This preliminary study was designed in a trial to delineate the size o
f the problem of ochratoxicosis and its relation to genesis of lesions
mounting to end stage renal disease (ESRD) or urothelial tumors in Eg
ypt. This study comprised five groups of patients having renal disease
s of different presentations; they are: patients with (ESRD) under con
servative medical treatment (group 1), patients with (ESRD) under trea
tment with regular hemodialysis (group 2), renal allograft recipients
(group 3), patients with nephrotic syndrome (group 4) and patients wit
h urothelial tumors (group 5). In addition, two reference groups: pote
ntial related donors for renal transplantation (group 6) and healthy c
ontrol with negative family history of renal disease (group 7). For al
l groups, laboratory, radiological and histopathological evaluation of
kidney status were carried out coupled with determination of ochratox
in A level in serum, in urine and in biopsy specimens of patients with
urothelial tumors. High ochratoxin serum levels were found in patient
s with ESRD (groups 1 and 2) (P < 0.01), higher serum levels were dete
cted in the group without dialysis (group 1) in comparison with the re
ference groups possibly due to ochratoxin. A clearance by dialysis. Oc
hratoxin A was detected in serum and urine of renal transplant recipie
nts (group 3) (P < 0.01) and especially higher levels were found in pa
tients with nephrotic syndrome (group 4) (P < 0.001). For the group wi
th urothelial turner (group 5), positive serum, urine and tissue biops
y specimens for ochratoxin levels were found (P < 0.01). The results c
ould lead to the conclusion that ochratoxin A could be correlated to t
he genesis of renal disease leading to (ESRD) or causing urothelial ca
ncer. A thorough and in depth study of the problem of ochratoxicosis a
nd renal disease causation in Egypt is now recommended.