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Polyoma Viremia Adversely Affects Renal Function at One Year in Kidney Transplant Recipients: Independent of Immunosuppressive Regimen

K. Nguyen, R. Weng, J. Foe-Parker, H. Ichii, C. Foster III

Div. Transplantation/Surgery, University of California, Irvine School of Medicine, Orange, Ca.

Meeting: 2013 American Transplant Congress

Abstract number: C1371

Background:

Polyoma virus (BKV) reactivation is a complication in renal transplant recipients that can lead to BKV nephropathy (BKVN) and allograft loss.

The purpose of this study is to evaluate induction therapy choice with Rabbit anti-thymocyte globulin (RATG) vs. Basiliximab (anti-IL2). A secondary endpoint is to determine whether maintenance IS regimen with or without long-term steroid therapy is an independent risk factor for BKV replication and if steroid avoidance may reduce the emergence of BKV in kidney transplant recipients.

Method:

A retrospective, single-center analysis of 243 kidney transplant recipients from July 1, 2005 – September 15, 2012 was performed. Induction IS was RATG or anti-IL2 along with maintenance IS consisted of TAC/MMF, CSA/MMF, TAC/ERL, SRL/MMF +/- prednisone. The incidence of BKV viremia, BKVN, serum creatinine at 6 months and 1 year, and allograft loss were analyzed.

Results:

90.5% (220) were BKV(-), 9.5% (23) BKV(+). Patient demographics and transplant characteristics were comparable except the BKV(+) patients had a lower BMI (p-0.027). The CSA/MMF group had a larger percent develop BKV(+), 13% vs 2.7% (p- 0.017). Induction IS regimen selection and maintenance steroid did not increase the incidence of BKV viremia. 13%(3) patients in the BKV(+) group developed BKVN and 52% were converted to Leflunomide. Creatinine Clearance (1-year) was statistically lower in the BKV(+) group vs. the BKV(-) Group, 54.8 ml/min vs. 69.7ml/min (P-0.037).

Patient Demographics
Characteristic BKV(+), n=23 BK (-) , n=220
Age (years) 46.1 45.6
BMI (kg/m2) 24.43 26.53 *
DGF 26% (6) 30% (67)
Male 78.3 %(18) 65%(143)
Female 21.74% (5) 35% (77)
African-American 8.7 % (2) 3.18% (7)
Asian-American 13 %(3) 19.5%(43)
Hispanic 21.7%(5) 17.7 %(39)
Caucasian 56.5%(13) 59.5% (131)
LDKT 39.1% (9) 33.2%(73)
DDKT 60.9% (14) 66.8%(147)
LDKT-Living Donor Kidney Transplant ; DDKT- Deceased Donor Kidney Transplant; *p<0.05
Immunosuppression
  BKV(+) BKV(-)
Type of Induction
RATG 39.1%(9) 39.1% (86)
Anti-IL2 60.9%(14) 60.9% (134)
Maintenance IS
Steroids-Yes 87%(20) 90%(198)
Steroids-No 13%(3) 10%(22)
TAC/MMF 82.6%(19) 92.3%(203)
CSA/MMF 13%(3) 2.73%(6)*
TAC/ERL 4.3%(1) 1.8% (4)
SRL/MMF 0 2.7% (6)
*P<0.05

Conclusion:

The choice of induction therapy did not increase the incidence of BKV viremia. The presence of BKV viremia adversely affected kidney transplant allograft function at one year.

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To cite this abstract in AMA style:

Nguyen K, Weng R, Foe-Parker J, Ichii H, III CFoster. Polyoma Viremia Adversely Affects Renal Function at One Year in Kidney Transplant Recipients: Independent of Immunosuppressive Regimen [abstract]. Am J Transplant. 2013; 13 (suppl 5). https://atcmeetingabstracts.com/abstract/polyoma-viremia-adversely-affects-renal-function-at-one-year-in-kidney-transplant-recipients-independent-of-immunosuppressive-regimen/. Accessed May 16, 2025.

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