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Elevated serum bilirubin levels are inversely associated with coronary artery atherosclerosis
Seung Joo Kang1, Donghee Kim, Hyo Eun Park
1Department of Internal Medicine, Healthcare Research Institute, Seoul National University, Hospital Healthcare System Gangnam Center, Seoul, South Korea.
Insights
High serum bilirubin levels are linked to lower rates of coronary atherosclerosis and calcified plaques. This suggests bilirubin may act as a protective biomarker against coronary artery disease.
Area of Science:
- Cardiology
- Biochemistry
- Preventive Medicine
Background:
- Inverse correlations between high serum bilirubin and cardiovascular disease are suggested.
- Anti-atherogenic effects of bilirubin require further establishment, particularly regarding coronary plaques and stenosis.
Purpose of the Study:
- To investigate the association between serum bilirubin levels and coronary atherosclerosis.
- To determine if bilirubin is linked to the presence and severity of coronary plaques and stenosis.
Main Methods:
- A cross-sectional study of 2862 men without cardiovascular disease who underwent coronary computed tomography (CT).
- Coronary atherosclerosis defined by stenotic lesions, classified by degree (<50% or ≥50%).
- Serum bilirubin levels categorized as normal (≤1.2 mg/dL) or elevated (>1.2 mg/dL).
Main Results:
- Elevated bilirubin levels were associated with lower prevalences of coronary atherosclerosis and stenosis ≥50%.
- Serum bilirubin showed an inverse association with total and calcified plaques in univariate analysis.
- After adjusting for risk factors, higher bilirubin levels demonstrated a dose-dependent inverse association with coronary atherosclerosis and calcified plaques.
Conclusions:
- Serum bilirubin levels are inversely associated with coronary atherosclerosis and calcified plaques in a dose-dependent manner.
- These findings suggest serum bilirubin may serve as a protective biomarker for coronary artery disease.
Background:
Inverse correlations of high serum bilirubin with metabolic and cardiovascular disease have been suggested. However, anti-atherogenic effects of bilirubin have not been well-established in terms of the presence of plaques and stenosis identified in coronary computed tomography (CT).
Methods:
A cross-sectional study was conducted on 2862 men who were free of cardiovascular disease and underwent coronary CT as part of a routine medical screening examination. Coronary stenotic lesions were considered to be incidences of coronary atherosclerosis, and stenosis was classified as stenosis <50% or ≥50%, according to degree of stenosis.
Results:
The prevalences of coronary atherosclerosis and stenosis ≥50% in subjects with elevated bilirubin levels (>1.2 mg/dL) were lower than those in subjects with normal bilirubin levels (≤1.2 mg/dL) (19.9% vs. 27.9%, p < 0.001, 8.5% vs. 10.3%, p = 0.044). Bilirubin was inversely associated with total plaques (odds ratio [OR] 0.59, 95% confidence interval [CI] 0.48-0.73 in the 4th quartile vs. 1st quartile) and calcified plaques (OR 0.60, 95% CI 0.49-0.75) in univariate analysis. After adjusting for traditional risk factors, it was found that coronary atherosclerosis (OR 0.73, 95% CI 0.56-0.94 in the 4th quartile vs. 1st quartile) and calcified plaque (OR 0.66, 95% CI 0.53-0.84) were inversely associated with the bilirubin grade in a dose-dependent manner.
Conclusions:
The serum bilirubin level was inversely associated with coronary atherosclerosis and calcified plaques in a dose-dependent manner. These results suggested that serum bilirubin could be used as a protective biomarker of coronary artery disease.
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