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Ann Biol Sci, 2017

ISSN: 2348-1927

August 23-24, 2017 | Toronto, Canada

Annual Conference on

MICROBIAL PATHOGENESIS, INFECTIOUS DISEASE,

ANTIMICROBIALS AND DRUG RESISTANCE

Arch Clin Microbiol, 8:5

DOI: 10.4172/1989-8436-C1-003

Background:

Glucose

6-phosphate

dehydrogenase

deficiency (G6PDd) is an X-linked hereditary genetic defect,

affecting an estimated 400 million people worldwide. Severe

clinical manifestations associated with G6PDd (e.g., chronic

hemolytic anemia) depends on the type of G6PD molecular

variants and exposure to hemolytic triggers (e.g., antimalarial

like Primaquine). However, a scarce study on G6PDd renders

the use of Primaquine for effective therapeutic treatment of

malaria.

Objectives:

To determine the availability and characterization

of selected molecular variants of G6PDd specific genes

among selected populations in malaria endemic area of

Amhara region, Ethiopia.

Methods:

Using a cross sectional study design, a total of

156 dried blood samples were randomly selected from 360

stored samples of national malaria indicator survey of 2011

starting from July 30/2014 to January 30/2015. Polymerase

chain reaction and restricted fragment length polymorphism

technique was applied to characterize G6PDd variants as

G6PD*A, G6PD*A- and/or G6PD*Mediterranean. Binary

logistic regression was applied to see association (P<0.05 is

significant) among different parameters.

Result:

Of 156 studied dried blood spot samples, 10 (6.4%)

had G6PD genotype available. G6PD*A (100%) was the

only genotype characterized, while neither G6PD*A- nor

G6PD*Mediterranean genotypes were detected. There was

no statistical significant difference between G6PDd and

other socio demographic and risk related variables (P>0.05).

Conclusion:

G6PD*A variant was the only G6PDd genotype

detected in this study. G6PD*A variant has almost (90%) the

same enzymatic activities with the wild type. Therefore, this

result supports the safe use of primaquine, especially the

single low dose for transmission interruption of Plasmodium

falciparum gametocyte and radical cure of

Plasmodium

vivax

, as a part of malaria elimination toolkit, among selected

populations in malaria endemic areas of Amhara region.

e

:

y_mamuye@yahoo.com

Molecular characterization of glucose-6-phosphate dehydrogenase deficiency specific variants in

Amhara region, Ethiopia

Yeshwondm Mamuye

1

and Getachew Abebe

2

1

St.Paul’s Hospital Millennium Medical College, Ethiopia

2

Asela University School of Laboratory, Ethiopia