Laboratoire d'hématologie moléculaire et cellulaire, Institut Pasteur de Tunis, 13 place Pasteur, Tunis-Le-Belvédère, Tunisia.
Blood Cells Mol Dis. 2013 Feb;50(2):110-4. doi: 10.1016/j.bcmd.2012.08.005. Epub 2012 Sep 7.
We screened 423 patients referred to our laboratory after hemolysis triggered by fava beans ingestion, neonatal jaundice or drug hemolysis. Others were asymptomatic but belonged to a family with a history of G6PD deficiency. The determination of enzymatic activity using spectrophotometric method, revealed 293 deficient (143 males and 150 females). The molecular analysis was performed by a combination of PCR-RFLP and DNA sequencing to characterize the mutations causing G6PD deficiency. 14 different genotypes have been identified : G6PD A(-) (376A>G;202G>A) (46.07%) and G6PD Med (33.10%) were the most common variants followed by G6PD Santamaria (5.80%), G6PD Kaiping (3.75%), the association [c.1311T and IVS11 93c] (3.75%), G6PD Chatham (2.04%), G6PD Aures (1.70%), G6PD A(-) Betica (0.68%), the association [ 376G;c.1311T;IVS11 93c] (0.68%), G6PD Malaga, G6PD Canton and G6PD Abeno respectively (0.34%). Two novel missense mutations were identified (c.920A>C: p.307Gln>Pro and c.968T>C: p.323 Leu>Pro). We designated these two class III variants as G6PD Tunis and G6PD Nefza. A mechanism which could account for the defective activity is discussed.
我们对 423 名因食用豆类、新生儿黄疸或药物性溶血而导致溶血的患者进行了筛查,他们被转至我们实验室。其他患者无症状,但来自有 G6PD 缺乏症病史的家族。使用分光光度法测定酶活性,发现 293 例酶活性缺乏(男 143 例,女 150 例)。采用 PCR-RFLP 和 DNA 测序相结合的方法进行分子分析,以确定引起 G6PD 缺乏症的突变。共鉴定出 14 种不同的基因型:G6PD A(-)(376A>G;202G>A)(46.07%)和 G6PD Med(33.10%)是最常见的变异体,其次是 G6PD Santamaria(5.80%)、G6PD Kaiping(3.75%)、[c.1311T 和 IVS11 93c] 联合突变(3.75%)、G6PD Chatham(2.04%)、G6PD Aures(1.70%)、G6PD A(-) Betica(0.68%)、[376G;c.1311T;IVS11 93c] 联合突变(0.68%)、G6PD Malaga、G6PD Canton 和 G6PD Abeno 分别为(0.34%)。发现了两种新的错义突变(c.920A>C:p.307Gln>Pro 和 c.968T>C:p.323 Leu>Pro)。我们将这两种 III 类变体分别命名为 G6PD Tunis 和 G6PD Nefza。讨论了一种可以解释其缺陷活性的机制。