Circulating Long Non-coding RNA ENST00000507296 Is a Prognostic Indicator in Patients with Dilated Cardiomyopathy

Xudong Zhang1, Xiang Nie1, Shuai Yuan1

  • 1Division of Cardiology, Department of Internal Medicine, Tongji Hospital, Tongji Medical College and Hubei Key Laboratory of Genetics and Molecular Mechanisms of Cardiologic Disorders, Huazhong University of Science and Technology, Wuhan, China.

Insights

Circulating long non-coding RNA ENST00000507296 shows promise as a prognostic biomarker for dilated cardiomyopathy (DCM). Lower levels of this biomarker correlate with improved event-free survival in DCM patients, aiding in disease management.

Area of Science:

  • Cardiovascular Research
  • Molecular Biology
  • Biomarker Discovery

Background:

  • Long non-coding RNAs (lncRNAs) are implicated in cardiovascular disease pathogenesis.
  • The utility of circulating lncRNAs as biomarkers for dilated cardiomyopathy (DCM) remains largely unexplored.

Purpose of the Study:

  • To investigate the potential of circulating lncRNAs as diagnostic and prognostic biomarkers for DCM.
  • To identify specific lncRNAs associated with DCM and its severity.

Main Methods:

  • Microarray profiling and real-time qPCR were used to screen and validate lncRNAs in controls and DCM patients.
  • lncRNA sequencing in heart-derived cells explored potential origins.
  • Receiver-operating characteristic (ROC) curve analysis assessed diagnostic accuracy.
  • Cox regression and Kaplan-Meier analyses evaluated prognostic value.

Main Results:

  • Eight candidate lncRNA biomarkers were identified, with five validated in a second cohort.
  • Circulating lncRNA ENST00000507296 levels correlated significantly with cardiac function.
  • Lower levels of ENST00000507296 were associated with higher event-free survival in DCM patients.

Conclusions:

  • Circulating lncRNA ENST00000507296 serves as a valuable prognostic biomarker for patients with DCM.
  • This finding supports the potential use of ENST00000507296 in monitoring DCM progression and patient outcomes.
Abstract

Related Concept Videos

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,...
548
Indicators02:39

Indicators

Certain organic substances change color in dilute solution when the hydronium ion concentration reaches a particular value. For example, phenolphthalein is a colorless substance in any aqueous solution with a hydronium ion concentration greater than 5.0 × 10−9 M (pH < 8.3). In more basic solutions where the hydronium ion concentration is less than 5.0 × 10−9 M (pH > 8.3), it is red or pink. Substances such as phenolphthalein, which can be used to determine the pH of a solution, are...
60.4K
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
9.9K
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

3.6K
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...
465
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...
512