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Plasma C-type natriuretic peptide levels in healthy children
S Del Ry1, M Cantinotti, M Cabiati
1CNR Institute of Clinical Physiology and Fondazione G. Monasterio, Laboratory of Cardiovascular Biochemistry, Pisa, Italy. delry@ifc.cnr.it
Insights
Plasma C-type natriuretic peptide (CNP) levels are significantly higher in infants and children than adults. This study establishes crucial reference intervals for CNP in newborns and children, vital for clinical applications.
Area of Science:
- Biochemistry
- Pediatrics
- Cardiovascular Research
Background:
- C-type natriuretic peptide (CNP) is increasingly recognized for its role in cardiovascular disease.
- Plasma CNP levels in adults correlate with disease severity, but reference values in infants are scarce.
Purpose of the Study:
- To determine the reference intervals for plasma CNP in healthy human newborns and infants.
- To establish age-specific reference ranges for CNP in pediatric populations.
Main Methods:
- Plasma CNP was measured using radioimmunoassay in 121 healthy children (newborns to 12 years) and 32 adults.
- Participants were stratified into distinct age groups: 0-3 days, 4-30 days, 1-12 months, 1-12 years, and adults.
Main Results:
- Plasma CNP levels were significantly higher in children (13.6 ± 1.2 pg/ml) compared to adults (7.4 ± 1.0 pg/ml).
- Distinct reference intervals were identified: newborns (0-3 days) 11.6 ± 2.1 pg/ml, newborns (4-30 days) 16.4 ± 3.7 pg/ml, infants (1-12 months) 15.4 ± 2.7 pg/ml, and children (1-12 years) 13.6 ± 2.3 pg/ml.
- CNP concentrations peaked between 4-5 days of life, declining progressively thereafter.
Conclusions:
- At least five distinct reference intervals for plasma CNP are recommended for pediatric use.
- These findings provide essential data for the clinical application of CNP in diagnosing and managing pediatric cardiovascular conditions.
Abstract:
C-type natriuretic peptide (CNP) is assuming increasing importance in cardiovascular disease, and in adults its plasma levels are related to clinical and functional disease severity. Data are scarce regarding the reference values for CNP in infancy. Aim of this study was to assess the reference intervals for CNP in human healthy newborns and infants. Plasma CNP was measured in 121 healthy children divided into: 41 newborns (age 0-3 days), 24 newborns (4-30 days), 22 infants (1-12 months) and 32 children (1-12 years). A group of 32 healthy adult subjects (age 64 ± 1 years) was also studied. CNP was measured by a specific radioimmunoassay. Between- and within-assay variability resulted ≤ 30 and 20%, respectively and analytical sensitivity 0.77 ± 0.05 pg/tube. Plasma CNP resulted significantly higher in children than in adult subjects (13.6 ± 1.2 pg/ml vs. 7.4 ± 1.0 pg/ml, p=0.030). When the results were analyzed as a function of the age the reference intervals for plasma CNP resulted: 11.6 ± 2.1 pg/ml for newborns (0-3 days), 16.4 ± 3.7 pg/ml for newborns (4-30 days), 15.4 ± 2.7 pg/ml for infants (1-12 months), 13.6 ± 2.3 pg/ml for children (1-12 years) [p=0.01 newborns (4-30 days) vs. adults; p=0.03 infants (1-12 months) vs. adults]. CNP showed the highest concentrations after 12h of life with a peak between 4 and 5 days of life and with a progressive decline afterwards. According to these data at least five different reference intervals for CNP determinations should be used. These observations may be helpful for future clinical application of CNP in human children.
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