Serum levels of 25-hydroxyvitamin D are important in establishing true vitamin D levels in humans. The purposes of this study were to develop a sensitive, specific liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for detection of 25-hydroxyvitamin D2 and D3 and establish reference intervals for these analytes. Chromatographic separation of 25(OH)D2 and 25(OH)D3 was achieved after adding deuterated Δ9-tetrahydrocannabinol (Δ9-THC-D 3) and organic extraction. The 3 ions were ionized using positive electrospray ionisation and detected in the multiple-reaction monitoring mode using mass (m)/charge (z) transitions of 318.15 > 196.20 (Δ 9-THC-D3), 401.15 > 365.2 [25(OH)D3], and 413.15 > 355.20 [25(OH)D2]. Reference interval study results were compared with current 25(OH)D recommendations. Elution of 25(OH)D2, 25(OH)D3, and Δ9-THC-D3 was achieved after 3.0 minutes (total run time, 6.0 minutes). Within- and between-run coefficients of variation were less than 11%. Deming regression of radioimmunoassay and LC-MS/MS methods for total 25(OH)D levels yielded a slope of 0.97 (95% confidence interval, 0.88-1.05) and y-intercept of -1.74 ng/mL. Reference intervals were less than recommended levels (D2, 0.0-12.1; D3, 5.5-41.4; total vitamin D, 6.0-43.5 ng/mL [0-30, 14-103, 15-109 nmol/L, respectively]) with no statistically significant differences in race, age, or sex. This LC-MS/MS method provides a rapid, accurate, sensitive, and cost-effective alternative to other methods for detection of 25(OH)D2 and 25(OH)D3 at nanomolar concentrations.
- 25-Hydroxyvitamin D
- Liquid chromatography tandem mass spectrometry
- Reference interval