Relationship of the proinflammatory cytokines to myocardial ischemia and dysfunction after uncomplicated coronary revascularization

The proinflammatory cytokines have been implicated in mediating myocardial dysfunction associated with myocardial infarction, severe congestive heart failure, and sepsis. We tested the hypothesis that cytokine levels are elevated after uncomplicated coronary artery bypass grafting and associated wit...

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Veröffentlicht in:The Journal of thoracic and cardiovascular surgery 1994-10, Vol.108 (4), p.626-635
Hauptverfasser: Hennein, Hani A., Ebba, Hailu, Rodriguez, Jorge L., Merrick, Scot H., Keith, Fraser M., Bronstein, Merrill H., Leung, Jacqueline M., Mangano, Dennis T., Greenfield, Lazar J., Rankin, J.Scott
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container_issue 4
container_start_page 626
container_title The Journal of thoracic and cardiovascular surgery
container_volume 108
creator Hennein, Hani A.
Ebba, Hailu
Rodriguez, Jorge L.
Merrick, Scot H.
Keith, Fraser M.
Bronstein, Merrill H.
Leung, Jacqueline M.
Mangano, Dennis T.
Greenfield, Lazar J.
Rankin, J.Scott
description The proinflammatory cytokines have been implicated in mediating myocardial dysfunction associated with myocardial infarction, severe congestive heart failure, and sepsis. We tested the hypothesis that cytokine levels are elevated after uncomplicated coronary artery bypass grafting and associated with episodes of postoperative myocardial ischemia and dysfunction. Coronary artery bypass grafting was performed under general anesthesia with moderate systemic hypothermia and cold-blood potassium cardioplegic solution. Tumor necrosis factor-α and interleukin-6 levels were determined by bioassays, and interleukin-8 levels were measured by a sandwich enzyme-linked immunosorbent assay. Myocardial function and ischemic episodes were assessed by intraoperative transesophageal echocardiography and perioperative 12-channel Holter monitoring. A total of 22 patients were studied, with no deaths or complications. Arterial tumor necrosis factor-α rose in a bimodal distribution, peaking at 2 and 18 to 24 hours after the operation (at 20.2 ± 6.4 pg/ml, [mean ± standard error of the mean]) and 5.8 ± 1.6 pg/ml, respectively; before cardiopulmonary bypass: 0.90 ± 0.20 pg/ml, p < 0.001 for both peaks) then progressively declined to levels before bypass. Arterial interleukin-6 was maximally elevated immediately on termination of cardiopulmonary bypass and peaked again 12 to 18 hours after cardiopulmonary bypass (at 7520 ± 2439 pg/ml and 6216 ± 1928 pg/ml, respectively; before bypass: 746 ± 187 pg/ml, p < 0.0001 for both peaks). Arterial interleukin-8 levels were more variable but followed a similar pattern, peaking in the early period after cardiopulmonary bypass and again at 16 to 18 hours after the operation (at 4110 ± 1403 pg/ml and 1760 ± 1145 pg/ml, respectively; before bypass: 461 ± 158. p < 0.05 for both peaks). By multivariate analysis, the aortic crossclamp time was independently predictive of postoperative cytokine levels. Left ventricular wall motion abnormalities were associated with both interleukin-6 and interleukin-8 levels, worsening scores being associated with increasing levels (for interleukin-6, p = 0.003; for interleukin-8, p = 0.05). Postoperative myocardial ischemic episodes were associated with interleukin-6 levels, six of seven (85%) patients with episodes of myocardial ischemia after a peak in interleukin-6 concentrations (p < 0.01). We conclude that proinflammatory cytokines are elevated after uncomplicated coronary revascularization and may contribute
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We tested the hypothesis that cytokine levels are elevated after uncomplicated coronary artery bypass grafting and associated with episodes of postoperative myocardial ischemia and dysfunction. Coronary artery bypass grafting was performed under general anesthesia with moderate systemic hypothermia and cold-blood potassium cardioplegic solution. Tumor necrosis factor-α and interleukin-6 levels were determined by bioassays, and interleukin-8 levels were measured by a sandwich enzyme-linked immunosorbent assay. Myocardial function and ischemic episodes were assessed by intraoperative transesophageal echocardiography and perioperative 12-channel Holter monitoring. A total of 22 patients were studied, with no deaths or complications. Arterial tumor necrosis factor-α rose in a bimodal distribution, peaking at 2 and 18 to 24 hours after the operation (at 20.2 ± 6.4 pg/ml, [mean ± standard error of the mean]) and 5.8 ± 1.6 pg/ml, respectively; before cardiopulmonary bypass: 0.90 ± 0.20 pg/ml, p &lt; 0.001 for both peaks) then progressively declined to levels before bypass. Arterial interleukin-6 was maximally elevated immediately on termination of cardiopulmonary bypass and peaked again 12 to 18 hours after cardiopulmonary bypass (at 7520 ± 2439 pg/ml and 6216 ± 1928 pg/ml, respectively; before bypass: 746 ± 187 pg/ml, p &lt; 0.0001 for both peaks). Arterial interleukin-8 levels were more variable but followed a similar pattern, peaking in the early period after cardiopulmonary bypass and again at 16 to 18 hours after the operation (at 4110 ± 1403 pg/ml and 1760 ± 1145 pg/ml, respectively; before bypass: 461 ± 158. p &lt; 0.05 for both peaks). By multivariate analysis, the aortic crossclamp time was independently predictive of postoperative cytokine levels. Left ventricular wall motion abnormalities were associated with both interleukin-6 and interleukin-8 levels, worsening scores being associated with increasing levels (for interleukin-6, p = 0.003; for interleukin-8, p = 0.05). Postoperative myocardial ischemic episodes were associated with interleukin-6 levels, six of seven (85%) patients with episodes of myocardial ischemia after a peak in interleukin-6 concentrations (p &lt; 0.01). We conclude that proinflammatory cytokines are elevated after uncomplicated coronary revascularization and may contribute to postoperative myocardial ischemia and segmental wall motion abnormalities. 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We tested the hypothesis that cytokine levels are elevated after uncomplicated coronary artery bypass grafting and associated with episodes of postoperative myocardial ischemia and dysfunction. Coronary artery bypass grafting was performed under general anesthesia with moderate systemic hypothermia and cold-blood potassium cardioplegic solution. Tumor necrosis factor-α and interleukin-6 levels were determined by bioassays, and interleukin-8 levels were measured by a sandwich enzyme-linked immunosorbent assay. Myocardial function and ischemic episodes were assessed by intraoperative transesophageal echocardiography and perioperative 12-channel Holter monitoring. A total of 22 patients were studied, with no deaths or complications. Arterial tumor necrosis factor-α rose in a bimodal distribution, peaking at 2 and 18 to 24 hours after the operation (at 20.2 ± 6.4 pg/ml, [mean ± standard error of the mean]) and 5.8 ± 1.6 pg/ml, respectively; before cardiopulmonary bypass: 0.90 ± 0.20 pg/ml, p &lt; 0.001 for both peaks) then progressively declined to levels before bypass. Arterial interleukin-6 was maximally elevated immediately on termination of cardiopulmonary bypass and peaked again 12 to 18 hours after cardiopulmonary bypass (at 7520 ± 2439 pg/ml and 6216 ± 1928 pg/ml, respectively; before bypass: 746 ± 187 pg/ml, p &lt; 0.0001 for both peaks). Arterial interleukin-8 levels were more variable but followed a similar pattern, peaking in the early period after cardiopulmonary bypass and again at 16 to 18 hours after the operation (at 4110 ± 1403 pg/ml and 1760 ± 1145 pg/ml, respectively; before bypass: 461 ± 158. p &lt; 0.05 for both peaks). By multivariate analysis, the aortic crossclamp time was independently predictive of postoperative cytokine levels. Left ventricular wall motion abnormalities were associated with both interleukin-6 and interleukin-8 levels, worsening scores being associated with increasing levels (for interleukin-6, p = 0.003; for interleukin-8, p = 0.05). Postoperative myocardial ischemic episodes were associated with interleukin-6 levels, six of seven (85%) patients with episodes of myocardial ischemia after a peak in interleukin-6 concentrations (p &lt; 0.01). We conclude that proinflammatory cytokines are elevated after uncomplicated coronary revascularization and may contribute to postoperative myocardial ischemia and segmental wall motion abnormalities. 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We tested the hypothesis that cytokine levels are elevated after uncomplicated coronary artery bypass grafting and associated with episodes of postoperative myocardial ischemia and dysfunction. Coronary artery bypass grafting was performed under general anesthesia with moderate systemic hypothermia and cold-blood potassium cardioplegic solution. Tumor necrosis factor-α and interleukin-6 levels were determined by bioassays, and interleukin-8 levels were measured by a sandwich enzyme-linked immunosorbent assay. Myocardial function and ischemic episodes were assessed by intraoperative transesophageal echocardiography and perioperative 12-channel Holter monitoring. A total of 22 patients were studied, with no deaths or complications. Arterial tumor necrosis factor-α rose in a bimodal distribution, peaking at 2 and 18 to 24 hours after the operation (at 20.2 ± 6.4 pg/ml, [mean ± standard error of the mean]) and 5.8 ± 1.6 pg/ml, respectively; before cardiopulmonary bypass: 0.90 ± 0.20 pg/ml, p &lt; 0.001 for both peaks) then progressively declined to levels before bypass. Arterial interleukin-6 was maximally elevated immediately on termination of cardiopulmonary bypass and peaked again 12 to 18 hours after cardiopulmonary bypass (at 7520 ± 2439 pg/ml and 6216 ± 1928 pg/ml, respectively; before bypass: 746 ± 187 pg/ml, p &lt; 0.0001 for both peaks). Arterial interleukin-8 levels were more variable but followed a similar pattern, peaking in the early period after cardiopulmonary bypass and again at 16 to 18 hours after the operation (at 4110 ± 1403 pg/ml and 1760 ± 1145 pg/ml, respectively; before bypass: 461 ± 158. p &lt; 0.05 for both peaks). By multivariate analysis, the aortic crossclamp time was independently predictive of postoperative cytokine levels. Left ventricular wall motion abnormalities were associated with both interleukin-6 and interleukin-8 levels, worsening scores being associated with increasing levels (for interleukin-6, p = 0.003; for interleukin-8, p = 0.05). Postoperative myocardial ischemic episodes were associated with interleukin-6 levels, six of seven (85%) patients with episodes of myocardial ischemia after a peak in interleukin-6 concentrations (p &lt; 0.01). We conclude that proinflammatory cytokines are elevated after uncomplicated coronary revascularization and may contribute to postoperative myocardial ischemia and segmental wall motion abnormalities. (J THORAC CARDIOVASC SURG 1994;108:626-35)</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>7934095</pmid><doi>10.1016/S0022-5223(94)70286-1</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Coronary Artery Bypass
Cytokines - blood
Cytokines - physiology
Echocardiography, Transesophageal
Heart Diseases - blood
Heart Diseases - surgery
Humans
Interleukin-6 - blood
Interleukin-8 - blood
Male
Middle Aged
Myocardial Ischemia - blood
Myocardial Ischemia - diagnostic imaging
Myocardial Ischemia - physiopathology
Postoperative Period
Time Factors
Tumor Necrosis Factor-alpha - analysis
Ventricular Dysfunction, Left - blood
Ventricular Dysfunction, Left - diagnostic imaging
Ventricular Dysfunction, Left - physiopathology
title Relationship of the proinflammatory cytokines to myocardial ischemia and dysfunction after uncomplicated coronary revascularization
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