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Comparative analysis of RBC membrane lipids in thalassemia, and iron deficiency anemia in relation to hypochromia and oxidant injury
Authors:S P Sanghani  V A Haldankar  K K Shalia  S K Bichlle
Institution:(1) Department of Biochemistry Mumbai Central, Topiwala National Medical College and B. Y. L. Nair Hospital, 40008 Mumbai;(2) Department Hematology Mumbai Central, Topiwala National Medical College and B. Y. L. Nair Hospital, 40008 Mumbai
Abstract:The effect of an intrinsic defect in the red cell and pronounced hypochromia on oxidative damage to RBC membrane lipids was compared in beta-thalassemia and iron deficiency anemia (IDA), which have a varied etiology but equivalent low hemogiobin content. The study was planned to correlate the etiology of the disorders to the severity of lipid imbalance and RBC hemolysis in membranes of both the conditions. Results indicated a fall of lysophosphatidylcholine(LPC), phosphatidylethanolamine(PE) and the unsaturated to saturated fatty acid ratio in both conditions, while phosphatidylcholine(PC) increased only in thalassemia. However, irrespective of the disease, sphingomyelin(SM), total cholesterol and phospholipid levels elevated and the hydrogen peroxide stress test indicated increased susceptibility of both pathologic RBCs to peroxidation. Present findings indicate that IDA and thalassemla, allow for considerable amounts of oxidative damage to membrane lipids, irrespective of their etiologles, and thus point hypochromia as an important contributor for inducing lipid imbalance and RBC hemolysis.
Keywords:Hypochromia  intrinsic defect  oxidation  RBC membrane  lipid imbalance
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