F. Kokot et al., INFLUENCE OF LONG-TERM ERYTHROPOIETIN TREATMENT ON INSULIN, GLUCAGON,PANCREATIC-POLYPEPTIDE, AND GASTRIN-SECRETION IN HEMODIALYZED PATIENTS, Nephrology, dialysis, transplantation, 9, 1994, pp. 35-39
As already reported short-term rHuEpo treatment influences plasma insu
lin, glucagon, pancreatic polypeptide (PP), and gastrin secretion in h
aemodialysed patients. The present study aimed to assess the influence
of long-term rHuEpo treatment on secretion of above mentioned hormone
s. A total of 27 haemodialysed patients and nine healthy subjects were
examined. Nine patients with uraemic anaemia were treated with rHuEpo
for 12 months (Epo group) while another nine patients did not receive
rHuEpo (non-Epo group), but were monitored biochemically and clinical
ly as patients of the Epo group. The third group (HD) comprised nine h
aemodialysed patients with a haematocrit value of greater-than-or-equa
l-to 30% without rHuEpo therapy. In all subjects plasma levels of insu
lin, glucagon, gastrin, and PP were estimated before and after adminis
tration of a test meal. Patients of the Epo group were examined before
and after 6 and 12 months of rHuEpo treatment (patients of the Epo gr
oup) or clinical monitoring (patients of the non-Epo group) respective
ly, while only one test was performed in patients of the HD group and
healthy subjects. Six months of rHuEpo treatment was followed by an in
crease of fasting insulinaemia and a decrease of basal plasma level of
glucagon and PP. At that time point rHuEpo therapy also increased the
response of insulin, glucagon, and gastrin to the test meal. After 12
months of rHuEpo therapy basal insulinaemia returned to the pretreatm
ent value while plasma levels of PP and glucagon were still lower than
pretreatment ones. After 12 months of rHuEpo therapy the response of
PP secretion to a test meal was higher while that of gastrin secretion
lower that the pretreatment ones. Our results suggest that rHuEpo tre
atment exerts a profound effect on secretion of insulin, gastrin, PP,
and glucagon secretion, which seems to be dependent upon duration of r
HuEpo therapy and not only, or exclusively, to improvement of the haem
atological status.