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Published on: December 11, 2016
Left ventricular ejection fraction and myocardial fibrosis in sudden cardiac death
Harri Silvola1, Lauri Holmstrom1, Lasse Pakanen2,3
1Research Unit of Biomedicine and Internal Medicine, Medical Research Center Oulu, University of Oulu, Oulu University Hospital, OYS Sydän, Kajaanintie 50, Oulu 90220, Finland.
Insights
Sudden cardiac death (SCD) risk is often assessed by left ventricular ejection fraction (LVEF). However, LVEF poorly correlates with myocardial fibrosis, a common finding in SCD victims, suggesting LVEF is an unreliable indicator of fibrosis.
Area of Science:
- Cardiology
- Pathology
- Forensic Medicine
Background:
- Left ventricular ejection fraction (LVEF) is a primary metric for assessing sudden cardiac death (SCD) risk.
- Myocardial fibrosis is increasingly recognized as a significant factor in various heart conditions.
Purpose of the Study:
- To determine the spectrum of LVEF in a population-based cohort of SCD victims.
- To evaluate the association between myocardial fibrosis and pre-SCD LVEF.
Main Methods:
- Analysis of autopsy-verified SCD cases (n=5869) from Northern Finland (1998-2017).
- Macroscopic and histological assessment of myocardial fibrosis extent.
- Evaluation of pre-mortem echocardiography data (LVEF) from electronic health records.
Main Results:
- A significant proportion of SCD victims exhibited myocardial fibrosis (substantial: 19.6%, moderate: 53.8%).
- Only 15.4% of SCD subjects had severely reduced LVEF (≤35%).
- A weak correlation (Spearman's ρ 0.21) was found between myocardial fibrosis extent and LVEF.
Conclusions:
- The prevalence of myocardial fibrosis is high among SCD victims, while severely reduced LVEF is less common.
- Left ventricular ejection fraction demonstrates a weak correlation with the extent of myocardial fibrosis.
- LVEF is an unreliable surrogate for assessing myocardial fibrosis in individuals who have experienced SCD.
Aims:
Left ventricular ejection fraction (LVEF) remains the key determinant in the evaluation for the risk of sudden cardiac death (SCD). Myocardial fibrosis has gained increasingly more interest in the context of various myocardial diseases. We determined the spectrum of LVEF and evaluated the association between myocardial fibrosis and pre-SCD LVEF in a population-based SCD cohort.
Methods And Results:
The Fingesture study and clinical data have been collected from consecutive autopsy-verified SCD victims from Northern Finland between 1998 and 2017 (n = 5869). The cause of death was verified in medicolegal autopsy in all subjects. Electronic health records were used to identify those with pre-mortem echocardiography data. The extent of myocardial fibrosis at autopsy was characterized macroscopically and from histology samples. The LVEF recorded median 2 years (interquartile range 1-5) prior to SCD was evaluated in 716 SCD subjects. Proportional LVEF values were as follows: 62.7% (n = 449) normal LVEF (≥50%), 21.9% (n = 157) mildly reduced LVEF (36-49%), and 15.4% (n = 110) severely reduced LVEF (≤35%). At autopsy 19.6% (n = 140) had substantial, 53.8% (n = 386) moderate, and 22.1% (n = 158) mild fibrosis, and 4.5% (n = 32) had no myocardial fibrosis. The extent of myocardial fibrosis and LVEF had poor correlation (Spearman's ρ 0.21, CI 0.141-0.285, P < 0.001). Only 21.4% of those with substantial fibrosis at autopsy had LVEF ≤35%.
Conclusion:
The proportion of SCD subjects with LVEF ≤35% is low, and the prevalence of myocardial fibrosis is high. The LVEF has a weak correlation with the extent of myocardial fibrosis. Our study suggests that LVEF is a poor surrogate of myocardial fibrosis in SCD victims.
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