Literature DB >> 14757390

Serum carnitine concentrations correlated to clinical outcome parameters in chronic hemodialysis patients.

A L Steiber1, L J Weatherspoon, L Spry, A T Davis.   

Abstract

Carnitine metabolism and the therapeutic use of carnitine has been a major area of interest in dialysis patients. The purpose of this study was to determine whether any correlations exist between carnitine status and selected clinical parameters in hemodialysis (HD) patients. This study was an observational study of data from patients receiving HD at a Midwest dialysis center. The subjects (n=49) were 60+/-16 (mean+/-SD) years of age and 48% male. Fifteen percent of the subjects had type 1 diabetes mellitus (DM), 29% had type 2 DM, and 25% had left ventricular hypertrophy (LVH). The serum-free and total carnitine, and acylcarnitine concentrations were: 40.3+11.8 microm/l, 22.8+/-7.3, and 17.5+/-5.9 microm/l, respectively. The serum acylcarnitine to free carnitine ratio (A/F) was 0.80+/-0.27. Blood urea nitrogen (BUN), parathyroid hormone and ejection fraction were positively correlated and age and left atrial dilation (cm) were negatively correlated with serum total carnitine (P<0.05). BUN and hematocrit were positively correlated (P<0.05) and age was negatively correlated with free carnitine. Subjects who used mannitol or were male had significantly higher concentrations of both free and total carnitine, respectively (P<0.05). Subjects using aspirin had lower concentrations of serum total carnitine (P<0.10). These results suggest certain subgroups of patients may need to be targeted for further studies with carnitine replacement therapy, i.e. long-term patients, older patients, patients with left verticular hypertrophy and left atrial enlargement, females and patients on aspirin therapy.

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Year:  2004        PMID: 14757390     DOI: 10.1016/s0261-5614(03)00085-2

Source DB:  PubMed          Journal:  Clin Nutr        ISSN: 0261-5614            Impact factor:   7.324


  5 in total

1.  A randomised, controlled clinical trial evaluating changes in therapeutic efficacy and oxidative parameters after treatment with propionyl L-carnitine in patients with peripheral arterial disease requiring haemodialysis.

Authors:  Salvatore Santo Signorelli; Pasquale Fatuzzo; Francesco Rapisarda; Sergio Neri; Margherita Ferrante; Gea Oliveri Conti; Roberto Fallico; Luigi Di Pino; Giuseppe Pennisi; Gabriella Celotta; Anzaldi Massimiliano
Journal:  Drugs Aging       Date:  2006       Impact factor: 3.923

2.  Metabolic profiling of PPARalpha-/- mice reveals defects in carnitine and amino acid homeostasis that are partially reversed by oral carnitine supplementation.

Authors:  Liza Makowski; Robert C Noland; Timothy R Koves; Weibing Xing; Olga R Ilkayeva; Michael J Muehlbauer; Robert D Stevens; Deborah M Muoio
Journal:  FASEB J       Date:  2008-10-22       Impact factor: 5.191

Review 3.  Mass Spectrometric Analysis of L-carnitine and its Esters: Potential Biomarkers of Disturbances in Carnitine Homeostasis.

Authors:  Judit Bene; Andras Szabo; Katalin Komlósi; Bela Melegh
Journal:  Curr Mol Med       Date:  2020       Impact factor: 2.222

Review 4.  Significance of Levocarnitine Treatment in Dialysis Patients.

Authors:  Hiroyuki Takashima; Takashi Maruyama; Masanori Abe
Journal:  Nutrients       Date:  2021-04-07       Impact factor: 5.717

5.  Neuroprotective effects of L-carnitine against oxygen-glucose deprivation in rat primary cortical neurons.

Authors:  Yu Jin Kim; Soo Yoon Kim; Dong Kyung Sung; Yun Sil Chang; Won Soon Park
Journal:  Korean J Pediatr       Date:  2012-07-17
  5 in total

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