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Updated: Jan 31, 2026

Orthotopic Liver Transplantation in Rats
Published on: July 1, 2012
Evolution of Biomarkers of Atherogenic Risk in Liver Transplantation Recipients
L M C Linhares1, C P Oliveira1, M R Alvares-da-Silva2
1Department of Gastroenterology (LIM-07/LIM-37), University of São Paulo School of Medicine, São Paulo, Brazil.
Insights
Cardiovascular disease is a major risk after liver transplantation. Atherogenic risk biomarkers significantly increased in liver transplant recipients (LTRs) within 48 months, preceding coronary plaque development.
Area of Science:
- Cardiology
- Transplantation Medicine
- Biomarker Research
Background:
- Cardiovascular disease (CVD) is a primary cause of mortality post-liver transplantation (LT).
- Understanding atherogenic risk evolution in liver transplant recipients (LTRs) is crucial for long-term outcomes.
Purpose of the Study:
- To evaluate the progression of atherogenic risk in LTRs.
- To assess changes in biomarkers of endothelial dysfunction, inflammation, and oxidative stress.
- To correlate these biomarkers with cardiac imaging findings.
Main Methods:
- Prospective study of 36 LTRs, followed for 48 months post-LT.
- Measurement of serum biomarkers: sICAM-1, sVCAM-1, serum amyloid A, and myeloperoxidase at 12 and 48 months.
- Cardiac computed tomography (CT) and coronary artery calcium score (CACS) performed at 12 months.
Main Results:
- Significant increases in sVCAM-1, sICAM-1, myeloperoxidase, and serum amyloid A were observed from 12 to 48 months post-LT (P < .001).
- Prevalence of metabolic syndrome risk factors increased during the study.
- Cardiac CT showed mild (19%) and moderate (25%) coronary artery disease.
Conclusions:
- Serum biomarkers indicating atherogenic risk significantly increase in LTRs.
- These biomarker elevations occur before the development of coronary plaques.
- No direct association was found between these biomarkers and metabolic syndrome or coronary artery calcium scores.
Background:
Cardiovascular disease is a major contributing factor to long-term mortality after liver transplantation (LT).
Methods:
This study evaluated the evolution of atherogenic risk in liver transplant recipients (LTRs). Thirty-six subjects were prospectively enrolled at 12 months and followed for 48 months after liver transplantation. Serum biomarkers of endothelial dysfunction (sICAM-1 and sVCAM-1), chronic inflammation (serum amyloid A), and oxidative stress (myeloperoxidase) were measured at 12 and 48 months after LT. Additionally, at 12 months all patients underwent a cardiac computed tomography (CT) scan and a coronary artery calcium score (CACS).
Results:
The prevalence of risk factors of metabolic syndrome (MS) increased over the course of the study. The patients' sVCAM-1 and sICAM-1 increased from 1.82 ± 0.44 ng/mL to 9.10 ± 5.82 ng/mL (P < .001) and 0.23 ± 0.09 ng/mL to 2.7 ± 3.3 ng/mL, respectively from month 12 to 48. Serum myeloperoxidase increased from 0.09 ± 0.07 ng/mL to 3.46 ± 3.92 ng/mL (P < .001) over the course of the study. Serum amyloid A also increased from 21.4 ± 40.7 ng/mL at entry to 91.5 ± 143.6 ng/mL at end of study (P < .001).
Conclusion:
No association between these biomarkers and MS was noted. The cardiac CT revealed mild and moderate disease in 19% and 25% of the cohort, respectively. No association between serum biomarkers and CACS was noted. Serum biomarkers of atherogenic risk increase rapidly in LTRs and precede coronary plaques.
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