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Iron status of inner-city African-American infants
Betsy Lozoff1, Mary Lu Angelilli, Jigna Zatakia
1Center for Human Growth and Development, University of Michigan, Ann Arbor, Michigan 48109, USA. blozoff@umich.edu
Insights
Assessing iron status in infants is complex. Different measurement methods yield varying iron deficiency prevalence rates, highlighting the need for better infant iron assessment tools.
Area of Science:
- Pediatric Nutrition
- Hematology
- Public Health
Background:
- Iron deficiency remains a significant concern in infant populations, particularly in urban settings.
- Accurate assessment of iron status in infants is crucial for early intervention and preventing long-term health consequences.
Observation:
- This study evaluated the iron status of 198 9-month-old inner-city infants, with 94% fed iron-fortified formula.
- A comprehensive panel of iron measures, including hemoglobin, free erythrocyte protoporphyrin (FEP), and body iron, were assessed.
- Lead and inflammation markers were also evaluated to contextualize iron status findings.
Findings:
- Elevated FEP levels were observed in 52.3% of infants, independent of lead exposure or inflammation.
- Iron deficiency prevalence varied significantly (2.5%–14.4%) based on the diagnostic criteria used (MCV, ferritin, Sweden/Honduras, or body iron).
- The immaturity of iron storage regulation in infants under one year makes ferritin-based estimates, including body iron, potentially unreliable.
Implications:
- The variability in prevalence estimates underscores the challenges in accurately diagnosing iron deficiency in young infants.
- Current diagnostic methods may not be sufficiently sensitive or specific for this age group.
- There is an urgent need for the development and validation of functional indicators to assess iron status in infants accurately.
Abstract:
The iron status of African-American infants continues to be subject to debate. We characterized the iron status of 198 9-month-old inner-city infants (94% fed iron-fortified formula) using a comprehensive panel of measures and assessing lead and inflammation markers. The proportion with iron deficiency was calculated based on three approaches (> or = 2 abnormal iron measures with or without anemia for MCV model--NHANES II, ferritin model--NHANES III, or Sweden/Honduras study) and a promising new measure-body iron, calculated from ferritin and transferrin receptor (TfR). There were no sex differences for any iron measure. Hb < 110 g/l was observed in 25%; Hb < or = 105 g/l in 10.1%. Free erythrocyte protoporphyrin (FEP) values were elevated without elevated lead concentrations or an inflammatory response: mean FEP = 86.6 microg/dl red blood cells [75.5 micromol/mol heme]; 52.3% were > 80 microg/dl (1.42 micromol/l), almost half of which were accompanied by a second abnormal iron measure. The estimated prevalence of iron deficiency was 14.4, 5.3, and 2.5% for the MCV model, ferritin model, and Sweden/Honduras cutoffs, respectively, and 4.1% for body iron < 0 mg/kg. Regulation of iron storage is immature at < 1 year of age, making estimates of iron deficiency that depend on ferritin, including body iron, suspect in this age period. Thus, the "true" prevalence of iron deficiency could not be established with confidence due to major differences in the results, depending on the guidelines used. Functional indicators of poor iron status in young infants are urgently needed.
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