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Published on: January 28, 2020
Atherogenic index as an associative marker for coronary artery disease
Basavaraj Utagi1, Dilip Johny2, Aditya Ojha3
1Department of Cardiology, Fortis Hospital, Cunningham Road, Bengaluru, Karnataka, India.
Insights
The atherogenic index of plasma (AIP) is a valuable, low-cost biomarker for assessing coronary artery disease (CAD) risk. AIP demonstrated superior diagnostic performance compared to other common biomarkers in patients with suspected CAD.
Area of Science:
- Cardiology
- Biomarkers
- Risk Stratification
Background:
- Coronary artery disease (CAD) presents a significant global health challenge.
- Effective risk stratification requires pragmatic, low-cost biomarkers.
- The atherogenic index of plasma (AIP), log(TG/HDL-C), is a lipid-derived indicator of cardiometabolic risk.
Purpose of the Study:
- To evaluate AIP as an associative marker for CAD.
- To compare the diagnostic performance of AIP with other commonly used biomarkers.
Main Methods:
- A case-control study involving 340 participants (211 cases, 129 controls) with angiography-confirmed CAD.
- Assessed AIP, uric acid, creatinine, neutrophil-to-lymphocyte ratio (NLR), TG/HDL-C, HbA1c, and ejection fraction.
- Used multivariable logistic regression and receiver operating characteristic (ROC) analysis for association and discrimination evaluation.
Main Results:
- AIP, uric acid, and creatinine were independently associated with CAD.
- AIP showed superior discriminatory ability compared to uric acid, creatinine, NLR, and HbA1c in ROC analysis.
- AIP values correlated with increased angiographic severity.
Conclusions:
- Readily available AIP provides incremental prognostic value in symptomatic patients with suspected CAD.
- Findings are hypothesis-generating and require validation in prospective, multicenter studies.
Background:
Coronary artery disease (CAD) is a significant global health burden, warranting pragmatic, low-cost biomarkers for effective risk stratification. The atherogenic index of plasma (AIP), calculated as log(TG/HDL-C), is a lipid-derived indicator of cardiometabolic risk. We evaluated AIP as an associative marker for CAD and compared its diagnostic performance with commonly used biomarkers.
Methods:
In a hospital-based, angiography-confirmed case-control cohort (n = 340; 211 cases, 129 controls), we assessed AIP alongside uric acid, creatinine, neutrophil-to-lymphocyte ratio (NLR), TG/HDL‑C, HbA1c, and ejection fraction. Group characteristics were summarized using descriptive statistics, chi-square tests, and ANOVA. Associations with CAD were examined using multivariable logistic regression adjusted for age, sex, body mass index, diabetes, hypertension, smoking status, and statin use. Discriminative performance was evaluated via receiver operating characteristic (ROC) analysis, with pairwise comparisons conducted using DeLong's test.
Results:
Values of AIP (OR 1.42, 95% CI 1.18-1.69; p = 0.012), uric acid (OR 1.20, 95% CI 1.02-1.42; p = 0.032), and creatinine (OR 1.69, 95% CI 1.03-2.76; p = 0.038) were independently associated with CAD. HbA1c, TG/HDL‑C, NLR, and ejection fraction were not significantly associated in multivariable models. Values of AIP increased with greater angiographic severity. In ROC analysis, AIP showed superior discriminatory ability to uric acid, creatinine, NLR, and HbA1c (all p < 0.05, DeLong test), and performed comparably to TG/HDL‑C, consistent with AIP being its log transformation.
Conclusion:
Readily available AIP offers incremental prognostic value in symptomatic patients with suspected CAD. These findings are hypothesis-generating; thus, thresholds should be interpreted cautiously pending prospective, multicenter studies.
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