Haemoglobin (Hb, HGB) is the iron-containing protein inside red blood cells that carries oxygen from the lungs to every tissue and returns part of the carbon dioxide. Its concentration in blood is the main laboratory criterion for anaemia (too little) and one of the key criteria for erythrocytosis / polycythaemia (too much).
Each red blood cell (erythrocyte) contains about 270 million haemoglobin molecules. Adult haemoglobin (HbA) is a tetramer of four globin chains — two α and two β — with a molecular mass of about 64.5 kDa. Every chain holds one haem group: a porphyrin ring with a single ferrous iron atom (Fe2+) that reversibly binds one molecule of oxygen. One haemoglobin molecule can therefore carry up to four O2 molecules.
In healthy adults about 95–98 % of haemoglobin is HbA (α2β2), 2–3.5 % is HbA2 (α2δ2) and less than 1 % is foetal haemoglobin HbF (α2γ2). Inherited changes in globin genes cause the haemoglobinopathies — sickle-cell disease (HbS) and the thalassaemias — which are among the most common monogenic disorders in the world.
Oxygen binding is cooperative: when one haem binds O2, the tetramer changes shape and the remaining sites bind oxygen more easily. This gives the oxygen–haemoglobin dissociation curve its typical S-shape. In the lungs (PO2 ≈ 100 mmHg) haemoglobin is about 97–98 % saturated; in working tissues, where PO2 falls to 20–40 mmHg, it releases a large share of its oxygen. The PO2 at which haemoglobin is 50 % saturated (P50) is about 26–27 mmHg.
Acidosis, higher CO2, fever and higher 2,3-bisphosphoglycerate shift the curve to the right (the Bohr effect), so oxygen is released more readily where it is needed. Alkalosis, hypothermia, carbon monoxide and foetal haemoglobin shift it to the left.
The oxygen content of arterial blood depends mostly on haemoglobin:
With Hb 15 g/dL and SaO2 98 %, arterial blood carries about 20 mL O2 per 100 mL. Halving haemoglobin halves this value, which is why anaemia reduces exercise capacity even when lung function and oxygen saturation are normal.
Haemoglobin is measured as part of the complete blood count, usually photometrically after converting all forms of haemoglobin to a stable coloured compound. Reference intervals depend on age, sex, pregnancy, altitude and the laboratory, so always compare the result with the range printed on the report. Typical values are shown below.
| Group | Typical reference range | Anaemia threshold (WHO) |
|---|---|---|
| Adult men | 13.5–17.5 g/dL (135–175 g/L) | <13.0 g/dL |
| Adult non-pregnant women | 12.0–15.5 g/dL (120–155 g/L) | <12.0 g/dL |
| Pregnant women | ≥11.0 g/dL (2nd trimester ≥10.5) | <11.0 g/dL (<10.5 in 2nd trimester) |
| Children 6–23 months | ≈10.5–13.5 g/dL | <10.5 g/dL |
| Children 2–4 years | ≈11.0–14.0 g/dL | <11.0 g/dL |
| Children 5–11 years | ≈11.5–15.5 g/dL | <11.5 g/dL |
| Newborns (first days) | 14–22 g/dL | age-specific |
Anaemia affected roughly one-third of the world's population in 2010 and is a major cause of years lived with disability, especially in women of reproductive age and young children. It is a sign, not a diagnosis: the cause must always be found. A practical first step is to look at the red-cell size (MCV) together with the reticulocyte count.
| Type (by MCV) | Main causes | Useful next tests |
|---|---|---|
| Microcytic MCV <80 fL | Iron deficiency (blood loss, poor intake, malabsorption, pregnancy), thalassaemia trait, anaemia of chronic inflammation, sideroblastic anaemia | Ferritin, transferrin saturation, CRP, haemoglobin electrophoresis |
| Normocytic MCV 80–100 fL | Acute blood loss, chronic kidney disease (low erythropoietin), chronic inflammation, haemolysis, bone-marrow failure or infiltration, early iron deficiency | Reticulocytes, creatinine/eGFR, LDH, bilirubin, haptoglobin, blood smear |
| Macrocytic MCV >100 fL | Vitamin B12 or folate deficiency, alcohol, liver disease, hypothyroidism, drugs (methotrexate, hydroxyurea), myelodysplastic syndromes | B12, folate, TSH, liver tests, reticulocytes |
A haemoglobin above the reference range means either less plasma (relative erythrocytosis) or a true increase in red-cell mass (absolute erythrocytosis). Absolute erythrocytosis is secondary when it is driven by erythropoietin, or primary when the bone marrow produces red cells on its own, as in polycythaemia vera.
| Mechanism | Examples |
|---|---|
| Relative (low plasma volume) | Dehydration, vomiting and diarrhoea, diuretics, burns, "stress" erythrocytosis |
| Secondary — chronic hypoxia | Smoking (carbon monoxide), living at high altitude, COPD, obstructive sleep apnoea, cyanotic congenital heart disease, high-affinity haemoglobin variants |
| Secondary — excess erythropoietin or androgens | Kidney cysts or tumours, liver cancer, after kidney transplantation, testosterone or anabolic steroid use, erythropoietin doping; SGLT2 inhibitors cause a modest rise |
| Primary | Polycythaemia vera — a myeloproliferative neoplasm; a JAK2 mutation is found in about 95–98 % of patients |
High haemoglobin makes blood more viscous. This raises the risk of arterial and venous thrombosis — stroke, myocardial infarction, deep-vein thrombosis and pulmonary embolism. Possible symptoms are headache, dizziness, blurred vision, a red face (plethora), itching after a warm bath, burning pain in the fingers and toes (erythromelalgia) and, in polycythaemia vera, an enlarged spleen.
haemoglobin is below 7–8 g/dL, falls rapidly, or is accompanied by chest pain, fainting, severe breathlessness, black or bloody stools, vomiting blood or heavy bleeding. Also seek urgent care if a high haemoglobin comes with sudden weakness of an arm or leg, speech problems, chest pain or a painful swollen leg.
haemoglobin is repeatedly below or above the reference range, even without symptoms. The doctor will usually repeat the full blood count and add ferritin, vitamin B12, folate, kidney function and other tests depending on the findings. Do not start iron supplements without testing: they can mask bleeding and are harmful in iron overload.
This article is for general information and does not replace a consultation with a doctor. Reference ranges vary between laboratories; interpret your result together with a healthcare professional who knows your history.
Published on 2 June 2019