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Clonal Hematopoiesis of Indeterminate Potential and Infarct Severity in ST-Elevation Myocardial Infarction (CHIP in STEMI)

2026年5月22日 更新者:Medical University Innsbruck

Clonal Hematopoiesis of Indeterminate Potential (CHIP) refers to the age-related expansion of hematopoietic stem cell clones carrying somatic mutations in leukemia-associated driver genes (e.g., DNMT3A, TET2, ASXL1) in the absence of a hematological malignancy. CHIP has been identified as an independent cardiovascular risk factor associated with increased rates of myocardial infarction, stroke, and cardiovascular mortality, likely mediated through enhanced inflammatory signaling in mutant macrophages and monocytes.

ST-elevation myocardial infarction (STEMI) is a life-threatening emergency requiring immediate reperfusion by primary percutaneous coronary intervention (PCI). Despite successful reperfusion, adverse cardiac remodeling and heart failure may occur depending on myocardial injury severity, microvascular obstruction (MVO), and intramyocardial hemorrhage (IMH) - phenomena substantially driven by ischemia-reperfusion injury and the inflammatory response.

The CHIP in STEMI study is a prospective, observational, single-center cohort study at the Medical University of Innsbruck investigating whether CHIP - detected by targeted next-generation sequencing - is associated with greater infarct severity and worse cardiac outcomes in STEMI patients undergoing primary PCI. The primary endpoint is the presence of MVO and/or IMH on cardiac MRI (CMR) at 5±2 days post-PCI. Secondary endpoints include infarct size, left and right ventricular function, major adverse cardiovascular events (MACE), and immune cell transcriptome profiling by single-cell RNA sequencing.

350 patients (18-75 years, minimum 90 female) will be enrolled over 36 months and followed for 4 years (2026-2030).

研究概览

详细说明

Background and Rationale:

CHIP mutations - particularly in TET2 and DNMT3A - promote a pro-inflammatory state in hematopoietic cells. Preclinical data demonstrate that TET2-deficient macrophages exhibit exaggerated NLRP3 inflammasome activation and IL-1β secretion, while DNMT3A mutations impair immune resolution after myocardial ischemia. This enhanced inflammatory signaling may worsen myocardial ischemia-reperfusion injury (IRI), thereby increasing MVO, IMH, and infarct size in CHIP carriers presenting with STEMI.

Study Design:

Prospective, observational, single-center cohort study. No intervention beyond standard of care.

Study Population:

350 patients aged 18-75 years with STEMI undergoing primary PCI at the University Clinic of Internal Medicine III - Cardiology and Angiology, Medical University of Innsbruck. A minimum of 90 female participants will be enrolled.

Key Inclusion Criteria:

  • Age 18-75 years
  • STEMI with symptom onset ≤12 hours before PCI
  • Successful primary PCI of culprit lesion
  • Written informed consent

Key Exclusion Criteria:

  • Prior myocardial infarction or known cardiomyopathy
  • Known hematological malignancy
  • Contraindication to CMR (pacemaker, severe claustrophobia, eGFR <30 mL/min/1.73m²)
  • Cardiogenic shock requiring mechanical circulatory support
  • Life expectancy <12 months due to non-cardiac cause
  • Pregnancy

Assessments:

  1. Cardiac MRI (CMR) at 5±2 days post-PCI: MVO, IMH, infarct size (%LVMM), LV/RV ejection fraction, volumes, mass
  2. Targeted next-generation sequencing (NGS) for CHIP mutations (VAF ≥2%): DNMT3A, TET2, ASXL1, and other driver genes
  3. Single-cell RNA sequencing (scRNA-seq) of PBMCs at baseline and 12-month follow-up
  4. Serial blood biomarkers: hsCRP, IL-6, IL-18, NT-proBNP, troponin T, complete blood count
  5. Clinical follow-up visits at 12, 24, and 48 months

Primary Endpoint:

Presence of microvascular obstruction (MVO) and/or intramyocardial hemorrhage (IMH) on CMR at 5±2 days post-PCI in CHIP carriers versus non-carriers.

Secondary Endpoints:

  • Infarct size (% left ventricular myocardial mass, %LVMM)
  • LV and RV ejection fraction, end-diastolic/systolic volumes, myocardial mass
  • MACE: all-cause mortality, non-fatal reinfarction, hospitalization for heart failure at 12, 24, and 48 months
  • Changes in CHIP mutation variant allele frequency (VAF) over time
  • Differential gene expression in immune cell subsets by scRNA-seq
  • Biomarker trajectories (NT-proBNP, hsCRP, IL-6)

Ethics and Regulatory:

The study protocol has been approved by the Research Ethics Committee of the Medical University of Innsbruck and is conducted in accordance with the Declaration of Helsinki and ICH-GCP guidelines. All participants provide written informed consent prior to study inclusion. The study is funded by the KLiF (Klinisch-Interne Forschung) program of the Medical University of Innsbruck.

研究类型

观察性的

注册 (估计的)

350

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

研究联系人备份

  • 姓名:Sebastian J Reinstadler, MD, PhD
  • 电话号码:+43 512 504 83772

学习地点

    • Tyrol
      • Innsbruck、Tyrol、奥地利、6020
        • Medical University of Innsbruck
        • 接触:
        • 接触:
          • Sebastian J Reinstadler, MD, PhD
          • 电话号码:+43 512 504 83772

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

是的

取样方法

非概率样本

研究人群

The study population will consist of adult female and male patients aged 18 to 75 years with a first acute ST-elevation myocardial infarction treated with primary percutaneous coronary intervention within 12 hours after symptom onset. Patients will be screened at the coronary care unit of the Medical University of Innsbruck. Eligible patients will be invited to participate after primary percutaneous coronary intervention and after assessment of inclusion and exclusion criteria. Standard clinical care and secondary prevention will be performed according to current guideline recommendations.

描述

Inclusion Criteria:

  • Diagnosis of first acute ST-elevation myocardial infarction according to current European Society of Cardiology guidelines
  • Symptoms consistent with ST-elevation myocardial infarction lasting more than 30 minutes and less than 12 hours before primary percutaneous coronary intervention
  • Treatment with primary percutaneous coronary intervention
  • Age 18 to 75 years
  • Written informed consent

Exclusion Criteria:

  • Prior myocardial infarction, coronary artery bypass grafting, or percutaneous coronary intervention
  • Persistent hemodynamic instability, Killip class greater than 2 including cardiogenic shock, or resuscitated cardiac arrest not allowing cardiac magnetic resonance imaging
  • Known active or prior malignancy, including hematologic malignancies or myelodysplastic syndromes
  • Prior oncologic treatment with chemotherapy, radiotherapy, or radioisotopes
  • Abnormal baseline complete blood count with clinically significant cytopenia, defined as leukocytes less than 3.0 x 10^9/L, platelets less than 100 x 10^9/L, or hemoglobin less than 10 g/dL
  • Chronic viral infection associated with systemic inflammation
  • Active autoimmune disease or chronic systemic inflammatory disorder
  • Chronic kidney disease with creatinine clearance less than 30 mL/min/1.73 m2
  • Contraindication to cardiac magnetic resonance imaging
  • Pre-ST-elevation myocardial infarction life expectancy of less than 1 year
  • Participation in an interventional trial
  • Limited possibility to attend follow-up examinations, for example residence abroad
  • Pregnancy

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
干预/治疗
STEMI Patients
Patients presenting with ST-elevation myocardial infarction (STEMI) who undergo successful primary percutaneous coronary intervention (PCI). All consecutive eligible patients are enrolled regardless of CHIP mutation status. This single cohort is analyzed based on CHIP presence/absence and specific CHIP mutation type (e.g., DNMT3A, TET2, ASXL1).
Participants will undergo blood sampling for assessment of clonal hematopoiesis of indeterminate potential by targeted next-generation sequencing and cardiac magnetic resonance imaging for assessment of myocardial injury, including microvascular obstruction, intramyocardial hemorrhage, infarct size, ventricular function, and myocardial tissue characteristics. Additional biomarker and inflammatory profiling will be performed according to the study protocol.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Occurrence of microvascular injury
大体时间:5 ± 2 days after primary percutaneous coronary intervention
Presence of microvascular injury, defined as microvascular obstruction and/or intramyocardial hemorrhage, assessed by cardiac magnetic resonance imaging in patients with ST-elevation myocardial infarction treated with primary percutaneous coronary intervention. The outcome will be analyzed according to the presence or absence of clonal hematopoiesis of indeterminate potential.
5 ± 2 days after primary percutaneous coronary intervention

次要结果测量

结果测量
措施说明
大体时间
Infarct size
大体时间:5 ± 2 days after primary percutaneous coronary intervention
Infarct size expressed as percentage of left ventricular myocardial mass, assessed by cardiac magnetic resonance imaging in patients with ST-elevation myocardial infarction treated with primary percutaneous coronary intervention. The outcome will be analyzed according to the presence or absence of clonal hematopoiesis of indeterminate potential.
5 ± 2 days after primary percutaneous coronary intervention
Left ventricular ejection fraction
大体时间:5 ± 2 days, 4 months, and 12 months after primary percutaneous coronary intervention
Left ventricular ejection fraction assessed by cardiac magnetic resonance imaging in patients with ST-elevation myocardial infarction treated with primary percutaneous coronary intervention.
5 ± 2 days, 4 months, and 12 months after primary percutaneous coronary intervention
All-cause mortality
大体时间:Within 12 months after study inclusion.
eath from any cause after study inclusion.
Within 12 months after study inclusion.
Hospitalization for heart failure
大体时间:Within 12 months after study inclusion.
Hospitalization due to new or worsening heart failure after study inclusion.
Within 12 months after study inclusion.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年6月20日

初级完成 (估计的)

2029年6月20日

研究完成 (估计的)

2030年6月20日

研究注册日期

首次提交

2026年5月22日

首先提交符合 QC 标准的

2026年5月22日

首次发布 (实际的)

2026年5月29日

研究记录更新

最后更新发布 (实际的)

2026年5月29日

上次提交的符合 QC 标准的更新

2026年5月22日

最后验证

2026年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • 1195/2024
  • KLP1365525 (其他赠款/资助编号:Austrian Science Fund)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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