Literature DB >> 24178641

Diet treatment of branched chain ketoaciduria studied by proton magnetic resonance spectroscopy.

G Pontoni1, F Rotondo, T M Vacchiano, L Pinto, V Perrotta, D D Pietra, M Cartenì-Farina, V Zappia.   

Abstract

A novel nuclear magnetic resonance method is proposed for the diagnosis and follow-up of patients affected by branched chain ketoaciduria. The method allows quantitation of the branched chain amino acids (BCAA's) such as leucine, isoleucine and valine and of related keto- and hydroxy acids by means of a single spectrum. The method implies short time of analysis, as opposed to the very long time required by the techniques currently in use (amino acid analyzer combined with gaschromatography/mass spectrometry of keto- and hydroxyacids), it is easy and suitable for adjustements of the dietary treatment even on a daily basis. The case of a 15 days old newborn child, presenting muscular hypertonicity was unambiguously diagnosed in few minutes by means of one single NMR spectrum of urine. More interestingly, NMR spectra of serum in the following days were suitable for quantitating amino-, and keto acids as well as other metabolites of relevance in the follow up of the dietary treatment of the disease. After a diet lacking of BCAA's, to eliminate keto acids, a low BCAA diet was introduced, that succeeded in keeping the serum levels of the three amino acids within the normal range, while dropping the related keto acids.

Entities:  

Year:  1996        PMID: 24178641     DOI: 10.1007/BF00805724

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  9 in total

Review 1.  A critical assessment of methods of measuring metabolite concentrations by NMR spectroscopy.

Authors:  P S Tofts; S Wray
Journal:  NMR Biomed       Date:  1988-02       Impact factor: 4.044

Review 2.  Nuclear magnetic resonance spectroscopy in the study of inborn errors of metabolism.

Authors:  R A Iles; R A Chalmers
Journal:  Clin Sci (Lond)       Date:  1988-01       Impact factor: 6.124

3.  Early diagnosis and dietetic management in newborn with maple syrup urine disease. Birth to six weeks.

Authors:  E R Naughten; I P Saul; G Roche; C Mullins
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

4.  High-resolution 1H-NMR spectroscopy of blood plasma for metabolic studies.

Authors:  R A Wevers; U Engelke; A Heerschap
Journal:  Clin Chem       Date:  1994-07       Impact factor: 8.327

5.  Newborn screening for maple syrup urine disease.

Authors:  S E Snyderman; C Sansaricq
Journal:  J Pediatr       Date:  1985-08       Impact factor: 4.406

6.  Organic acids and branched-chain amino acids in body fluids before and after multiple exchange transfusions in maple syrup urine disease.

Authors:  Y Shigematsu; K Kikuchi; T Momoi; M Sudo; Y Kikawa; K Nosaka; M Kuriyama; S Haruki; K Sanada; N Hamano
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

7.  Possibilities of selective screening for inborn errors of metabolism using high-resolution 1H-FT-NMR spectrometry.

Authors:  W Lehnert; D Hunkler
Journal:  Eur J Pediatr       Date:  1986-09       Impact factor: 3.183

8.  Alpha-keto and alpha-hydroxy branched-chain acid interrelationships in normal humans.

Authors:  L J Hoffer; A Taveroff; L Robitaille; O A Mamer; M L Reimer
Journal:  J Nutr       Date:  1993-09       Impact factor: 4.798

9.  Practical methods to estimate whole body leucine oxidation in maple syrup urine disease.

Authors:  L J Elsas; N P Ellerine; P D Klein
Journal:  Pediatr Res       Date:  1993-05       Impact factor: 3.756

  9 in total

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