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Exchangeable Zinc Pool Size at Birth in Pakistani Small for Gestational Age and Appropriate for Gestational Age
Shabina Ariff1, Nancy F Krebs2, Jamie E Westcott2
1Aga Khan University, Karachi, Pakistan.
Insights
Small for gestational age (SGA) infants do not have lower zinc stores at birth. However, Pakistani infants showed lower zinc levels compared to US infants, suggesting maternal nutrition impacts fetal zinc transfer.
Area of Science:
- Nutritional science
- Pediatrics
- Human physiology
Background:
- Small for gestational age (SGA) infants face higher risks of illness and poor growth.
- Zinc supplementation may benefit SGA infants, but their susceptibility to zinc deficiency is unclear.
Purpose of the Study:
- To compare zinc endowment in term SGA and appropriate for gestational age (AGA) infants.
- To investigate if SGA infants have a higher susceptibility to zinc deficiency.
Main Methods:
- A longitudinal study in Pakistan compared exchangeable zinc pools (EZPs) in SGA and AGA infants.
- Zinc stable isotopes were administered intravenously to measure EZP size at birth and 6 months.
Main Results:
- No significant difference in EZP was found between SGA and AGA infants at birth or 6 months.
- EZP declined significantly relative to body weight in both groups by 6 months.
- Pakistani infants had lower birth EZP than US AGA infants.
Conclusions:
- Results do not support a difference in zinc endowment between SGA and AGA infants in Pakistan.
- Findings suggest reduced in utero zinc transfer linked to maternal nutrition.
- This may increase susceptibility to postnatal zinc deficiency in SGA infants.
Objectives:
Small for gestational age (SGA) infants are more susceptible to infectious morbidity and growth faltering compared to their appropriate for gestational age (AGA) counterparts. Zinc supplementation of SGA infants may be beneficial but the underlying susceptibility to zinc deficiency of SGA infants has not been examined.
Methods:
In a community-based, observational, longitudinal study in a peri-urban settlement of Karachi, Pakistan, we compared the size of the exchangeable zinc pools (EZPs) in term SGA and AGA infants at birth and at 6 months of age, hypothesizing that the EZP would be lower in the SGA group. To measure EZP size, a zinc stable isotope was intravenously administered within 48 hours of birth (n = 17 and 22) at 6 months (n = 11 and 14) in SGA and AGA infants, respectively. Isotopic enrichment in urine was used to determine EZP.
Results:
No significant difference was detected in the mean (±standard deviation) EZP between SGA and AGA infants at birth, with values of 9.8 ± 3.5 and 10.1 ± 4.1 mg/kg, respectively (P = 0.86), or at 6 months. Longitudinal EZP measurements demonstrated a significant decline in EZP relative to body weight in both groups at 6 months (P < 0.001). Mean EZP (adjusted for body weight) size at birth for the combined Pakistani groups was significantly lower than AGA infants at birth in the United States (P = 0.017).
Conclusions:
These results did not support a difference in zinc endowment between SGA and AGA Pakistani infants. They, however, do suggest lower in utero zinc transfer to the fetus in a setting where poor maternal nutritional status may confer a high susceptibility to postnatal zinc deficiency.
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