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Serum N-glycan profiling can predict biopsy-proven graft rejection after living kidney transplantation.

Authors :
Soma O
Hatakeyama S
Yoneyama T
Saito M
Sasaki H
Tobisawa Y
Noro D
Suzuki Y
Tanaka M
Nishimura SI
Harada H
Ishida H
Tanabe K
Satoh S
Ohyama C
Source :
Clinical and experimental nephrology [Clin Exp Nephrol] 2020 Feb; Vol. 24 (2), pp. 174-184. Date of Electronic Publication: 2019 Nov 25.
Publication Year :
2020

Abstract

Background: To evaluate whether serum N-glycan profile can be used as a diagnostic marker of graft rejection after living-donor kidney transplants (KT).<br />Methods: We retrospectively examined 174 KT recipients at five medical centers. N-Glycan levels were analyzed in postoperative serum samples using glycoblotting combined with mass spectrometry. We developed an integrated score to predict graft rejection based on a combination of age, gender, immunological risk factors, and serum N-glycan levels at post-KT day D1 and D7. Rejection-free survival rates stratified by the sum of integrated scores (D1 + D7) were evaluated using Kaplan-Meier curves.<br />Results: Of 174, 52 showed graft rejection (Rejection-pos. group) and 122 recipients did not show graft rejection (Rejection-neg. group). The integrated scores were significantly higher in the Rejection-pos. group than those of the Rejection-neg. group. Area-under-curve (AUC) value of integrated scores at post-KT D1, and D7 were 0.84 and 0.84, respectively. The sum of integrated scores (D1 + D7) ≥ 0.50 identified graft rejection with 81% sensitivity and 80% specificity; with an AUC value of 0.87. Recipients with higher sum of integrated scores (D1 + D7 ≥ 0.5) had significantly shorter rejection-free survival than those with lower scores.<br />Conclusion: Evaluation of serum N-glycosylation profiles can identify recipients who are prone to rejection.

Details

Language :
English
ISSN :
1437-7799
Volume :
24
Issue :
2
Database :
MEDLINE
Journal :
Clinical and experimental nephrology
Publication Type :
Academic Journal
Accession number :
31768865
Full Text :
https://doi.org/10.1007/s10157-019-01820-8