We investigated a new ELISA for measuring activated factor XII (FXIIa)
in plasma. The intra-assay coefficient of variation was 3.5% and 5.1%
for plasma containing 2.5 and 8.2 ng/ml FXIIa. The inter-assay coeffi
cient of variation was 6.2% and 6.6%. FXIIa correlated with age in wom
en older than 55 years (r=0.55, P=0.0003). Mean levels in the whole po
pulation of 160 healthy individuals included in this study were not di
fferent between men and women, but women younger than 55 years had low
er levels than older women and men of the corresponding age. In a grou
p of 25 healthy centenarians FXIIa was significantly higher (3.2 ng/ml
, 95% CI 2.3-3.6) than in controls (2.1 ng/ml, 95% CI 1.8-2.4). Increa
sed levels were also found in pregnancy, with higher levels in the thi
rd trimester (4.7 ng/ml, 95% CI 3.9-5.5) than in the first trimester (
2.9 ng/ml, 95% CI 2.2-3.9). FXIIa was unmeasurable in patients with FX
II deficiency, but normal in patients with FXI deficiency and C1-inhib
itor deficiency. FXIIa was significantly higher than in normal control
s in patients with severe sepsis (3.9 ng/ml, 95% CI 2.8-5.4) and septi
c shock (5.4 ng/ml, 95% CI 3.7-7.7). After treatment with thrombolytic
agents, a marked increase of FXIIa was found in patients with myocard
ial infarction. In conclusion, the immunoassay of FXIIa permits to stu
dy more directly the contact phase of blood coagulation in situations
in which the involvement of this system may play a pathophysiological
role.