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Association Between Serum Atherogenic Index and Cardiovascular Disease in Early Adulthood: A Cohort Study
Mianwang He1, Nana Yin2, Chi Wang3
1Department of Neurology, Chinese PLA General hospital, Chinese PLA Medical School, Beijing, China.
Insights
Higher atherogenic index of plasma (AIP) is linked to increased cardiovascular disease (CVD) and stroke risk in young adults. AIP can help identify individuals at higher risk for early cardiovascular events.
Area of Science:
- Cardiology
- Preventive Medicine
- Biomarkers
Background:
- The atherogenic index of plasma (AIP) is a novel marker for atherogenic risk.
- Its association with cardiovascular disease (CVD) and mortality in young adults is not well-established.
Purpose of the Study:
- To determine if AIP independently predicts CVD (including stroke) and all-cause mortality in young adults.
- To assess AIP's utility in early cardiovascular risk stratification.
Main Methods:
- Analysis of 64,416 participants aged 18-44 without prior CVD from the Kailuan Study (2006-2016).
- AIP calculated at baseline, with participants stratified into quartiles.
- Multivariable Cox models used to estimate hazard ratios (HRs) for CVD, stroke, and all-cause mortality, adjusted for multiple risk factors.
Main Results:
- Over a mean follow-up of 14.65 years, higher AIP quartiles (Q2-Q4) were associated with increased risk of CVD and stroke compared to the lowest quartile (Q1).
- HRs for CVD ranged from 1.16 to 1.36, and for stroke from 1.14 to 1.26.
- No significant association was found between AIP and all-cause mortality after adjustment.
Conclusions:
- Elevated AIP is an independent predictor of increased CVD and stroke risk in young adults.
- AIP shows potential as a valuable biomarker for early cardiovascular risk assessment in this demographic.
Background:
The atherogenic index of plasma (AIP), calculated as log(triglycerides/high-density lipoprotein cholesterol), is a novel marker of atherogenic risk, but its association with cardiovascular disease (CVD) and mortality in early adulthood remains unclear.
Objectives:
This study aimed to investigate whether AIP independently predicts the risk of CVD (including stroke) and all-cause mortality in young adults.
Methods:
We analyzed 64,416 participants aged 18-44 years without prior CVD from the Kailuan Study (2006-2016). AIP was calculated at baseline, and participants were categorized into quartiles. The primary outcomes were incident CVD, stroke, and all-cause mortality, ascertained through December 2023. Multivariable Cox models adjusted for traditional risk factors, lipids, renal function, and medication use were used to estimate HRs.
Results:
Over a mean follow-up of 14.65 years (Q1-Q3: 10.60-16.90 years), 1,853 CVD events, 1,571 stroke events, and 1,332 cases of all-cause mortality occurred. After full adjustment, compared with the lowest AIP quartile (Q1), the HRs for CVD in Q2-Q4 were 1.16 (95% CI: 0.99-1.36), 1.29 (95% CI: 1.11-1.50), and 1.36 (95% CI: 1.17-1.59), respectively. Corresponding HRs for stroke were 1.14 (95% CI: 0.97-1.35), 1.21 (95% CI: 1.03-1.43), and 1.26 (95% CI: 1.07-1.49). No significant association was found between AIP and all-cause mortality after multivariable adjustment. Sensitivity and competing risk analyses supported the robustness of these findings.
Conclusions:
Higher AIP is independently associated with increased risks of CVD and stroke in young adults. AIP may serve as a useful biomarker for early cardiovascular risk stratification in this population.
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