Reference spectrophotometric values for glucose-6-phosphate dehydrogenase activity in two-to six-month-old infants on the Thailand-Myanmar border.

G6PD deficiency G6PD testing Plasmodium vivax infants malaria elimination paediatric G6PD reference values

Journal

Wellcome open research
ISSN: 2398-502X
Titre abrégé: Wellcome Open Res
Pays: England
ID NLM: 101696457

Informations de publication

Date de publication:
2022
Historique:
accepted: 08 01 2024
medline: 26 2 2024
pubmed: 26 2 2024
entrez: 26 2 2024
Statut: epublish

Résumé

Glucose-6-phosphate dehydrogenase (G6PD) deficiency represents a barrier to the full deployment of anti-malarial drugs for vivax malaria elimination and of first-line antibiotics. Lack of established reference ranges for G6PD activity in breast-fed infants puts them at risk of drug-induced haemolysis and restricts access to safe treatment of their mothers. The present work was undertaken to establish age-specific G6PD normal values using the gold standard spectrophotometric assay to support the future clinical use of tafenoquine in lactating women and safer antibiotic treatment in infants. Spectrophotometric results collected at the Thai-Myanmar border from 78 healthy infants between the ages of 2 and 6 months showed a trend of decreased enzymatic activity with increasing age (which did not reach statistical significance when comparing 2-3 months old against 4-6 months old infants) and provided a reference normal value of 100% activity for infants 2-6 months old of 10.18IU/gHb. Normal reference G6PD activity in 2-6-month-old infants was approximately 140% of that observed in G6PD normal adults from the same population. Age specific G6PD activity thresholds should be used in paediatric populations to avoid drug-induced haemolysis. Primaquine and tafenoquine are 8-aminoquinolines used to provide radical cure from dormant stages of malaria vivax; recurrence from dormant malaria parasite causes morbidity and mortality especially in women who are not eligible for treatment while pregnant and breastfeeding. Subjects with glucose-6-phosphate dehydrogenase (G6PD) deficiency are susceptible to dose-dependent drug-induced haemolysis when treated with several drugs including antibiotics and 8-aminoquinolines. G6PD testing is necessary before use of these drugs. Adult normal reference values for G6PD enzymatic activity exist for adults and are used to provide safe radical cure with different regimens of primaquine and tafenoquine. We have collected data in infants to establish normal reference values of G6PD enzymatic activity in infants aged 2-6 months. These results will be used in future to carry out clinical trials where breast-feeding women of a malaria endemic area will be treated with 8-aminoquinolines. Inclusion of mothers and their babies will be based on already established reference values in adult and these newly established values for infants. An added benefit for infants is that age-specific reference values established with this study will be used more widely to provide safer antibiotic treatment.

Sections du résumé

Background UNASSIGNED
Glucose-6-phosphate dehydrogenase (G6PD) deficiency represents a barrier to the full deployment of anti-malarial drugs for vivax malaria elimination and of first-line antibiotics. Lack of established reference ranges for G6PD activity in breast-fed infants puts them at risk of drug-induced haemolysis and restricts access to safe treatment of their mothers.
Methods UNASSIGNED
The present work was undertaken to establish age-specific G6PD normal values using the gold standard spectrophotometric assay to support the future clinical use of tafenoquine in lactating women and safer antibiotic treatment in infants.
Results UNASSIGNED
Spectrophotometric results collected at the Thai-Myanmar border from 78 healthy infants between the ages of 2 and 6 months showed a trend of decreased enzymatic activity with increasing age (which did not reach statistical significance when comparing 2-3 months old against 4-6 months old infants) and provided a reference normal value of 100% activity for infants 2-6 months old of 10.18IU/gHb.
Conclusions UNASSIGNED
Normal reference G6PD activity in 2-6-month-old infants was approximately 140% of that observed in G6PD normal adults from the same population. Age specific G6PD activity thresholds should be used in paediatric populations to avoid drug-induced haemolysis.
Primaquine and tafenoquine are 8-aminoquinolines used to provide radical cure from dormant stages of malaria vivax; recurrence from dormant malaria parasite causes morbidity and mortality especially in women who are not eligible for treatment while pregnant and breastfeeding. Subjects with glucose-6-phosphate dehydrogenase (G6PD) deficiency are susceptible to dose-dependent drug-induced haemolysis when treated with several drugs including antibiotics and 8-aminoquinolines. G6PD testing is necessary before use of these drugs. Adult normal reference values for G6PD enzymatic activity exist for adults and are used to provide safe radical cure with different regimens of primaquine and tafenoquine. We have collected data in infants to establish normal reference values of G6PD enzymatic activity in infants aged 2-6 months. These results will be used in future to carry out clinical trials where breast-feeding women of a malaria endemic area will be treated with 8-aminoquinolines. Inclusion of mothers and their babies will be based on already established reference values in adult and these newly established values for infants. An added benefit for infants is that age-specific reference values established with this study will be used more widely to provide safer antibiotic treatment.

Autres résumés

Type: plain-language-summary (eng)
Primaquine and tafenoquine are 8-aminoquinolines used to provide radical cure from dormant stages of malaria vivax; recurrence from dormant malaria parasite causes morbidity and mortality especially in women who are not eligible for treatment while pregnant and breastfeeding. Subjects with glucose-6-phosphate dehydrogenase (G6PD) deficiency are susceptible to dose-dependent drug-induced haemolysis when treated with several drugs including antibiotics and 8-aminoquinolines. G6PD testing is necessary before use of these drugs. Adult normal reference values for G6PD enzymatic activity exist for adults and are used to provide safe radical cure with different regimens of primaquine and tafenoquine. We have collected data in infants to establish normal reference values of G6PD enzymatic activity in infants aged 2-6 months. These results will be used in future to carry out clinical trials where breast-feeding women of a malaria endemic area will be treated with 8-aminoquinolines. Inclusion of mothers and their babies will be based on already established reference values in adult and these newly established values for infants. An added benefit for infants is that age-specific reference values established with this study will be used more widely to provide safer antibiotic treatment.

Identifiants

pubmed: 38406309
doi: 10.12688/wellcomeopenres.18417.2
pmc: PMC10884598
doi:

Types de publication

Journal Article

Langues

eng

Pagination

273

Informations de copyright

Copyright: © 2024 Bancone G et al.

Déclaration de conflit d'intérêts

No competing interests were disclosed.

Auteurs

Germana Bancone (G)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, 63110, Thailand.
Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7LG, UK.

Day Day Poe (DD)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, 63110, Thailand.

Gornpan Gornsawun (G)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, 63110, Thailand.

Phyu Phyu Htway (PP)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, 63110, Thailand.

Mary Ellen Gilder (ME)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, 63110, Thailand.

Laypaw Archasuksan (L)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, 63110, Thailand.

Kesinee Chotivanich (K)

Mahidol-Oxford Tropical Medicine Research Unit (MORU), Faculty of Tropical Medicine, Mahidol University, Bangkok, 10400, Thailand.

Rose McGready (R)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, 63110, Thailand.
Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7LG, UK.

Francois Nosten (F)

Shoklo Malaria Research Unit, Mahidol-Oxford Tropical Medicine Research Unit, Faculty of Tropical Medicine, Mahidol University, Mae Sot, 63110, Thailand.
Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7LG, UK.

Classifications MeSH