Frequency of low carnitine levels in children on dialysis

Alejandra Aguilar-Kitsu1, Pilar Ibarra-Cazares, Leticia Mendoza-Guevara

  • 1Hospital de Pediatria, Centro Médico Nacional Siglo XXI, IMSS, México.

Insights

Low serum carnitine is common in pediatric patients undergoing dialysis. This study found high frequencies of low carnitine levels in children on peritoneal dialysis (PD) and hemodialysis (HD).

Area of Science:

  • Pediatric Nephrology
  • Nutritional Biochemistry
  • Renal Replacement Therapy

Background:

  • Carnitine is essential for fatty acid metabolism.
  • Dialysis patients may have altered carnitine levels due to nutritional status and dialysis losses.
  • Understanding carnitine status in pediatric dialysis patients is crucial for metabolic health.

Purpose of the Study:

  • To determine the prevalence of low serum carnitine levels in pediatric patients undergoing peritoneal dialysis (PD) and hemodialysis (HD).
  • To investigate potential correlations between carnitine levels, dialysis modality, and dietary intake.

Main Methods:

  • Prospective cross-sectional study of 100 pediatric patients (<17 years) on PD or HD for >3 months.
  • Exclusion of patients with primary carnitine deficiency.
  • Measurement of serum total, free, and acylcarnitine; assessment of carnitine intake via a 4-day food diary.

Main Results:

  • 75% of patients exhibited lower-than-normal serum carnitine levels; 29% met criteria for deficiency.
  • No significant difference in carnitine levels was observed between PD and HD groups.
  • No correlation found between free carnitine levels and duration of dialysis or estimated carnitine intake.

Conclusions:

  • A high frequency of low serum carnitine levels exists in pediatric patients on chronic dialysis.
  • Dialysis modality (PD vs. HD) did not influence carnitine status in this cohort.
  • Further investigation into carnitine supplementation strategies for pediatric dialysis patients is warranted.

Related Concept Videos

Chronic Kidney Disease III: Interprofessional Care01:28

Chronic Kidney Disease III: Interprofessional Care

Chronic kidney disease (CKD) requires collaborative and comprehensive management. CKD progresses through stages and can lead to end-stage kidney disease (ESKD) if untreated. Interprofessional collaboration and patient education are crucial, enabling patients to manage their health and improve their quality of life.Diagnostic approach for chronic kidney diseaseThe diagnosis of CKD primarily focuses on the glomerular filtration rate (GFR), which assesses kidney function by measuring how well...
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses a challenge in...
Chronic Kidney Disease II: Clinical Manifestations01:24

Chronic Kidney Disease II: Clinical Manifestations

Chronic Kidney Disease (CKD) progressively impairs multiple body systems due to the accumulation of uremic toxins, which disrupt cellular functions across various organs.Neurologic symptomsNeurologic symptoms often arise early in CKD, as uremic toxin buildup drives changes in cognitive and motor functions. Patients frequently experience fatigue, headache, confusion, difficulty concentrating, and, in severe cases, seizures. Peripheral neuropathy commonly manifests as burning sensations in the...
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test01:22

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test

In clinical practice, the direct measurement of hepatic blood flow to evaluate liver function presents significant challenges due to the intricate and specialized nature of the necessary techniques. Consequently, healthcare professionals often rely on empirical estimates derived from thorough patient examinations and liver function tests to gauge liver health. Among the tools at their disposal, the Child–Pugh and MELD scoring systems stand out for their ability to categorize and assess the...
Serum Studies: Renal Function Tests01:24

Serum Studies: Renal Function Tests

Renal function tests are crucial for assessing kidney health, monitoring disease progression, and evaluating the kidneys' efficiency in waste elimination, fluid balance, and electrolyte regulation. These tests offer critical insights into kidney function, even though routine measurements may appear normal until there is a significant decline in the glomerular filtration rate or GFR. Typically, signs of kidney impairment only become evident when the GFR falls to about 50% of its normal level.
Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...