The prevalence of glucose-6-phosphate dehydrogenase deficiency in Trat province, eastern Thailand

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Nattaphol Prakobkaew
Surachat Buddhisa

Abstract

The most prevalent X-linked enzymopathy in Thailand is glucose-6-phosphate dehydrogenase (G6PD) deficiency. The eastern Thailand border region is at risk of developing drug-resistant malaria and the frequency of G6PD deficiency and the characterization of G6PD variants are unclear. A fluorescent spot test (FST), quantitative G6PD activity assay, and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) to identify common G6PD variants were used to evaluate the prevalence of G6PD deficiency. G6PD deficiency was found in 12.06% of the population. Females with an FST of 6.43% were intermediate, whereas females with an FST of 1.61% were deficient, and men with an FST of 4.02% were deficient. G6PD Viangchan was the most common variant, followed by G6PD Mahidol, according to PCR-RFLP results. G6PD activity in the heterozygotes females were more than 60% of normal activity. In G6PD deficient samples, there is a strong negative correlation between G6PD activity and hemoglobin, hematocrit. The frequency of G6PD deficiency in the region is important for G6PD diagnosis and potentially useful for implementing appropriate anti-malarial drug treatment.

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1.
Prakobkaew N, Buddhisa S. The prevalence of glucose-6-phosphate dehydrogenase deficiency in Trat province, eastern Thailand. Arch AHS [Internet]. 2022 Aug. 26 [cited 2024 Dec. 19];34(2):35-43. Available from: https://he01.tci-thaijo.org/index.php/ams/article/view/255535
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Original article

References

Bancone G, Chu CS, Somsakchaicharoen R, Chowwiwat N, Parker DM, Charunwatthana P, et al. Characterization of G6PD genotypes and phenotypes on the northwestern Thailand-Myanmar border. PLoS One 2014; 9(12): 1-11.

Valencia SH, Ocampo ID, Arce-Plata MI, Recht J, Arévalo-Herrera M. Glucose-6-phosphate dehydrogenase deficiency prevalence and genetic variants in malaria endemic areas of Colombia. Malar J 2016; 15(1): 1-9.

Phompradit P, Kuesap J, Chaijaroenkul W, Rueangweerayut R, Hongkaew Y, Yamnuan R, et al. Prevalence and distribution of glucose-6-phosphate dehydrogenase (G6PD) variants in Thai and Burmese populations in malaria endemic areas of Thailand. Malar J 2011; 10: 1-8.

Henriques G, Phommasone K, Tripura R, Peto TJ, Raut S, Snethlage C, et al. Comparison of glucose-6 phosphate dehydrogenase status by fluorescent spot test and rapid diagnostic test in Lao PDR and Cambodia. Malar J 2018; 17(1): 1-7.

Matsuoka H, Thuan DTV, Van Thien H, Kanbe T, Jalloh A, Hirai M, et al. Seven different glucose-6-phosphate dehydrogenase variants including a new variant distributed in Lam Dong Province in southern Vietnam. Acta Med Okayama 2007; 61(4): 213-9.

Canavati SE, Lawford HLS, Fatunmbi BS, Lek D, Top-Samphor N, Leang R, et al. Establishing research priorities for malaria elimination in the context of the emergency response to artemisinin resistance framework-the Cambodian approach. Malar J 2016; 15(1): 1-10.

Kittisares K, Palasuwan D, Noulsri E, Palasuwan A. Thalassemia trait and G6PD deficiency in Thai blood donors. Transfus Apher Sci 2019; 58(2): 201-6.

Bancone G, Chu CS, Somsakchaicharoen R, Chowwiwat N, Parker DM, Charunwatthana P, et al. Characterization of G6PD Genotypes and Phenotypes on the Northwestern Thailand-Myanmar Border. PLoS One 2014; 9(12): 1-11.

Sathupak S, Leecharoenkiat K, Kampuansai J. Prevalence and molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Lue ethnic group of northern Thailand. Sci Reports 2021; 11(1): 1-9.

Nuchprayoon I, Sanpavat S, Nuchprayoon S. Glucose-6-phosphate dehydrogenase (G6PD) mutations in Thailand: G6PD Viangchan (871G>A) is the most common deficiency variant in the Thai population. Hum Mutat 2002; 19(2): 1-6.

Laosombat V, Sattayasevana B, Janejindamai W, Viprakasit V, Shirakawa T, Nishiyama K, et al. Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind). Blood Cells Mol Dis 2005; 34(2): 191-6.

Domingo GJ, Satyagraha AW, Anvikar A, Baird K, Bancone G, Bansil P, et al. G6PD testing in support of treatment and elimination of malaria: Recommendations for evaluation of G6PD tests. Malar J 2013; 12(1): 1-12.

Nuchprayoon I, Louicharoen C, Charoenvej W. Glucose-6-phosphate dehydrogenase mutations in Mon and Burmese of southern Myanmar. J Hum Genet 2008; 53(1): 48-54.

Dechyotin S, Sakunthai K, Khemtonglang N, Yamsri S, Sanchaisuriya K, Kitcharoen K, et al. Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in Females from Previously Malaria Endemic Regions in Northeastern Thailand and Identification of a Novel G6PD Variant. Mediterr J Hematol Infect Dis 2021; 13(1): 1-9.

Bancone G, Menard D, Khim N, Kim S, Canier L, Nguong C, et al. Molecular characterization and mapping of glucose-6-phosphate dehydrogenase (G6PD) mutations in the Greater Mekong Subregion. Malar J 2019; 8(1): 1-15.

World Health Organization. Updating the WHO G6PD classification of variants and the International Classification of Diseases, 11th Revision (ICD-11) Background and rationale. Geneva: WHO; 2019.

Arese P, Gallo V, Pantaleo A, Turrini F. Life and death of glucose-6-phosphate dehydrogenase (G6PD) deficient erythrocytesrole of redox stress and band 3 modifications. Transfus Med Hemotherapy 2012; 39(5): 328-34.

Ajlaan SK, Al-Naama LM, Al-Naama MM. Correlation between normal glucose-6-phosphate dehydrogenase level and haematological parameters. East Mediterr Heal J 2000; 6(2-3): 391-5.

Bancone G, Kalnoky M, Chu CS, Chowwiwat N, Kahn M, Malleret B, et al. The G6PD flow cytometric assay is a reliable tool for diagnosis of G6PD deficiency in women and anaemic subjects. Sci Rep 2017; 7(1): 1-8.

Kurth F, Lingscheid T, Steiner F, Stegemann MS, Bélard S, Menner N, et al. Hemolysis after Oral Artemisinin Combination Therapy for Uncomplicated Plasmodium falciparum Malaria. Emerg Infect Dis 2016; 22(8): 1381-6.

Chu CS, Bancone G, Nosten F, White NJ, Luzzatto L. Primaquine-induced haemolysis in females heterozygous for G6PD deficiency. Malar J 2018; 17(1): 1-9.