el-Hazmi M A, Warsy A S
Trop Geogr Med. 1987 Jan;39(1):32-5.
Sickle cell haemoglobin (Hb S) and glucose-6-phosphate dehydrogenase (G-6-PD) deficiency occur at a variable prevalence in different regions of Saudi Arabia. The interaction between the two genes was investigated in 1859 Saudi males in different regions where the two genes were known to exist at both a high and a low frequency. The frequency of G-6-PD deficiency was the highest in the sickle cell anaemia (SS) cases. Furthermore, in all areas except Tehamat-Aseer (on the Red Sea), the frequency of G-6-PD deficiency was greater in the sickle cell heterozygotes (AS) than in the normal (AA) individuals. The interaction between G-6-PD deficiency and sickle cell gene in the homozygotes and heterozygotes may provide additional benefit against environmental and genetical factors, and may play a role in the amelioration of sickle cell disease in Saudis.
镰状细胞血红蛋白(Hb S)和葡萄糖-6-磷酸脱氢酶(G-6-PD)缺乏症在沙特阿拉伯不同地区的患病率各不相同。在沙特阿拉伯不同地区的1859名男性中,对这两种基因之间的相互作用进行了研究,在这些地区,已知这两种基因在高频率和低频率下均有存在。G-6-PD缺乏症的频率在镰状细胞贫血(SS)病例中最高。此外,在除红海沿岸的泰哈马特-阿西尔之外的所有地区,镰状细胞杂合子(AS)中G-6-PD缺乏症的频率高于正常(AA)个体。纯合子和杂合子中G-6-PD缺乏症与镰状细胞基因之间的相互作用可能会提供额外的抵御环境和遗传因素的益处,并可能在沙特人镰状细胞病的改善中发挥作用。