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Gestational age and age at sampling influence metabolic profiles in premature infants
Reese H Clark1, Amy S Kelleher2, Donald H Chace2
1Pediatrix-Obstetrix Center for Research, Education and Quality, Sunrise, Florida reese_clark@pediatrix.com.
Insights
Gestational and chronological age significantly impact amino acid and acylcarnitine profiles in premature infants. These findings are crucial for interpreting metabolic screening tests in this vulnerable population.
Area of Science:
- Biochemistry
- Neonatology
- Metabolomics
Background:
- Premature infants often have altered metabolic profiles due to immaturity.
- Accurate interpretation of metabolic screening tests is vital for early diagnosis of inborn errors of metabolism.
Purpose of the Study:
- To investigate how gestational age and chronological age affect amino acid and acylcarnitine profiles in premature infants.
- To establish reference values for metabolic profiles in preterm neonates.
Main Methods:
- Metabolic profiles, including 15 amino acids and 35 acylcarnitines, were analyzed in infants born between 23 and 31 weeks of gestation.
- Samples were collected within 24 hours of birth and on approximately days 7, 28, and 42, or at discharge.
- Standard newborn screening techniques were employed, with analysis conducted by a central laboratory.
Main Results:
- Of 995 infants studied, 21.5% had abnormal metabolic profiles; none were diagnosed with inborn errors of metabolism.
- Both gestational age and postbirth chronological age significantly influenced the metabolic profiles.
- Infants born earlier (23-26 weeks gestation) had higher rates of abnormal profiles (29%) compared to those born later (29-31 weeks gestation, 17%). Abnormalities were most frequent on day 7 for the earliest gestations (21%).
Conclusions:
- The study highlights the complexity of interpreting metabolic profiles in preterm infants due to immaturity.
- The data provide essential reference values for understanding metabolism and improving screening for inborn errors of metabolism in preterm neonates.
Objective:
To describe the influence that gestational age and chronological age have on amino acid and acylcarnitine profiles in an at-risk population of premature infants.
Methods:
Metabolic profiles (15 amino acids and 35 acylcarnitines) were obtained by using standard newborn techniques on infants born between 23 and 31 completed weeks of gestation. The profiles were drawn within the first 24 hours after birth and on approximately days 7, 28, and 42 of life or at discharge. A single, central, contract laboratory analyzed and managed the samples.
Results:
We studied 995 patients; none was subsequently diagnosed with an inborn error of metabolism. Of the 3579 samples, there were 257 (7.2%) amino acid or acylcarnitine alerts reported in 214 infants (21.5% of infants studied). Both gestational age and postbirth chronological age significantly influenced the metabolic profile. Twenty-nine percent of infants at 23 to 26 weeks' gestational age had an abnormal metabolic profile compared with 17% of infants at 29 to 31 weeks' gestational age (P < .01). On the day of birth, 12% of the profiles were abnormal compared with 2% on day 28 (P < .01). The highest rate of abnormal values occurred on day 7 in the infants 23 to 26 weeks' gestational age (21%).
Conclusions:
These results demonstrate the complexity of understanding the impact of immaturity and disease on metabolic profiles used to screen for inborn errors of metabolism. Our data provide reference values for studies aimed at better understanding metabolism in preterm infants.
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