Genetic association studies in β-hemoglobinopathies.

Abstract

Characterization of the molecular basis of the β-thalassemias and sickle cell disease (SCD) clearly showed that individuals with the same β-globin genotypes can have extremely diverse clinical severity. Two key modifiers, an innate ability to produce fetal hemoglobin and coinheritance of α-thalassemia, both derived from family and population studies, affect the pathophysiology of both disorders at the primary level. In the past 2 decades, scientific research had applied genetic approaches to identify additional genetic modifiers. The review summarizes recent genetic studies and key genetic modifiers identified and traces the story of fetal hemoglobin genetics, which has led to an emerging network of globin gene regulation. The discoveries have provided insights on new targets for therapeutic intervention and raise possibilities of developing fetal hemoglobin predictive diagnostics for predicting disease severity in the newborn and for integration into prenatal diagnosis to better inform genetic counseling.

• Authors: Swee Lay Thein
• Journal: Hematology. American Society of Hematology. Education Program (Hematology Am Soc Hematol Educ Program) Vol. 2013 Pg. 354-61 ( 2013) ISSN: 1520-4383 [Electronic] United States
• PMID: 24319204 (Publication Type: Journal Article, Review)

Chemical References

• Fetal Hemoglobin

Topics

• Anemia, Sickle Cell (diagnosis, genetics, therapy)
• Fetal Hemoglobin (genetics)
• Genome-Wide Association Study
• Humans
• beta-Thalassemia (diagnosis, genetics, therapy)