Source:http://linkedlifedata.com/resource/pubmed/id/20408814
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2010-6-4
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pubmed:abstractText |
Ca2+ cycling plays a critical role in heart failure and lethal arrhythmias. As susceptibility to sudden cardiac death is considered to be a heritable trait in general population, we have therefore investigated whether potentially functional variants of genes encoding RyR2 (ryanodine receptor 2) and the L-type Ca2+ channel are related to the risk of ventricular arrhythmias and sudden cardiac death in CHF (chronic heart failure) in a case-control study. We found that the A allele of rs3766871 in RYR2 was associated with an increased risk of ventricular arrhythmias in patients with CHF {odds ratio, 1.66 [95% CI (confidence interval), 1.21-2.26]; P=0.002}. During a median follow-up period of 32 months in 1058 (85.0%) patients, 296 (28.0%) patients died from heart failure, of whom 141 (47.6%) had sudden cardiac death. After adjustment for age, gender and suspected risk factors, patients carrying the A allele of rs3766871 had an increased risk of cardiac death {HR (hazard ratio), 1.53 [95% CI, 1.11-2.12]; P=0.010} and sudden cardiac death [HR, 1.92 (95% CI, 1.25-2.94); P=0.003]. Patients carrying the A allele of rs790896 in RYR2 had a reduced risk of sudden cardiac death [HR, 0.65 (95% CI, 0.45-0.92); P=0.015]. In conclusion, the A allele of rs3766871 in RYR2 not only associates with ventricular arrhythmias, but also serves as an independent predictor of sudden cardiac death, and the A allele of rs790896 in RYR2 is a protective factor against sudden cardiac death in patients with CHF.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1470-8736
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
119
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
215-23
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pubmed:dateRevised |
2010-9-23
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pubmed:meshHeading |
pubmed-meshheading:20408814-Adult,
pubmed-meshheading:20408814-Aged,
pubmed-meshheading:20408814-Arrhythmias, Cardiac,
pubmed-meshheading:20408814-Base Sequence,
pubmed-meshheading:20408814-Death, Sudden, Cardiac,
pubmed-meshheading:20408814-Epidemiologic Methods,
pubmed-meshheading:20408814-Female,
pubmed-meshheading:20408814-Genetic Predisposition to Disease,
pubmed-meshheading:20408814-Heart Failure,
pubmed-meshheading:20408814-Humans,
pubmed-meshheading:20408814-Male,
pubmed-meshheading:20408814-Middle Aged,
pubmed-meshheading:20408814-Polymorphism, Single Nucleotide,
pubmed-meshheading:20408814-Prognosis,
pubmed-meshheading:20408814-Ryanodine Receptor Calcium Release Channel
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pubmed:year |
2010
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pubmed:articleTitle |
Common RyR2 variants associate with ventricular arrhythmias and sudden cardiac death in chronic heart failure.
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pubmed:affiliation |
Center for Arrhythmia Diagnosis and Treatment, Fu Wai Cardiovascular Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100037, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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