death (see Chapter 2).
Fig. 1.4 Diagrammatic representation of the sites and rates of synthesis of different haemoglobins in the embryonic and fetal periods and during infancy.
From Bain (2020)37.
Fig. 1.5 First trimester (8 weeks) fetal blood film showing the large size of the erythroblasts (compare with Fig. 1.6) typical of those derived from the yolk sac. These erythroblasts contain mainly embryonic globins. Note the high proportion of red cells that are nucleated and the absence of white blood cells. May–Grünwald–Giemsa (MGG), ×40 objective.
Fig. 1.6 Second trimester (14 weeks) fetal blood film showing typical erythroblasts derived from definitive haematopoiesis. These erythroblasts contain mainly fetal haemoglobin. Note the smaller size of the erythroblasts and the higher proportion of enucleated red cells compared with the first trimester (Fig. 1.5). MGG, ×40.
The production of adult haemoglobin (haemoglobin A; α2β2) begins during the second trimester and remains at low levels until 30–32 weeks post‐conception, when haemoglobin A production starts to increase concomitantly with a fall in haemoglobin F production. The net result is an average haemoglobin F in term babies of 70–80% and haemoglobin A of 25–30%.39,40 After birth, haemoglobin F falls, to approximately 2% by the age of 12 months, with a corresponding increase in haemoglobin A. The molecular control of this change from haemoglobin F to haemoglobin A is termed globin switching. In recent years, there has been considerable research into the genes involved in globin switching (e.g. BCL11A) in order to identify strategies to delay or reverse this physiological switch after birth and so maintain haemoglobin F production for children affected by severe β globin disorders such as sickle cell disease or thalassaemia major.41,42
The timing of globin switching depends on post‐conceptional age rather than postnatal age. In fact, in term babies there is little change in haemoglobin F in the first 15 days after birth, but in preterm babies who are not transfused, haemoglobin F may remain at the same level for the first 6 weeks of life before haemoglobin A production starts to increase. This delay in haemoglobin A production (i.e. the switch from γ globin production to β globin production) can make the diagnosis of β globin disorders in the neonatal period difficult, particularly in preterm infants. This is in contrast to α globin disorders, which are almost invariably evident at birth since α globin chains are essential for the production of all but the very earliest embryonic haemoglobins (see Fig. 1.4 and Table 1.1).
Red blood cell lifespan and the red blood cell membrane in the fetus and neonate
Neonatal red blood cells, particularly in preterm babies, have a shorter lifespan than adult red blood cells. Red cell lifespan is inversely proportional to gestational age at birth. Studies over 50 years ago using isotopically labelled red blood cells estimated red blood cell lifespans for preterm infants at 35–50 days, compared with 60–70 days for term infants and 120 days for healthy adults.35 More recent estimates, using mathematical modelling and transfusion of autologous cord blood cells, have also calculated the red cell lifespan in preterm neonates to be approximately 50 days.43
The reasons for a lower red cell lifespan in neonates, although not fully understood, are thought to include the many biochemical and functional differences in the membrane of neonatal versus adult red blood cells (see Table 1.1). Known differences between neonatal and adult red blood cells include increased resistance to osmotic lysis, increased mechanical fragility, increased total lipid content with an altered lipid profile, increased insulin‐binding sites and reduced expression of blood group antigens such as A, B and I.35 Together these differences translate into the characteristic morphological differences seen in neonatal blood films, particularly in preterm neonates (Figs 1.7–1.9), and are associated with accelerated red cell membrane loss44 leading to reduced red cell lifespan. Indeed, the distinctive geometry of neonatal red blood cells and the membrane deformability of some of the irregularly shaped cells have been compared to the properties of red blood cells in the inherited red cell membrane disorders.45
Fig. 1.7 Normal blood film at term. MGG, ×40.
Fig. 1.8 Normal preterm red cells at different gestational ages: (a) baby born at 28 weeks’ gestation showing echinocytes, polychromatic macrocytes and one nucleated red blood cell (NRBC); (b) baby born at 25 weeks’ gestation showing numerous echinocytes, echinocytic fragments and one NRBC. Note that anisocytosis and poikilocytosis is greater at 25 weeks than at 28 weeks. MGG, ×100.
Fig. 1.9 Blood film of a normal preterm baby (born at 28 weeks’ gestation) showing a degree of erythroblastosis. MGG, ×40.
Red blood cell metabolism in the fetus and neonate
There are major differences between the metabolism of fetal or neonatal red blood cells and that of adult red blood cells. These differences affect not only the functional properties of the red cells of healthy fetuses and neonates but also the clinical impact of inherited and acquired red cell disorders. Both the glycolytic pathway and the pentose phosphate pathway are affected (see Table 1.1). Overall, glycolysis and glucose consumption are lower in neonatal red blood cells than in adult red blood cells. This occurs despite the increased activity of most glycolytic pathway enzymes, such as glucose‐6‐phosphate dehydrogenase (G6PD), pyruvate kinase and lactate dehydrogenase (LDH), and is thought to be the result of reduced phosphofructokinase activity. Neonatal red cells also have less ability to generate the reduced
