Evidence map›Paper›PMID 17906856›Full record

Trial reportEuropean journal of clinical pharmacology2007

Influence of SLCO1B1, 1B3, 2B1 and ABCC2 genetic polymorphisms on mycophenolic acid pharmacokinetics in Japanese renal transplant recipients.

Masatomo Miura, Shigeru Satoh, Kazuyuki Inoue, Hideaki Kagaya, Mitsuru Saito, Takamitsu Inoue, Toshio Suzuki, Tomonori Habuchi

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in European journal of clinical pharmacology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 149 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. An integrated sampling strategy for therapeutic mycophenolic acid monitoring in lung transplant recipients.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2025
    Article
  6. Article
  7. The Impact ofJournal of personalized medicine · 2024
    Article
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  9. Review
  10. Article
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  19. Observational
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Masatomo MiuraDepartment of Pharmacy, Akita University Hospital, Akita, Japan.
Shigeru Satoh
Kazuyuki Inoue
Hideaki Kagaya
Mitsuru Saito
Takamitsu Inoue
Toshio Suzuki
Tomonori Habuchi
Akita University · JPAkita University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe investigated the association between mycophenolic acid (MPA) pharmacokinetics and organic anion-transporting polypeptide (OATP/SLCO)1B1, 1B3, 2B1 and multidrug resistance-association protein 2 (MRP2/ABCC2) genetic polymorphisms and diarrhea.

methodsEighty-seven renal allograft recipients were given repeated doses of mycophenolate mofetil every 12 h at a designated time (09:00 and 21:00). The pharmacokinetics of MPA were analyzed on day 28 posttransplantation.

resultsThe dose-adjusted area under the cuve (AUC)(6-12) of MPA, an estimate of enterohepatic recirculation, was greater in SLCO1B3 T334G GG (or G699A AA) carriers than in TT carriers (or G699A GG) (40 vs. 25 ng h/mL per milligram, respectively, P = 0.0497). None of the polymorphism of SLCO1B1, SLCO2B1, or ABCC2 C-24T were associated with MPA pharmacokinetics or diarrhea. However, the oral clearance of MPA in recipients having both the SLCO1B3 T334G GG genotype and the ABCC2 C-24T T allele was significantly lower than in patients having both the SLCO1B3 T334G TT and ABCC2 C-24T CC genotypes (0.15 vs. 0.18 L/h per kilogram, respectively, P = 0.0010).

conclusionsMPA excretion into bile in patients with SLCO1B3 T334G GG (or G699A AA) was higher than in those with T334G TT (or G699A GG), probably resulting in a higher AUC(6-12) value of MPA. MPA uptake into hepatocytes and excretion into bile at first pass may be greater in SLCO1B3 T334G GG carriers than in TT carriers. In addition, the ABCC2 C-24T polymorphism also seems to be associated with enhanced enterohepatic circulation of MPA. The SLCO1B3 and ABCC2 transporters rather than uridine diphosphate-glucuronosyltransferase (UGT) may partly affect interindividual variety in plasma MPA concentration.

Indexed as

Kidney TransplantationPolymorphism, GeneticAdultAntibiotics, AntineoplasticArea Under CurveATP-Binding Cassette, Sub-Family C ProteinsFemaleGenotypeHumansImmunosuppressive AgentsJapanLiver-Specific Organic Anion Transporter 1MaleMembrane Transport ProteinsMiddle AgedMultidrug Resistance-Associated Protein 2ABCC2 protein, humanAntibiotics, AntineoplasticATP-Binding Cassette, Sub-Family C ProteinsImmunosuppressive AgentsLiver-Specific Organic Anion Transporter 1Membrane Transport ProteinsMultidrug Resistance-Associated Protein 2Mycophenolic AcidOrganic Anion TransportersOrganic Anion Transporters, Sodium-IndependentSLCO1B1 protein, humanSLCO1B3 protein, humanSLCO2B1 protein, humanSolute Carrier Organic Anion Transporter Family Member 1B3Tacrolimus

Identifiers

PMID17906856
OpenAlexW2084711681

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.