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Association Between Atherogenic Index of Plasma and Risk of Cardiovascular Disease: A Dose-Response Meta-Analysis of
Taifeng Chen1, Jinliang Liang1, Yaqin Su1
1Department of Biostatistics and Epidemiology, School of Public Health, Shenzhen University Medical School, Shenzhen, China.
Insights
Elevated atherogenic index of plasma (AIP) is linked to increased cardiovascular disease (CVD) morbidity and mortality. This association shows a dose-response relationship, indicating AIP
Area of Science:
- Cardiovascular Medicine
- Biomarkers
- Epidemiology
Background:
- The atherogenic index of plasma (AIP) is a lipid parameter.
- Cardiovascular disease (CVD) remains a leading cause of mortality worldwide.
- Understanding predictive markers for CVD is crucial for public health.
Purpose of the Study:
- To systematically evaluate the correlation between AIP and CVD morbidity and mortality.
- To investigate the potential dose-response relationship between AIP levels and CVD outcomes.
Main Methods:
- A comprehensive literature search was conducted across major databases (PubMed, Embase, Web of Science, CNKI, WanFang, VIP) until January 2026.
- Included studies were cohort studies analyzing AIP and CVD incidence or death.
- Pooled relative risks (RRs) and 95% confidence intervals (CIs) were calculated, with restricted cubic splines used to assess dose-response relationships.
Main Results:
- Analysis of 24 studies revealed significantly higher CVD morbidity (RR=1.35) and mortality (RR=1.49) in the highest AIP groups.
- A per-unit increase in AIP was associated with a 47% increase in CVD morbidity (RR=1.47) and a 42% increase in CVD mortality (RR=1.42).
- Linear dose-response relationships were observed between AIP and both CVD morbidity (p=0.659) and mortality (p=0.619).
Conclusions:
- Elevated AIP is correlated with increased CVD morbidity and mortality.
- A significant dose-response relationship exists, suggesting AIP as a potential predictor for CVD.
- These findings support AIP's role in early clinical identification and intervention for high-risk populations.
Objective:
To systematically evaluate the correlations between atherogenic index of plasma (AIP) and the morbidity and mortality of cardiovascular disease (CVD) and investigate the potential dose-response relationship.
Methods:
We comprehensively searched the PubMed, Embase, and Web of Science Core Collection, CNKI, WanFang, and VIP for relevant literature until January 31, 2026. The included studies were cohort studies. The pooled relative risk (RR) and 95% confidence interval (CI) for dose-response relationships were calculated. The linear/nonlinear relationships were evaluated by using restricted cubic splines.
Results:
A total of 24 studies were included for the analysis. The pooled RRs for CVD morbidity and mortality in the highest versus lowest AIP group were 1.35 (95% CI: 1.25 to 1.45) and 1.49 (95% CI: 1.19 to 1.87), respectively. For per 1-unit increase in AIP, the risk of CVD morbidity and mortality increased by 47% (RR = 1.47, 95% CI: 1.32 to 1.64) and 42% (RR = 1.42, 95% CI: 1.18 to 1.71), respectively. Dose-response results showed linear associations between AIP and CVD morbidity (pnon-linearity = 0.659), as well as between AIP and CVD mortality (pnon-linearity = 0.619).
Conclusion:
This dose-response meta-analysis revealed a correlation between elevated AIP and the morbidity and mortality of CVD. The association has a dose-response profile between AIP and CVD morbidity, suggesting that AIP may serve as a potential predictor of CVD and provide an important basis for early clinical identification and intervention in populations at high risk of CVD.
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