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Effect of mycophenolate mofetil on hematological side effects incidence in renal transplant recipients.

Clinical transplantation
January 1, 2013
Joanna Sobiak et al. (5 authors)
Comparative StudyJournal ArticleHuman Study
Study Details

Study Goal

The researchers aimed to assess the relationship between mycophenolate mofetil (MMF) metabolites and hematopoietic adverse effects, including iron-related outcomes, in renal transplant recipients.

Results Summary

The study found that anemia was more frequent in MMF-treated patients, with higher plasma iron concentrations observed, but iron supplementation was ineffective in patients with declined renal function. MPAG pharmacokinetic parameters negatively correlated with hemoglobin and hematocrit, suggesting MPAG may predict MMF-induced anemia.

Population

Renal transplant recipients in the late post-transplant period (n = 61 MMF-treated patients out of 106 total participants).

Effective Dosage

Not specified

Duration

Not specified

Interactions

None mentioned

Extracted Claims (9)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Mycophenolate mofetil (MMF)
increase
hematological toxicity
solid organ transplantation patients
-
frequently causes
#1
Mycophenolate mofetil (MMF)
increase
anemia
renal transplant recipients
30.7% vs. 20.0%
more frequently observed
#2
Mycophenolate mofetil (MMF)
increase
plasma iron concentrations
patients treated with MMF
32.9 ± 9.4 μmol/L vs. 28.7 ± 9.4 μmol/L
significantly higher
#3
iron supplementation
increase
anemia
patients with anemia
48.2% vs. 20.3%
more frequently applied
#4
MPAG pharmacokinetic parameters
decrease
hemoglobin
renal transplant recipients
-
correlated negatively
#5
MPAG pharmacokinetic parameters
decrease
hematocrit
renal transplant recipients
-
correlated negatively
#6
MPAG pharmacokinetic parameters
increase
anemia
patients with anemia
-
higher
#7
extensive iron supplementation
no change
anemia
renal transplant recipients with deteriorated renal function
-
may be ineffective
#8
declined renal function
increase
anemia
renal transplant recipients
-
associated with
#9
Abstract

Mycophenolate mofetil (MMF), an immunosuppressant administered after solid organ transplantation, is generally well tolerated; however, it frequently causes hematological toxicity. In this study, we aimed to assess the relation between the pharmacokinetic parameters of MMF metabolites (mycophenolic acid [MPA] and 7-O-MPA glucuronide [MPAG]) and the adverse effects on the hematopoietic system in renal transplant recipients. The four-h pharmacokinetic profiles of MPA and MPAG were determined using the HPLC method for MMF-treated patients (n = 61) among 106 renal transplant recipients (during the late post-transplant period) participating in the study. Anemia was more frequently observed in the study group compared with the control group (30.7% vs. 20.0%) and although the difference was insignificant, plasma iron concentrations were significantly higher in patients treated with MMF (32.9 ± 9.4 μmol/L vs. 28.7 ± 9.4 μmol/L; p = 0.032). Iron supplementation was more frequently applied to patients with anemia (48.2%) compared with patients with hemoglobin within the norm (20.3%; p = 0.005). As all MPAG pharmacokinetic parameters correlated negatively with hemoglobin and hematocrit, and MPAG pharmacokinetic parameters were higher in patients with anemia, MPAG may be the predicting factor of MMF side effects. In renal transplant recipients, especially with deteriorated renal function, extensive iron supplementation may be ineffective as anemia was associated with declined renal function and was not caused by low iron concentration.

Medical Subject Headings (MeSH)
AdultAgedAnemiaCase-Control StudiesFemaleFollow-Up StudiesGlomerular Filtration RateHematopoietic SystemHumansImmunosuppressive AgentsIncidenceKidney Failure, ChronicKidney Function TestsKidney TransplantationMaleMiddle AgedMycophenolic AcidPrognosisRisk FactorsYoung Adult
Study Links
Quality Scores
SafetyNot Assessed
Efficacy30/10
Quality65/10
Citation Metrics
Total Citations15
Citations/Year1.3
Relative Citation Ratio0.72
NIH Percentile38.5%
Research Impact Scores
APT Score0.50
Weight Score1.32
Normalized Score0.45
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