2013, Number 1
Risk factors for seropositivity for human herpesvirus-8 in patients with chronic renal failure in transplant waiting list and in renal transplant recipients
Bostock IC, Alberú J, Salazar-Nando A, Huante-Pérez A, Cervantes M, León-García D, Figueroa-Granados V, Gabilondo B, Morales-Buenrostro LE, Vilatobá CM, Soto-Ramírez LE
Language: Spanish
References: 12
Page: 15-19
PDF size: 72.57 Kb.
ABSTRACT
The prevalence of human herpes virus-8 antibodies has a great geographic variability in the general population and in pre- and post-kidney transplant recipients, and is associated with the development of Kaposi’s sarcoma. In Mexico, human herpes virus-8 seroprevalence in 307 blood donors was 0.65%. Aim: To investigate: 1) human herpes virus-8 seroprevalence, and 2) associated risk factors for seropositivity, in a) 156 chronic renal failure patients (pts) randomly selected from a waiting list for cadaveric transplantation, and b) 118 kidney transplant recipients with functioning grafts at diverse post-Kidney transplant follow up. Methods: Demographic data were obtained for kidney transplant recipients from clinical files and by a self-administered questionnaire for sexual practices; in chronic renal failure pts, data were obtained by direct interview. Serum samples from all pts were tested for IgG antibodies using an ELISA commercial kit. Data analyzed: chronic renal failure group: mean age 36 ± 13 years, 50% male, overall mean time on dialysis 43 ± 47 mos (20.5% hemodialysis, 56% CAPD, 18.6% both, 5 none), blood transfusion history (BT) 78%, previous kidney transplant 9%. Kidney transplant recipients group: mean age 30 ± 11 years, 55% male, mean time post-kidney transplant follow up 111 ± 70 mos, pre-kidney transplant overall time on dialysis 22 ± 21.8 mos (37% hemodialysis, 35.6% CAPD, 23% both, 4% none), blood transfusion 79%, triple drug immunosuppressive therapy 76%. Results: human herpes virus-8 IgG antibodies were detected in 6/156 (3.8%) and in 4/118 (3.4%) chronic renal failure and kidney transplant recipients patients, respectively. There were no risk factors significantly associated with human herpes virus-8 antibodies in the chronic renal failure group. However, in kidney transplant recipients patients, multivariate analysis demonstrated hemodialysis to be a significant risk factor (p = 0.03), and a blood transfusion showed a trend towards statistical significance (p = 0.06); on the other hand, by univariate analysis a blood transfusion was a significant risk factor (p = 0.04), and hemodialysis showed a trend (p = 0.089). Conclusions: Chronic renal failure patients, regardless of having received a kidney transplant, had a high risk for human herpes virus-8 infection (› 5 times of the prevalence among healthy blood donors). The exposure to blood products was a risk factor for this infection in kidney transplant recipients; the lack of significance of this factor in chronic renal failure group could be related to the low number of infected pts studied. Although the kidney transplant recipients studied remain free of Kaposi’s sarcoma, they should be closely monitored.REFERENCES