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THALASSEMIA

THALASSEMIA. Hope Y. Agbemenyah . Thalassemia syndromes. The hemoglobin is critical for gaseous exchange and transportation between tissues. Hemoglobins are encoded in two tightly linked gene clusters;

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THALASSEMIA

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  1. THALASSEMIA Hope Y. Agbemenyah

  2. Thalassemia syndromes • The hemoglobin is critical for gaseous exchange and transportation between tissues. • Hemoglobins are encoded in two tightly linked gene clusters; • the α-like globin genes are clustered on chromosome 16, and the β-like genes on chromosome 11. • The α-like cluster consists of two α-globin genes and a single copy of the ζ-gene. • The non-α gene cluster consists of a single ε gene, the Gγ and Aγ fetal globin genes, and the adult δ and β genes. • Thalassemias are heterogeneous group of inherited haemoglobinopathies due to mutations leading impaired α- orβ- globin biosynthesis. -diminished production of adult haemoglobin tetramers HbA (α2β2): hypochromic and microcytic anemia. -increased cell membrane damage or ineffective erythropoiesis or both

  3. Demographics and Epidemiology Certain ancestry: endemic in the Mediterranean basin, Middle East, Asian and tropical Africa and the Indian subcontinent ancestry. Distribution parallels that of Plasmodium falciparum

  4. Molecular Pathogenesis • Mutations • Trancriptional: Promoter region mutations • Inability to recruit transcription factors eg GATA-1, NFE-2, the SWI/SNF-like protein called ATRX • Posttranscriptional: mRNA processing • Splicing mutations some normal beta globin • β+- Thalassemia (reduced but detectable β-globin synthesis) • Translational: Chain termination mutation • de-novo stop codon and indel blocking translation • βo- Thalassemia (absent β-globin) • Deletion: α-Thalassemia • Deletion: α-Thalassemia • Other causes • α-protein stabilizing protein (AHSP)

  5. Classifications • α-Thalassemias • due to deletions that cause reduced or lack of synthesis of alpha globin chain. • hence unpaired gamma globins (fetal) or beta (adults) • these are soluble so hemolysis and ineffective erythropoiesis is less severe than beta thalassemia.

  6. Classifications • β-Thalassemias • variable mutations leading to increased levels of alpha globin proteins • accumulation of highly insoluble unpaired α chains. They form toxic inclusion bodies that kill developing erythroblasts in the marrow, few escape with membrane damaging insoluble α chains that undergo extravascular lyses • Provoking compensatory erythroid hyperplasia but the marrow is sabotaged by ineffective erythropoiesis. • Persistence of anemia causes exuberant extramedullaryerythropoietic tissues recruitment

  7. Clinical presentations • Despite differences in the molecular mechanisms underlying the cause of the disease patients generally present common symptoms of • severe tissue hypoxia, hemolytic anemia, marked hepatomegaly, marked erythroidhyperplasia, iron overload • Other symptoms include fatigue, weakness, pale appearance, excessive hemolysis leading to yellowish discoloration of skin (jaundice), facial bone deformities, dark urine. The signs and symptoms the patient experiences depend on the type and severity of thalassemia. • Hyperplasia of bone marrow and extramedullary erythropoiesis

  8. Diagnosis • β-Thalassemia major: basis of severe microcytic anemia, ineffective erythropoiesis- hepatosplenomegaly, and elevated levels of HbF, HbA2 or both • Intermedia exhibit similar stigmata but can survive without chronic hypertransfusion • Minor: profound microcytosis and hypochromia with target cells, but only minimal or mild anemia. Mean corpuscular volume is rarely >75fL; hematocrit is rarely <30-33%. Hb electrophoresis reveals normal/elevated HbA2 or normal/elevated HbF • α-thalassemia trait- mild hypochromia and microcytosisusually without anemia • Hb electrophoresis • Microcytosis and hypochromia • Reduction in HbA and increase in Hb F • Increased RBC count for such level of anemia

  9. Diagnosis • Blood smear shows • Anisocytosis(marked variation in size) • Poikilocytosis (variation in shape) • Target cells ( accumulation of Hb in the center of the cell) • Basophilic stippling • Enlargement of cheekbones and other bony prominence

  10. Treatment • Blood transfusion and as complication you treat iron overload iron chelator- deferoxamine or deferasirox • Cardiac disease resulting from progressive iron overload and secondary hemochromatosis- an important cause of death • Regular monitoring of extramedullary hematopoiesis and spleen size (Splenectomy) • Hydroxyurea (established) and HDACi (worth testing experimentally) indicated in patients with extramedullaryhematopoiesis and leg ulcers • Allogenic stem cells transplantation is the only curative therapy • Vitamin D supplementation • Gene therapy, lentiviral constructs expressing corresponding correct gene • Premature Termination Codon treatment by the use of aminoglycosides

  11. Prevention Antenatal diagnosis DNA diagnosis by PCR amplification of fetal DNA obtained by amniocentesis or chorionic villus biopsy which is then hybridized to allele-specific oligonucleotide probes This examination is only appropriate if both parents are known to be carriers (β-Thalassemia minor) and will accept a termination Seek genetic counseling if a carrier of α-Thalassemia gene Assisted reproductive therapy

  12. Differential Diagnoses Anemia of Chronic Disease and Renal Failure Lead Nephropathy Lead poisoning SideroblasticAnemias

  13. Case • A 10-month-old boy of Arabic extraction is brought to the physician by his parents who complain that their child is failing to thrive. Physical examination reveals splenomegaly and jaundice. A CBC shows a microcytic, hypochromic anemia (hemoglobin = 7.4 g/dL). Fetal hemoglobin accounts for most of the hemoglobin. A peripheral blood smear is shown in the image. Which of the following is the appropriate diagnosis? • What is the pathogenesis of splenomegaly seen in the patient described above

  14. Adriana is a 7-year-old who lives with her parents in a surburban community. Her parents brought her to the united states from their homeland in Greece when she was 1 year old. At the of 3, she was in the 10th percentile for her height and weight, pale and her hemoglobin was 5.8 g/dL. Following further diagnostic studies, she was diagnosed with beta-thalassemia major. Over the course of the next 4 years, Adriana was hospitalized every 1-2 months so she could be transfused with packed red blood cells. • Case study • During a routine follow-up visit at the hematology clinic, Adriana’s laboratory results were as follows: • Hemoglobin: 10 g/dL • Total serum iron: 150 g/L • As hematologist, you discuss planned treatment with Adriana and her parents

  15. What are the clinical manifestations of b-Thalassemia? • What are the priorities of care for Adriana? • Which options are available for Adriana to prevent life-long blood transfusion?

  16. References • http://www.ncbi.nlm.nih.gov/pubmed/7290983 • http://www.sciencedirect.com/science/article/pii/S0891584914001907 • http://www.thalassemia.com • http://www.thalassemia.org • http://www.thalassemia.org.cy • Pathology by Kumar and Robbins • Harrison’s principles of internal medicine 17thed McGraw-Hill • Davidson’s principles and practice of internal medicine 20thed McGraw-Hill

  17. Vielen Dank fuereureAufmerksamkeit

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