A prospective cross‐sectional study of BK virus infection in non‐renal solid organ transplant recipients with chronic renal dysfunction

Transplant Infectious Disease - Tập 8 Số 2 - Trang 102-107 - 2006
Todd D. Barton1, Emily A. Blumberg1, Alden Doyle2, Vivek N. Ahya3, James Ferrenberg4, Susan C. Brozena5, Ajit P. Limaye6
1Department of Medicine, Division of Infectious Diseases, University of Pennsylvania, Philadelphia, Pennsylvania, USA
2Department of Medicine, Division of Renal, Electrolytes, & Hypertension, University of Pennsylvania, Philadelphia, Pennsylvania, USA,
3Department of Medicine, Divisions of Pulmonary & Critical Care Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA,
4Fred Hutchinson Cancer Research Center, Seattle, Washington, USA
5Department of Medicine, Division of Cardiovascular Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA,
6Departments of Laboratory Medicine & Medicine, University of Washington, Seattle, Washington, USA

Tóm tắt

Abstract: Background: Polyomavirus (primarily BK virus [BKV]) infection is an important cause of chronic renal dysfunction in renal transplant recipients, but its possible contribution to chronic renal dysfunction in non‐renal solid organ transplant (NRSOT) recipients has not been fully explored.

Methods: We performed a prospective, cross‐sectional study of consecutive NRSOT recipients with unexplained chronic renal dysfunction of at least a 3 months duration. Medical records were reviewed, and polymerase chain reaction was used to amplify BKV‐specific sequences from serum and urine samples. The potential associations between various demographic and transplant variables and BKV infection were assessed.

Results: Thirty‐four consecutive NRSOT recipients (23 lung, 8 liver, 2 heart, 1 heart–lung) with chronic renal dysfunction were enrolled at a median of 3.5 years (range 0.3–12.5 years) post transplantation. Five of the 34 (15%) patients had BKV viruria (range 1040–1.8 × 106 copies/mL), but none had BKV viremia. BK viruria was associated with mycophenolate mofetil use (5 of 19 [26%] vs. 0 of 15, P=0.03) and a history of cytomegalovirus disease (3 of 4 [75%] vs. 2 of 30 [7%], P<0.01). However, the mean estimated creatinine clearance was similar in patients with or without BKV viruria (49 vs. 47 mL/min).

Conclusions: BKV viruria was present in a proportion of NRSOT patients with otherwise unexplained chronic renal dysfunction. The possibility that BKV infection might contribute to chronic renal dysfunction in this setting warrants further investigation.

Từ khóa


Tài liệu tham khảo

10.1016/S1473-3099(03)00770-9

Ramos E, 2002, BK virus nephropathy diagnosis and treatment, experience at the University of Maryland renal transplant program, 143

Kazory A, 2003, Renal transplantation and polyomavirus infection, recent clinical facts and controversies, 5, 65

10.1046/j.1523-1755.2003.00103.x

10.1056/NEJM200005043421802

10.1056/NEJMoa020439

10.1016/S1053-2498(02)00412-6

10.1053/jlts.2003.50113

10.1046/j.1523-1755.2002.00361.x

10.1056/NEJMoa021744

10.1097/00007890-200204270-00030

10.1034/j.1600-6143.2003.00126.x-i1

10.1097/01.TP.0000119156.52197.CA

10.1086/320711

10.1128/JCM.42.3.1176-1180.2004

10.1016/S0041-1345(00)01889-3

10.1097/01.TP.0000061597.09830.49

10.1056/NEJM200005043421809

Mylonakis E, 2001, BK virus in solid organ transplant recipients, an emerging syndrome, 72, 1587

10.1111/j.1600-6143.2005.00742.x

Puliyanda D, 2003, Heart and liver transplant recipients are at a low risk for polyoma virus BK viremia and nephropathy [abstract], Am J Transplant, 3, 510