The Journal of Nutritional Biochemistry
Volume 18, Issue 12 , Pages 827-831, December 2007

A simple rapid immunoassay for S-adenosylhomocysteine in plasma

  • Antonieta Capdevila

      Affiliations

    • Department of Biochemistry, Vanderbilt University Medical Center, Nashville, TN 37532, USA
  • ,
  • Raymond F. Burk

      Affiliations

    • Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37532, USA
  • ,
  • Joshua Freedman

      Affiliations

    • Department of Psychiatry, UCLA School of Medicine, Los Angeles, CA, USA
  • ,
  • Frank Frantzen

      Affiliations

    • Axis-Shield ASA, P.O. Box 6073, Morkved, N-8031 Bodø, Norway
  • ,
  • Ingrid Alfheim

      Affiliations

    • Bio-Medisink Innovasjon AS, Gaustadallén 21, N-0349, Oslo
  • ,
  • Conrad Wagner

      Affiliations

    • Department of Biochemistry, Vanderbilt University Medical Center, Nashville, TN 37532, USA
    • Department of Veterans Affairs Medical Center, Nashville, TN 37212, USA
    • Corresponding Author InformationCorresponding author. Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232, USA. Tel.: +1 615 343 9866; fax: +1 615 343 0704.

Received 1 August 2006; received in revised form 1 December 2006; accepted 3 January 2007. published online 18 May 2007.

Abstract 

The measurement of plasma S-adenosylhomocysteine is a more sensitive indicator of the risk for vascular disease than is plasma homocysteine. Because the level of S-adenosylhomocysteine is normally in the nanomolar range, it has been difficult to measure and necessitated the development of complex fluorometric and mass-spectrophotometric methods. We have now adapted an existing immunoassay used for the measurement of homocysteine to the measurement of S-adenosylhomocysteine in plasma. This assay is sensitive down to the level of less than 0.1 pmol, and there is no interference by S-adenosylmethionine. The assay is carried out in microplates, allows the measurement of 12 samples per plate and can easily be carried out in a 4-h period. The method is applicable to plasma samples having S-adenosylhomocysteine concentrations ranging from 10 to 150 nM without dilution. The mean value for 16 normal subjects by this method was 18.9±1.4 nM (S.E.M.), compared with 17.8±1.4 nM obtained by a previously described method using two high-performance liquid chromatography columns with fluorescence derivatization. Mean values for seven cirrhotic patients were 46.5±3.3 nM by this new method compared with 44.6±5.3 by the former method. The ease and speed of this method should allow the widespread measurement of this important metabolite in laboratories without access to sophisticated equipment.

Keywords: S-adenosylhomocysteine, Immunoassay, Plasma, Vascular disease, Human

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 This study was supported by the Research Service of the Department of Veterans Affairs, Washington, DC, USA, and grant #DK15298 to C.W. and #ES02497 to R.F.B. from the National Institutes of Health, US Public Health Service, Bethesda, MD, USA.

PII: S0955-2863(07)00046-0

doi:10.1016/j.jnutbio.2007.01.003

The Journal of Nutritional Biochemistry
Volume 18, Issue 12 , Pages 827-831, December 2007