Key result
CHIP is linked to ~83% higher 30-day mortality or renal failure in post-AMI cardiogenic shock.
Why the study?
Does clonal hematopoiesis of indeterminate potential worsen clinical outcomes in patients with cardiogenic shock complicating acute myocardial infarction?
Cohort (n=446)
Yes
Does clonal hematopoiesis of indeterminate potential worsen clinical outcomes in patients with cardiogenic shock complicating acute myocardial infarction?
Answers are grounded in this paper and cite their sources.
CHIP operates as an independent prognostic factor associated with worse short-term outcomes in patients suffering from cardiogenic shock complicating acute myocardial infarction.
BACKGROUND Clonal hematopoiesis of indeterminate potential (CHIP) is common in elderly individuals and is associated with an increased risk of both hematologic malignancies and cardiovascular disease. The impact of CHIP on the outcomes for patients with cardiogenic shock (CS) complicating acute myocardial infarction (AMI) remains undetermined. OBJECTIVES The purpose of this study was to determine the prognostic impact of CHIP in CS after AMI. METHODS Blood samples were obtained at randomization from 446 patients included in the CULPRIT-SHOCK (Culprit Lesion Only vs Multivessel Percutaneous Coronary Intervention in Cardiogenic Shock; NCT01927549) trial. CHIP was assessed using a next-generation sequencing approach targeting the most commonly mutated genes; the primary outcome at 30 days comprised all-cause mortality and renal replacement therapy. RESULTS CHIP variants at ≥2% variant allele frequency were detected in 29% (n = 129), most commonly in the DNMT3A or TET2 genes, which harbored 47% and 36% of all mutations, respectively. Compared to non-CHIP patients, CHIP carriers were older and had decreased renal function and increased levels of N-terminal pro-B-type natriuretic peptide and inflammatory biomarkers. CHIP carriers had worse short-term outcomes measured either as mortality or as the combined clinical endpoint of mortality or severe renal failure within 30 days. Association of CHIP with the combined endpoint was independent of age and biomarkers reflecting kidney function, heart failure severity, and inflammation (OR: 1.83; 95% CI: 1.05-3.21; P = 0.03) but not significant regarding all-cause mortality (OR: 1.67; 95% CI: 0.96-2.90; P = 0.069). CONCLUSIONS CHIP is frequent among AMI and CS patients and is associated with impaired clinical outcome. CHIP assessment may facilitate risk stratification in patients with CS and imply novel treatment targets. (Culprit Lesion Only vs Multivessel Percutaneous Coronary Intervention in Cardiogenic Shock [CULPRIT-SHOCK]; NCT01927549).
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Böhme et al. (2022) conducted a cohort in Cardiogenic shock complicating acute myocardial infarction (n=446). Clonal hematopoiesis of indeterminate potential (CHIP) vs. Non-CHIP carriers was evaluated on Combined endpoint of all-cause mortality and renal replacement therapy at 30 days (OR 1.83, 95% CI 1.05-3.21, p=0.03). Clonal hematopoiesis of indeterminate potential increased the 30-day risk of all-cause mortality or severe renal failure (OR 1.83) in patients with cardiogenic shock after acute myocardial infarction.
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