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Detection of Endothelial Cell Specific Molecule-1 According to Allograft Status After Kidney Transplantation.

J.-W. Seo, S.-Y. Kim, Y.-G. Kim, Y.-H. Jeong, Y.-H. Lee, J.-Y. Moon, T.-W. Lee, C.-G. Ihm, S.-H. Lee.

Division of Nephrology, Department of Internal Medicine, College of Medicine, Kyung Hee University, Seoul, Republic of Korea.

Meeting: 2016 American Transplant Congress

Abstract number: D10

Keywords: Endothelial cells, Kidney transplantation, Rejection

Session Information

Date: Tuesday, June 14, 2016

Session Name: Poster Session D: Antibody Mediated Rejection: Session #2

Session Time: 6:00pm-7:00pm

 Presentation Time: 6:00pm-7:00pm

Location: Halls C&D

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To investigate urine ESM-1(endothelial cell specific molecule-1) as well as plasma ESM-1 level from renal allograft recipients, we show whether there is the difference of ESM-1 level according to allograft status.

We measured plasma and urine ESM-1 in 116 patients with underwent KTP. The concentration of ESM-1 was analyzed by enzyme linked immunosorbent assay (ELISA). According to allograft status, Groups are divided as stable, cellular rejection (CR), acute antibody-mediated rejection (AMR), long term good survival, and chronic AMR. We compared variables associated with graft status including plasma and urine ESM-1 between groups.

The distribution of plasma ESM-1 was not significantly different between all groups according to allograft status (p=0.131). On the other hand, the distribution of urine ESM-1 to creatinine ratio (urine ESM-1/Cr) was significantly different between all groups according to allograft status (p<0.001). In subgroup analysis, the distribution of urine ESM-1/Cr of stable group was significantly different from both CR and AMR groups. However, urine ESM-1/Cr of CR group was not significantly different from AMR group (p=0.063). Area under the curve (AUC) for differentiating AMR from CR was 0.774 (p<0.001).

Urine ESM-1 may reflect the possibility as biomarker of antibody-mediated rejection. Elevated urine ESM-1 level was associated with severity of glomerulitis, interstial fibrosis, glomerulopathy, arteriolar hyaline thickening, and peritubular capilaritis.

CITATION INFORMATION: Seo J.-W, Kim S.-Y, Kim Y.-G, Jeong Y.-H, Lee Y.-H, Moon J.-Y, Lee T.-W, Ihm C.-G, Lee S.-H. Detection of Endothelial Cell Specific Molecule-1 According to Allograft Status After Kidney Transplantation. Am J Transplant. 2016;16 (suppl 3).

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To cite this abstract in AMA style:

Seo J-W, Kim S-Y, Kim Y-G, Jeong Y-H, Lee Y-H, Moon J-Y, Lee T-W, Ihm C-G, Lee S-H. Detection of Endothelial Cell Specific Molecule-1 According to Allograft Status After Kidney Transplantation. [abstract]. Am J Transplant. 2016; 16 (suppl 3). https://atcmeetingabstracts.com/abstract/detection-of-endothelial-cell-specific-molecule-1-according-to-allograft-status-after-kidney-transplantation/. Accessed March 8, 2021.

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