Finnish Genetic Study for Arrhythmic Events (FinGesture)

Beskrivning

The Fingesture study (Finnish Genetic Study for Arrhythmic Events) has collected clinical and autopsy data from 5869 successive sudden cardiac death (SCD) victims from the geographical defined area of Oulu University Hospital District in Northern Finland since 1998. A medicolegal autopsy was performed on all SCD victims in the Department of Forensic Medicine, University of Oulu, Oulu, Finland, and the National Institute for Health and Welfare, Oulu, Finland by experienced forensic pathologists, making use of contemporary guidelines for diagnosis of the death cause. The hearts of the SCD victims were meticulously inspected, including measurements of cardiac weight macroscopic dissection and examination of the myocardium, coronary arteries and valves, and histological examination of three to five myocardial samples. The genetic data includes whole exome sequencing of 223 SCD victims who have either primary myocardial fibrosis or myocardial fibrosis accompanied by hypertrophy.
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Publiceringsår

2024

Typ av data

Upphovspersoner

Sini Skarp Orcid -palvelun logo - Medarbetare

Sisätautien tutkimusyksikkö - Upphovsperson, Utgivare

Juhani Junttila - Medarbetare

Projekt

Övriga uppgifter

Vetenskapsområden

Genetik, utvecklingsbiologi, fysiologi; Allmänmedicin, inre medicin och annan klinisk medicin

Språk

engelska, finska

Öppen tillgång

Begränsad tillgång

Licens

Creative Commons Attribution 4.0 International (CC BY 4.0)

Nyckelord

genetics, cardiovascular diseases, Arrythmias, exome sequencing, Sudden cardiac death

Ämnesord

exomsekvensering, fibros, genetik, hjärt-kärlsjukdomar, hjärtstillestånd, kardiologi, plötslig död

Temporal täckning

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