Cytomegalovirus prevention strategies and the risk of BK polyomavirus viremia and nephropathy
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
LO1503
National Sustainability Program I - International
Ministry of Education, Youth and Sports of the Czech Republic - International
Charles University Research Fund - International
CZ.02.1.01/0.0/0.0/16_019/0000787
Fighting INfectious Diseases - International
European Regional Development Fund - International
PubMed
31220412
DOI
10.1111/ajt.15507
PII: S1600-6135(22)09221-8
Knihovny.cz E-zdroje
- Klíčová slova
- clinical research/practice, clinical trial, infection and infectious agents - viral: BK/JC/polyoma, infection and infectious agents - viral: cytomegalovirus (CMV), infectious disease, kidney transplantation/nephrology,
- MeSH
- chronické selhání ledvin komplikace chirurgie MeSH
- cytomegalovirové infekce prevence a kontrola MeSH
- Cytomegalovirus MeSH
- dospělí MeSH
- infekce onkogenními viry prevence a kontrola MeSH
- lidé středního věku MeSH
- lidé MeSH
- multivariační analýza MeSH
- polyomavirové infekce virologie MeSH
- premedikace MeSH
- přežívání štěpu MeSH
- proporcionální rizikové modely MeSH
- prospektivní studie MeSH
- randomizované kontrolované studie jako téma MeSH
- rizikové faktory MeSH
- transplantace ledvin škodlivé účinky MeSH
- valaciclovir terapeutické užití MeSH
- valganciklovir terapeutické užití MeSH
- viremie etiologie MeSH
- virus BK MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- valaciclovir MeSH
- valganciklovir MeSH
Polyomavirus BK (BKV) is the cause of polyomavirus-associated nephropathy resulting in premature graft loss. There are limited data regarding the role of cytomegalovirus (CMV) infection and its prevention in developing BKV viremia and PVAN. In a prospective study, we analyzed 207 consecutive renal transplant recipients previously enrolled in 2 randomized trials evaluating different CMV prevention regimens with routine screening for BKV and CMV. Of these, 59 received valganciclovir and 100 valacyclovir prophylaxis; 48 patients were managed by preemptive therapy. At 3 years, the incidence of BKV viremia and PVAN was 28% and 5%, respectively. CMV DNAemia developed in 55% and CMV disease in 6%. Both BKV viremia (42% vs 23% vs 21%, P = .006) and PVAN (12% vs 2% vs 2%, P = .011) were increased in patients treated with valganciclovir prophylaxis compared to valacyclovir and preemptive therapy. Using multivariate Cox proportional hazard regression, valganciclovir prophylaxis was independent predictor of BKV viremia (hazard ratio [HR] = 2.38, P = .002) and PVAN (HR = 4.73, P = .026). In contrast, the risk of subsequent BKV viremia was lower in patients with antecedent CMV DNAemia (HR = 0.50, P = .018). These data suggest valganciclovir prophylaxis may be associated with increased risk of BKV viremia and PVAN. CMV DNAemia did not represent a risk for BKV.
Zobrazit více v PubMed
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