circRNA basic information
circBase ID: hsa_circ_0001535
Name: hsa_circ_FAM13B
Synonym: circFAM13B
Host Gene: FAM13B
Genomic location(hg19): -
Genomic location(hg38): -
Subcellular localization: not tested
 
 
 
 
 
 
 
Disease basic information
MONDO ID:
0005542
MONDO name: acute coronary syndrome
Disease details: acute coronary syndrome / ACS
Disease DO ID:
-
Disease MeSH ID:
D054058
Disease NCIt ID:
C53652
Disease ICD11 ID:
-
Disease OMIM ID:
-
Species: Human
Species details: Homo sapiens
Tissue specimen:

platelets

Cell lines:

-

In vivo animal model:

-

circRNA-disease information
Expression pattern:
DS
Associated gene: P2Y12 receptor
Associated microRNA: miR-126
Biological function: Associated with ticagrelor antiplatelet responsiveness and predicts adverse ischemic events in ticagrelor-treated ACS patients.
Molecular mechanism: Not investigated; bioinformatics prediction suggested potential binding sites on miR-126 and a hypothesized effect on P2Y12 receptor expression.
Biological pathway or process:

drug response (other); ceRNA regulation (other)

Detected method:
Q
Validation methods:

RT-qPCR; Clinical Sample Validation; Cohort Study; Survival Analysis; ROC Analysis

Clinical significance:

High circFAM13B expression (> 1.05) predicts a higher risk of adverse ischemic events and improves prediction when combined with clinical risk factors.

Description:

In ticagrelor-treated ACS patients, platelet-derived circFAM13B level is associated with antiplatelet responsiveness (HTPR) and independently predicts adverse ischemic events during follow-up. A miR-126/P2Y12-related mechanism is proposed only by bioinformatics prediction and hypothesis, without experimental validation.

Confidence score:

0.4992

Other information
Title:

Platelet-derived circFAM13B associated with anti-platelet responsiveness of ticagrelor in patients with acute coronary syndrome.

Journal: Thrombosis journal
Published: 2024
PubMed ID: 38907258
Study type:

clinical study

Data availability: The data used to support the findings of this study are available from the corresponding author (yintong301@163.com) upon request.
Code availability: -