Literature DB >> 19102038

Vasovagal syncope: state or trait?

Anna Serletis Bizios1, Robert S Sheldon.   

Abstract

PURPOSE OF REVIEW: The absence of a satisfactory comprehensive theory for vasovagal syncope has prompted attention towards a possible genetic origin. There are several features of this trait that suggest a genetic origin. The purposes of this review are to present a rationale for considering a genetic origin and critically summarize recent findings. RECENT
FINDINGS: Key characteristics that suggest a genetic origin are incomplete effect in the population, a persistent clinical phenotype, and the absence of obvious infectious or autoimmune causes. There are familial pedigrees of vasovagal syncope, and statistical analyses of the impact of family history on the likelihood of an individual fainting that suggest an autosomal dominant transmission with incomplete penetrance. There is also evidence of sex-specific penetrance. Early candidate gene studies point towards involvement of sympathetic signal transduction in the physiologic cascade.
SUMMARY: Several epidemiologic characteristics of vasovagal syncope suggest that it may have a genetic origin.

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Year:  2009        PMID: 19102038     DOI: 10.1097/hco.0b013e32831ba05f

Source DB:  PubMed          Journal:  Curr Opin Cardiol        ISSN: 0268-4705            Impact factor:   2.161


  2 in total

1.  Dominant Transmission Observed in Adolescents and Families With Orthostatic Intolerance.

Authors:  Jennifer E Posey; Rebecca Martinez; Jeremy E Lankford; James R Lupski; Mohammed T Numan; Ian J Butler
Journal:  Pediatr Neurol       Date:  2016-09-24       Impact factor: 3.372

2.  Arg389Gly β1-adrenergic receptor polymorphism and susceptibility to syncope during tilt test.

Authors:  Monika Zelazowska; Małgorzata Lelonek; Wojciech Fendler; Tadeusz Pietrucha
Journal:  Arch Med Sci       Date:  2014-05-13       Impact factor: 3.318

  2 in total

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