In a prospective study of 61 emergency department patients with suspected ACS, we compared a novel plasma immunoassay for PO4-cTnI to cTnI overall and in a subgroup with symptoms ≤ 4 h duration (n = 31). Admission PO4-cTnI and cTnI assays (thresholds determined by ROC curve) were analyzed in a blinded fashion against the clinical, ECG and coronary angiographic diagnosis of ACS.
Overall, PO4-cTnI sensitivity was significantly higher than cTnI (82%vs. 50%, respectively, P < 0.05) and PO4-cTnI specificity was 81%(n = 61). Addition of PO4-cTnI to cTnI improved sensitivity to 91%vs. 50%for cTnI alone (P < 0.001). In the ≤ 4 h subgroup (n = 31), PO4-cTnI sensitivity was significantly higher than cTnI (79%vs. 26%, respectively, P < 0.01) and PO4-cTnI specificity was 75%. In the same ≤ 4 h subgroup, addition of PO4-cTnI to cTnI improved sensitivity to 84%vs. 26%for cTnI alone (P = 0.001).
The results suggest that PO4-cTnI, alone or in combination with cTnI, warrants further investigation as a sensitive, cardiac-specific diagnostic tool for early ACS.