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Genetic and Epigenetic Factors of Takotsubo Syndrome: A Systematic Review.
Ferradini, Valentina; Vacca, Davide; Belmonte, Beatrice; Mango, Ruggiero; Scola, Letizia; Novelli, Giuseppe; Balistreri, Carmela Rita; Sangiuolo, Federica.
  • Ferradini V; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.
  • Vacca D; Tumor Immunology Unit, Department of Health Sciences, University of Palermo, 90134 Palermo, Italy.
  • Belmonte B; Tumor Immunology Unit, Department of Health Sciences, University of Palermo, 90134 Palermo, Italy.
  • Mango R; Cardiology Unit, Department of Emergency and Critical Care, Policlinico Tor Vergata, 00133 Rome, Italy.
  • Scola L; Department of Biomedicine, Neuroscience and Advanced Diagnostics (Bi.N.D.), University of Palermo, 90134 Palermo, Italy.
  • Novelli G; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.
  • Balistreri CR; Department of Biomedicine, Neuroscience and Advanced Diagnostics (Bi.N.D.), University of Palermo, 90134 Palermo, Italy.
  • Sangiuolo F; Department of Biomedicine and Prevention, University of Rome Tor Vergata, Via Montpellier 1, 00133 Rome, Italy.
Int J Mol Sci ; 22(18)2021 Sep 13.
Article in English | MEDLINE | ID: covidwho-1409701
ABSTRACT
Takotsubo syndrome (TTS), recognized as stress's cardiomyopathy, or as left ventricular apical balloon syndrome in recent years, is a rare pathology, described for the first time by Japanese researchers in 1990. TTS is characterized by an interindividual heterogeneity in onset and progression, and by strong predominance in postmenopausal women. The clear causes of these TTS features are uncertain, given the limited understanding of this intriguing syndrome until now. However, the increasing frequency of TTS cases in recent years, and particularly correlated to the SARS-CoV-2 pandemic, leads us to the imperative necessity both of a complete knowledge of TTS pathophysiology for identifying biomarkers facilitating its management, and of targets for specific and effective treatments. The suspect of a genetic basis in TTS pathogenesis has been evidenced. Accordingly, familial forms of TTS have been described. However, a systematic and comprehensive characterization of the genetic or epigenetic factors significantly associated with TTS is lacking. Thus, we here conducted a systematic review of the literature before June 2021, to contribute to the identification of potential genetic and epigenetic factors associated with TTS. Interesting data were evidenced, but few in number and with diverse limitations. Consequently, we concluded that further work is needed to address the gaps discussed, and clear evidence may arrive by using multi-omics investigations.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Genetic Heterogeneity / Genetic Predisposition to Disease / Epigenesis, Genetic / Takotsubo Cardiomyopathy / COVID-19 Type of study: Diagnostic study / Prognostic study / Reviews / Systematic review/Meta Analysis Topics: Long Covid / Variants Limits: Humans Language: English Year: 2021 Document Type: Article Affiliation country: Ijms22189875

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Genetic Heterogeneity / Genetic Predisposition to Disease / Epigenesis, Genetic / Takotsubo Cardiomyopathy / COVID-19 Type of study: Diagnostic study / Prognostic study / Reviews / Systematic review/Meta Analysis Topics: Long Covid / Variants Limits: Humans Language: English Year: 2021 Document Type: Article Affiliation country: Ijms22189875