Time-Weighted Cumulative High-Sensitivity C-Reactive Protein and Risk of Cardiac Conduction Block: Findings from a
Mo Zhang1,2, Dou Shi1, Yixiu Chen2,3
1Graduate School, Hebei North University, Zhangjiakou City, Hebei Province, 075000, People's Republic of China.
Insights
Elevated cumulative exposure to high-sensitivity C-reactive protein (cumhsCRP) significantly increases the risk of cardiac conduction block (CCB). This finding highlights inflammation
Area of Science:
- Cardiology
- Inflammation Research
- Preventive Medicine
Background:
- Chronic low-grade inflammation is a known risk factor for cardiovascular events.
- High-sensitivity C-reactive protein (hsCRP) is a key biomarker of inflammation.
Purpose of the Study:
- To investigate the association between cumulative hsCRP exposure and new-onset cardiac conduction block (CCB).
- To evaluate the dose-response relationship between time-weighted cumulative hsCRP and CCB risk.
Main Methods:
- Prospective community-based cohort study of 48,703 participants.
- Analysis of time-weighted cumulative hsCRP over an average of 6.36 years.
- Cox proportional hazards models and restricted cubic spline analysis to assess CCB risk.
Main Results:
- A total of 803 new-onset CCB cases were identified over 9.24 years.
- Elevated cumulative hsCRP (≥ 2 mg/L) was independently associated with a 24% increased risk of CCB (HR: 1.24, 95% CI: 1.07-1.44).
- A linear association was observed between cumulative hsCRP and CCB risk.
Conclusions:
- Cumulative exposure to hsCRP is an independent predictor of CCB development.
- This association is particularly noted for left bundle branch block and left anterior fascicular block.
- Findings offer insights for CCB prevention strategies targeting inflammation.
Purpose:
Chronic low-grade inflammation is increasingly recognized as a contributing factor in the development of cardiovascular events. This study aimed to evaluate the association between time-weighted cumulative exposure to high-sensitivity C-reactive protein (cumhsCRP) and the risk of new-onset cardiac conduction block (CCB).
Patients And Methods:
A total of 48,703 participants from a prospective community-based cohort were included. The average exposure time for cumhsCRP was 6.36 years. Participants were stratified into two groups: cumhsCRP < 2 mg/L and cumhsCRP ≥ 2 mg/L. The incidence of new-onset cardiac conduction block and its subtypes was identified through standard 12-lead electrocardiograms. Cox proportional hazards models were used to assess the relationship between cumhsCRP levels and incident CCB risk, adjusting for potential confounders. A restricted cubic spline curve further explored the dose-response pattern.
Results:
During a mean follow-up period of 9.24 years, 803 cases of new-onset CCB were documented (incidence rate: 1.65%). After full multivariable adjustment, individuals in the cumhsCRP ≥ 2 mg/L group exhibited a significantly higher risk of CCB compared to those with cumhsCRP < 2 mg/L (HR: 1.24, 95% CI: 1.07-1.44). The RCS analysis suggested a linear association between log-transformed cumhsCRP and CCB risk (p for non-linearity = 0.294).
Conclusion:
Elevated cumulative exposure to high-sensitivity C-reactive protein is independently associated with an increased risk of developing CCB, especially left bundle branch block and left anterior fascicular block. This study will provide new insights into the prevention of CCB.
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