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The clinical role of combined circulating complement C1q and AIP for CAD with LDL-C level below 1.8mmol/L
Chenyujun Hu1, Zehao Zhao1, Shutong Dong1
1Department of Cardiology, Beijing Anzhen Hospital, Beijing Institute of Heart Lung and Blood Vessel Disease, Beijing Key Laboratory of Precision Medicine of Coronary Atherosclerotic Disease, Clinical center for coronary heart disease, Capital Medical University, Capital Medical University, Beijing, 100029, China.
Insights
Higher circulating complement C1q levels and the atherogenic index of plasma (AIP) are positively correlated with coronary artery disease (CAD) risk, even in patients with low LDL-C. This suggests a combined marker for cardiovascular disease.
Area of Science:
- Cardiovascular Research
- Immunology
- Lipid Metabolism
Background:
- Circulating complement C1q is increasingly recognized for its role in atherosclerosis.
- The atherogenic index of plasma (AIP) is an emerging lipid marker.
- The combined role of C1q and AIP in coronary artery disease (CAD), especially in patients with low LDL-C, remains unclear.
Purpose of the Study:
- To investigate the interplay between C1q and AIP in relation to CAD.
- To evaluate the combined predictive value of C1q and AIP for CAD risk.
Main Methods:
- Stratified 7270 patients into non-CAD and CAD groups based on coronary angiography.
- Employed restricted cubic spline and logistic regression analyses to assess the association between C1q, AIP, and CAD.
- Utilized receiver operating characteristic analysis for predictive assessment.
Main Results:
- Patients with CAD exhibited higher C1q levels and an inverse trend in AIP compared to the non-CAD group.
- A significant negative correlation was found between C1q and AIP.
- Logistic regression revealed significant associations between CAD and C1q/AIP; lower C1q levels correlated with increased CAD risk (OR 1.661-2.314).
Conclusions:
- A notable positive correlation exists between the combination of C1q and AIP and CAD.
- The findings suggest C1q and AIP may serve as combined biomarkers for cardiovascular risk assessment.
Background:
In the past few years, circulating complement C1q involvement in atherosclerosis has garnered growing research interest in addition to the emerging recognition of the novel lipid marker named atherogenic index of plasma (AIP). Nevertheless, among patients experiencing low-density lipoprotein cholesterol (LDL-C) levels less than 1.8mmol/L, the interplay between C1q combined with the AIP for coronary artery disease (CAD) is ambiguous.
Methods:
Patients were stratified into a non-CAD and CAD group according to their coronary angiography. The association between C1q in conjunction with the AIP and CAD was explored using restricted cubic spline analyses and logistic regression models. To assess how it predicted, a receiver operating characteristic analysis was undertaken.
Results:
A total of 7270 patients comprised 1476 non-CAD patients and 5794 patients diagnosed with CAD were analyzed. A comparison of the two groups showed that the C1q levels were notably higher compared to the CAD group, while AIP exhibited an inverse trend. Across quartiles of C1q, the AIP demonstrated a decline with increasing C1q levels, and significant differences were observed between the groups. A correlation analysis underscored a notable negative correlation between the two variables. Univariate and multivariate logistic regression analyses revealed significant associations between CAD and the C1q quartile groups/AIP. Furthermore, compared with the Q4 group, a decrease in the C1q levels corresponded to an escalation in CAD risk, with the odds ratio rising from 1.661 to 2.314.
Conclusions:
In conclusion, there appears to be a notable positive correlation between the combination of C1q with the AIP and CAD.
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