Left ventricular remodeling in hypertrophic cardiomyopathy patients with atrial fibrillation

Hongwei Tian1, Jingang Cui1, Chengzhi Yang1

  • 1State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.

Insights

Left ventricular remodeling and larger left atrial size are significant predictors of atrial fibrillation (AF) in hypertrophic cardiomyopathy (HCM) patients. These findings suggest that left ventricular remodeling contributes to AF development in HCM.

Area of Science:

  • Cardiology
  • Cardiovascular Imaging
  • Electrophysiology

Background:

  • Atrial fibrillation (AF) is a common complication in hypertrophic cardiomyopathy (HCM).
  • Left atrial (LA) structural remodeling is linked to AF in HCM.
  • The role of left ventricular (LV) remodeling in AF presence within HCM patients remains under-evaluated.

Purpose of the Study:

  • To investigate the effect of LV remodeling on AF presence in HCM patients.
  • To assess LV remodeling using cardiovascular magnetic resonance (CMR).

Main Methods:

  • 394 HCM patients (293 HOCM, 101 NOHCM) were analyzed.
  • Patients were categorized into HCM with AF (n=50) and HCM without AF (n=344).
  • Data collected from hospital records; LV remodeling index (LVRI) and LA diameter assessed via CMR.

Main Results:

  • HCM patients with AF had significantly larger LA diameter and higher LVRI compared to those without AF.
  • LVRI positively correlated with LA size.
  • LVRI and LA size were independent determinants of AF in HCM, even after adjusting for age and LV end-diastolic mass index.

Conclusions:

  • HCM patients with AF exhibit increased LA diameter, LVRI, and age.
  • LV remodeling and LA size are strong, independent predictors of AF in HCM.
  • LV remodeling may play a contributing role in the development of AF in HCM patients.
Abstract

Related Concept Videos

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...
490
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...
555
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
Nucleosome Remodeling02:54

Nucleosome Remodeling

Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
11.2K
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,...
568