[Diagnosis of "fish odor syndrome" by urine nuclear magnetic resonance proton spectrometry]

Ann Dermatol Venereol. 1998 Mar;125(3):210-2.
[Article in French]

Abstract

Background: Trimethylaminuia is an unusual observation, often termed fish odor syndrome. The condition results from reduced ability to oxidize trimethylamine (TMA), which has a fishy odor, into odorless trimethylamine N-oxide (TMAO).

Method: Proton nuclear magnetic resonance spectroscopy (MRS) was used as a simple and rapid method to detect TMA and TMAO in the same urine sample without pretreatment. Subjects were considered to have deficient N-oxidation of TMA if the TMAO/TMA ratio was greater than 80 p. 100 (heterozygous) or 65 p. 100 (homozygous).

Discussion: Direct proton RRS analysis of urine is well suited for diagnosis of fish odor syndrome. It can be used to detect heterozygous patients and also provides an easily implemented follow-up tool.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Genetic Carrier Screening / methods
  • Genetic Diseases, Inborn / genetics
  • Genetic Diseases, Inborn / prevention & control
  • Genetic Diseases, Inborn / urine*
  • Humans
  • Magnetic Resonance Spectroscopy / methods*
  • Methylamines / urine*
  • Oxidants / urine*
  • Reproducibility of Results
  • Syndrome

Substances

  • Methylamines
  • Oxidants
  • trimethyloxamine
  • trimethylamine