INFLUENCE OF LONG-TERM ERYTHROPOIETIN TREATMENT ON INSULIN, GLUCAGON,PANCREATIC-POLYPEPTIDE, AND GASTRIN-SECRETION IN HEMODIALYZED PATIENTS

Citation
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
Citations number
10
Categorie Soggetti
Urology & Nephrology
ISSN journal
09310509
Volume
9
Year of publication
1994
Supplement
3
Pages
35 - 39
Database
ISI
SICI code
0931-0509(1994)9:<35:IOLETO>2.0.ZU;2-H
Abstract
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.