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Sökning: id:"swepub:oai:lup.lub.lu.se:bab4e6bd-9055-4d58-83fc-927ad8fea57d" > Association of comm...

Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction

Jabbari, Reza (författare)
Copenhagen University Hospital
Jabbari, Javad (författare)
Copenhagen University Hospital
Glinge, Charlotte (författare)
Copenhagen University Hospital
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Risgaard, Bjarke (författare)
Copenhagen University Hospital
Sattler, Stefan (författare)
Copenhagen University Hospital
Winkel, Bo Gregers (författare)
Copenhagen University Hospital
Terkelsen, Christian Juhl (författare)
Aarhus University Hospital
Tilsted, Hans Henrik (författare)
Aalborg University
Jensen, Lisette Okkels (författare)
Odense University Hospital
Hougaard, Mikkel (författare)
Odense University Hospital
Haunsø, Stig (författare)
Copenhagen University Hospital
Engstrøm, Thomas (författare)
Lund University,Lunds universitet,Kardiologi,Sektion II,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Cardiology,Section II,Department of Clinical Sciences, Lund,Faculty of Medicine,Copenhagen University Hospital
Albert, Christine M. (författare)
Harvard University,Brigham and Women's Hospital / Harvard Medical School
Tfelt-Hansen, Jacob (författare)
Copenhagen University Hospital
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 (creator_code:org_t)
2017-11-21
2017
Engelska.
Ingår i: BMC Medical Genetics. - : Springer Science and Business Media LLC. - 1471-2350. ; 18:1
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background: Cohort studies have revealed an increased risk for ventricular fibrillation (VF) and sudden cardiac death (SCD) in patients with atrial fibrillation (AF). In this study, we hypothesized that single nucleotide polymorphisms (SNP) previously associated with AF may be associated with the risk of VF caused by first ST-segment elevation myocardial infarction (STEMI). Methods: We investigated association of 24 AF-associated SNPs with VF in the prospectively assembled case-control study among first STEMI-patients of Danish ancestry. Results: We included 257 cases (STEMI with VF) and 537 controls (STEMI without VF). The median age at index infarction was 60 years for the cases and 61 years for the controls (p = 0.100). Compared to the control group, the case group was more likely to be male (86% vs. 75%, p = 0.001), have a history of AF (7% vs. 2%, p = 0.006) or hypercholesterolemia (39% vs. 31%, p = 0.023), and a family history of sudden death (40% vs. 25%, p < 0.001). All 24 selected SNPs have previously been associated with AF. None of the 24 SNPs were associated with the risk of VF after adjustment for age and sex under additive genetic model of inheritance in the logistic regression model. Conclusion: In this study, we found that the 24 AF-associated SNPs may not be involved in increasing the risk of VF. Larger VF cohorts and use of new next generation sequencing and epigenetic may in future identify additional AF and VF risk loci and improve our understanding of genetic pathways behind the two arrhythmias.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Nyckelord

Atrial fibrillation
Genetics
Myocardial infarction
Single nucleotide polymorphisms
ST-elevation myocardial infarction
Sudden cardiac death
Ventricular fibrillation

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