The Genetic Landscape of Patent Foramen Ovale: A Systematic Review.
Atrial Septal Defects
Congenital Heart Defects
paradoxical embolism
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
06 12 2021
06 12 2021
Historique:
received:
06
11
2021
revised:
30
11
2021
accepted:
03
12
2021
entrez:
24
12
2021
pubmed:
25
12
2021
medline:
17
2
2022
Statut:
epublish
Résumé
Patent Foramen Ovale (PFO) is a common postnatal defect of cardiac atrial septation. A certain degree of familial aggregation has been reported. Animal studies suggest the involvement of the Notch pathway and other cardiac transcription factors (GATA4, TBX20, NKX2-5) in Foramen Ovale closure. This review evaluates the contribution of genetic alterations in PFO development. We systematically reviewed studies that assessed rare and common variants in subjects with PFO. The protocol was registered with PROSPERO and followed MOOSE guidelines. We systematically searched English studies reporting rates of variants in PFO subjects until the 30th of June 2021. Among 1231 studies, we included four studies: two of them assessed the
Identifiants
pubmed: 34946902
pii: genes12121953
doi: 10.3390/genes12121953
pmc: PMC8700998
pii:
doi:
Substances chimiques
GATA4 Transcription Factor
0
GATA4 protein, human
0
Homeobox Protein Nkx-2.5
0
NKX2-5 protein, human
0
Types de publication
Journal Article
Systematic Review
Langues
eng
Sous-ensembles de citation
IM
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