Circulating Proteome Analysis Identifies Reduced Inflammation After Initiation of Hemodynamic Support with Either Veno-Arterial Extracorporeal Membrane Oxygenation or Impella in Patients with Cardiogenic Shock.
Nikolaos A DiakosLija SwainShreyas BhaveXiaoying QiaoTowia LibermannJillian HaywoodSiya GoelShiva AnnamalaiMichele EspositoHaval ChweichAnthony FaugnoNavin K KapurPublished in: Journal of cardiovascular translational research (2024)
In-hospital mortality associated with cardiogenic shock (CS) remains high despite the use of percutaneous assist devices. We sought to determine whether support with VA-ECMO or Impella in patients with CS alters specific components of the plasma proteome. Plasma samples were collected before device implantation and 72 h after initiation of support in 11 CS patients receiving ECMO or Impella. SOMAscan was used to detect 1305 circulating proteins. Sixty-seven proteins were changed after ECMO (18 upregulated and 49 downregulated, p < 0.05), 38 after Impella (10 upregulated and 28 downregulated, p < 0.05), and only eight proteins were commonly affected. Despite minimal protein overlap, both devices were associated with markers of reduced inflammation and increased apoptosis of inflammatory cells. In summary, ECMO and Impella are associated with reduced expression of inflammatory markers and increased markers of inflammatory cell death. These circulating proteins may serve as novel targets of therapy or biomarkers to tailor AMCS use.
Keyphrases
- extracorporeal membrane oxygenation
- acute respiratory distress syndrome
- oxidative stress
- cell death
- cell cycle arrest
- respiratory failure
- induced apoptosis
- endoplasmic reticulum stress
- poor prognosis
- genome wide
- signaling pathway
- bone marrow
- dna methylation
- mesenchymal stem cells
- amino acid
- left ventricular assist device
- replacement therapy