The integrity and stability of specimens under different storage conditions for glucose-6-phosphate dehydrogenase deficiency screening using WST-8
نویسندگان
چکیده
• The first report comparing the stability of three different G6PD sample types (normal controls, heterozygous females and deficient individuals) under storage conditions. Specimens with normal activity, both EDTA blood DBS, can be stored at −20 °C for up to 1 year controlled Blood samples from as DBS conditions year. activity in significantly decreased over storage. Accurate measurement glucose-6-phosphate dehydrogenase (G6PD) is critical malaria treatment misclassification deficiency could cause serious harm patients. should assessed on day collection. Otherwise, specimens suitable prevent loss activity. Here, we integrity testing females, individuals using water-soluble tetrazolium salts (WST-8) assay. were ethylenediaminetetraacetic acid (EDTA) whole dried spots (DBS) various temperatures (37 °C, room temperature, 4 -20 °C) humidity (with without desiccant). stable when conditions, 85% 91% presence desiccant, respectively. showed greater enzyme after desiccant. rapidly lost all tested. However, reduction did not interfere classification. Samples will allow accurate enable safe effective use antimalarial drugs such primaquine tafenoquine.
منابع مشابه
Evaluation of glucose-6-phosphate dehydrogenase stability in blood samples under different collection and storage conditions.
To the Editor: Fujimoto et al. (1 ) reported that the stability of galactose 1-phosphate in dried blood spots for neonatal screening was adversely affected by humidity and temperature, especially when low-value samples are evaluated. We extend these findings to glucose-6-phosphate dehydrogenase (G-6-PD; EC 1.1.1.49) activity, deficiency of which is by far the most common genetic disease worldwi...
متن کاملGlucose-6-Phosphate Dehydrogenase Deficiency and Neonatal Hyperbilirubinemia
Background: Jaundice is affecting over 60-80 percent of neonates in the first week of life. Glucose-6-phosphate dehydrogenase (G6PD) deficiency, which is an important cause of pathologic hyperbilirubinemia, can lead to hemolytic anemia, jaundice and kernicterus. The present study was performed to determine the prevalence of G6PD deficiency among icteric neonates in Shirvan, Iran. Methods: This...
متن کاملNeonatal screening for glucose-6-phosphate dehydrogenase deficiency: sex distribution.
Eight hundred and six newborn infants at high risk for glucose-6-phosphate dehydrogenase (G-6-PD) deficiency were screened; 30.2% of the boys and 10.4% of the girls had severe G-6-PD deficiency. Surprisingly, 14% of the enzyme deficient girls had a father from a low risk ethnic group. Girls of high risk mothers should be screened for G-6-PD deficiency regardless of paternal origin.
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LABORATORY DATA biochemical markers metabolic defect chromosomal assignment chromosome X localization chromosome Xq localization chromosome Xq28 localization gene, structural-functional anomalies G6PD (G6PD1) glucose-6-phosphate dehydrogenase, gene chr.Xq28 gene analysis-DNA analysis myelo-erythropoietic disorders glucose-6-phosphate dehydrogenase deficiency haemolytic anaemia isolated hematopo...
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Out of 20 patients with viral hepatitis whose glucose-6phosphate dehydrogenase (G-6-PD) levels were normal, 14 had clinical evidence of a mild to moderate degree of haemolysis but in all the patients studied the half life of chromium-51-labelled red cells was shortened. Out of 18 viral hepatitis patients deficient in G-6-PD 17 had clinical evidence of haemolysis, and in eight this was more seve...
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ژورنال
عنوان ژورنال: Acta Tropica
سال: 2021
ISSN: ['1873-6254', '0001-706X']
DOI: https://doi.org/10.1016/j.actatropica.2021.105864