PMID- 19775428 OWN - NLM STAT- MEDLINE DCOM- 20091202 LR - 20240117 IS - 1532-429X (Electronic) IS - 1097-6647 (Print) IS - 1097-6647 (Linking) VI - 11 IP - 1 DP - 2009 Sep 23 TI - Infarct evolution in man studied in patients with first-time coronary occlusion in comparison to different species - implications for assessment of myocardial salvage. PG - 38 LID - 10.1186/1532-429X-11-38 [doi] AB - BACKGROUND: The time course of infarct evolution, i.e. how fast myocardial infarction (MI) develops during coronary artery occlusion, is well known for several species, whereas no direct evidence exists on the evolution of MI size normalized to myocardium at risk (MaR) in man. Despite the lack of direct evidence, current literature often refers to the "golden hour" as the time during which myocardial salvage can be accomplished by reperfusion therapy. Therefore, the aim of the present study was to investigate how duration of myocardial ischemia affects infarct evolution in man in relation to previous animal data. Consecutive patients with clinical signs of acute myocardial ischemia were screened and considered for enrollment. Particular care was taken to assure uniformity of the patients enrolled with regard to old MI, success of revascularization, collateral flow, release of biochemical markers prior to intervention etc. Sixteen patients were ultimately included in the study. Myocardium at risk was assessed acutely by acute myocardial perfusion single photon emission computed tomography (MPS) and by T2 imaging (T2-STIR) cardiovascular magnetic resonance (CMR) after one week in 10 of the 16 patients. Infarct size was measured by late gadolinium enhancement (LGE) at one week. RESULTS: The time to reach 50% MI of the MaR (T50) was significantly shorter in pigs (37 min), rats (41 min) and dogs (181 min) compared to humans (288 min). There was no significant difference in T50 when using MPS compared to T2-STIR (p = 0.53) for assessment of MaR (288 +/- 23 min vs 310 +/- 22 min, T50 +/- standard error). The transmural extent of MI increased progressively as the duration of ischemia increased (R2 = 0.56, p < 0.001). CONCLUSION: This is the first study to provide direct evidence of the time course of acute myocardial infarct evolution in relation to MaR in man with first-time MI. Infarct evolution in man is significantly slower than in pigs, rats and dogs. Furthermore, infarct evolution assessments in man are similar when using MPS acutely and T2-STIR one week later for determination of MaR, which significantly facilitates future clinical trials of cardioprotective therapies in acute coronary syndrome by the use of CMR. FAU - Hedstrom, Erik AU - Hedstrom E AD - Department of Clinical Physiology, Lund University Hospital, SE-221 85 Lund, Sweden. erik.hedstrom@med.lu.se FAU - Engblom, Henrik AU - Engblom H FAU - Frogner, Fredrik AU - Frogner F FAU - Astrom-Olsson, Karin AU - Astrom-Olsson K FAU - Ohlin, Hans AU - Ohlin H FAU - Jovinge, Stefan AU - Jovinge S FAU - Arheden, Hakan AU - Arheden H LA - eng PT - Comparative Study PT - Journal Article DEP - 20090923 PL - England TA - J Cardiovasc Magn Reson JT - Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance JID - 9815616 SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Animals MH - Coronary Occlusion/*complications/diagnosis/therapy MH - Disease Models, Animal MH - Disease Progression MH - Dogs MH - Female MH - Humans MH - Magnetic Resonance Imaging MH - Male MH - Middle Aged MH - Myocardial Infarction/diagnosis/*etiology/therapy MH - Myocardial Perfusion Imaging/methods MH - Myocardial Reperfusion MH - Myocardial Revascularization MH - Myocardium/*pathology MH - Rats MH - Species Specificity MH - Swine MH - Time Factors MH - Tomography, Emission-Computed, Single-Photon PMC - PMC2758877 EDAT- 2009/09/25 06:00 MHDA- 2009/12/16 06:00 PMCR- 2009/09/23 CRDT- 2009/09/25 06:00 PHST- 2009/05/13 00:00 [received] PHST- 2009/09/23 00:00 [accepted] PHST- 2009/09/25 06:00 [entrez] PHST- 2009/09/25 06:00 [pubmed] PHST- 2009/12/16 06:00 [medline] PHST- 2009/09/23 00:00 [pmc-release] AID - S1097-6647(23)00519-7 [pii] AID - 1532-429X-11-38 [pii] AID - 10.1186/1532-429X-11-38 [doi] PST - epublish SO - J Cardiovasc Magn Reson. 2009 Sep 23;11(1):38. doi: 10.1186/1532-429X-11-38.