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A Method to Evaluate Fetal Erythropoiesis from Postnatal Survival of Fetal RBCs
Authors:Denison J. Kuruvilla  John A. Widness  Demet Nalbant  Robert L. Schmidt  Donald M. Mock  Peter Veng-Pedersen
Affiliation:.Department of Pharmaceutical Sciences and Experimental Therapeutics, College of Pharmacy, University of Iowa, 115 S. Grand Ave. S227, Iowa City, Iowa 52242 USA ;.Department of Pediatrics, College of Medicine, University of Iowa, Iowa City, Iowa USA ;.Departments of Biochemistry and Molecular Biology, University of Arkansas for Medical Sciences, Little Rock, Arkansas USA ;.Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas USA
Abstract:Fetal RBCs are produced during a period of very rapid growth and stimulated erythropoiesis under hypoxic intrauterine conditions. Fetal RBC life span varies with gestational age (GA) and is shorter than that in healthy adults. Due to the special kinetic properties of life span-based survival of human RBCs, a mathematical model-based kinetic analysis of the survival of fetal RBCs shortly after birth provides a unique opportunity to “look backward in time” to evaluate fetal erythropoiesis. This work introduces a novel method that utilizes postnatal in vivo RBC survival data collected within 2 days after birth to study both nonsteady-state (non-SS) in utero RBC production and changing fetal RBC life span over time. The effect of changes in erythropoiesis rate and RBC life span and the effect of multiple postnatal phlebotomies on the RBC survival curves were investigated using model-based simulations. This mathematical model, which considers both changes in the rate of erythropoiesis and RBC life span and which accurately accounts for the confounding effect of multiple phlebotomies, was applied to survival curves for biotin-labeled RBCs from ten anemic very low birth weight preterm infants. The estimated mean fetal RBC production rate scaled by body weight was 1.07 × 107 RBCs/day g, and the mean RBC life span at birth was 52.1 days; these values are consistent with reported values. The in utero RBC life span increased at a rate of 0.51 days per day of gestation. We conclude that the proposed mathematical model and its implementation provide a flexible framework to study in utero non-SS fetal erythropoiesis in newborn infants.KEY WORDS: cord blood RBCs, fetal erythropoiesis, fetal RBC life span, fetal RBC production, red blood cells
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