Glucose-6-phosphate Dehydrogenase Deficiency and Thalassaemia Trait
نویسندگان
چکیده
There is now evidence that an increase in the low-density serum lipoproteins plays a part in the causation of degenerative vascular disease (Gofman, Jones, Lindgren, Lyon, Elliott, and Strisower, 1950; Kannel, Dawber, Kagan, Revotskie, and Stokes, 1961). Studies of serum cholesterol in different ethnic groups has shown important differences (Adlersberg and Schaefer, 1959), but it cannot yet be decided if these differences are caused by genetic factors, by diet, or by other environmental influences (Adlersberg, Schaefer, Steinberg, and Wang, 1956). Choremis, Kyriakides, and Papadakis (1961), studying children with Cooley's anaemia and sicklecell anaemia, reported decreased values of serum lipids as determined by chemical analysis. Westerman, Pierce, and Jensen (1964) also found plasma total lipid, total phospholipid, and total cholesterol concentrations to be significantly lower in patients with sickle-cell anaemia than in a group of normal subjects. Fessas, Stamatoyannopoulos, and Keys (1963) described reduced levels of cholesterol and 5-lipoprotein in carriers of the thalassaemia trait. On the other hand in Negroes with glucose-6phosphate dehydrogenase (G6PD) deficiency serum cholesterol levels are reported to be higher as compared with age-matched controls (Tarlov, Brewer, and Swanson, 1961). In the Greek population we have a relatively large number of people with the thalassaemia trait, as well as people with G6PD deficiency. In view of this, we carried out a study of serum lipoproteins in carriers of the thalassaemia trait and in G6PD deficient subjects, in order to confirm the existence of any significant differences in the serum lipoproteins between these two groups.
منابع مشابه
Thalassaemia and glucose-6-phosphate dehydrogenase deficiency in sickle-cell disorder patients in Taiz, Yemen.
A pilot study was conducted to determine the prevalence and haematological characteristics of the interaction between thalassaemia or/and glucose-6-phosphate dehydrogenase (G6PD) deficiency in patients with sickle-cell disorder (SCD) in Taiz city, Yemen, where the prevalence of sickle-cell trait (HbAS) is 8.2%. Blood samples were collected from 31 SCD patients. Complete blood count and haemoglo...
متن کاملPrevalence of thalassaemia, iron-deficiency anaemia and glucose-6-phosphate dehydrogenase deficiency among Arab migrating nomad children, southern Islamic Republic of Iran.
This study investigated the prevalence of iron-deficiency anaemia, glucose-6-phosphate dehydrogenase (G6PD) deficiency and β-thalassaemia trait among Arab migrating nomad children in southern Islamic Republic of Iran. Blood samples were analysed from 134 schoolchildren aged < 18 years (51 males, 83 females). Low serum ferritin (< 12 ng/dL) was present in 17.9% of children (21.7% in females and ...
متن کاملGenetic red cell disorders and severity of falciparum malaria in Myanmar.
A hospital-based survey was undertaken to investigate the relationship between the incidence and severity of malaria infection and various red cell disorders in Myanmar. The mean parasitaemia levels of patients with alpha- or beta-thalassaemia trait or with severe glucose-6-phosphate dehydrogenase (G6PD) deficiency were lower than those of individuals with normal haemoglobin AA or with heterozy...
متن کاملSerum lipoproteins in schoolboys in relation to glucose-6-phosphate dehydrogenase deficiency and thalassaemia trait.
There is now evidence that an increase in the low-density serum lipoproteins plays a part in the causation of degenerative vascular disease (Gofman, Jones, Lindgren, Lyon, Elliott, and Strisower, 1950; Kannel, Dawber, Kagan, Revotskie, and Stokes, 1961). Studies of serum cholesterol in different ethnic groups has shown important differences (Adlersberg and Schaefer, 1959), but it cannot yet be ...
متن کاملGlucose-6-Phosphate Dehydrogenase Deficiency Associated with Thalassemia and Sickle Cell Anemia in an Iranian Family
Sickle cell-thalassemia associated with glucose- 6-phosphate dehydrogenese deficiency is reported in an Iranian family. The father had sickle trait and G.6.P.D. deficiency, the mother minor thalassemia, one of the sons siclc:le ceH-thailasemiia., the oth-er sickle cell trait; the daughter had sickle cell-thalassemia and was carrier of G.6.P.D. deficiellcy.
متن کامل