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Cumulative remnant cholesterol as a causal risk factor for ischemic heart disease: A prospective cohort study
Xuemei Zhao1, Yifei Wang1, Wei Li1
1Department of Cardiology, Tangshan Workers' Hospital, China; Hebei Medical University, China.
Insights
Elevated cumulative remnant cholesterol (cumRC) significantly increases the risk of ischemic heart disease (IHD). Monitoring and managing cumRC is crucial for preventing IHD events.
Area of Science:
- Cardiovascular Medicine
- Lipid Metabolism
- Epidemiology
Background:
- Baseline remnant cholesterol (RC) is linked to ischemic heart disease (IHD).
- The long-term impact of cumulative RC on incident IHD requires further investigation.
Purpose of the Study:
- To examine the association between cumulative remnant cholesterol (cumRC) and the risk of developing IHD.
Main Methods:
- Analysis of 42,639 participants from the Kailuan Study (2006-2010) excluding those with prior MI, coronary revascularization, or cancer.
- Cumulative RC (cumRC) calculated by average RC multiplied by assessment interval.
- Participants categorized into quartiles based on cumRC levels; IHD risk assessed using multivariable Cox proportional hazard models.
Main Results:
- Over 9.97 years, 1,205 IHD events occurred.
- IHD risk increased with higher cumRC quartiles (Q4 vs. Q1: HR 1.69 [1.42-2.01]).
- Elevated cumRC showed a consistent association with heightened IHD risk across analyses.
Conclusions:
- Higher cumulative remnant cholesterol is a significant predictor of increased ischemic heart disease risk.
- Regular monitoring and management of remnant cholesterol levels may be vital for IHD prevention strategies.
Background:
While previous studies have established a significant correlation between baseline remnant cholesterol (RC) and ischemic heart disease (IHD), the enduring impact of RC on incident IHD remains to be elucidated. This study aimed to investigate the association between cumulative remnant cholesterol(cumRC) and IHD susceptibility.
Methods:
Participating from the Kailuan Study (2006-2010) were enrolled, excluding those with prior myocardial infarction, coronary artery revascularization and cancer across three consecutive examinations. The cumRC derived by multiplying the average RC with the interval between the two consecutive assessments. Participants were segmented into quartiles based on cumRC levels: Q1 (cumRC < 2.69 mmol/l); Q2 (2.69 ≤ cumRC < 4.04 mmol/l); Q3(4.04 ≤ cumRC < 5.65 mmol/l) and Q4 (cumRC ≥ 5.65 mmol/l). The correlation between cumRC and IHD risk was ascertained by using multivariable Cox proportional hazard models.
Result:
The analysis encompassed 42,639 participants. Over an average tracking period of 9.97 years, 1,205 instances of IHD were identified. IHD susceptibility augmented with rising cumRC quartiles. After adjusting for potential confounders, the hazard ratios for IHD events were 1.06 (0.88-1.29) for Q2, 1.30 (1.08-1.56) for Q3 and 1.69 (1.42-2.01) for Q4, relative to Q1. Elevated cumRC was significantly associated with a heightened IHD risk, a trend consistent in both subgroup and sensitivity analyses.
Conclusion:
Elevated cumRC significantly correlates with a higher risk of IHD, suggesting that consistent monitoring and regulation of RC might be instrumental in IHD prevention.
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