Abstract
Objective
Deficiencies of citrulline and arginine have been associated with adverse outcomes in preterm-infants and data regarding enteral supplementation in preterm infants is limited.
Study design
This randomized -trial [NCT03649932] included 42 preterm infants (gestational age ≤33 weeks) randomized to receive enteral L-citrulline in low (100 mg/kg/day), medium (200 mg/kg/day) and high-dose (300 mg/kg/day) groups for 7 days. Plasma citrulline and arginine levels were obtained pre-and-post supplementation and efficacy was determined by a significant increase in levels after supplementation. A p < 0.05 was considered significant. Safety monitoring included blood-pressure-monitoring as well as complications and death during hospitalization.
Results
A total of 40/42 (95%) of the recruits completed the 7-day supplementation with no adverse events. Plasma-citrulline levels increased significantly in all three groups while plasma-arginine levels increased significantly in the high-dose group.
Conclusion
Enteral L-citrulline supplementation in preterm infants is safe and effective in increasing plasma citrulline and arginine levels.
Clinical trial registration
NCT03649932 https://clinicaltrials.gov/ct2/show/NCT03649932.
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Data availability
Deidentified individual participant data (including data dictionaries) will be made available in addition to study protocols, the statistical analysis plan, and the informed consent form. The data will be made available upon publication to researchers who provide a methodologically sound proposal for use in achieving the goals of the approved proposal. Proposals should be submitted to skjain@utmb.edu.
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AQ, MQM, SB drafted the initial manuscript, and reviewed and revised the manuscript. AQ, MQM, SB, and MEF-F obtained consent, collected data, carried out the initial analyses, and reviewed and revised the manuscript. AQ and SKJ conceptualized and designed the study, coordinated and supervised data collection, and critically reviewed the manuscript for important intellectual content. All authors approved the final manuscript as submitted and agree to be accountable for all aspects of the work.
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The study was approved by the Institutional Review Board at the University of Texas Medical Branch, Galveston, TX. Consent was obtained from patients prior to induction into the study. The study was in accordance with the Declaration of Helsinki.
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Qasim, A., Mehdi, M.Q., Bhatia, S. et al. Enteral L-citrulline supplementation in preterm infants is safe and effective in increasing plasma arginine and citrulline levels—a pilot randomized trial. J Perinatol (2023). https://doi.org/10.1038/s41372-023-01761-x
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DOI: https://doi.org/10.1038/s41372-023-01761-x