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Associations of plasma hepcidin with mortality risk in patients with coronary artery disease
Xinrui Li1, Ding Ding1, Yuan Zhang2
1Guangdong Provincial Key Laboratory of Food, Nutrition and Health, Department of Nutrition, School of Public Health, Sun Yat-sen University, Guangzhou, Guangdong, China.
Insights
High hepcidin levels predict mortality in acute coronary syndrome (ACS) patients. This finding suggests hepcidin may serve as a valuable biomarker for risk stratification in ACS.
Area of Science:
- Cardiovascular Medicine
- Biomarker Discovery
- Atherosclerosis Research
Background:
- Hepcidin, a key regulator of iron metabolism, is implicated in atherosclerosis.
- The prognostic value of hepcidin in coronary artery disease (CAD) mortality is not well-established.
- This study investigates hepcidin's association with mortality in CAD patients, with and without acute coronary syndrome (ACS).
Purpose of the Study:
- To determine the relationship between plasma hepcidin levels and all-cause and cardiovascular disease (CVD) mortality.
- To assess the predictive value of hepcidin in patients with stable CAD and ACS.
Main Methods:
- A cohort of 759 ACS patients and 526 stable CAD patients was followed for an average of 4.1 years.
- Plasma hepcidin levels were measured and correlated with mortality outcomes.
- Statistical analyses, including multivariable regression and risk reclassification, were performed after adjusting for CVD risk factors and inflammatory markers.
Main Results:
- Increased plasma hepcidin was significantly associated with higher all-cause and CVD mortality in ACS patients.
- Multivariable-adjusted hazard ratios demonstrated a dose-response relationship between hepcidin tertiles and mortality.
- Inclusion of hepcidin improved cardiovascular risk prediction models, showing significant net reclassification improvement.
Conclusions:
- Plasma hepcidin is a positive predictor of mortality in patients with ACS.
- Hepcidin emerges as a potential novel biomarker for enhanced risk prediction in ACS patients.
Background:
Increased blood hepcidin may be associated with the presence and promotion of atherosclerosis, the association of hepcidin with mortality among coronary artery disease (CAD) patients remains unknown. We sought to assess the relationship of hepcidin and all-cause and cardiovascular disease (CVD) mortality among CAD patients with and without acute coronary syndrome (ACS).
Methods And Results:
This study included 759 patients with ACS and 526 patients with stable CAD. After an average follow-up of 4.1 years, 154 deaths were recorded, 114 were due to CVD. After adjusting for CVD risk factors and inflammatory markers, the plasma hepcidin was positively associated with all-cause and CVD mortality in the ACS patients, the multivariable-adjusted hazard ratios (HRs) across tertiles of hepcidin were 1.00, 2.18 (95% CI 1.23-3.94), and 2.82 (95% CI 1.59-5.12) for all-cause mortality (Ptrend=0.006), and 1.00, 2.20 (95% CI 1.12-4.05), and 2.64 (95% CI 1.41-5.65) for CVD mortality (Ptrend=0.01). The C-index and net reclassification improvement when including hepcidin in traditional CVD models were 1.6% and 21.5% for all-cause mortality, 1.4% and 23.5% for CVD mortality, respectively, (P<0.001).
Conclusions:
Plasma hepcidin was positively associated with mortality in ACS patients. Hepcidin may be a potential biomarker for risk prediction in ACS patients.
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