Interaction of Sickle Cell Trait and Glucose-6-Phosphate Dehydrogenase Deficiency in Cameroon
| Autor: | Shelly C. Bernstein, James E. Bowman, L K Noche |
|---|---|
| Rok vydání: | 1980 |
| Předmět: |
Male
Genetics Hemoglobin s medicine.medical_specialty Sickle cell trait Anemia Hemoglobin Sickle Dehydrogenase Anemia Sickle Cell Biology medicine.disease Sickle Cell Trait Glucosephosphate Dehydrogenase Deficiency Endocrinology Internal medicine parasitic diseases medicine Humans Cameroon Hemoglobin Genetics (clinical) Glucose-6-phosphate dehydrogenase deficiency |
| Zdroj: | Human Heredity. 30:7-11 |
| ISSN: | 1423-0062 0001-5652 |
| Popis: | The prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency and sickle cell trait was determined in 371 Cameroonian males and 668 male blood donors in Chicago. The number of males with both sickle cell trait and G6PD deficiency was significantly greater than expected (p less than 0.05) in Cameroon. The number of males with both sickle cell trait and G6PD deficiency in the Chicago population also exceeded the exptected number, although this was not statistically significant (p greater than 0.30). A young red cell population associated with the sickle cell gene leading to elevated G6PD levels in G6PD-deficient males suggests that sickle hemoglobin may exert a beneficial effect on G6PD deficiency, rather than the opposite, as had previously been proposed. These red cells may be better able to deal with oxidative stress, which can precipitate severe hemolytic disease in G6PD deficiency. |
| Databáze: | OpenAIRE |
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