el-Hazmi M A, Bahakim H M, Warsy A S, al-Momen A, al-Wazzan A, al-Fawwaz I, Huraib S, Harakati M
College of Medicine & King Khalid Hospital, King Saud University, Riyadh, Saudi Arabia.
Mol Cell Biochem. 1993 Jul 7;124(1):17-22. doi: 10.1007/BF01096377.
Sickle cell anaemia (SCA) exhibits significant variations in clinical presentation in different populations for which several genetic factors including SCA-associated alpha- and beta-thalassaemias, G-6-PD deficiency and elevated Hb F level have been implicated as possible ameliorating factors. Saudi Arabia is unique in that mild and severe forms of the disease occur at a high frequency. We investigated the G gamma/A gamma ratio and Hb F level and correlated these values with the severity of SCA. The results showed that Hb F level varies significantly in both groups of patients with no evident correlation with the mild clinical manifestations. However, G gamma/A gamma ratio correlated significantly with the disease severity where a high ratio was observed in patients with the mild and a low ratio in patients with the severe disease. The results are evaluated and discussed in the light of correlation studies and regression analysis.
镰状细胞贫血(SCA)在不同人群中的临床表现存在显著差异,包括与SCA相关的α和β地中海贫血、葡萄糖-6-磷酸脱氢酶(G-6-PD)缺乏症以及血红蛋白F(Hb F)水平升高在内的多种遗传因素被认为是可能的改善因素。沙特阿拉伯的独特之处在于,该疾病的轻度和重度形式都有较高的发病率。我们研究了Gγ/Aγ比值和Hb F水平,并将这些值与SCA的严重程度进行关联。结果显示,两组患者的Hb F水平差异显著,且与轻度临床表现无明显相关性。然而,Gγ/Aγ比值与疾病严重程度显著相关,轻度患者中该比值较高,重度患者中该比值较低。我们根据相关性研究和回归分析对结果进行了评估和讨论。