Related Experiment Video
Updated: May 29, 2026

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
Reduced plasma APJ levels and APLNR G212A polymorphism in Syrian patients with coronary artery disease
Maisaa Hassan Abd-Alkareem1, Hussam Eddin Mohammed Shibli2, Faizeh Ali Alquobaili1
1Department of Biochemistry and Microbiology, Faculty of Pharmacy, Damascus University, Damascus, Syrian Arab Republic.
Insights
Reduced plasma APJ levels were found in Syrian coronary artery disease (CAD) patients, suggesting a weakened protective role for the apelin/APJ system. The apelin receptor G212A polymorphism showed no significant association with CAD risk in this population.
Area of Science:
- Cardiovascular Research
- Genetics
- Biomarkers
Background:
- Coronary artery disease (CAD) is a major global health concern.
- The apelin/apelin receptor (APJ) system plays a role in cardiovascular regulation.
- This study is the first in a Syrian population to examine the apelin/APJ system in relation to CAD.
Purpose of the Study:
- To investigate the association of the apelin receptor G212A polymorphism with CAD susceptibility.
- To assess plasma apelin receptor (APJ) levels in Syrian CAD patients and controls.
- To explore the role of the apelin/APJ system in the pathophysiology of CAD.
Main Methods:
- Case-control study involving 108 CAD patients and 114 healthy controls.
- Plasma APJ levels measured using enzyme-linked immunosorbent assay (ELISA).
- Apelin receptor G212A genotype and allele frequencies determined by PCR-restriction fragment length polymorphism (PCR-RFLP).
Main Results:
- Plasma APJ levels were significantly lower in CAD patients compared to controls (p < 0.005).
- Lower plasma APJ levels were independently associated with CAD and hypertension.
- No statistically significant association was found between the apelin receptor G212A polymorphism and CAD risk (p > 0.05).
Conclusions:
- Significantly reduced plasma APJ levels in Syrian CAD patients suggest a diminished protective role of the apelin/APJ system.
- The apelin receptor G212A polymorphism was not significantly associated with CAD risk in this cohort.
- Plasma APJ may serve as a potential biomarker for CAD, emphasizing the need for population-specific genetic studies.
Background:
Coronary artery disease (CAD) remains a leading global cause of mortality. The apelin/apelin receptor (APJ) system has emerged as a novel pathway implicated in cardiovascular regulation and disease progression. This pioneering case-control study, the first conducted in a Syrian population, investigated the association of the apelin receptor G212A polymorphism and plasma APJ levels with CAD susceptibility.
Methods:
The participants comprised 108 CAD patients confirmed by angiography and 114 healthy controls. Plasma APJ levels were quantified via enzyme-linked immunosorbent assay (ELISA), and the apelin receptor G212A genotype and allele frequencies were determined using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The study was registered on ClinicalTrials.gov (Identifier: NCT05562687).
Results:
Plasma APJ levels were significantly lower in CAD patients compared to controls (p < 0.005). Multivariable regression analysis further revealed that plasma APJ levels were independently associated with CAD and hypertension. While the heterozygous GA genotype and the A allele showed higher frequencies in CAD patients, no statistically significant association of the G212A polymorphism was observed between the patient and control groups (p > 0.05). Notably, the homozygous mutant AA genotype was not detected in any study participant.
Conclusion:
Our findings indicate significantly reduced plasma APJ levels in Syrian CAD patients, suggesting a diminished protective role of the apelin/APJ system in disease pathophysiology. Despite observed trends, the apelin receptor G212A polymorphism was not significantly associated with CAD risk in this specific cohort. This highlights the potential of plasma APJ as a biomarker and underscores the importance of population-specific genetic studies.
Related Concept Videos
Pharmacogenetics of Drug Targets: β₂-Adrenergic Receptors, Apo E, Thymidylate Synthase
Pharmacogenomics: Identification of New Drug Targets
Acute Coronary Syndrome III: Diagnostic Studies
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Coronary Artery Disease II: Pathophysiology
Acute Coronary Syndrome II: Pathophysiology and Clinical Manifestations