Brian J Sandri1,2, Gabriele R Lubach3, Eric F Lock4, Pamela J Kling5, Michael K Georgieff1,2, Christopher L Coe3, Raghavendra B Rao1,2. 1. Division of Neonatology, Department of Pediatrics, University of Minnesota, Minneapolis, MN, USA. 2. Center for Neurobehavioral Development, University of Minnesota, Minneapolis, MN, USA. 3. Harlow Center for Biological Psychology, University of Wisconsin, Madison, WI, USA. 4. Division of Biostatistics, School of Public Health, University of Minnesota, Minneapolis, MN, USA. 5. Division of Neonatology, Department of Pediatrics, University of Wisconsin, Madison, WI, USA.
Abstract
BACKGROUND: The effects of infantile iron deficiency anemia (IDA) extend beyond hematological indices and include short- and long-term adverse effects on multiple cells and tissues. IDA is associated with an abnormal serum metabolomic profile, characterized by altered hepatic metabolism, lowered NAD flux, increased nucleoside levels, and a reduction in circulating dopamine levels. OBJECTIVES: The objective of this study was to determine whether the serum metabolomic profile is normalized after rapid correction of IDA using iron dextran injections. METHODS: Blood was collected from iron-sufficient (IS; n = 10) and IDA (n = 12) rhesus infants at 6 months of age. IDA infants were then administered iron dextran and vitamin B via intramuscular injections at weekly intervals for 2 to 8 weeks. Their hematological and metabolomic statuses were evaluated following treatment and compared with baseline and a separate group of age-matched IS infants (n = 5). RESULTS: Serum metabolomic profiles assessed at baseline and after treatment via HPLC/MS using isobaric standards identified 654 quantifiable metabolites. At baseline, 53 metabolites differed between IS and IDA infants. Iron treatment restored traditional hematological indices, including hemoglobin and mean corpuscular volume, into the normal range, but the metabolite profile in the IDA group after iron treatment was markedly altered, with 323 metabolites differentially expressed when compared with an infant's own baseline profile. CONCLUSIONS: Rapid correction of IDA with iron dextran resulted in extensive metabolic changes across biochemical pathways indexing the liver function, bile acid release, essential fatty acid production, nucleoside release, and several neurologically important metabolites. The results highlight the importance of a cautious approach when developing a route and regimen of iron repletion to treat infantile IDA.
BACKGROUND: The effects of infantile iron deficiency anemia (IDA) extend beyond hematological indices and include short- and long-term adverse effects on multiple cells and tissues. IDA is associated with an abnormal serum metabolomic profile, characterized by altered hepatic metabolism, lowered NAD flux, increased nucleoside levels, and a reduction in circulating dopamine levels. OBJECTIVES: The objective of this study was to determine whether the serum metabolomic profile is normalized after rapid correction of IDA using iron dextran injections. METHODS: Blood was collected from iron-sufficient (IS; n = 10) and IDA (n = 12) rhesus infants at 6 months of age. IDA infants were then administered iron dextran and vitamin B via intramuscular injections at weekly intervals for 2 to 8 weeks. Their hematological and metabolomic statuses were evaluated following treatment and compared with baseline and a separate group of age-matched IS infants (n = 5). RESULTS: Serum metabolomic profiles assessed at baseline and after treatment via HPLC/MS using isobaric standards identified 654 quantifiable metabolites. At baseline, 53 metabolites differed between IS and IDA infants. Iron treatment restored traditional hematological indices, including hemoglobin and mean corpuscular volume, into the normal range, but the metabolite profile in the IDA group after iron treatment was markedly altered, with 323 metabolites differentially expressed when compared with an infant's own baseline profile. CONCLUSIONS: Rapid correction of IDA with iron dextran resulted in extensive metabolic changes across biochemical pathways indexing the liver function, bile acid release, essential fatty acid production, nucleoside release, and several neurologically important metabolites. The results highlight the importance of a cautious approach when developing a route and regimen of iron repletion to treat infantile IDA.
Authors: Brian J Sandri; Jonathan Kim; Gabriele R Lubach; Eric F Lock; Candace Guerrero; LeeAnn Higgins; Todd W Markowski; Pamela J Kling; Michael K Georgieff; Christopher L Coe; Raghavendra B Rao Journal: Am J Physiol Regul Integr Comp Physiol Date: 2022-03-10 Impact factor: 3.210
Authors: Brian J Sandri; Jonathan Kim; Gabriele R Lubach; Eric F Lock; Candace Guerrero; LeeAnn Higgins; Todd W Markowski; Pamela J Kling; Michael K Georgieff; Christopher L Coe; Raghavendra B Rao Journal: Data Brief Date: 2022-09-11