INTERLEUKIN-8 (IL-) AS AN EARLY PREDICTOR OF AM1 AND STUDY THE EFFECT OF THROMBOLYTIC THERAPY ON ITS LEVEL
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IL-8 is a cytokine and a potent chemoattractant for neutrophils. Infiltration of the myocardium by neutrophils is observed in patients with coronary artery disease. IL-8 regulate and activate neutrophils in acute inflammation. Also, IL-8 has a regulatory role in ischemic and reperfused myocardium. To evaluate the usefulness of IL-8 for early detection ofA.M.I and to detect the effect of thrombolytic therapy on the level of IL-8. We measure serum CK-MB, total leukocytic count and serum IL-8 levels in group I (14 patients with AMI who have received streptokinase), group II (13 patients with AMI who have not received thrombolytic therapy) at 0, 3, 12 and 24 hours after admission and group III (15 halthy control subjects, serum IL-8 concentration measured by enzyme linked immunosorbent assay (ELISA) maximal level of IL-8 in the 27 patients with AM! (349 21-. 291 pg/ml) significantly (P < 0.01) exceeded those in the control group (4.4 1. 2.2 pg/ml). Peak of serum level of IL-8 reached earlier. Than total leukocytic count and serum level of CK-MB in all patients with AM! (27) (5.5, 16.5, 15 hrs respectively). IL-8 is an early markers ofAMI. There was highly significant differences between group! (patients with A.MI who have received thrombolytic therapy) and group!! (patients with AMI who have not received thrombolytic therapy) as regard maximal serum level of CK-MB and total leukocytic count (119.01- 11.2 I.U/L VS 93.0 ± 17.5) (P < 0.01) and 14.1 ±2.3x 103/mm3 VS 12-2.3 (Pc 0.05) respectively However there was no significant difference between group (I) therapy and group p as regard maximal level o f IL-8 (380 1- 308 VS 318 1 275 pg/ml, P > 0.05 respectively, but there was significant difference between group land H as regard time of maximal rise of IL-8 (4.5 ± 1.2 VS 6.5 ± 3.2 hrs) (P < 0.05) respectively. Conclusion IL-8 may be an early diagnostic tool for detection AM; also thrombolytic therapy cause earlier and higher peaking and repaid decrease of serum IL-8 in patients with AM!