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Abstract
Because total cholesterol levels have been found to be lower in patients affected
by thalassemia major and intermedia, we examined the plasma lipid pattern of 628 beta-thalassemia
trait carriers and 4552 controls in order to evaluate whether the plasma lipid impairment
is also present in the heterozygous state. Total cholesterol and low density lipoprotein
(LDL)-cholesterol levels were significantly lower in betathalassemia trait carriers
when compared to controls, whereas plasma triglycerides and high density lipoprotein
(HDL)-cholestrol levels did not differ between the two groups. We suggest that accelerated
erythropoiesis and increased uptake of LDL by macrophages and histiocytes of the reticuloendothelial
system are the main determinants of low plasma cholesterol levels in heterozygous
thalassemia.
Keywords
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References
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Article info
Publication history
Accepted:
September 29,
1988
Received in revised form:
September 1,
1988
Received:
March 16,
1988
Identification
Copyright
© 1989 Published by Elsevier Inc.