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The association between IL-17A and IL-23R polymorphisms and coronary artery disease risk in a Middle Eastern Chinese
Qiang Zhao1,2, Huaxin Jiang3, Teng Ma2
1Department of Cardiology, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, China.
Insights
Genetic variations in IL-17A and IL-23R are linked to coronary artery disease (CAD) risk. This study found specific polymorphisms in IL-17A (rs2275913) and IL-23R (rs6682925) associated with increased CAD susceptibility.
Area of Science:
- Genetics
- Cardiovascular Medicine
- Immunology
Background:
- Interleukin-17A (IL-17A) and Interleukin-23 Receptor (IL-23R) gene polymorphisms may influence gene expression and susceptibility to coronary artery disease (CAD).
- Previous research on the association between IL-17A/IL-23R polymorphisms and CAD risk has yielded inconclusive results.
Purpose of the Study:
- To investigate the association between specific polymorphisms in the IL-17A and IL-23R genes and the risk of developing coronary artery disease (CAD).
Main Methods:
- A hospital-based case-control study involving 191 CAD patients and 131 controls.
- Genotyping of IL-17A rs2275913 and IL-23R rs6682925 polymorphisms was performed using the Sequenom MassARRAY platform.
- Patient and control groups were assessed using SXscore, and biochemical parameters like FPG, HbA1C, HDL, ApoA1, and Lp(a) were analyzed.
Main Results:
- Patients with CAD exhibited higher FPG and HbA1C levels, and lower HDL and ApoA1 levels compared to controls. Lp(a) levels were significantly lower in controls than in cases.
- The IL-17A rs2275913 (AA vs GG: OR=2.16; AG/AA vs GG: OR=1.81) and IL-23R rs6682925 (CC vs TT: OR=1.91) polymorphisms were associated with an increased risk of CAD.
- Subgroup analysis indicated that the IL-23R rs6682925 polymorphism was significantly associated with increased CAD risk in patients with a high SXscore (CT/CC vs TT: OR=3.72).
Conclusions:
- Type 2 Diabetes Mellitus (T2DM), elevated Lp(a), and reduced HDL-c and ApoA1 are identified as risk factors for CAD.
- The IL-17A rs2275913 and IL-23R rs6682925 polymorphisms may play a role in the susceptibility to developing coronary artery disease.
Background:
Polymorphisms in IL-17A and IL-23R may affect the expression of these genes and could contribute to a patient's susceptibility to coronary artery disease (CAD). Although this association was investigated by previous studies, the relationship remains unclear.
Method:
We conducted this hospital-based case-control study to determine whether polymorphisms in these two genes could be associated with a risk of CAD. A total of 191 patients and 131 controls, as determined by SXscore, were enrolled in this study. The genotyping was performed with the Sequenom MassARRAY platform.
Results:
The results showed that that the FPG and HbA1C levels were higher in patients with CAD than in the controls. In addition, the HDL and ApoA1 levels were significantly higher in the controls than in the cases. In contrast, the Lp(a) level was significantly lower in the controls than in the patients. The IL-17A rs2275913 and IL-23R rs6682925 polymorphisms were associated with an increased risk of CAD (rs2275913: AA vs GG: crude OR = 2.16, 95% CI = 1.08-4.30; AG/AA vs GG: crude OR = 1.81, 95% CI = 1.04-3.15; rs6682925 CC vs TT: crude OR = 1.91, 95% CI = 1.00-3.63). The subgroup analysis by SXscore revealed that the IL-23R rs6682925 polymorphism (CT/CC vs TT: crude OR = 3.72, 95% CI = 1.19-11.66) was associated with an increased risk of CAD in patients with a high SXscore.
Conclusion:
This study suggested that T2DM, Lp(a), HDL-c, and ApoA1 were risk factors of CAD and that the IL-17A rs2275913 and IL-23R rs6682925 polymorphisms may contribute to susceptibility to CAD.
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