BK polyomavirus DNAemia in pancreas transplant recipients compared to pancreas–kidney recipients

Author:

Yetmar Zachary A.1,Kudva Yogish C.2ORCID,Seville Maria Teresa3,Bosch Wendelyn4,Dean Patrick G.5,Huskey Janna L.6,Budhiraja Pooja6ORCID,Jarmi Tambi7ORCID,Kukla Aleksandra8ORCID,Beam Elena1ORCID

Affiliation:

1. Division of Public Health Infectious Diseases, and Occupational Medicine Department of Medicine Mayo Clinic Rochester Minnesota USA

2. Division of Endocrinology Diabetes Metabolism & Nutrition Department of Medicine Mayo Clinic Rochester Minnesota USA

3. Division of Infectious Diseases Department of Medicine Mayo Clinic Phoenix Arizona USA

4. Division of Infectious Diseases Department of Medicine Mayo Clinic Jacksonville Florida USA

5. Division of Transplantation Surgery Department of Surgery Mayo Clinic Rochester Minnesota USA

6. Division of Nephrology Department of Medicine Mayo Clinic Phoenix Arizona USA

7. Department of Transplantation Mayo Clinic Jacksonville Florida USA

8. Division of Nephrology and Hypertension Department of Medicine Mayo Clinic Rochester Minnesota USA

Abstract

AbstractBackgroundBK polyomavirus (BKV) infection is a common complication of kidney transplantation. While BKV has been described in non‐kidney transplant recipients, data are limited regarding its epidemiology and outcomes in pancreas transplant recipients.MethodsWe conducted a retrospective cohort study of adults who underwent pancreas transplantation from 2010–2020. The primary outcome was BKV DNAemia. Secondary outcomes were estimated glomerular filtration rate (eGFR) reduction by 30%, eGFR < 30 mL/min/1.73 m2, endstage kidney disease, and pancreas allograft failure. Cox regression with time‐dependent variables was utilized.ResultsFour hundred and sixty‐six patients were analyzed, including 74, 46, and 346 with pancreas transplant alone (PTA), pancreas‐after‐kidney, or simultaneous pancreas–kidney transplants, respectively. PTA recipients experienced a lower incidence of BKV DNAemia (8.8% vs. 32.9%; p < .001) and shorter duration of DNAemia (median 28.0 vs. 84.5 days). No PTA recipients with BKV DNAemia underwent kidney biopsy or developed endstage kidney disease. Lymphopenia, non‐PTA transplantation, and older age were associated with BKV DNAemia, which itself was associated with pancreas allograft failure (adjusted hazard ratio 2.14, 95% confidence interval 1.27–3.60; p = .004). Among PTA recipients, BKV DNAemia was not associated with eGFR reduction or eGFR < 30 mL/min/1.73 m2.ConclusionsBKV DNAemia was common among PTA recipients, though lower than a comparable group of pancreas–kidney recipients. However, BKV DNAemia was not associated with adverse native kidney outcomes and no PTA recipients developed endstage kidney disease. Conversely, BKV DNAemia was associated with pancreas allograft failure. Further studies are needed to estimate the rate of BKV nephropathy in this population, and further evaluate long‐term kidney outcomes.

Funder

National Center for Advancing Translational Sciences

Publisher

Wiley

Subject

Transplantation

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