Use of a novel high-sensitivity troponin T, I and MPO, NT-proBNP assays
Use of a novel high-sensitivity troponin T, I and MPO, NT-proBNP assays
to detect myocardial injury in patients
to detect myocardial injury in patients
with atrial fibrillation treated by direct-current cardioversion
with atrial fibrillation treated by direct-current cardioversion
C. Le Goff
C. Le Goff
11, C.Garweg
, C.Garweg
22, J-F. Kaux
, J-F. Kaux
33, P.Melon
, P.Melon
22, P. Lancellotti
, P. Lancellotti
22, L. Pierard
, L. Pierard
22, J-P.Chapelle
, J-P.Chapelle
111 Department of Clinical Chemistry of the University of Liege, Liège, Belgium 2 Department of Cardiology, CHU Sart-Tilman, Liège, Belgium
3 Department of Motricity Sciences of the University of Liege and CHU Sart-Tilman, Liège, Belgium
Introduction:
Novel high-sensitive cardiac troponin T (hsTnT) and I (TnI II) assays have the potential to detect myocardial injury with a higher sensitivity. The aim of the study was to assess the level of hsTnT and TnI II in patients with atrial fibrillation (AF) as compared to control and following direct current cardioversion. Levels of NT-proBNP, myeloperoxydase (MPO) and hs-CRP were concomitantly measured.
Methods:
HsTnT, NT-proBNP, hs-CRP and TnI II determinations were realized on heparin plasma of 27 patients with AF successfully treated by cardioversion and 64 control subjects.
MPO quantification was performed on the EDTA plasma samples. All assays were performed before (T0) and 4 hours (T+4h) after cardioversion.
Results:
The levels of hsTnT (Fig.1) and TnI II (Fig.2) were increased in patients with AF compared to controls (p<0.005). Between T0 and T+4h, we observed an increased of TnI II (p=0.36) (Fig. 5) but not for hsTnT (p=0.5) (Fig. 6). Cardioversion was not associated with any statistically change in hsTnT and TnII levels. AF patients also had higher proBNP level (Fig. 3) than controls (p<0.001) and increased level of hs-CRP (p=0.08) (Fig. 4). NT-proBNP levels decreased between T0 and T+4h (Fig.7). For hsCRP, no change was observed between T0 and T+4h (Fig.8). MPO levels were not increased between T0 and T+4h (Fig. 9).
Fig. 1 : hs TnT (µg/L) - Comparison controls with AF patients
Fig. 2 : TnI (µg/L) - Comparison controls with AF patients
Fig.9 : MPO (ng/.mL) - Comparison between T0 and T+4h in AF patients Fig. 4 : hs CRP (mg/L) - Comparison
controls with AF patients
Fig. 3: NT-proBNP (ng/L) - Comparison controls with AF patients
Fig. 6 : hs TnT (µg/L) - Comparison between T0 and T+4h in AF patients Fig. 5 : TnI (µg/L) - Comparison
between T0 and T+4h in AF patients
Fig. 7 : NT-proBNP (ng/L) - Comparison between T0 and T+4h in AF patients
Fig.8 : hsCRP (ng/.mL) - Comparison between T0 and T+4h in AF patients
Conclusions:
Our results showed that patients with persistent AF had increased plasmatic concentration of hsTnT and TnI II reflecting the presence of myocardial damage that was not further modified by cardioversion. In our population, AF was associated with increased level of NT-proBNP and sign of inflammation as reflected by elevated hs-CRP plasmatic concentration. MPO assays cannot be used in this case.
160 140 120 100 80 60 40 20 MPO_T0 MPO_T1 0,07 0,06 0,05 0,04 0,03 0,02 0,01 0,00 hsTnT_T0 hsTnT_T1 5000 4000 3000 2000 1000 0 NT_proBNP_ctrl NT_proBNP_cardio 0,09 0,08 0,07 0,06 0,05 0,04 0,03 0,02 0,01 0,00 TnI_ctrl TnI_cardio 0,14 0,12 0,10 0,08 0,06 0,04 0,02 0,00 TnI_T0 TnI_T1 160 140 120 100 80 60 40 20 0 hsCRP_T0 hsCRP_T1 5000 4000 3000 2000 1000 0 NT_proBNP_T0 NT_proBNP_T1 160 140 120 100 80 60 40 20 0 hsCRP_ctrl hsCRP_cardio 0,06 0,05 0,04 0,03 0,02 0,01 0,00 hsTnT_ctrl hsTnT_cardio