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

22. maj 2026 opdateret af: 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).

Studieoversigt

Detaljeret beskrivelse

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.

Undersøgelsestype

Observationel

Tilmelding (Anslået)

350

Kontakter og lokationer

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Studiekontakt

Undersøgelse Kontakt Backup

  • Navn: Sebastian J Reinstadler, MD, PhD
  • Telefonnummer: +43 512 504 83772

Studiesteder

    • Tyrol
      • Innsbruck, Tyrol, Østrig, 6020
        • Medical University of Innsbruck
        • Kontakt:
        • Kontakt:
          • Sebastian J Reinstadler, MD, PhD
          • Telefonnummer: +43 512 504 83772

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ja

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

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.

Beskrivelse

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

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Kohorter og interventioner

Gruppe / kohorte
Intervention / Behandling
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.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Occurrence of microvascular injury
Tidsramme: 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

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Infarct size
Tidsramme: 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
Tidsramme: 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
Tidsramme: Within 12 months after study inclusion.
eath from any cause after study inclusion.
Within 12 months after study inclusion.
Hospitalization for heart failure
Tidsramme: Within 12 months after study inclusion.
Hospitalization due to new or worsening heart failure after study inclusion.
Within 12 months after study inclusion.

Samarbejdspartnere og efterforskere

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Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

20. juni 2026

Primær færdiggørelse (Anslået)

20. juni 2029

Studieafslutning (Anslået)

20. juni 2030

Datoer for studieregistrering

Først indsendt

22. maj 2026

Først indsendt, der opfyldte QC-kriterier

22. maj 2026

Først opslået (Faktiske)

29. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

29. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

22. maj 2026

Sidst verificeret

1. maj 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 1195/2024
  • KLP1365525 (Andet bevillings-/finansieringsnummer: Austrian Science Fund)

Plan for individuelle deltagerdata (IPD)

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