- Research article
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Jeddah, Kingdom of Saudi Arabia
BMC Research Notesvolume 4, Article number: 436 (2011)
The development of polymerase chain reaction (PCR)-based methods for the detection of known mutations has facilitated detecting specific red blood cell (RBC) enzyme deficiencies. We carried out a study on glucose-6-phosphate dehydrogenase (G6PD) deficient subjects in Jeddah to evaluate the molecular characteristics of this enzyme deficiency and the frequency of nucleotide1311 and IVS-XI-93 polymorphisms in the glucose-6-phosphate dehydrogenase gene.
A total of 1584 unrelated Saudis (984 neonates and 600 adults) were screened for glucose-6-phosphate dehydrogenase deficiency. The prevalence of glucose-6-phosphate dehydrogenase deficiency was 6.9% (n = 110). G6PD Mediterranean mutation was observed in 98 (89.1%) cases, G6PD Aures in 11 (10.0%) cases, and G6PD Chatham in 1 (0.9%) case. None of the samples showed G6PD A‾ mutation. Samples from 29 deficient subjects (25 males and 4 females) were examined for polymorphism. The association of two polymorphisms of exon/intron 11 (c.1311T/IVS-XI-93C) was observed in 14 (42.4%) of 33 chromosomes studied. This association was found in 9 (31.0%) carriers of G6PD Mediterranean and in 4 (13.8%) carriers of G6PD Aures.
The majority of mutations were G6PD Mediterranean, followed by G6PD Aures and < 1% G6PD Chatham. We conclude that 1311T is a frequent polymorphism in subjects with G6PD Mediterranean and Aures variants in Jeddah.
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common enzymopathies, accounting for over 400 million cases worldwide [1–3]. Most cases of glucose-6-phosphate dehydrogenase deficiency occur in males . Affected individuals are usually asymptomatic, and go through life without being aware of their deficiency. They are, however, at risk of having acute hemolytic crises in response to infection, eating fava beans, and to drugs having a high oxidation potential .
Based on biochemical properties, ethnic origin, and clinical presentation, more than 400 variants of glucose-6-phosphate dehydrogenase have been distinguished in the past. Characterization at the DNA level reduced this number to about 182; these are distributed among 4 classes based on activity and clinical manifestation . In the Kingdom of Saudi Arabia, studies have described the prevalence of glucose-6-phosphate dehydrogenase deficiency and associated enzyme variants, with G6PD Mediterranean found to be the most common [7–10]. In the current study, 110 cases of glucose-6-phosphate dehydrogenase deficiency were studied at the molecular level to evaluate the molecular heterogeneity of this deficiency and the frequency of the silent C/T polymorphism at nt 1311 in glucose-6-phosphate dehydrogenase deficient subjects in the Jeddah area.
Unrelated Saudi adults and neonates were screened for glucose-6-phosphate dehydrogenase deficiency. For adults, blood samples were collected from the general population; this included blood donors, university students, and health-care workers. All neonates delivered from February 2002 to June 2002 at King Abdulaziz University Hospital and King Fahd Armed Force Hospital in Jeddah were also screened for glucose-6-phosphate dehydrogenase deficiency. Consent was obtained from the participants or their parents prior to conducting the research. The study was approved by the Biomedical Ethical Research Committee of the Faculty of Medicine of King Abdulaziz University (Reference No. 530-11)
Red blood cell glucose-6-phosphate dehydrogenase activity was measured with quantitative kits that use Sigma glucose-6-phosphate dehydrogenase H control (Sigma Medical, USA). The kits use the chemical reaction described by Beutler , with NADPH production measured at 340 nm in kinetic mode (change in optical density per minute). Values < 4.6 U/g Hb were considered deficient [11, 12].
Genomic DNA was extracted from peripheral blood leukocytes of the deficient subjects by standard methods (proteinase K digestion, phenol/isoamyl alcohol/chloroform extraction and ethanol precipitation) [11, 13].
The most frequent glucose-6-phosphate dehydrogenase variants were determined by restriction fragment length polymorphism (RFLP). The G6PD Aures mutation is located in exon 3 (c.143T > C, p.Ile48Thr), G6PD A‾ mutations are located in exon 4 (c.202 G > A, p.Val68 > Met) and exon 5 (c.376A > G, p.Asn126Asp), and G6PD Mediterranean is in exon 6 (c.563C > T, p.Ser188Phe). Therefore, these DNA fragments were amplified using primers as listed in Table 1. For the reactions, 500 ng DNA were amplified on a GeneAmp® PCR System 2700 thermal cycler (Applied BioSystems, Foster City, CA, USA) with 1.25 U AmpliTaq® DNA Polymerase (Roche, New Jersey, NJ, USA) and 10 pmol of each primer, 0.2 mM of each dNTP, and1.5 mM MgCl2. The final buffer comprised 16.6 mM (NH4)2SO4, 67 mM Tris-Cl, pH 8.8, 1.5 mM MgCl2, 67 mM Na2EDTA, pH 8.0, 70 μg BSA, and 10 mM β-mercaptoethanol. An initial denaturation step at 94°C for 5 minutes was followed by 35 cycles of denaturation at 94°C for 10 seconds, annealing at 61°C for 30 seconds, and extension at 72°C for 30 seconds. A final extension at 72°C for 7 minutes completed the cycling reaction. For RFLP studies, 18 μl of each PCR product was restricted according to the manufacturer's recommendation with 20 IU of each corresponding enzyme. Exon 3 was cleaved with BglII, exon 4 with NlaIII, exon 5 with FokI, and exon 6 with MboII. Ten microliters of the digestion products were size fractionated by electrophoresis through polyacrylamide gels (6%), stained with ethidium bromide (0.25 μg/ml), and analyzed by UV transillumination.
For molecular characterization of the remaining glucose-6-phosphate dehydrogenase deficient subjects and also for evaluating the frequency of nucleotide 1311C > T polymorphism, the glucose-6-phosphate dehydrogenase gene was entirely sequenced. Samples from glucose-6-phosphate dehydrogenase deficient patients were sent to the Department of Biochemistry and Genetics, Henri Mondor University Hospital, Creteil, France for gene sequencing. Different DNA fragments were amplified using primers as listed in Table 1. The amplification reaction was performed using 10% (v/v) dimethylsulphoxide (DMSO) with 35 cycles of 1 minute denaturation at 94°C, 1 minute annealing at 56°C, and 1 minute extension at 72°C, followed by a final extension of 7 minute at 72°C. Nucleotide sequencing of the PCR products was performed with the forward and reverse primers using the BigDye® Terminator v3.1 Sequencing Kit (Applied BioSystems) and analyzed on an automated sequencer (ABI PRISM® 3100 Genetic Analyzer; Applied BioSystems) [3, 14, 15].
A total of 1584 Saudis (984 neonates and 600 adults) were screened for glucose-6-phosphate dehydrogenase deficiency. One hundred and ten subjects (6.9%), including 42 adults (36 males and 6 females) and 68 neonates (58 males and 10 females) were deficient. G6PD Mediterranean mutation was observed in 98 (89.1%) cases, G6PD Aures in 11 (10.0%) cases, and G6PD Chatham in 1 (0.9%) case. None of the samples showed G6PD A‾ mutation (Table 2). Samples from 29 deficient subjects (25 males and 4 females) were examined for polymorphism. The nucleotide 1311T (p.Tyr437Tyr) polymorphism was observed in 14 (42.4%) of 33 chromosomes studied (25 males and 4 females), and it was associated with G6PD Mediterranean (n = 9; 31.0%) and G6PD Aures (n = 4; 13.8%) (Table 2).
The availability of molecular studies by PCR and glucose-6-phosphate dehydrogenase gene sequencing allows accurate diagnosis and characterization of glucose-6-phosphate dehydrogenase deficiency. In this study, we characterized the molecular defects of the glucose-6-phosphate dehydrogenase gene in deficient patients living in Jeddah. We identified 3 variants; G6PD Mediterranean, G6PD Aures and G6PD Chatham (Table 2).
Most of the patients (89.1%) in this study had the G6PD Mediterranean mutation. Similarly, other authors found a high prevalence of G6PD Mediterranean among glucose-6-phosphate dehydrogenase deficient Saudis in a study conducted in Jeddah [8, 9]. These studies, however, reported a lower frequency compared with our study; 51.1% and 38.1%, respectively. In one report evaluating the frequency of glucose-6-phosphate dehydrogenase mutation in 47 patients in Jeddah, 96% of the patients showed C > T substitution at codon 188 of the glucose-6-phosphate dehydrogenase gene, characteristic of the Mediterranean type . Another study from the Al-Hassa and Al-Qatif areas of Saudi Arabia's Eastern Province also showed G6PD Mediterranean as the most frequent variant, with a prevalence of 45.9% and 36.5% for these 2 areas . Studies conducted in several other areas of the Persian Gulf region have also reported a high prevalence of the Mediterranean variant; 55.5% in the Al-Ain District of United Arab Emirates , 72.9% in Kuwait , 65.2% in Oman , and 72.8% in Zanjan Province in Iran .
G6PD Aures was first described in Saudi Arabia by Niazi et al.  in 1996. In the current study we identified G6PD Aures in 10% of the cases (Table 2). Similar results were reported from Taif, in the Makkah province of Saudi Arabia, with 12.3% of 49 deficient Saudis having G6PD Aures. The prevalence was slightly higher in the United Arab Emirates (16.6%)  and much lower in Kuwait (1.4%) .
The G6PD A¯ variant was absent in our sample. Warsy and El-Hazmi  identified the G6PD A¯ in a study conducted in several provinces in Saudi Arabia. The central province had the lowest frequency (0.0325 in males and 0.0242 in females for A+ , 0.0074 in males and 0.0009 in females for A¯ ). This report primed us to authenticate the data by sequencing all the samples. However a larger sample size is needed for the verification of absence of G6PD A¯ mutation.
The low prevalence (0.9%) of G6PD Chatham mutation in this study was less than that reported in another study  from Taif, where the authors found a prevalence of 4.1%. The lower prevalence observed in our study could be due to the fact that we had a larger sample size (110) compared with 49 in their study.
In this study, the association of two polymorphisms, a silent C/T at nt 1311 (p.Tyr437Tyr) and T/C at nt IVS-XI-93, was studied by direct sequencing of exon and intron 11 of the glucose-6-phosphate dehydrogenase gene. The c.1311T/IVS-XI-93C polymorphism was identified in 42.2% of 33 chromosomes studied. This result is comparable to that obtained from studies conducted in Bahraini and Pakistani populations . On the other hand, Kurdi-Haidar et al.  reported the frequency of the c.1311T/IVS-XI-93C polymorphism in only 14% of the subjects in a study conducted in Saudi Arabia. This can be explained by the low number of X chromosomes studied by the authors. The 1311T polymorphism is frequently observed in Indian and Middle East populations . Conversely, it is less frequent in American and non Mediterranean European countries [22, 24].
The presence of the dual mutation (c.1311T/IVS-XI-93C) has been proposed to be linked to glucose-6-phosphate dehydrogenase deficiency. This association was frequently observed with G6PD Mediterranean and G6PD Aures[25, 26].
Molecular analysis of glucose-6-phosphate dehydrogenase deficiency in this study conducted in Jeddah revealed a higher prevalence of G6PD Mediterranean (89.1%) and Aures (10.0%) compared with other studies from Saudi Arabia. The absence of the African variant suggests further studies with a larger sample size are warranted. The nucleotide 1311T is a frequent polymorphism observed in Saudi Arabia.
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The authors would like to thank King Abdulaziz University for funding this study. Professor Henri Wajcman collaborated in the study and reviewed the manuscript. Bushra M. Jarullah and Dr. Mohammed S. Al Muhayawi entered the data and collected data for the literature.
The authors declare that they have no competing interests.
SKJ, as the principal investigator, designed and wrote the proposal for the study, and submitted it to the research committee of King Abdulaziz University in April 2006. EA helped supervise gel documentation and sequencing of glucose-6-phosphate dehydrogenase in his laboratory. JJ performed the molecular procedure with the assistance of SKJ. KM conducted the gene sequence analysis of the 42 samples. All authors contributed to writing the manuscript.