Glucose-6-phosphate dehydrogenase deficiency (G6PD) as a risk factor of male neonatal sepsis

Z Rostami-Far1, K Ghadiri2, M Rostami-Far3

  • 1Department of Biology, Sanandaj Branch, Islamic Azad University, Sanandaj, Iran.

Insights

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is more common in neonates with sepsis, suggesting it

Area of Science:

  • Pediatrics
  • Neonatology
  • Genetics

Background:

  • Neonatal sepsis affects male infants more frequently, with unknown causes.
  • Glucose-6-phosphate dehydrogenase (G6PD) is crucial for white blood cell (WBC) function in fighting infections.
  • NADPH, produced via the pentose phosphate pathway involving G6PD, is essential for WBCs' antimicrobial respiratory burst.

Purpose of the Study:

  • To investigate the prevalence of G6PD deficiency in neonates diagnosed with sepsis.
  • To explore the association between G6PD deficiency and neonatal sepsis risk.

Main Methods:

  • A comparative study involving 76 neonates with sepsis and 1214 healthy neonates.
  • G6PD deficiency was identified using the fluorescent spot test.
  • White blood cell counts and neutrophil percentages were analyzed in relation to G6PD status.

Main Results:

  • The prevalence of G6PD deficiency was significantly higher in the sepsis group compared to the control group (p=0.03).
  • While WBC counts and neutrophil percentages were lower in G6PD deficient neonates, the differences were not statistically significant (p=0.77 and p=0.86, respectively).

Conclusions:

  • G6PD deficiency emerges as a significant risk factor for developing neonatal sepsis.
  • The findings support G6PD deficiency as a potential explanation for the higher incidence of sepsis in male infants.
  • Routine newborn screening for G6PD deficiency is recommended to identify at-risk infants.

Related Concept Videos

Glucose Transporters01:27

Glucose Transporters

Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
27.9K
Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
967
Pathophysiology of Diabetes01:20

Pathophysiology of Diabetes

Diabetes mellitus is a chronic metabolic disorder characterized by hyperglycemia. The four categories of diabetes are type 1 diabetes, type 2 diabetes, other specific types of diabetes, and gestational diabetes.
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
4.0K
Diabetes Mellitus: Type 2 and Gestational01:22

Diabetes Mellitus: Type 2 and Gestational

Type 2 diabetes, characterized by insulin resistance, arises when the insulin receptors on cells lose responsiveness to insulin, diminishing the cell's capacity to take up glucose, resulting in elevated blood glucose levels. To receive a diagnosis of Type 2 diabetes, a series of blood glucose tests are necessary to assess whether the blood glucose falls within normal parameters. If the result is out of the normal range, a patient may be diagnosed as prediabetic or diabetic, depending on the...
5.3K
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
306
Hypoglycemia and Glucagon01:15

Hypoglycemia and Glucagon

Without prolonged fasting, healthy individuals maintain blood glucose levels above 3.5 mM due to a well-adapted neuroendocrine counterregulatory system that effectively prevents acute hypoglycemia, a potentially life-threatening condition. The primary clinical scenarios for hypoglycemia encompass diabetes treatment, inappropriate production of endogenous insulin or insulin-like substances by tumors, and the use of glucose-lowering agents in non-diabetic individuals. Notably, hypoglycemia in the...
1.1K