ArticleFrontiers in pharmacology2026
Developmental age and clinical illness drive
Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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9 authors.
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Abstract
Background: Caffeine is the standard therapy for apnea of prematurity and used near-universally in preterm infants. Interindividual variability in clearance, exposure, and clinical responses persists in neonates. CYP1A2 is the primary enzyme responsible for caffeine metabolism in adults, but the enzyme activity in neonates has historically been considered negligible. Methods: Scavenged plasma samples from neonates receiving caffeine therapy in a neonatal intensive care unit were analyzed to quantify caffeine and paraxanthine concentrations. The caffeine metabolic ratio (CMR) was used as a functional biomarker of Results: Thirty-one neonates (186 plasma samples) were recruited for this study. Paraxanthine was detectable in all samples, demonstrating measurable CYP1A2 activity. CMR increased with postmenstrual age even after adjusting for clinical covariates ( Conclusion: These findings provide the first
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