“…21 Its release kinetics are different from those of TnT. In patients with acute myocardial infarction, serum levels of H-FABP return to normal by 24 h after the onset of myocardial infarction, 22 which suggests that H-FABP is rapidly cleared from circulation following leakage from the cytosol.…”
Section: Differences In Tnt and H-fabp Myocardial Damage Markersmentioning
“…21 Its release kinetics are different from those of TnT. In patients with acute myocardial infarction, serum levels of H-FABP return to normal by 24 h after the onset of myocardial infarction, 22 which suggests that H-FABP is rapidly cleared from circulation following leakage from the cytosol.…”
Section: Differences In Tnt and H-fabp Myocardial Damage Markersmentioning
“…H-FABP was initially reported to be rapidly released from injured myocardium (50 ). Because of the recent redefinition of MI (51 ), biochemical markers have become even more important for assessment of suspected cardiac ischemia patients with non-ST-segment elevation.…”
Section: Clinical Interpretation Of Plasma H-fabp Concentrationsmentioning
Background: A biomarker that reliably detects myocardial ischemia in the absence of necrosis would be useful for initial identification of unstable angina patients and for differentiating patients with chest pain of an etiology other than coronary ischemia, and could provide clinical utility complementary to that of cardiac troponins, the established markers of necrosis.
“…It is a powerful regulator of the mitochondrial beta-oxidative system in the heart 9 . It was first noted to be a marker of myocardial infarction (MI) in 1988 [10][11] , it is rapidly released from the cytosol into the circulation after myocardial ischemia and necrosis 12 . H-FABP was shown to be associated with chronic heart failure patients 13 .…”
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