Background/Aim: Decreased sensitivity to the hypoglycaemic action of insuli
n is an almost universal phenomenon in uraemic patients, and it is attribut
ed either to uraemic toxins or to anaemia or even to secondary hyperparathy
roidism. Considering the conflicting data of few existing studies, we exami
ned the influence of erythropoietin (EPO) treatment on insulin resistance a
nd tested the probable correlation of this influence with sympathetic nervo
us system (SNS) activity. Methods: We studied 8 non-obese, non-diabetic, st
able dialysis patients using the euglycaemic insulin clamp technique before
administration of EPO (phase A), 10 days after (phase B), and after the co
rrection of the haematocrit level, at least 8 weeks later (phase C). We est
imated the indices (glucose infusion rate, mg/kg/min), M/G (glucose clearan
ce), and M/I (tissue sensitivity to insulin), and we measured haematocrit,
haemoglobin, triglyceride, ferritin, EPO, and fasting insulin levels in eac
h phase. During each phase, we tested the SNS activity using the response o
f blood pressure to persistent handgrip and the response of blood pressure
to the standing position. Results: Our patients appeared to have an increas
ed insulin resistance in phase A (M-A = 6.24 +/- 1.01) which was significan
tly improved 10 days after the beginning of EPO treatment and before the ri
se of haematocrit (M-B = 7.71 +/- 1.54, p < 0.05). There was no further imp
rovement in phase C. Indices M/G and M/I behaved similarly. The serum trigl
yceride levels decreased in response to the increased insulin sensitivity.
The patients studied did not demonstrate fasting hyperinsulinaemia, while t
he SNS activity was abnormal and remained unchanged throughout the study pe
riod in spite of some individual improvement. Conclusions: Our study proves
the beneficial effect of EPO treatment on insulin resistance in dialysis p
atients which could be attributed to the EPO itself and not to the correcti
on of anaemia and is accompanied by improvement in triglyceride levels. Ame
lioration of insulin resistance did not influence the SNS activity, making
the association between EPO treatment and SNS-derived changes in blood pres
sure quite improbable. Copyright (C) 2000 S. Karger AG. Basel.