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MEDICC Review  2012 

Use of cuban recombinant human erythropoietin in Parkinson's disease treatment

DOI: 10.1590/S1555-79602012000100003

Keywords: parkinson disease, erythropoietin, recombinant proteins, neuroprotective agents, clinical trial, safety, ior-epocim, cuba.

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Abstract:

introduction recombinant human erythropoietin is used primarily to treat anemia. there is evidence of its neuroprotective capacity from preclinical studies in parkinson's disease and other neurodegenerative diseases. recombinant human erythropoietin produced in cuba (ior-epocim) is registered and approved for use in humans in cuba and in a number of other countries. objective assess safety and possible neuroprotective effect of ior-epocim in a group of parkinson's disease patients. methods a three-phase exploratory study (proof of concept) was conducted from august 2008 to april 2009: preliminary assessment, treatment (weeks 1-5), and post-treatment (weeks 6-35). participants were 10 parkinson's disease patients (8 men, 2 women) from the outpatient clinic at the international neurological restoration center, all at least one year post onset, aged 47-65 years. the ior-epocim was administered subcutaneously in a once-weekly dose (60 iu/kg body weight) for five weeks. therapy with patients' antiparkinsonian drugs was maintained throughout the study, except during motor examination, conducted following a 12-hour withdrawal (off condition). safety was evaluated primarily by recording adverse events (by intensity and causality) from start of treatment until the study's completion. hematological parameters and blood pressure were also measured because of their direct relationship to the medication's action. to evaluate possible neuroprotective activity, variables were included related to patients' motor function and cognitive and affective status, measured using internationally recognized scales. all variables were evaluated before, during and after treatment. data were processed using a fixed-effects linear model, with a repeated-measures design (significance level p < 0.05). results three patients experienced mild adverse events (precordial discomfort and hypertension in one; leg fatigue in another; renal colic in a third), with a possible causal relationship in the firs

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