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Non-invasive Optical Measurement of Cerebral Metabolism and Hemodynamics in Infants
Published on: March 14, 2013
Caffeine metabolism in premature infants
S al-Alaiyan1, S al-Rawithi, D Raines
1Department of Pediatrics, Section of Neonatology, MBC-58, P.O. Box 3354, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.
Insights
Caffeine metabolism in premature infants matures with postnatal age, primarily via N7-demethylation. Female infants exhibit higher metabolic rates, indicating gender influences caffeine processing.
Area of Science:
- Pharmacokinetics and Drug Metabolism
- Neonatal Physiology
- Pediatric Pharmacology
Background:
- Caffeine is a common treatment for apnea of prematurity.
- Individual variations in hepatic enzyme activity affect caffeine metabolism.
- Understanding factors influencing caffeine metabolism is crucial for optimizing therapy in neonates.
Purpose of the Study:
- To investigate the impact of postnatal age (PNA), birth weight (BW), study weight (SW), gestational age (GA), postconceptual age (PCA), and gender on caffeine metabolism maturation in premature infants.
- To identify the predominant caffeine metabolic pathways in this population.
Main Methods:
- Oral administration of caffeine base (10 mg/kg loading, 2 mg/kg maintenance).
- Measurement of plasma caffeine and metabolite concentrations on day 5 post-loading dose.
- Calculation of molar concentration ratios for N3-, N7-, N1-, and Nall- demethylation, clearance (CL), and %caffeine (%CAF) in 80 premature infants.
Main Results:
- Caffeine metabolic activity (N3-, N7-, Nall- pathways) increased with PNA, while %CAF decreased.
- No significant differences in N1-pathway or CL were observed across PNA groups.
- Female infants showed significantly higher %CAF and N1-, N3-, Nall- metabolic rates compared to males; PNA was significantly related to %CAF and Nall- demethylation.
Conclusions:
- N7-demethylation is the primary pathway for caffeine metabolism in premature infants.
- Caffeine metabolism maturation progresses with postnatal age in infants under 60 days, independent of BW, GA, PCA, and SW.
- Female neonates exhibit accelerated caffeine metabolism compared to males.
Abstract:
Caffeine has been used frequently in the treatment and prevention of apnea of prematurity. The metabolism of caffeine depends on the activities of the hepatic enzymes that vary from one infant to another. The objective of this study was to determine the influence of postnatal age (PNA), birth weight (BW), study weight (SW), gestational age (GA), postconceptual age (PCA), and gender on the maturation of caffeine metabolism in premature infants. The caffeine base was administered orally as a loading dose of 10 mg/kg, followed by a maintenance dose of 2 mg/kg every 24 hours. The steady-state concentration of caffeine and metabolites was measured in plasma taken on the 5th-day postloading dose. The molar concentration ratios for the N3 (N3-), N7 (N7-), N1 (N1-), and all methyl (Nall-) demethylation processes; clearance (CL); and the percentage of molar concentration of caffeine found in plasma to that of the total caffeine and metabolites (%CAF) were calculated from samples collected from 80 neonatal infants. The 48 male and 32 female premature infants had median (range) BW (g), GA (weeks), SW (g), PCA (weeks), and PNA (days) of 1300 (650-2260), 30 (24-34), 1630 (980-2670), 34 (29-40), and 28 (5-60), respectively. The median (range) of the ratios for the %CAF, CL, and the N3-, N7-, N1-, and Nall- were 86.9 (52.9-99.0), 0.127 (0.046-0.503) ml.kg-1.min-1, 0.032 (0-0.438), 0.070 (0.007-0.471), 0.026 (0-0.283), and 0.0463 (0.003-0.303), respectively. When the patients were stratified into four PNA age groups, each older group showed a consistently higher level of caffeine metabolic activity for the N3-, N7-, and Nall- pathways with a corresponding decrease in the %CAF, whereas no significant differences were seen for the N1-pathway or for CL. No pattern of significant differences between the demethylation process ratios, %CAF, or CL was seen between groups of infants when they were stratified according to BW, SW, PCA, or GA. The female infants were found to have significantly higher rates of caffeine metabolism as shown by %CAF, N1-, N3-, and Nall- processes but not the N7-. Multivariate linear regression analysis by two methods demonstrated that PNA is significantly related to %CAF and Nall-, whereas the female patients had higher levels of metabolic activity for the %CAF and N1- process. The authors conclude that the N7-demethy-lation process is the predominate caffeine metabolic process in premature infants. Furthermore, the maturation of the caffeine metabolism in premature infants with a PNA of less than 60 days increases with postnatal age, regardless of birth weight, gestational age, postconceptual age, and study weight. The female neonatal patients demonstrated a higher rate of caffeine metabolism than the males.
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