4.8 Article

Persistent Long-Term Structural, Functional, and Metabolic Changes After Stress-Induced (Takotsubo) Cardiomyopathy

期刊

CIRCULATION
卷 137, 期 10, 页码 1039-1048

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCULATIONAHA.117.031841

关键词

broken heart syndrome; cardiac energetics; cardiopulmonary exercise testing; stress-induced cardiomyopathy; takotsubo

资金

  1. British Heart Foundation [PG/15/108/31928] Funding Source: researchfish
  2. Chief Scientist Office [CGA/16/04] Funding Source: researchfish
  3. British Heart Foundation [PG/15/108/31928, PG/15/108/31928, CH/09/002] Funding Source: Medline
  4. Wellcome Trust [WT103782AIA] Funding Source: Medline
  5. Chief Scientist Office [CGA/16/04, CGA-16-4] Funding Source: Medline

向作者/读者索取更多资源

BACKGROUND: Takotsubo cardiomyopathy is an increasingly recognized acute heart failure syndrome precipitated by intense emotional stress. Although there is an apparent rapid and spontaneous recovery of left ventricular ejection fraction, the long-term clinical and functional consequences of takotsubo cardiomyopathy are ill-defined. METHODS: In an observational case-control study, we recruited 37 patients with prior (> 12-month) takotsubo cardiomyopathy, and 37 age-, sex-, and comorbidity-matched control subjects. Patients completed the Minnesota Living with Heart Failure Questionnaire. All participants underwent detailed clinical phenotypic characterization, including serum biomarker analysis, cardiopulmonary exercise testing, echocardiography, and cardiac magnetic resonance including cardiac P-31-spectroscopy. RESULTS: Participants were predominantly middle-age (6411 years) women (97%). Although takotsubo cardiomyopathy occurred 20 (range 13-39) months before the study, the majority (88%) of patients had persisting symptoms compatible with heart failure (median of 13 [range 0-76] in the Minnesota Living with Heart Failure Questionnaire) and cardiac limitation on exercise testing (reduced peak oxygen consumption, 241.3 versus 31 +/- 1.3 mL/kg/min, P<0.001; increased VE/Vco(2) slope, 31 +/- 1 versus 26 +/- 1, P=0.002). Despite normal left ventricular ejection fraction and serum biomarkers, patients with prior takotsubo cardiomyopathy had impaired cardiac deformation indices (reduced apical circumferential strain, -16 +/- 1.0 versus -23 +/- 1.5%, P<0.001; global longitudinal strain, -17 +/- 1 versus -20 +/- 1%, P=0.006), increased native T1 mapping values (1264 +/- 10 versus 1184 +/- 10 ms, P<0.001), and impaired cardiac energetic status (phosphocreatine/-adenosine triphosphate ratio, 1.3 +/- 0.1 versus 1.9 +/- 0.1, P<0.001). CONCLUSIONS: In contrast to previous perceptions, takotsubo cardiomyopathy has long-lasting clinical consequences, including demonstrable symptomatic and functional impairment associated with persistent subclinical cardiac dysfunction. Taken together our findings demonstrate that after takotsubo cardiomyopathy, patients develop a persistent, long-term heart failure phenotype.

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