Literature DB >> 19360272

[Neurocardiogenic syncope and hereditarity].

Mariana Cristina S Azevedo1, Juarez N Barbisan, Erlon Oliveira Abreu Silva.   

Abstract

OBJECTIVE: To investigate a possible familial predisposition in neurocardiogenic syncope.
METHODS: Cross-sectional survey with 252 subjects, with positive familial history for syncope, who underwent head-up tilt-test (TT) at Instituto de Cardiologia do Rio Grande do Sul, between September 2001 and September 2005. The relationship between familial history for neurocardiogenic syncope and TT result was analysed.
RESULTS: Familial history for neurocardiogenic syncope was identified in 40% (49/126 cases) of subjects with positive tilt-test results and 25% (31/126 ) of those with negative TT.
CONCLUSION: There is a correlation between familial history for neurocardiogenic syncope and its occurence. A genetic component can possibly explain this relationship.

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Year:  2009        PMID: 19360272     DOI: 10.1590/s0104-42302009000100009

Source DB:  PubMed          Journal:  Rev Assoc Med Bras (1992)        ISSN: 0104-4230            Impact factor:   1.209


  1 in total

1.  Alteration of gene expression profiling including GPR174 and GNG2 is associated with vasovagal syncope.

Authors:  Yu-Juan Huang; Zai-wei Zhou; Miao Xu; Qing-wen Ma; Jing-bin Yan; Jian-yi Wang; Quo-qin Zhang; Min Huang; Liming Bao
Journal:  Pediatr Cardiol       Date:  2014-11-01       Impact factor: 1.655

  1 in total

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