DEHYDROEPIANDROSTERONE SULFATE QUANTIFICATION IN SERUM USING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY MASS-SPECTROMETRY AND A DEUTERATED INTERNAL STANDARD - A TECHNIQUE SUITABLE FOR ROUTINE USE OR AS A REFERENCE METHOD

A thermospray high-performance liquid chromatography/mass spectrometry method for determination of serum dehydroepiandrosterone sulfate is described. The steroid was measured intact using [7,7-H-2(2)]dehydroepiandrosterone sulfate as internal standard. The analysis was carried out in the negative ion mode by determining the peak height ratio of the molecular anions of the analyte and internal standard. The method was used to determine the steroid in serum from 15 male and female normal adults and the following values were obtained: males, 272 +/- 45-mu-g/dl (range, 197 to 331-mu-g/dl) and females, 215 +/- 67-mu-g/dl (range, 107 to 347-mu-g/dl). In addition, dehydroepiandrosterone sulfate was measured by high-performance liquid chromatography/mass spectrometry and radioimmunoassay (a commercial kit) on 25 individuals of all age groups. There was strong correlation between the values obtained, but the radioimmunoassay values were generally double those obtained by high-performance liquid chromatography/mass spectrometry. Three other steroid sulfates, androsterone sulfate, epiandrosterone sulfate, and androst-5-ene-3-beta, 17-beta-diol sulfate, were also assayed. In males, these had mean values of 112, 44, and 13-mu-g/dl and, in females, they had mean values of 84, 25, and 6-mu-g/dl, respectively. Radioimmunoassay cross-reactivity measurement for these steroids (as reference compounds) showed that they were unlikely to contribute greatly to the discrepancy between radioimmunoassay and high-performance liquid chromatography/mass spectrometry values.