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. 2014 Jul 14;14:33. doi: 10.1186/1472-6890-14-33

Table 2.

DHEA sulfate immunoassay cross-reactivity

Compound Plasma/serum concentrations Cross-reactivity in Roche assay Likelihood of clinically significant cross-reactivity
DHEA sulfate
• Up to 6,070 ng/mL (infants) [31]
100%
High (assay target)
• 5 – 4,070 ng/mL (females > 1 year old) [31]
• 5–4,920 ng/mL (males > 1 year old) [31]
Pregnenolone sulfate
• 21 – 84 ng/mL (adult controls) [32]
2.1%
Low, possible minor effect around time of parturition.
• Up to 1,580 ng/mL in pregnancy [33]
17-Hydroxyprogesterone
• 0.1 – 2.0 ng/mL (pediatric controls) [22]
0.08%
Low, possible minor effect in 21-hydroxylase deficiency.
• Up to 1,005 ng/mL (21-hydroxylase deficiency) [22]
17-Hydroxypregnenolone
• Up to 4.3 ng/ml in healthy females [34,35]
0.05%
Low
• Up to 4.8 ng/mL in healthy males [34,35]
  • Up to 100 ng/mL in premature infants [36]