Key result
Mild therapeutic hypothermia significantly increased MCP-1 levels after rewarming on day 3 compared to normothermia (125.7 vs 12.3 pg/mL; p=0.011) in patients with cardiogenic shock complicating AMI.
Why the study?
Little is known about the effect of mild therapeutic hypothermia on the inflammatory response, specifically MCP-1 levels, in patients with cardiogenic shock complicating acute myocardial infarction.
Does mild therapeutic hypothermia affect MCP-1 levels in patients with cardiogenic shock complicating acute myocardial infarction?
RCT (n=40)
1:1 ratio
Does mild therapeutic hypothermia affect MCP-1 levels in patients with cardiogenic shock complicating acute myocardial infarction?
Absolute Event Rate: 125.7% vs 12.3%
p-value: p=0.011
Mild therapeutic hypothermia in cardiogenic shock complicating AMI leads to a significant increase in MCP-1 levels after rewarming, though not during the cooling phase.
MTH shows no effect on MCP-1 in CS complicating AMI; leaves open whether hypothermia modulates inflammation in this population.
Background: There is evidence that monocyte chemoattractant protein-1 (MCP-1) levels reflect the intensity of the inflammatory response in patients with cardiogenic shock (CS) complicating acute myocardial infarction (AMI) and have a predictive value for clinical outcomes. However, little is known about the effect of mild therapeutic hypothermia (MTH) on the inflammatory response in patients with CS complicating AMI. Therefore, we conducted a biomarker study to investigate the effect of MTH on MCP-1 levels in patients with CS complicating AMI. Methods: In the randomized mild hypothermia in cardiogenic shock (SHOCK-COOL) trial, 40 patients with CS complicating AMI were enrolled and assigned to MTH (33 °C) for 24 h or normothermia at a 1:1 ratio. Blood samples were collected at predefined time points at the day of admission/day 1, day 2 and day 3. Differences in MCP-1 levels between and within the MTH and normothermia groups were assessed. Additionally, the association of MCP-1 levels with the risk of all-cause mortality at 30 days was analyzed. Missing data were accounted for by multiple imputation as sensitivity analyses. Results: There were differences in MCP-1 levels over time between patients in MTH and normothermia groups (P for interaction = 0.013). MCP-1 levels on day 3 were higher than on day 1 in the MTH group (day 1 vs day 3: 21.2 [interquartile range, 0.25–79.9] vs. 125.7 [interquartile range, 87.3–165.4] pg/mL; p = 0.006) and higher than in the normothermia group at day 3 (MTH 125.7 [interquartile range, 87.3–165.4] vs. normothermia 12.3 [interquartile range, 0–63.9] pg/mL; p = 0.011). Irrespective of therapy, patients with higher levels of MCP-1 at hospitalization tended to have a decreased risk of all-cause mortality at 30 days (HR, 2.61; 95% CI 0.997–6.83; p = 0.051). Conclusions: The cooling phase of MTH had no significant effect on MCP-1 levels in patients with CS complicating AMI compared to normothermic control, whereas MCP-1 levels significantly increased after rewarming. Trial registration: NCT01890317.
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Cheng et al. (2022) conducted an RCT in Cardiogenic shock complicating acute myocardial infarction (n=40). Mild therapeutic hypothermia vs. Normothermia was evaluated on MCP-1 levels on day 3 (p=0.011). Mild therapeutic hypothermia significantly increased MCP-1 levels after rewarming on day 3 compared to normothermia (125.7 vs 12.3 pg/mL; p=0.011) in patients with cardiogenic shock complicating AMI.
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