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Two Trajectories of Post-DSA eGFR after Kidney Transplant

J. Beaumont,1 K. Briley,2 A. Maldonado,3 C. Haisch,2 P. Bolin,2 S. Kendrick,4 H. Jones,4 K. McLawhorn,4 D. Leeser,2 L. Rebellato,2 M. Everly.1

1Terasaki Research Institute, Los Angeles, CA
2East Carolina University, Greenville, NC
3Vidant Medical Center, Greenville, NC
4Eastern Nephrology Associates, Greenville, NC.

Meeting: 2018 American Transplant Congress

Abstract number: 513

Keywords: Glomerular filtration rate (GFR), Graft failure, IgG

Session Information

Session Name: Concurrent Session: Kidney Complications: Antibody & Late Outcomes

Session Type: Concurrent Session

Date: Tuesday, June 5, 2018

Session Time: 4:30pm-6:00pm

 Presentation Time: 5:30pm-5:42pm

Location: Room 4B

A clearer understanding of the patterns of glomerular filtration rate (GFR) decline following donor-specific antibody (DSA) development and the factors that might be associated with a faster decline in function are needed. Herein, we study post-DSA GFR decline in 52 DSA-positive renal transplant patients.

Methods: We performed a retrospective analysis of de novo DSA positive transplant patients transplanted at a single transplant center between 11/1999 and 4/2011. All patients underwent frequent HLA IgG serial antibody monitoring by LABScreen® single antigen beads with IgG3 testing after DSA was found positive. Only patients with an eGFR>50 at the time of DSA were included in the analysis. Latent class mixed models were fit to all available eGFR measurements post-DSA. The number of latent classes was identified based on BIC. After patients were classified according to posterior probabilities, variables associated with class membership were identified.

Results: A total of 52 patients were included in the analysis. Two latent classes were identified (Figure): patients with stable eGFR post-DSA (n=28) and patients with rapidly declining eGFR post-DSA (n=24). Patients in the declining trajectory (compared to the stable eGFR cohort) were more likely to have had a living donor (33% vs 7%), have experienced an acute rejection episode (71% vs 25%), have IgG3+ DSA (65% vs 9%), died during follow-up (38% vs 14%), or experience graft failure (58% vs 25%). There were not substantial differences between the classes in age at transplant, race, gender, or delayed graft function.

Conclusion: Our findings support the idea that patients may take clear clinical courses after the onset of DSA. Those who develop or have a history of acute rejection and those who have IgG3 positive DSA are more likely to have a fast decline in eGFR and proceed to allograft failure and possibly death.

CITATION INFORMATION: Beaumont J., Briley K., Maldonado A., Haisch C., Bolin P., Kendrick S., Jones H., McLawhorn K., Leeser D., Rebellato L., Everly M. Two Trajectories of Post-DSA eGFR after Kidney Transplant Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Beaumont J, Briley K, Maldonado A, Haisch C, Bolin P, Kendrick S, Jones H, McLawhorn K, Leeser D, Rebellato L, Everly M. Two Trajectories of Post-DSA eGFR after Kidney Transplant [abstract]. https://atcmeetingabstracts.com/abstract/two-trajectories-of-post-dsa-egfr-after-kidney-transplant/. Accessed May 16, 2025.

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