Related Experiment Video
Updated: Apr 28, 2026

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
Association between PON1 rs662 polymorphism and coronary artery disease
1Cardiovascular Research Institute and Department of Cardiology, Shenyang Northern Hospital, Shenyang, China.
Low paraoxonase 1 (PON1) expression in coronary arteries is linked to coronary artery disease (CAD). The PON1 Q192R polymorphism, particularly the 192R allele, is a significant risk factor for CAD in the Chinese Han population.
Area of Science:
- Cardiovascular Research
- Biochemistry
- Genetics
Background:
- Paraoxonase 1 (PON1) is a plasma enzyme that plays a role in inhibiting atherosclerosis.
- PON1 expression is found in human aortic tissue and influences atherosclerosis progression.
- PON1 is associated with susceptibility to coronary artery disease (CAD).
Purpose of the Study:
- To investigate PON1 immunohistochemistry in human coronary arteries.
- To determine PON1 polymorphisms and plasma status.
- To analyze the association between PON1 and CAD risk.
Main Methods:
- Immunohistochemical staining detected PON1 expression in coronary artery tissues.
- Polymerase chain reaction direct sequencing identified PON1 polymorphisms in 2456 Chinese Han individuals.
- Serum PON1 activity and concentrations were measured using spectrophotometry and ELISA.
Main Results:
- PON1 expression was lower in atherosclerotic arteries compared to normal arteries.
- The PON1 Q192R polymorphism significantly affected CAD risk (P=0.001).
- Carriers of the 192R allele had a higher risk of CAD, and serum PON1 levels were reduced in CAD patients.
Conclusions:
- Reduced PON1 expression in atherosclerotic coronary arteries is associated with CAD.
- The PON1 Q192R polymorphism is significantly linked to CAD susceptibility in the Chinese Han population.
- The 192R allele may serve as an independent predictor for CAD.
Related Concept Videos
Coronary Artery Disease II: Pathophysiology
Single Nucleotide Polymorphisms-SNPs
Coronary Artery Disease I: Introduction
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Pharmacogenetics of Drug Transporters: P-Glycoprotein and Solute Carrier Transporters
Coronary Artery Disease III: Clinical Manifestations

