Anemia in kidney transplants without erythropoietic agents: levels of erythropoietin and iron parameters

Transplant Proc. 2012 Nov;44(9):2590-2. doi: 10.1016/j.transproceed.2012.09.044.

Abstract

Aim: To study the association between hemoglobin, endogenous erythropoietin (EPO) levels and ferric parameters in kidney recipients not treated with EPO-stimulating agents.

Materials and methods: Transverse study of 219 kidney transplant outpatients. The median time after transplantation was 54 months (P(25-75), 23-107). We assessed blood counts, ferric parameters, EPO levels, renal function (MDRD-4), and adjuvant treatment. We performed a linear regression analysis to predict hemoglobin.

Results: Median EPO values were 14.05 mUI/mL (P(25-75) = 10.2-19.7). Applying the formulas described by Beguin, kidney transplant recipients showed a low observed/expected ratio of erythropoietin and of transferrin. Considering anemia to be an hemoglobin of < 12 g/dL in women and < 13 g/dL in men, 24.2% of subjects were anemic (n = 53), including 2.3% with hemoglobin < 11 g/dL. Anemic patients displayed worse renal function (49.2 ± 18.5 versus 55.46 ± 16.58 mL/min/1.73 m(2) in nonanemic; P = .021). There were no differences in C-reactive protein. The patients receiving a combination of angiotensin-converting enzyme inhibitors (ACEI) and angiotensin II receptor blockers (ARB) showed the highest prevalence of anemia compared with other groups (42.9%, P = .027). EPO levels were significantly lower among patients treated with these drugs (P = .041), without differences in transferrin and ferritin. The percentage of anemic patients treated with mammalian target of rapamycin inhibitors (mTORi) was 31% versus 22.2% among those not receiving these immunosuppressants (P = .23). Although there were no differences in hemoglobin levels, patients treated with mTORi, showed higher EPO levels (P = .005) and lower mean corpuscular volume (P < .001). Regarding the etiology of chronic kidney disease, less frequently anemic patients were those with polycystic kidney disease (8.6% versus 26.7% in the rest, P = .021). The formula obtained by multiple linear regression to calculate hemoglobin was: hemoglobin = 11829-0909 log (EPG level) - 0455 (if female) + 0.010 0.013 transferrin + 0.013 creatinine clearance (r = .424, P < .001).

Conclusions: Treatment with ACEI and/or ARBs seemed to produce a defect in the synthesis of EPO, while those treated with mTORi, a hyporesponsive state.

MeSH terms

  • Adult
  • Aged
  • Anemia / blood*
  • Anemia / epidemiology*
  • Angiotensin II Type 1 Receptor Blockers / adverse effects
  • Angiotensin-Converting Enzyme Inhibitors / adverse effects
  • Biomarkers / blood
  • Cross-Sectional Studies
  • Erythropoietin / blood*
  • Female
  • Ferritins / blood
  • Hemoglobins / analysis
  • Humans
  • Immunosuppressive Agents / adverse effects
  • Incidence
  • Iron / blood*
  • Kidney / physiopathology
  • Kidney Transplantation / adverse effects*
  • Linear Models
  • Male
  • Middle Aged
  • Protein Kinase Inhibitors / adverse effects
  • Risk Factors
  • Spain / epidemiology
  • TOR Serine-Threonine Kinases / antagonists & inhibitors
  • Time Factors
  • Transferrin / analysis

Substances

  • Angiotensin II Type 1 Receptor Blockers
  • Angiotensin-Converting Enzyme Inhibitors
  • Biomarkers
  • EPO protein, human
  • Hemoglobins
  • Immunosuppressive Agents
  • Protein Kinase Inhibitors
  • Transferrin
  • Erythropoietin
  • Ferritins
  • Iron
  • MTOR protein, human
  • TOR Serine-Threonine Kinases