Journals / Gazi Medical Journal / 2006 / Cilt: 17 - Sayı: 3

Valproik asit kullanan idiyopatik epilepsili çocuklarda açil karnitin profillerinin değerlendirilmesi

Analysis of acylcarnitine profiles in children with idiopathic epilepsy using valproic acid

Pages
157–159
Publication Date
2022-10-19
DOI
—
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

A statistical comparison of these acylcarnitines between subjects and controls showed a statistically significant effect (p

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Purpose: To evaluate whether valproic acid (VPA) treatment in children with epilepsy affects the plasma fatty acylcarnitine esters.
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Key Findings & Data:Materials and Methods: Fifty children (mean age, 10±3.9) with epilepsy receiving VPA treatment for at least one year were evaluated along with 110 children of similar age as a control group.
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Conclusion & Impact:A statistical comparison of these acylcarnitines between subjects and controls showed a statistically significant effect (p
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Purpose: To evaluate whether valproic acid (VPA) treatment in children with epilepsy affects the plasma fatty acylcarnitine esters. Materials and Methods: Fifty children (mean age, 10±3.9) with epilepsy receiving VPA treatment for at least one year were evaluated along with 110 children of similar age as a control group. Levels of free carnitine and acylcarnitine profiles were studied with tandem mass spectrometry (Tan-dem-MS). Results: Free camitine levels were within the normal limits. Valproic acid was found to affect the levels of the following individual acylcarnitines (medians): C4-acylcarnitine (0.56 umol/L; controls 0.39 umol/L), 3-hyd-roxy-isovalerylcamitine (C5-OH) (0.23 umol/L; controls 0.14 umol/L), C14-acylcarnitine (0.11 umol/L; controls 0.16 umol/L), C16-acylcarnitine (0.76 umol/L; controls 2.5 umol/L), C16-OH-acylcarnitine (0.04 umol/L; controls 0.07umol/L), and Cl8:1-acylcarnitine (0.8 umol/L; controls 0.97 umol/L). A statistical comparison of these acylcarnitines between subjects and controls showed a statistically significant effect (p

Özet

Amaç: Valproik asit (VPA) tedavisi alan epilepsili çocuklarda plazma açil-karnitin düzeylerinin etkilenip etkilenmeyeceğini araştırmak amaçlı yapıl­mıştır. Materyals ve Metods: En az bir yıldır VPA tedavisi alan 50 epilepsili çocuk (ortalama yaş, 10±3.9) ve benzer yaştaki 110 çocuk control grubu olarak incelenmiştir. Serbest karnitin ve açilkarnitin düzeyleri Tandem Mass Spe­ctrometry (Tandem-MS) yöntemi kullanılarak ölçülmüştür. Sonuçlar: Serbest karnitin düzeyleri normal olarak saptanmıştır. Valproik asitin aşağıda belirtilen açilkarnitin düzeylerini kontrol grubu ile karşılaş­tırıldığında istatistiksel olarak anlamlı bir şekilde etkilediği (p

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Cite This Article

SERDAROĞLU, A., HASANOĞLU, A., TÜMER, L., HİRFANOĞLU, T., BİRBEROĞLU, G., CANSU, A., GÜCÜYENER, K. (2022). Valproik asit kullanan idiyopatik epilepsili çocuklarda açil karnitin profillerinin değerlendirilmesi. Gazi Medical Journal, Cilt: 17 - Sayı: 3, 157–159. https://ajindex.com/articles/520433

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References (16)

  1. Chung S, Choi J, Hyun T. Alterations in the carnitine metabolism in epileptic children treated with valproic acid. J Korean Med Sci 1997
  2. Segade SR, Pena CA, Tutor JC. Carnitine deficiency associated with anticonvulsant therapy. ClinChimActa 1989
  3. Arrigoni ME, Caso V: Carnitine protects mitochondria and removes toxic acyls from xenobiotics. Drugs Exp Clin Res 2001
  4. Nishida N, Sugimoto T, Araki A. Carnitine metabolism in valproate- treated rats: the effect of L-carnitine supplementation. Ped Res 1987
  5. Camina MF, Rozas I, Gomez JM. Short-term effects of administra­ tion of anticonvulsant drugs on free carnitine and acylcarnitine in mouse serum and tissues. Br J Pharmacol 1991
  6. Beghi E, Bizzi A, Codegoni. Valproate, carnitine metabolism, and bi­ ochemical indicators of liver function. Epilepsia 1990
  7. Riva R, Albani F, Gobbi G. Carnitine disposition before and during valproate therapy in patients with epilepsy. Epilepsia 1993
  8. Laub MC, Brunner IP, Jaeger G. Serum carnitine during valproic acid therapy. Epilepsia 1986
  9. Eyer F, Felgenhauer N, Gempel K. Acute valproate poisoning: phar- macokinetics, alteration in fatty acid metabolism, and changes du­ ring therapy. J Clin Psychopharmacol 2005
  10. Silva MF, Jakobs C, Duran M. Valproate induces in vitro accumula­ tion of long-chain fatty acylcarnitines. Mol Genet Metab 2001
  11. Matsuda I, Ohtani Y, Ninomiya N. Renal handling of carnitine in children with carnitine deficiency and hyperamonemia associated with valproate therapy. J Pediatr 1986
  12. Camina MF, Rozas I, Gago C. Alteration of renal carnitine metabo­ lism by anticonvulsant treatment. Neurol 1991
  13. Silva MFB, Selhorst J, Overmans H. Characterization of plasma acylcarnitines in patients under valproate monotherapy using ESI- MS/MS. Clin Biochem 2001
  14. Chace DH, Hillman SL, Va Hove JLK, Naylor EW. Rapid diagno­ sis of MCAD deficiency: quantative analysis of octanocarnitines in newborn blood spots by tandem mass spectrometry. Clin Chem. 1997
  15. Moreno FA, Macey H, Schreiber B. Carnitine levels in valproic acid- treated psychiatric patients: a cross-sectional study. J Clin Psychiatry 2005
  16. Murakami K, Sugimoto T, Nishida N. Carnitine metabolism and morphometric change of liver mitochondria in valproate-treated rats. Neuropediatrics 1990