Left atrial cardiomyopathy: association with atrial fibrillation and stroke recurrence

Laura B H Friderichsen1, Bjørn S Larsen2,3, Mark Aplin3

  • 1Faculty of Health and Medical Sciences, Department of Biomedical Sciences, University of Copenhagen, SUND, BMI, Blegdamsvej 3B, 2200 København N, Copenhagen, Denmark. Laura.friderichsen@sund.ku.dk.

Insights

Reduced left atrial emptying fraction (LAEF) and enlarged left atrium are linked to recurrent stroke or new atrial fibrillation (AF). LA fibrosis was not associated with these outcomes in stroke patients. Further research is needed on LAEF as a modifiable risk factor.

Area of Science:

  • Cardiology
  • Neurology
  • Medical Imaging

Background:

  • Left atrial (LA) dysfunction is implicated in stroke pathogenesis.
  • Understanding LA structural and functional markers may predict adverse cardiovascular events.
  • Atrial fibrillation (AF) is a common complication and cause of stroke.

Purpose of the Study:

  • To investigate the association between LA dysfunction markers and stroke recurrence or new-onset AF.
  • To differentiate the predictive value of LA emptying fraction (LAEF), LA volumes, and LA fibrosis.
  • To analyze these associations in patients with stroke of undetermined etiology or large/small-vessel disease.

Main Methods:

  • Cardiac magnetic resonance imaging (MRI) with late gadolinium enhancement was used.
  • LA Emptying Fraction (LAEF), LA volumes, and LA fibrosis were quantified.
  • 91 patients with recent stroke (<30 days) and no known AF were followed.

Main Results:

  • A lower LAEF was significantly associated with an increased risk of stroke recurrence or new-onset AF (HR 1.41 per 5% decrease).
  • LA enlargement (increased LA volumes) also predicted the primary endpoint (HR 1.98 per 5 ml/m2 increase).
  • LA fibrosis showed no significant association with the combined endpoint or its components.

Conclusions:

  • LAEF and LA enlargement are significant predictors of recurrent stroke or new-onset AF in stroke patients.
  • LA fibrosis is not associated with these adverse outcomes in this cohort.
  • LAEF may represent a modifiable risk factor for reducing stroke recurrence and new AF onset.
Abstract

Related Concept Videos

Amyloid Fibrils03:03

Amyloid Fibrils

Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
Amyloid deposits were observed as early as 1639 in the liver and the spleen.   In 1854, Rudolph Virchow performed iodine staining,...
11.9K
Amyloid Fibrils03:03

Amyloid Fibrils

6.4K
ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias01:25

ECG Interpretation of Arrhythmias II: Atrial, Junctional and Ventricular Arrhythmias

Arrhythmia is a condition characterized by an irregular heart rhythm, with ECG changes that differ based on its origin and nature. The types of arrhythmias discussed below include atrial, junctional, and ventricular arrhythmias.Atrial ArrhythmiasPremature Atrial Complexes (PACs): PACs are early atrial beats caused by stress, caffeine, alcohol, electrolyte imbalances, hypoxia, hyperthyroidism, or certain medications (e.g., bronchodilators and decongestants). The ECG shows early P waves with an...
533
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
549
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
467
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
519