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Synergistic impact of pre-sensitization and delayed graft function on allograft rejection in deceased donor kidney transplantationopen access

Authors
Lee, HanbiPark, YohanBan, Tae HyunSong, Sang HeonSong, Seung HwanYang, JaeseokAhn, CurieYang, Chul WooChung, Byung HaKong, J.M.Kwon, O.J.Kim, D.G.Jung, C.-W.Kim, Y.H.Kim, J.K.Kim, C.-D.Min, J.W.Park, S.K.Park, Y.H.Berm, P.J.Park, J.H.Park, J.-W.Shin, H.S.Yoon, H.E.Lee, K.W.Lee, D.R.Lee, D.W.Lee, S.Y.Lee, S.-H.Lee, S.H.Lee, J.J.Pyo, L.J.Lee, J.-H.Jeon, J.S.Jun, H.Jeong, K.Chung, K.Y.Cho, H.R.Ki, J.M.Chae, D.-W.Choi, S.J.N.Han, D.J.Han, S.Huh, K.H.
Issue Date
Dec-2021
Publisher
Nature Research
Citation
Scientific Reports, v.11, no.1, pp.1 - 11
Indexed
SCIE
SCOPUS
Journal Title
Scientific Reports
Volume
11
Number
1
Start Page
1
End Page
11
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/140243
DOI
10.1038/s41598-021-95327-6
ISSN
2045-2322
Abstract
The aim of this study is to investigate whether or not delayed graft function (DGF) and pre-transplant sensitization have synergistic adverse effects on allograft outcome after deceased donor kidney transplantation (DDKT) using the Korean Organ Transplantation Registry (KOTRY) database, the nationwide prospective cohort. The study included 1359 cases between May 2014 and June 2019. The cases were divided into 4 subgroups according to pre-sensitization and the development of DGF post-transplant [non-pre-sensitized-DGF(−) (n = 1097), non-pre-sensitized-DGF(+) (n = 127), pre-sensitized-DGF(−) (n = 116), and pre-sensitized-DGF(+) (n = 19)]. We compared the incidence of biopsy-proven allograft rejection (BPAR), time-related change in allograft function, allograft or patient survival, and post-transplant complications across 4 subgroups. The incidence of acute antibody-mediated rejection (ABMR) was significantly higher in the pre-sensitized-DGF(+) subgroup than in other 3 subgroups. In addition, multivariable cox regression analysis demonstrated that pre-sensitization combined with DGF is an independent risk factor for the development of acute ABMR (hazard ratio 4.855, 95% confidence interval 1.499–15.727). Moreover, DGF and pre-sensitization showed significant interaction (p-value for interaction = 0.008). Pre-sensitization combined with DGF did not show significant impact on allograft function, and allograft or patient survival. In conclusion, the combination of pre-sensitization and DGF showed significant synergistic interaction on the development of allograft rejection after DDKT.
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