Genetic and Epigenetic Factors of Takotsubo Syndrome: A Systematic Review.
Biomarkers
/ analysis
COVID-19
/ complications
DNA Copy Number Variations
/ immunology
Epigenesis, Genetic
/ immunology
Genetic Heterogeneity
Genetic Loci
/ immunology
Genetic Predisposition to Disease
Heart Ventricles
/ immunology
Humans
Medical History Taking
Polymorphism, Single Nucleotide
/ immunology
SARS-CoV-2
/ immunology
Takotsubo Cardiomyopathy
/ diagnosis
TTS management
Takotsubo cardiomyopathy (TTS)
biomarkers
genetic and epigenetic factors
specific and effective treatments
systematic review
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
13 Sep 2021
13 Sep 2021
Historique:
received:
27
07
2021
revised:
02
09
2021
accepted:
11
09
2021
entrez:
28
9
2021
pubmed:
29
9
2021
medline:
6
10
2021
Statut:
epublish
Résumé
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.
Identifiants
pubmed: 34576040
pii: ijms22189875
doi: 10.3390/ijms22189875
pmc: PMC8471495
pii:
doi:
Substances chimiques
Biomarkers
0
Types de publication
Journal Article
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
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