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导致心肌梗死后并发心源性休克的克隆性造血的影响。

Impact of Clonal Hematopoiesis in Patients With Cardiogenic Shock Complicating Acute Myocardial Infarction.

机构信息

Medical Clinic and Policlinic 1, Hematology, Cellular Therapy and Hemostaseology, Leipzig University Hospital, Leipzig, Germany.

Heart Center Leipzig at University of Leipzig, Department of Internal Medicine/Cardiology and Leipzig Heart Institute, Leipzig, Germany.

出版信息

J Am Coll Cardiol. 2022 Oct 18;80(16):1545-1556. doi: 10.1016/j.jacc.2022.08.740.

Abstract

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).

摘要

背景

不确定潜能的克隆性造血(CHIP)在老年人中很常见,并且与血液系统恶性肿瘤和心血管疾病的风险增加有关。CHIP 对急性心肌梗死(AMI)并发心源性休克(CS)患者结局的影响仍不确定。

目的

本研究旨在确定 CHIP 在 AMI 后 CS 中的预后影响。

方法

从 CULPRIT-SHOCK(罪犯病变仅与多血管经皮冠状动脉介入治疗在心源性休克中的比较;NCT01927549)试验中随机纳入的 446 例患者中采集血液样本。使用靶向最常见突变基因的下一代测序方法评估 CHIP;30 天的主要结局包括全因死亡率和肾脏替代治疗。

结果

≥2%变异等位基因频率的 CHIP 变异在 29%(n=129)中检测到,最常见于 DNMT3A 或 TET2 基因,分别占所有突变的 47%和 36%。与非 CHIP 患者相比,CHIP 携带者年龄较大,肾功能下降,N 末端脑利钠肽前体和炎症生物标志物水平升高。CHIP 携带者短期预后较差,表现为死亡率或 30 天内死亡率或严重肾衰竭的联合临床终点。CHIP 与联合终点的关联独立于年龄和反映肾功能、心力衰竭严重程度和炎症的生物标志物(OR:1.83;95%CI:1.05-3.21;P=0.03),但与全因死亡率无显著相关性(OR:1.67;95%CI:0.96-2.90;P=0.069)。

结论

CHIP 在 AMI 和 CS 患者中很常见,与临床结局受损相关。CHIP 评估可能有助于 CS 患者的风险分层,并暗示新的治疗靶点。(罪犯病变仅与多血管经皮冠状动脉介入治疗在心源性休克中的比较;CULPRIT-SHOCK;NCT01927549)。

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