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Reduced Complications after Arterial Reconnection in a Rat Model of Orthotopic Liver Transplantation
Published on: November 7, 2020
Association Between Survival After Living Donor Liver Transplantation and Recipient Systemic Inflammation and Body
Jae Hwan Kim1, Yeon Ju Kim2, Hye-Mee Kwon2
1Department of Anesthesiology and Pain Medicine, Inje University Haeundae Paik Hospital, Busan 48108, Republic of Korea.
Preoperative sarcopenia and high systemic inflammatory status (SIS), measured by neutrophil-to-lymphocyte ratio (NLR), significantly increase mortality risk in liver transplant recipients. Combining these factors offers a practical way to predict survival post-transplant.
Area of Science:
- Hepatology
- Transplantation Surgery
- Geriatrics
Background:
- Preoperative sarcopenia is a known predictor of poor outcomes in liver transplantation (LT).
- Systemic inflammatory status (SIS) is implicated in skeletal muscle loss, suggesting a combined effect with sarcopenia on LT prognosis.
- Assessing both SIS and sarcopenia may improve risk stratification for LT recipients.
Purpose of the Study:
- To investigate the relationship between SIS and skeletal muscle index (SMI) with mortality in living donor liver transplantation (LDLT) recipients.
- To evaluate the combined prognostic value of sarcopenia and SIS for short-term and long-term survival after LDLT.
Main Methods:
- Retrospective analysis of 3387 adult LDLT recipients.
- Neutrophil-to-lymphocyte ratio (NLR > 3) used as a marker for SIS.
- Skeletal muscle index (SMI) calculated from CT scans with sex-specific cut-offs.
- Univariate and multivariable Cox proportional hazard analyses performed.
Main Results:
- Decreasing SMI correlated with increasing NLR.
- Both increasing NLR and decreasing SMI showed a dose-dependent association with 90-day mortality.
- Sarcopenia combined with NLR > 3 independently predicted higher 90-day and overall mortality (HRs 2.48 and 1.81, respectively).
- The association between sarcopenia and mortality persisted across subgroups, notably higher in women.
Conclusions:
- Sarcopenia and systemic inflammation (NLR > 3) significantly increase 90-day and overall mortality risk post-LT, nearly doubling the hazard.
- These readily available biomarkers provide a practical index for predicting LT survival.
- Addressing these potentially modifiable factors could represent a therapeutic target for improving post-LT outcomes.
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