Table 1.

Main causes of absolute iron deficiency/iron deficiency anemia

Type of causeConditionPathophysiologic mechanism
Increased iron requirements Infants, preschool children, adolescents Rapid growth 
Pregnant women: second and third trimesters Expansion of maternal and fetal erythroid mass 
ESA treatment Acute expansion of erythroid mass 
Low iron intake Malnutrition* Insufficient dietary iron: low heme iron or scarcely bioavailable iron (eg, chelated by phytates) 
Vegetarians, vegans 
Decreased intestinal iron absorption Gastrectomy, duodenal bypass, bariatric surgery Decreased absorptive surface 
Gluten-induced enteropathy 
Autoimmune atrophic gastritis Increased pH 
Helicobacter pylori infection Increased pH and blood loss 
Drugs: proton pump inhibitors, H2 blockers Blocking of gastric acid secretion 
Genetic IRIDA High serum hepcidin levels 
Chronic blood loss Hookworm infestation* Bleeding from gastrointestinal tract 
 Gastrointestinal benign and malignant lesions  
 Salicylates, corticosteroids, nonsteroidal anti-inflammatory drugs  
 Heavy menses, hematuria Bleeding from genitourinary system 
 Intravascular hemolysis (PNH, march hemoglobinuria) Urinary loss of hemoglobin (iron) 
 Drugs: anticoagulants, antiplatelet compounds Systemic bleeding 
 Defects of hemostasis (hereditary hemorrhagic telangectasia, von Willebrand disease)  
 Frequent blood donors Repeated blood letting 
Multiple causes (absolute iron deficiency associated with inflammation) Chronic infections in malnutrition* Reduced intake, increased proinflammatory cytokines 
Chronic kidney disease Decreased iron absorption, increased blood loss, reduced hepcidin excretion and increased production, drugs, ESAs 
Chronic systolic heart failure Decreased iron absorption, increased inflammation, blood loss 
Inflammatory bowel diseases Decreased iron absorption, increased blood loss, high hepcidin 
Postoperative anemia of major surgery Blood loss, increased proinflammatory cytokines 
Type of causeConditionPathophysiologic mechanism
Increased iron requirements Infants, preschool children, adolescents Rapid growth 
Pregnant women: second and third trimesters Expansion of maternal and fetal erythroid mass 
ESA treatment Acute expansion of erythroid mass 
Low iron intake Malnutrition* Insufficient dietary iron: low heme iron or scarcely bioavailable iron (eg, chelated by phytates) 
Vegetarians, vegans 
Decreased intestinal iron absorption Gastrectomy, duodenal bypass, bariatric surgery Decreased absorptive surface 
Gluten-induced enteropathy 
Autoimmune atrophic gastritis Increased pH 
Helicobacter pylori infection Increased pH and blood loss 
Drugs: proton pump inhibitors, H2 blockers Blocking of gastric acid secretion 
Genetic IRIDA High serum hepcidin levels 
Chronic blood loss Hookworm infestation* Bleeding from gastrointestinal tract 
 Gastrointestinal benign and malignant lesions  
 Salicylates, corticosteroids, nonsteroidal anti-inflammatory drugs  
 Heavy menses, hematuria Bleeding from genitourinary system 
 Intravascular hemolysis (PNH, march hemoglobinuria) Urinary loss of hemoglobin (iron) 
 Drugs: anticoagulants, antiplatelet compounds Systemic bleeding 
 Defects of hemostasis (hereditary hemorrhagic telangectasia, von Willebrand disease)  
 Frequent blood donors Repeated blood letting 
Multiple causes (absolute iron deficiency associated with inflammation) Chronic infections in malnutrition* Reduced intake, increased proinflammatory cytokines 
Chronic kidney disease Decreased iron absorption, increased blood loss, reduced hepcidin excretion and increased production, drugs, ESAs 
Chronic systolic heart failure Decreased iron absorption, increased inflammation, blood loss 
Inflammatory bowel diseases Decreased iron absorption, increased blood loss, high hepcidin 
Postoperative anemia of major surgery Blood loss, increased proinflammatory cytokines 

ESA, erythropoiesis-stimulating agent; H2 antagonists, histamine receptor blockers; IRIDA, iron-refractory iron deficiency anemia; PNH, paroxysmal nocturnal hemoglobinuria.

*

More common in developing countries.

Rarely resulting from gene mutations other than TMPRSS6.100 

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