Polycythaemia in infants of diabetic mothers: β-hydroxybutyrate stimulates erythropoietic activity
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Published on: September 9, 2014
Insights
Elevated maternal beta-hydroxybutyrate (β-OHB) in diabetic pregnancies is linked to infant polycythaemia. This suggests β-OHB may independently drive red blood cell production in newborns.
Area of Science:
- Perinatal Medicine
- Endocrinology
- Neonatology
Background:
- Infants of diabetic mothers (IDMs) are at increased risk for polycythaemia.
- Intrauterine hyperinsulinaemia is a suspected cause of polycythaemia in IDMs.
- The role of maternal metabolic factors, such as beta-hydroxybutyrate (β-OHB), is less understood.
Purpose of the Study:
- To investigate the association between elevated maternal β-OHB levels and polycythaemia in infants of diabetic mothers.
- To explore whether β-OHB contributes to polycythaemia independently of intrauterine hyperinsulinaemia and erythropoietin.
Main Methods:
- Maternal glycosylated haemoglobin and β-OHB levels were measured in late gestation.
- Infant birth weight, cord blood insulin, fetal haemoglobin, and haematocrit were assessed.
- Infant venous blood samples were analyzed for haematocrit levels 4 hours post-delivery.
Main Results:
- Mothers with diabetes had significantly higher β-OHB and glycosylated haemoglobin levels.
- Infants of diabetic mothers exhibited higher birth weights, cord blood insulin, fetal haemoglobin, and haematocrit.
- A strong positive correlation was found between maternal β-OHB levels and infant polycythaemia.
- Cord blood erythropoietin levels were similar between groups.
Conclusions:
- Elevated maternal β-OHB is strongly correlated with polycythaemia in infants of diabetic mothers.
- β-OHB may independently stimulate erythropoiesis, contributing to polycythaemia pathogenesis.
- These findings highlight β-OHB as a potential key factor in polycythaemia development in IDMs.
Abstract:
This study tested whether elevated maternal β-hydroxybutyrate (β-OHB) levels contribute to polycythaemia in infants of diabetic mothers. Pregnant diabetic women (n = 27) and non-diabetic controls (n = 20) and their singleton infants were included. Maternal glycosylated haemoglobin and β-OHB levels were studied at 34-36 weeks' gestation; levels were significantly higher in mothers with diabetes than in controls. Birth weights and cord blood levels of insulin and fetal haemoglobin were significantly higher in infants from diabetic mothers compared with control infants, as were haematocrit levels in venous blood samples taken from each infant at 4 h following delivery. Cord blood erythropoietin levels were similar in both groups. There was a positive strong correlation between maternal β-OHB levels and polycythaemia in newborn infants, indicating that β-OHB could activate erythropoiesis independently from intrauterine hyperinsulinaemia and/or erythropoietin levels, and may be important in the pathogenesis of polycythaemia in infants born to diabetic mothers.
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