The difference between means for group 1 and groups 2, 3 and 4 is highly significant (P < 0.001). Therefore the enzymatic defect in Greek people is not limited to the erythrocytes but can be also demonstrated in leucocytes.
对以下一组希腊人的白细胞中葡萄糖-6-磷酸脱氢酶(G-6-PD)活性进行了研究。第1组:43名男童和16名男学生,酶活性平均值分别为27.7±16.6单位和24.6±5.6单位。第2组:15名从未经历过急性溶血发作的G-6-PD缺乏男童,平均值为10.8±4.6单位。第3组:19名患蚕豆病期间及溶血危机后3个月的G-6-PD缺乏男童,平均值分别为8±4单位和9.2±1.9单位。第4组:第3组儿童的19名母亲,根据定义为G-6-PD缺乏症携带者,平均值为18.2±8.2单位。第1组与第2、3、4组平均值之间的差异非常显著(P<0.001)。因此,希腊人的酶缺陷不仅限于红细胞,在白细胞中也可表现出来。