In a prospective study, 40 maintenance hemodialysis patients, randomiz
ed in two equal groups, were treated with recombinant human erythropoi
etin (rHuEPO) for their renal anemia, for a period of 2 years. One gro
up was treated for 2 years, while the other was untreated control duri
ng the first year, but received rHuEPO during the second year of the s
tudy. Anemia was corrected in all treated patients and hematocrit main
tained between 30 and 35 vol% by low-dose subcutaneous treatment with
Recormon(R) (Boehringer Mannheim GmbH, Germany), according to the stud
y protocol. Bone marrow biopsy (BMB), from the posterior iliac crest,
was taken by the method of Jamshidi from 32 patients. Fourteen patient
s from the control group were biopsied twice: once at baseline and the
second time at 12 months of treatment, while 15 patients from the oth
er group were biopsied only once, at 24 months of rHuEPO treatment. Th
e biopsies were embedded in wax and in epoxy resin, and after staining
for light and electron microscopy, they were semiquantitatively exami
ned for several parameters: cellularity, myeloid:erythroid (M:E) ratio
, megakaryocytes, fatty tissue, megaloblasts, and marrow iron. Cellula
rity of the bone marrow increased significantly at 12 months of treatm
ent and it remained so at 24 months. M:E ratio was significantly reduc
ed indicating expansion of the erythroid pool, both at 12 and 24 month
s of therapy. The number of megakaryocytes in the bone marrow increase
d significantly at 12 months and remained high at 24 months of treatme
nt, while fatty tissue was significantly reduced at 12 and 24 months c
ompared to the baseline values. There was no significant change in the
percentage of megaloblasts in the bone marrow. Hemosiderin was reduce
d after treatment indicating mobilization of the bone marrow iron stor
es upon treatment with rHuEPO, We concluded that rHuEPO had a benefici
al long-term effect on bone marrow.