TY - JOUR
T1 - Usefulness of Adiponectin to Predict Myocardial Salvage Following Successful Reperfusion in Patients With Acute Myocardial Infarction
AU - Shibata, Rei
AU - Numaguchi, Yasushi
AU - Matsushita, Kunihiro
AU - Sone, Takahito
AU - Kubota, Ryuji
AU - Ohashi, Taiki
AU - Ishii, Masakazu
AU - Kihara, Shinji
AU - Walsh, Kenneth
AU - Ouchi, Noriyuki
AU - Murohara, Toyoaki
N1 - Funding Information:
Dr. Shibata received grants from the Japanese Ministry of Education, the Nakashima Foundation, and the Aichi D.R.G. Foundation, Japan. Dr. Ouchi was supported by an American Heart Association Scientist Development Grant, Northeast Affiliate, Framingham, Massachusetts. Dr. Kihara was supported by a Grant-in-Aid for Scientific Research on Priority Areas, Japan.
PY - 2008/6/15
Y1 - 2008/6/15
N2 - Adiponectin is an adipose-derived plasma protein that demonstrates beneficial actions on myocardial injury under ischemic conditions. Circulating endothelial progenitor cells are reported to associate with rescue of cardiac damage after acute myocardial infarction (AMI). We examined whether circulating adiponectin level affects myocardial function and injury in patients with AMI. A total of 48 patients who underwent successful reperfusion treatment after AMI were enrolled. Cardiac function and perfusion defect were assessed by scintigraphic images of iodine-123 β-methyl iodophenyl pentadecanoic acid in the acute phase and technetium-99m tetrofosmin in the long-term phase. Plasma adiponectin levels were measured by enzyme-linked immunosorbent assay at day 7 after AMI. Plasma adiponectin levels associated positively with myocardial salvage index representing the proportion of initial perfusion defect rescued by reperfusion and recovery of ejection fraction in the long-term phase and negatively with final infarct size. A positive correlation was also observed between adiponectin levels and number of circulating CD34+ cells as determined by flow cytometry and between myocardial salvage index and recovery of ejection fraction independently associated with circulating CD34+ cell levels. In conclusion, plasma adiponectin levels predict improvement of cardiac damage and function after reperfusion therapy in patients with AMI, suggesting that adiponectin could serve as a biomarker for assessment of myocardial injury after AMI.
AB - Adiponectin is an adipose-derived plasma protein that demonstrates beneficial actions on myocardial injury under ischemic conditions. Circulating endothelial progenitor cells are reported to associate with rescue of cardiac damage after acute myocardial infarction (AMI). We examined whether circulating adiponectin level affects myocardial function and injury in patients with AMI. A total of 48 patients who underwent successful reperfusion treatment after AMI were enrolled. Cardiac function and perfusion defect were assessed by scintigraphic images of iodine-123 β-methyl iodophenyl pentadecanoic acid in the acute phase and technetium-99m tetrofosmin in the long-term phase. Plasma adiponectin levels were measured by enzyme-linked immunosorbent assay at day 7 after AMI. Plasma adiponectin levels associated positively with myocardial salvage index representing the proportion of initial perfusion defect rescued by reperfusion and recovery of ejection fraction in the long-term phase and negatively with final infarct size. A positive correlation was also observed between adiponectin levels and number of circulating CD34+ cells as determined by flow cytometry and between myocardial salvage index and recovery of ejection fraction independently associated with circulating CD34+ cell levels. In conclusion, plasma adiponectin levels predict improvement of cardiac damage and function after reperfusion therapy in patients with AMI, suggesting that adiponectin could serve as a biomarker for assessment of myocardial injury after AMI.
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U2 - 10.1016/j.amjcard.2008.02.057
DO - 10.1016/j.amjcard.2008.02.057
M3 - Article
C2 - 18549845
AN - SCOPUS:44749092057
SN - 0002-9149
VL - 101
SP - 1712
EP - 1715
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 12
ER -