Your browser doesn't support javascript.
loading
Acute Response in the Noninfarcted Myocardium Predicts Long-Term Major Adverse Cardiac Events After STEMI.
Shanmuganathan, Mayooran; Masi, Ambra; Burrage, Matthew K; Kotronias, Rafail A; Borlotti, Alessandra; Scarsini, Roberto; Banerjee, Abhirup; Terentes-Printzios, Dimitrios; Zhang, Qiang; Hann, Evan; Tunnicliffe, Elizabeth; Lucking, Andrew; Langrish, Jeremy; Kharbanda, Rajesh; De Maria, Giovanni Luigi; Banning, Adrian P; Choudhury, Robin P; Channon, Keith M; Piechnik, Stefan K; Ferreira, Vanessa M.
Afiliação
  • Shanmuganathan M; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of R
  • Masi A; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom.
  • Burrage MK; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John
  • Kotronias RA; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
  • Borlotti A; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom.
  • Scarsini R; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
  • Banerjee A; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom.
  • Terentes-Printzios D; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
  • Zhang Q; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom.
  • Hann E; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom.
  • Tunnicliffe E; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom.
  • Lucking A; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
  • Langrish J; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
  • Kharbanda R; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
  • De Maria GL; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
  • Banning AP; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
  • Choudhury RP; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom.
  • Channon KM; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, United Kingdom. Electronic address: keith.channon@cardiov.ox.ac.uk.
  • Piechnik SK; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of Research Excellence, University of Oxford, Oxford, United Kingdom.
  • Ferreira VM; Acute Vascular Imaging Centre (AVIC), University of Oxford, John Radcliffe Hospital, Oxford, United Kingdom; Oxford Centre for Clinical Magnetic Resonance Research (OCMR), John Radcliffe Hospital, National Institute for Health Research (NIHR) Oxford Biomedical Research Centre, Oxford BHF Centre of R
JACC Cardiovasc Imaging ; 16(1): 46-59, 2023 01.
Article em En | MEDLINE | ID: mdl-36599569
ABSTRACT

BACKGROUND:

Acute ST-segment elevation myocardial infarction (STEMI) has effects on the myocardium beyond the immediate infarcted territory. However, pathophysiologic changes in the noninfarcted myocardium and their prognostic implications remain unclear.

OBJECTIVES:

The purpose of this study was to evaluate the long-term prognostic value of acute changes in both infarcted and noninfarcted myocardium post-STEMI.

METHODS:

Patients with acute STEMI undergoing primary percutaneous coronary intervention underwent evaluation with blood biomarkers and cardiac magnetic resonance (CMR) at 2 days and 6 months, with long-term follow-up for major adverse cardiac events (MACE). A comprehensive CMR protocol included cine, T2-weighted, T2∗, T1-mapping, and late gadolinium enhancement (LGE) imaging. Areas without LGE were defined as noninfarcted myocardium. MACE was a composite of cardiac death, sustained ventricular arrhythmia, and new-onset heart failure.

RESULTS:

Twenty-two of 219 patients (10%) experienced an MACE at a median of 4 years (IQR 2.5-6.0 years); 152 patients returned for the 6-month visit. High T1 (>1250 ms) in the noninfarcted myocardium was associated with lower left ventricular ejection fraction (LVEF) (51% ± 8% vs 55% ± 9%; P = 0.002) and higher NT-pro-BNP levels (290 pg/L [IQR 103-523 pg/L] vs 170 pg/L [IQR 61-312 pg/L]; P = 0.008) at 6 months and a 2.5-fold (IQR 1.03-6.20) increased risk of MACE (2.53 [IQR 1.03-6.22]), compared with patients with normal T1 in the noninfarcted myocardium (P = 0.042). A lower T1 (<1,300 ms) in the infarcted myocardium was associated with increased MACE (3.11 [IQR 1.19-8.13]; P = 0.020). Both noninfarct and infarct T1 were independent predictors of MACE (both P = 0.001) and significantly improved risk prediction beyond LVEF, infarct size, and microvascular obstruction (C-statistic 0.67 ± 0.07 vs 0.76 ± 0.06, net-reclassification index 40% [IQR 12%-64%]; P = 0.007).

CONCLUSIONS:

The acute responses post-STEMI in both infarcted and noninfarcted myocardium are independent incremental predictors of long-term MACE. These insights may provide new opportunities for treatment and risk stratification in STEMI.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infarto Miocárdico de Parede Anterior / Intervenção Coronária Percutânea / Infarto do Miocárdio com Supradesnível do Segmento ST Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infarto Miocárdico de Parede Anterior / Intervenção Coronária Percutânea / Infarto do Miocárdio com Supradesnível do Segmento ST Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article