Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymopathy in the
human population, especially those living in malaria endemic areas. Decreased G6PD enzymatic
activity is associated with 8-aminoquinolines-induced hemolysis leading to severe complication, and
malaria elimination challenge, especially in Plasmodium vivax malaria. This study was conducted to
the enzyme G6PD activity deficiency in population are living in malaria endemic zone in Tuy Duc
district, Dak Nong province. Method: In order to inform the safer use of 8-aminoquinolines, a crosssectional study which included 2,809 subjects was conducted using a quantitative CareStart™ G6PD
biosensor (AccessBio, USA). Results: The results showed that the normal value of G6PD activity
is 9.03 IU/g Hb, the adjusted male median is 8.78 IU/g Hb, the 30% and 80% cut-off values were
2.63 IU/g Hb and 7.02 IU/g Hb, respectively. The overall prevalence of G6PD deficiency of study
population was 2,31%, with the figures for male and female were 3.65% and 1.49%, respectively. The
prevalence of G6PD deficiency was significantly different among ethnic minority groups (p<0.005).
Conclusions: The quantitative test should include point-of-care G6PD activity testing in clinical
practice of vivax malaria to allow the safe use of 8-aminoquinolines for radical treatment.
ASSESSMENT OF QUANTITATIVE POINT-OF-CARE G6PD ACTIVITY BY USING CARESTART BIOSENSOR IN MALARIA ENDEMIC ZONE OF TUY DUC DISTTRICT, DAK NONG PROVINCE
12
Views
0
Downloads
Keywords
G6PD deficiency, Plasmodium vivax, CareStart™ G6PD biosensor.
Abstract
References
[1]
Tạ Thị Tĩnh, Lê Minh Đạo, Nguyễn Minh
Google Scholar
[2]
Hùng, Trần Thị Uyên, Thiếu enzyme glucose-6-
Google Scholar
[3]
phosphate dehydrogenase trong một số nhóm dân
Google Scholar
[4]
tộc khác nhau tại Việt Nam. Hội nghị Quốc gia về
Google Scholar
[5]
Sốt rét, Ký sinh trùng và Côn trùng (2001-2005),
Google Scholar
[6]
Nhà xuất bản Y học, 2006.
Google Scholar
[7]
Bancone G, Menard D, Khim N et al., Molecular
Google Scholar
[8]
characterization and mapping of glucose-6-
Google Scholar
[9]
phosphate dehydrogenase (G6PD) mutations
Google Scholar
[10]
in the Greater Mekong Subregion. Malaria
Google Scholar
[11]
journal, 18(1), 2009.
Google Scholar
[12]
Chu CS, Freedman DO, Tafenoquine and
Google Scholar
[13]
G6PD: A primer for clinicians. Journal of travel
Google Scholar
[14]
medicine, 26(4), taz023, 2019.
Google Scholar
[15]
Domingo GJ, Satyagraha AW, Anvikar A et
Google Scholar
[16]
al., G6PD testing in support of treatment and
Google Scholar
[17]
elimination of malaria: Recommendations
Google Scholar
[18]
for evaluation of G6PD tests, Malaria
Google Scholar
[19]
Journal, 12:391, 2013.
Google Scholar
[20]
Oo NN, Bancone G, Maw LZ et al., Validation
Google Scholar
[21]
of G6PD point-of-care tests among healthy
Google Scholar
[22]
volunteers in Yangon, Myanmar. PloS
Google Scholar
[23]
one, 11(4):e0152304, 2016.
Google Scholar
[24]
Pfeffer DA, Ley B, Howes RE et al., Quantification
Google Scholar
[25]
of glucose-6-phosphate dehydrogenase activity
Google Scholar
[26]
by spectrophotometry: A systematic review and
Google Scholar
[27]
meta-analysis. PLoS Med 17(5): e1003084, 2020.
Google Scholar
[28]
Rueangweerayut R, Bancone G, Harrell EJ et
Google Scholar
[29]
al., Hemolytic potential of tafenoquine in female
Google Scholar
[30]
volunteers heterozygous for G6PD deficiency
Google Scholar
[31]
(G6PD Mahidol variant) versus G6PD-normal
Google Scholar
[32]
volunteers. The American Journal of Tropical
Google Scholar
[33]
Medicine and Hygiene, 97(3):702-711, 2017.
Google Scholar
[34]
WHO, Point-of-care G6PD testing to support
Google Scholar
[35]
safe use of primaquine for the treatment of vivax
Google Scholar
[36]
malaria. WHO Evidence review group meeting
Google Scholar
[37]
report, WHO/UNAIDSbuilding, 2015.
Google Scholar
[38]
WHO, Guide to G6PD deficiency rapid diagnostic
Google Scholar
[39]
testing to support P. vivax radical cure, 2018.
Google Scholar
[40]
WHO, World Malaria Report 2020, 2020.
Google Scholar