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Are low birth weight children predisposed to renal loss of carnitine?
Piotr Tomasz Protas1, Alina Kępka2, Agnieszka Rybi-Szuminska1
1Department of Pediatrics and Nephrology, Medical University of Białystok, Białystok, Poland.
Insights
Low birth weight infants show higher urinary excretion of l-carnitine (LC) and acetyl-carnitine (ALC), suggesting potential renal dysfunction. This increased excretion negatively correlates with birth weight and estimated glomerular filtration rate (eGFR).
Area of Science:
- Pediatric Nephrology
- Biochemistry
- Neonatology
Background:
- Plasma carnitine homeostasis is primarily regulated by renal tubular reabsorption.
- Renal function and carnitine metabolism may be compromised in low birth weight (LBW) infants.
- Disturbances in carnitine excretion could indicate underlying renal dysfunction in LBW neonates.
Purpose of the Study:
- To investigate whether altered excretion of l-carnitine (LC) and acetyl-carnitine (ALC) in low birth weight (LBW) children is associated with renal dysfunction.
- To assess the relationship between birth weight, renal function (eGFR), and urinary carnitine levels in LBW infants.
Main Methods:
- A comparative study involving 59 LBW infants and 22 normal birth weight infants.
- Urine samples were collected and analyzed spectrophotometrically for free and esterified carnitine levels.
- Subjects were categorized into three age groups: 0-3 months, 4-12 months, and over 1 year.
Main Results:
- LBW infants exhibited significantly higher urinary excretion of free LC, total LC, and ALC compared to controls across all age groups.
- A significant negative correlation was observed between birth weight and urinary levels of free LC/cr, total LC/cr, and ALC/cr.
- In children over 12 months, a strong negative correlation was found between estimated glomerular filtration rate (eGFR) and urinary free LC/cr, total LC/cr, and ALC/cr.
Conclusions:
- Elevated urinary excretion of LC and ALC in LBW infants suggests potential renal tubular dysfunction.
- The negative correlation between carnitine excretion, birth weight, and eGFR supports the hypothesis of impaired renal handling of carnitines in LBW infants.
- These findings highlight the need for monitoring renal function in LBW infants due to altered carnitine metabolism.
Abstract:
Aim: The plasma homeostasis of both free and esterified carnitines is mostly regulated by renal tubular reabsorption, which may be disturbed in low birth weight children. The aim of study was to check whether disturbances in excretion of l-carnitine (LC) and its main ester, acetyl-carnitine (ALC), may be the result of renal dysfunction in low birth weight children (LBW).Methods: This study included 59 LBW children (2165 g [1490-2440]) and 22 children with normal birth weight as a reference group (3500 g [3275-3650]). Subjects were divided into three groups: 0-3 months, 4-12 months and over 1 year at the time of testing. Urinary levels of carnitine were measured spectrophotometrically.Results: The urine excretion of Free LC, Free LC/cr, Total LC and Total LC/cr. Were significantly higher in 0-3 and 4-12-month old LBW infants study groups when compared to the reference groups. We found statistically significant higher urine excretion of ALC and ALC/cr. in all age groups of LBW infants compared to the reference group. There was a negative correlation between birth weight and free LC/cr. (r= -0.3, p < .05), Total LC/cr. (r= -0.34, p < .05), and ALC/cr. (r= -39, p < .05), and in the children >12-month-old strong negative correlation between eGFR and free LC/cr. (r= -0.6, p < .05), Total LC/cr. (r= -0.61, p < .05), ALC/cr. (r= -0.61, p < .05.)Conclusion: Higher urine excretion of both LC and ALC and its negative correlation with birth weight and eGFR may reflect some degree of renal dysfunction in LBW infants.
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