Email updates

Keep up to date with the latest news and content from BMC Hematology and BioMed Central.

Open Access Research article

Molecular characterization of glucose-6-phosphate dehydrogenase deficient variants in Baghdad city - Iraq

Bassam MS Al-Musawi1, Nasir Al-Allawi2*, Ban A Abdul-Majeed1, Adil A Eissa2, Jaladet MS Jubrael3 and Hanan Hamamy4

Author Affiliations

1 Department of Pathology, College of Medicine, University of Baghdad, Baghdad, Iraq

2 Department of Pathology, College of Medicine, University of Dohuk, Azadi Hospital road, 1014 AM Dohuk, Iraq

3 Scientific Research Center, University of Dohuk, Dohuk, Iraq

4 Department of Genetic Medicine and Development, Geneva University Hospital, Geneva, Switzerland

For all author emails, please log on.

BMC Blood Disorders 2012, 12:4  doi:10.1186/1471-2326-12-4

Published: 27 March 2012

Abstract

Background

Although G6PD deficiency is the most common genetically determined blood disorder among Iraqis, its molecular basis has only recently been studied among the Kurds in North Iraq, while studies focusing on Arabs in other parts of Iraq are still absent.

Methods

A total of 1810 apparently healthy adult male blood donors were randomly recruited from the national blood transfusion center in Baghdad. They were classified into G6PD deficient and non-deficient individuals based on the results of methemoglobin reduction test (MHRT), with confirmation of deficiency by subsequent enzyme assays. DNA from deficient individuals was studied using a polymerase chain reaction-Restriction fragment length polymorphism (PCR-RFLP) for four deficient molecular variants, namely G6PD Mediterranean (563 C→T), Chatham (1003 G→A), A- (202 G→A) and Aures (143 T→C). A subset of those with the Mediterranean variant, were further investigated for the 1311 (C→T) silent mutation.

Results

G6PD deficiency was detected in 109 of the 1810 screened male individuals (6.0%). Among 101 G6PD deficient males molecularly studied, the Mediterranean mutation was detected in 75 cases (74.3%), G6PD Chatham in 5 cases (5.0%), G6PD A- in two cases (2.0%), and G6PD Aures in none. The 1311 silent mutation was detected in 48 out of the 51 G6PD deficient males with the Mediterranean variant studied (94.1%).

Conclusions

Three polymorphic variants namely: the Mediterranean, Chatham and A-, constituted more than 80% of G6PD deficient variants among males in Baghdad. Iraq. This observation is to some extent comparable to other Asian Arab countries, neighboring Turkey and Iran.

Keywords:
G6PD deficiency; Arabs; Baghdad; Iraq; G6PD Mediterranean; G6PD Chatham