Table 1. Biomarkers indicating systemic severe MC activation in patients.
Biomarker | Specificity for MCs | Sensitivity in anaphylaxis | Commonly used in daily practice |
---|---|---|---|
Tryptase | ++* | +** | ++ |
Plasma histamine | +/– | + | |
Urinary histamine metabolites*** | +/– | ++ | ++ |
PGD2 metabolites**** | +/– | ++ | + |
Urinary cysLT levels | –/+ | ++ | +/– |
Heparin | +++ | –/+***** | – |
DAO | –****** | ++ | – |
Basophils express very low amounts of tryptase, but MCs are a primary and major source of the enzyme.
The relatively low sensitivity of tryptase qualifies as a biomarker of massive MC activation and thus as a criterion of MCAS.
Relevant 24-h urinary histamine metabolites include N-methylhistamine and N-methylimidazoleacetic acid.
Among PGD2 metabolites, the most commonly measured substance is urinary 11β-prostaglandinF2α.
An increase in heparin is usually not measurable during an anaphylactic episode, unless the burden of MCs is very high (like in MC leukemia).
So far it is not known whether the increased DAO levels measured in patients during anaphylaxis are derived from MCs or (also) other cell types.
cysLT, cysteinyl leukotriene; DAO, diamino-oxidase; MCAS, mast cell activation syndrome; PGD2, prostaglandin D2; MC, mast cell.