Beta-thalassemia pathophysiology: Difference between revisions
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===Pathogenesis=== | ===Pathogenesis=== | ||
Beta thalassemia is a hereditary disease affecting hemoglobin. As with about half of all hereditary diseases, an inherited mutation damages the assembly of the messenger-type RNA (mRNA) that is transcribed from a chromosome. DNA contains both the instructions (genes) for stringing amino acids together into proteins, as well as stretches of DNA that play important roles in regulating produced protein levels. | Beta thalassemia is a hereditary disease affecting [[hemoglobin]]. As with about half of all hereditary diseases, an inherited mutation damages the assembly of the [[messenger-type RNA]] (mRNA) that is transcribed from a chromosome. [[DNA]] contains both the instructions (genes) for stringing amino acids together into proteins, as well as stretches of DNA that play important roles in regulating produced protein levels. | ||
In thalassemia, an additional, contiguous length or a discontinuous fragment of non-coding instructions is included in the mRNA. This happens because the mutation obliterates the boundary between the intronic and exonic portions of the DNA template. Because all the coding sections may still be present, normal hemoglobin may be produced and the added genetic material, if it produces pathology, instead disrupts regulatory functions enough to produce anemia. Hemoglobin's normal alpha and beta subunits each have an iron-containing central portion (heme) that allows the protein chain of a subunit to fold around it. Normal adult hemoglobin contains 2 alpha and 2 beta subunits. Thalassemia typically affects only the mRNAs for production of the beta chains (hence the name). Since the mutation may be a change in only a single base (single-nucleotide polymorphism), | In thalassemia, an additional, contiguous length or a discontinuous fragment of non-coding instructions is included in the [[mRNA]]. This happens because the mutation obliterates the boundary between the intronic and exonic portions of the DNA template. Because all the coding sections may still be present, normal hemoglobin may be produced and the added genetic material, if it produces pathology, instead disrupts regulatory functions enough to produce anemia. Hemoglobin's normal alpha and beta subunits each have an iron-containing central portion (heme) that allows the protein chain of a subunit to fold around it. Normal adult hemoglobin contains 2 alpha and 2 beta subunits. Thalassemia typically affects only the mRNAs for production of the beta chains (hence the name). Since the mutation may be a change in only a single base ([[single-nucleotide polymorphism]]), ongoing efforts seek [[gene therapies]] to make that single correction<ref name="pmid33626255">{{cite journal |vauthors=Taher AT, Musallam KM, Cappellini MD |title=β-Thalassemias |journal=N Engl J Med |volume=384 |issue=8 |pages=727–743 |date=February 2021 |pmid=33626255 |doi=10.1056/NEJMra2021838 |url=}}</ref><ref name="pmid19918805">{{cite journal |vauthors=Ward AJ, Cooper TA |title=The pathobiology of splicing |journal=J Pathol |volume=220 |issue=2 |pages=152–63 |date=January 2010 |pmid=19918805 |pmc=2855871 |doi=10.1002/path.2649 |url=}}</ref>. | ||
Beta-globin is an indispensable component of hemoglobin that is functioning alongside the alpha chain. In normal individuals, hemoglobin has two alpha-globin chains and two beta-globin chains (α2β2). In beta-thalassemia, the mutated gene of HBB is affecting the encoded beta-globin chains<ref name="pmid29333256">{{cite journal |vauthors=Fibach E, Rachmilewitz EA |title=Pathophysiology and treatment of patients with beta-thalassemia - an update |journal=F1000Res |volume=6 |issue= |pages=2156 |date=2017 |pmid=29333256 |pmc=5749127 |doi=10.12688/f1000research.12688.1 |url=}}</ref>. The pattern of these impaired genes can cause different pathologic conditions as shown in the table below<ref name="pmid35492364">{{cite journal |vauthors=Sanchez-Villalobos M, Blanquer M, Moraleda JM, Salido EJ, Perez-Oliva AB |title=New Insights Into Pathophysiology of β-Thalassemia |journal=Front Med (Lausanne) |volume=9 |issue= |pages=880752 |date=2022 |pmid=35492364 |pmc=9041707 |doi=10.3389/fmed.2022.880752 |url=}}</ref><ref name="pmid11605169">{{cite journal |vauthors=Rund D, Rachmilewitz E |title=Pathophysiology of alpha- and beta-thalassemia: therapeutic implications |journal=Semin Hematol |volume=38 |issue=4 |pages=343–9 |date=October 2001 |pmid=11605169 |doi=10.1016/s0037-1963(01)90028-9 |url=}}</ref>: | [[Beta-globin]] is an indispensable component of [[hemoglobin]] that is functioning alongside the alpha chain. In normal individuals, [[hemoglobin]] has two [[alpha-globin]] chains and two [[beta-globin]] chains (α2β2). In beta-thalassemia, the mutated gene of [[HBB]] is affecting the encoded [[beta-globin]] chains<ref name="pmid29333256">{{cite journal |vauthors=Fibach E, Rachmilewitz EA |title=Pathophysiology and treatment of patients with beta-thalassemia - an update |journal=F1000Res |volume=6 |issue= |pages=2156 |date=2017 |pmid=29333256 |pmc=5749127 |doi=10.12688/f1000research.12688.1 |url=}}</ref>. The pattern of these impaired genes can cause different pathologic conditions as shown in the table below<ref name="pmid35492364">{{cite journal |vauthors=Sanchez-Villalobos M, Blanquer M, Moraleda JM, Salido EJ, Perez-Oliva AB |title=New Insights Into Pathophysiology of β-Thalassemia |journal=Front Med (Lausanne) |volume=9 |issue= |pages=880752 |date=2022 |pmid=35492364 |pmc=9041707 |doi=10.3389/fmed.2022.880752 |url=}}</ref><ref name="pmid11605169">{{cite journal |vauthors=Rund D, Rachmilewitz E |title=Pathophysiology of alpha- and beta-thalassemia: therapeutic implications |journal=Semin Hematol |volume=38 |issue=4 |pages=343–9 |date=October 2001 |pmid=11605169 |doi=10.1016/s0037-1963(01)90028-9 |url=}}</ref>: | ||
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Maryam Hadipour, M.D.[2]
Overview
Beta-Thalassemia is an inherited disorder in hemoglobulin production due to a variety of genetic mutations in the gene responsible for Beta-globin production (HBB gene, on chromosome 11). The effects of beta-thalassemia on red blood cell morphology and function are significantly detrimental. Beta-Thalassemia contributes to abnormal hemoglobin and red blood cells (RBCs) that have impaired function in efficient oxygen delivery to different body tissues, which is called the state of anemia. As mutated genes are passed down, the shortage of functional red blood cells begins affecting the body from early infancy, and the lifelong persistence of insufficiency in beta-globin production results in chronic anemia. Hepatosplenomegaly, delayed developmental milestones, jaundice, bone problems, and different infections might happen in early infancy.
Pathophysiology
Pathogenesis
Beta thalassemia is a hereditary disease affecting hemoglobin. As with about half of all hereditary diseases, an inherited mutation damages the assembly of the messenger-type RNA (mRNA) that is transcribed from a chromosome. DNA contains both the instructions (genes) for stringing amino acids together into proteins, as well as stretches of DNA that play important roles in regulating produced protein levels. In thalassemia, an additional, contiguous length or a discontinuous fragment of non-coding instructions is included in the mRNA. This happens because the mutation obliterates the boundary between the intronic and exonic portions of the DNA template. Because all the coding sections may still be present, normal hemoglobin may be produced and the added genetic material, if it produces pathology, instead disrupts regulatory functions enough to produce anemia. Hemoglobin's normal alpha and beta subunits each have an iron-containing central portion (heme) that allows the protein chain of a subunit to fold around it. Normal adult hemoglobin contains 2 alpha and 2 beta subunits. Thalassemia typically affects only the mRNAs for production of the beta chains (hence the name). Since the mutation may be a change in only a single base (single-nucleotide polymorphism), ongoing efforts seek gene therapies to make that single correction[1][2].
Beta-globin is an indispensable component of hemoglobin that is functioning alongside the alpha chain. In normal individuals, hemoglobin has two alpha-globin chains and two beta-globin chains (α2β2). In beta-thalassemia, the mutated gene of HBB is affecting the encoded beta-globin chains[3]. The pattern of these impaired genes can cause different pathologic conditions as shown in the table below[4][5]:
| Type of Beta Thalassemia | Hemoglobin Chain Composition (genotype) | Severity |
|---|---|---|
| β thalassemia minor | α2β+/α2β+ or α2β+/α2β0 | Mild |
| β thalassemia major | α2β0/α2β0 | Sever |
| Thalassemia intermedia | Variable (can be similar to Major variant or may have some residual beta globin production) | Variable (milder than the Major variant but more severe than Beta Thalassemia Minor) |
Then a cascade of events would contribute to ineffective erythropoiesis and reduced hemoglobin production or impaired hemoglobin stability, hemolysis, and increased erythropoietin production (the hormone secreted by the kidney in response to low oxygen levels). Most other pathologic manifestations happen due to iron overload following the transfusions needed for the treatment [6].
- Hemolysis may happen due to the destruction of ineffective RBCs in the bone marrow, spleen, and blood, causing various consequences as well as hepatosplenomegaly[7].
- Extramedullary hematopoiesis might happen following the expansion of the bone marrow due to an increased need for erythropoiesis and increased erythropoietin production[6].
- Biliary lithiasis or gallstones would frequently happen due to products of hemolysis, excess iron, and liver damage[8].
- Endocrine disturbances might happen due to chronic anemia and low oxygen levels in the blood and iron overload[9]; followed by changes in the normal pattern of secretion of various hormones as well as[9]:
- Growth hormone: It causes delayed growth and development.
- Hypothalamic-pituitary-gonadal axis hormones: It causes hypogonadism.
- Thyroid stimulating hormone: It causes hypothyroidism.
- Parathyroid hormone (PTH): It causes parathyroid dysfunction.
- Adrenal hormones dysfunction.
Genetics
The genetic mutations present in β thalassemias are very diverse, and a number of different mutations can cause reduced or absent β globin synthesis. Two major groups of mutations can be distinguished[10][11][1]:
- Nondeletion forms: These defects generally involve a single base substitution or small deletion or inserts near or upstream of the β globin gene. Most commonly, mutations occur in the promoter regions preceding the beta-globin genes. Less often, abnormal splice variants are believed to contribute to the disease.
- Deletion forms: Deletions of different sizes involving the β globin gene produce different syndromes such as (βo) or hereditary persistence of fetal hemoglobin syndromes.
The severity of the disease depends on the nature of the mutation[12].
- Mutations are characterized as (βo) if they prevent any formation of β chains.
- Mutations are characterized as (β+) if they allow some β chain formation to occur.
- Alleles without a mutation that reduces function is characterized as (β). (Note that the "+" in β+ is relative to βo, not β.)
In either case there is a relative excess of α chains, but these do not form tetramers: rather, they bind to the red blood cell membranes, producing membrane damage, and at high concentrations they form toxic aggregates.
References
- ↑ 1.0 1.1 Taher AT, Musallam KM, Cappellini MD (February 2021). "β-Thalassemias". N Engl J Med. 384 (8): 727–743. doi:10.1056/NEJMra2021838. PMID 33626255 Check
|pmid=value (help). - ↑ Ward AJ, Cooper TA (January 2010). "The pathobiology of splicing". J Pathol. 220 (2): 152–63. doi:10.1002/path.2649. PMC 2855871. PMID 19918805.
- ↑ Fibach E, Rachmilewitz EA (2017). "Pathophysiology and treatment of patients with beta-thalassemia - an update". F1000Res. 6: 2156. doi:10.12688/f1000research.12688.1. PMC 5749127. PMID 29333256.
- ↑ Sanchez-Villalobos M, Blanquer M, Moraleda JM, Salido EJ, Perez-Oliva AB (2022). "New Insights Into Pathophysiology of β-Thalassemia". Front Med (Lausanne). 9: 880752. doi:10.3389/fmed.2022.880752. PMC 9041707 Check
|pmc=value (help). PMID 35492364 Check|pmid=value (help). - ↑ Rund D, Rachmilewitz E (October 2001). "Pathophysiology of alpha- and beta-thalassemia: therapeutic implications". Semin Hematol. 38 (4): 343–9. doi:10.1016/s0037-1963(01)90028-9. PMID 11605169.
- ↑ 6.0 6.1 Forget BG (March 1993). "The pathophysiology and molecular genetics of beta thalassemia". Mt Sinai J Med. 60 (2): 95–103. PMID 8469250.
- ↑ Shinar E, Rachmilewitz EA (1990). "Differences in the pathophysiology of hemolysis of alpha- and beta-thalassemic red blood cells". Ann N Y Acad Sci. 612: 118–26. doi:10.1111/j.1749-6632.1990.tb24297.x. PMID 2291541.
- ↑ Goldfarb A, Grisaru D, Gimmon Z, Okon E, Lebensart P, Rachmilewitz EA (1990). "High incidence of cholelithiasis in older patients with homozygous beta-thalassemia". Acta Haematol. 83 (3): 120–2. doi:10.1159/000205186. PMID 2109449.
- ↑ 9.0 9.1 Isik P, Yarali N, Tavil B, Demirel F, Karacam GB, Sac RU, Fettah A, Ozkasap S, Kara A, Tunc B (October 2014). "Endocrinopathies in Turkish children with Beta thalassemia major: results from a single center study". Pediatr Hematol Oncol. 31 (7): 607–15. doi:10.3109/08880018.2014.898724. PMID 24854890.
- ↑ Thein SL (May 2018). "Molecular basis of β thalassemia and potential therapeutic targets". Blood Cells Mol Dis. 70: 54–65. doi:10.1016/j.bcmd.2017.06.001. PMC 5738298. PMID 28651846.
- ↑ Finotti A, Breda L, Lederer CW, Bianchi N, Zuccato C, Kleanthous M, Rivella S, Gambari R (2015). "Recent trends in the gene therapy of β-thalassemia". J Blood Med. 6: 69–85. doi:10.2147/JBM.S46256. PMC 4342371. PMID 25737641.
- ↑ Jaing TH, Chang TY, Chen SH, Lin CW, Wen YC, Chiu CC (November 2021). "Molecular genetics of β-thalassemia: A narrative review". Medicine (Baltimore). 100 (45): e27522. doi:10.1097/MD.0000000000027522. PMC 8589257 Check
|pmc=value (help). PMID 34766559 Check|pmid=value (help).