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Published on: August 9, 2024
Circulating lncRNA IFNG-AS1 expression correlates with increased disease risk, higher disease severity and elevated
1Department of Cardiothoracic Surgery, Huangshi Central Hospital, Edong Healthcare Group, Affiliated Hospital of Hubei Polytechnic University, Huangshi, China.
Insights
Long, non-coding RNA IFNG-AS1 is upregulated in coronary artery disease (CAD) patients, correlating with disease risk, severity, and inflammation. Other tested lncRNAs showed no significant associations.
Area of Science:
- Biochemistry
- Molecular Biology
- Cardiovascular Research
Background:
- Coronary artery disease (CAD) poses a significant global health burden.
- Understanding the molecular mechanisms underlying CAD is crucial for developing effective diagnostic and therapeutic strategies.
- Long non-coding RNAs (lncRNAs) are emerging as key regulators in various diseases, including cardiovascular conditions.
Purpose of the Study:
- To investigate the association of circulating long, non-coding RNA (lncRNA) IFNG-AS1, lncRNA ANRIL, and lncRNA ITSN1 expressions with disease risk, severity, and inflammatory cytokine levels in coronary artery disease (CAD) patients.
- To determine the potential of these lncRNAs as biomarkers for CAD.
Main Methods:
- A case-control study involving 191 participants (102 CAD patients, 89 controls) undergoing coronary angiography.
- Quantitative polymerase chain reaction (qPCR) was used to measure plasma lncRNA IFNG-AS1, lncRNA ANRIL, and lncRNA ITSN1 expressions.
- Serum levels of inflammatory cytokines (TNF-α, IL-1β, IL-6, IL-8, IL-10, IL-17) were assessed using ELISA, and Gensini Score evaluated CAD severity.
Main Results:
- Circulating lncRNA IFNG-AS1 was significantly upregulated in CAD patients compared to controls (P < .001).
- lncRNA IFNG-AS1 expression showed a strong predictive value for CAD risk (AUC = 0.755) and was positively correlated with disease severity (Gensini Score, P = .009).
- lncRNA IFNG-AS1 levels were positively associated with inflammatory markers (hs-CRP, TNF-α, IL-6) and negatively with IL-10, while lncRNA ANRIL and lncRNA ITSN1 showed no significant correlations.
Conclusions:
- Circulating lncRNA IFNG-AS1 expression is a potential biomarker for increased risk and severity of coronary artery disease.
- Elevated lncRNA IFNG-AS1 levels are associated with heightened systemic inflammation in CAD patients.
- lncRNA ANRIL and lncRNA ITSN1 do not appear to be significantly associated with CAD risk or severity in this cohort.
Background:
This study aimed to investigate the associations of circulating long, non-coding (lncRNA) IFNG-AS1, lncRNA ANRIL and lncRNA ITSN1 relative expressions with disease risk, severity and inflammatory cytokines levels in coronary artery disease (CAD) patients.
Methods:
One hundred and ninety-one patients suspected of CAD who underwent coronary angiography were consecutively enrolled in this casecontrol study, and divided into CAD patients (N = 102) and controls (N = 89) according to coronary angiographic results. Blood samples of all participants were collected. Plasma lncRNA IFNG-AS1, lncRNA ANRIL and lncRNA ITSN1 expressions were detected using quantitative polymerase chain reaction (qPCR). Serum tumor necrosis factor-α (TNF-α), interleukin (IL)-1β (IL-1β), IL-6, IL-8, IL-10, and IL-17 were assessed using enzyme-linked immunosorbent assay (ELISA). Gensini Score was used to evaluate the disease severity of CAD patients.
Results:
LncRNA IFNG-AS1 relative expression in CAD patients was upregulated compared with that in controls (P < .001), and the receiver operating characteristic (ROC) curve showed that the area under curve (AUC) of lncRNA-IFNG-AS1 for predicting the risk of CAD was 0.755 (95% CI: 0.688-0.821). lncRNA IFNG-AS1 relative expression was remarkably associated with Gensini Score (r = .259, P = .009). Additionally, lncRNA IFNG-AS1 relative expression was positively associated with high-sensitivity C-reactive protein (hs-CRP) (r = .283, P = .004), TNF-α (r = .269, P = .006), and IL-6 levels (r = .425, P < .001), while it was negatively correlated with IL-10 level (r = -.263, P = .008). lncRNA ANRIL or lncRNA ITSN1 was not correlated with CA D risk, Gensini Score, hs-CRP, ESR, TNF-α, IL-1β, IL-6, IL-8, IL-10, or IL-17 levels (all P > .05).
Conclusion:
Circulating lncRNA IFNG-AS1 expression correlates with increased disease risk, higher disease severity and elevated inflammation in CAD patients.
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