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Role of iron deficiency anemia in the propagation of beta thalassemia gene

Role of iron deficiency anemia in the propagation of beta thalassemia gene. Microcytic hypochromic. normal rbc. Usman, M., Moinuddin, M., Ahmed, S.A. (2011) Korean J Hematol 46: 41-44 . Background. Normal hemoglobin is HbA , a 2 b 2 , carries oxygen

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Role of iron deficiency anemia in the propagation of beta thalassemia gene

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  1. Role of iron deficiency anemia in the propagation of beta thalassemia gene Microcytic hypochromic normal rbc Usman, M., Moinuddin, M., Ahmed, S.A. (2011) Korean J Hematol 46: 41-44

  2. Background • Normal hemoglobin is HbA, a2b2, carries oxygen • Other forms are HbA2a2d2 ; HbFa2g2 (normally gone at birth) • b-thalassemia is autosomal recessive defect in production of b-chain of hemoglobin • Thalassemia major is homozygote for mutant b-chain • Thalassemia minor is heterozygote carrier (trait, BTT) • Diagnosis shows microcytichypochromic anemia, nucleated rbc, decreased HbA, increased HbA2 and HbF; • Molecular diagnosis (PCR) can test for common mutations

  3. Background • Severe disease, shortened life expectancy • One of most common genetic disorders in Pakistan • Treatment of thalassemia requires many transfusions • Complications from iron overload, chelation therapy • Preventive program is based on identification of carriers: elevation of HbA2 >3.5% • However, iron deficiency anemia (IDA) decreases amount of hemoglobin -> HbA2 seems normal in person with BTT and IDA.

  4. Experimental plan • Test large number of women for BTT and IDA • Blood tests, hemoglobin electrophoresis, • Molecular diagnosis for common mutations (PCR) • Determine whether any BTT and IDA patients • Treat the IDA patients with oral iron, and see if HbA2 levels change.

  5. Results • 34 of 200 women were anemic • Hb electrophoresis showed 16 BTT (inc HbA2) • Molecular diagnosis confirmed these 16 also 8 more - those 8 had BTT and IDA • 10 just had IDA (serum ferritin levels)

  6. PCR identifies common mutations in HbB gene

  7. Molecular spectrum of mutations identified • Table 1

  8. Iron treatment restores HbA2 levels in patients with IDA; also reveals BTT in the BTT-IDA patient Table 2

  9. Conclusions • b-thalassemia is a serious disease, autosomal recessive, most common genetic disorder in Pakistan • Preventive efforts require identification of carriers (BTT) • As increased level of HbA2 because less b chain • Iron deficiency anemia (IDA) results in lower Hb overall, and also HbA2 • IDA in patient with BTT can mask the carrier state. • Any patient suspected of BTT should be tested for iron deficiency, which is corrected by iron treatment

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