scholarly journals Kidney Allograft Function Is a Confounder of Urine Metabolite Profiles in Kidney Allograft Recipients

Metabolites ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 533
Author(s):  
Karsten Suhre ◽  
Darshana M. Dadhania ◽  
John Richard Lee ◽  
Thangamani Muthukumar ◽  
Qiuying Chen ◽  
...  

Noninvasive biomarkers of kidney allograft status can help minimize the need for standard of care kidney allograft biopsies. Metabolites that are measured in the urine may inform about kidney function and health status, and potentially identify rejection events. To test these hypotheses, we conducted a metabolomics study of biopsy-matched urine cell-free supernatants from kidney allograft recipients who were diagnosed with two major types of acute rejections and no-rejection controls. Non-targeted metabolomics data for 674 metabolites and 577 unidentified molecules, for 192 biopsy-matched urine samples, were analyzed. Univariate and multivariate analyses identified metabolite signatures for kidney allograft rejection. The replicability of a previously developed urine metabolite signature was examined. Our study showed that metabolite profiles can serve as biomarkers for discriminating rejection biopsies from biopsies without rejection features, but also revealed a role of estimated Glomerular Filtration Rate (eGFR) as a major confounder of the metabolite signal.

2018 ◽  
Vol 104 (6) ◽  
pp. 1229-1239 ◽  
Author(s):  
Youssra Haouami ◽  
Tarak Dhaouadi ◽  
Imen Sfar ◽  
Mongi Bacha ◽  
Tahar Gargah ◽  
...  

Metabolomics ◽  
2018 ◽  
Vol 14 (9) ◽  
Author(s):  
Miriam Banas ◽  
Sindy Neumann ◽  
Johannes Eiglsperger ◽  
Eric Schiffer ◽  
Franz Josef Putz ◽  
...  

Radiology ◽  
1979 ◽  
Vol 132 (3) ◽  
pp. 667-672 ◽  
Author(s):  
Hedvig Hricak ◽  
Luis H. Toledo-Pereyra ◽  
William R. Eyler ◽  
Beatrice L. Madrazo ◽  
Michael Zammit

2008 ◽  
Vol 40 (10) ◽  
pp. 3390-3392 ◽  
Author(s):  
J. Karczewski ◽  
M. Karczewski ◽  
M. Glyda ◽  
K. Wiktorowicz

2015 ◽  
Vol 27 (2) ◽  
pp. 626-636 ◽  
Author(s):  
Karsten Suhre ◽  
Joseph E. Schwartz ◽  
Vijay K. Sharma ◽  
Qiuying Chen ◽  
John R. Lee ◽  
...  

2008 ◽  
Vol 86 (Supplement) ◽  
pp. 506
Author(s):  
M Karczewski ◽  
J Karczewski ◽  
M Glyda

2017 ◽  
Vol 29 (2) ◽  
pp. 620-635 ◽  
Author(s):  
Carmen Lefaucheur ◽  
Denis Viglietti ◽  
Luis G. Hidalgo ◽  
Lloyd E. Ratner ◽  
Serena M. Bagnasco ◽  
...  

Complement-activating anti-HLA donor-specific antibodies (DSAs) are associated with impaired kidney transplant outcome; however, whether these antibodies induce a specific rejection phenotype and influence response to therapy remains undetermined. We prospectively screened 931 kidney recipients for complement-activating DSAs and used histopathology, immunostaining, and allograft gene expression to assess rejection phenotypes. Effector cells were evaluated using in vitro human cell cultures. Additionally, we assessed the effect of complement inhibition on kidney allograft rejection phenotype and the clinical response to complement inhibition in 116 independent kidney recipients with DSAs at transplant receiving rejection prophylaxis with eculizumab or standard of care (plasma exchange and intravenous Ig) at ten international centers. The histomolecular rejection phenotype associated with complement-activating DSA was characterized by complement deposition and accumulation of natural killer cells and monocytes/macrophages in capillaries and increased expression of five biologically relevant genes (CXCL11, CCL4, MS4A7, MS4A6A, and FCGR3A) indicative of endothelial activation, IFNγ response, CD16-mediated natural killer cell activation, and monocyte/macrophage activation. Compared with standard of care, eculizumab specifically abrogated this histomolecular rejection phenotype and associated with a decreased 3-month rejection incidence rate in patients with complement-activating DSAs (56%; 95% confidence interval [95% CI], 38% to 74% versus 19%; 95% CI, 8% to 35%; P=0.001) but not in those with noncomplement-activating DSAs (9%; 95% CI, 2% to 25% versus 13%; 95% CI, 2% to 40%; P=0.65). In conclusion, circulating complement-activating anti-HLA DSAs are associated with a specific histomolecular kidney allograft rejection phenotype that can be abrogated by complement inhibition.


2016 ◽  
Vol 21 (4) ◽  
pp. 721-731 ◽  
Author(s):  
Akihiro Tsuchimoto ◽  
Toshiaki Nakano ◽  
Shoko Hasegawa ◽  
Kosuke Masutani ◽  
Yuta Matsukuma ◽  
...  

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