Evidence map›Paper›PMID 29243113›Full record

SynthesisEuropean journal of clinical pharmacology2018

Effect of UGT2B7 genotypes on plasma concentration of valproic acid: a meta-analysis.

Ping Wang, Xiao-Qian Lin, Wen-Ke Cai, Gui-Li Xu, Meng-Di Zhou, Mei Yang, Gong-Hao He

Abstract readMeta-AnalysisReview
PubMed Publisher
In one paragraph

Synthesis in European journal of clinical pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 3 pooled it
6.9field-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

23 citing papers in PubMed, 3 syntheses or guidelines pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Hydrocodone, Oxycodone, and Morphine Metabolism and Drug-Drug Interactions.The Journal of pharmacology and experimental therapeutics · 2023
    Review
  7. Article
  8. Cannabis Pharmacogenomics: A Path to Personalized Medicine.Current issues in molecular biology · 2023
    Review
  9. Article
  10. Review
  11. Valproic acid autoinduction: a case-based review.International journal of bipolar disorders · 2021
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Observational
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

7 authors at 2 institutions in 1 country.

Ping WangDepartment of Pharmacy, Kunming General Hospital of PLA, 212 Daguan Rd, Kunming, 650032, China.
Xiao-Qian LinDepartment of Pharmacy, Kunming General Hospital of PLA, 212 Daguan Rd, Kunming, 650032, China.
Wen-Ke CaiDepartment of Cardio-Thoracic Surgery, Kunming General Hospital of PLA, Kunming, 650032, China.
Gui-Li XuDepartment of Pharmacy, Kunming General Hospital of PLA, 212 Daguan Rd, Kunming, 650032, China.
Meng-Di ZhouDepartment of Pharmacy, Kunming General Hospital of PLA, 212 Daguan Rd, Kunming, 650032, China.
Mei YangDepartment of Pharmacy, Kunming General Hospital of PLA, 212 Daguan Rd, Kunming, 650032, China.
Gong-Hao HeDepartment of Pharmacy, Kunming General Hospital of PLA, 212 Daguan Rd, Kunming, 650032, China. gonghow@hotmail.com.
The First Hospital of Kunming · CNDali University · CN

Funding

National Natural Science Foundation of China 81460560the Applied Basic Research Program of Yunnan Province 2017FB134
6 · The paper itself

Abstract

purposeValproic acid (VPA) is one of the most widely used antiepileptic drugs. Recently, increasing evidence suggested that polymorphisms in UGT2B7 gene were associated with VPA pharmacokinetics, but results remained controversial. Therefore, a meta-analysis was performed to derive a more precise evaluation between C802T, C161T, and G211T polymorphisms and plasma concentration of VPA.

methodsThe PubMed, EMBASE, and the Cochrane library databases were searched for eligible studies. Articles meeting the inclusion criteria were comprehensively reviewed, and the available data were accumulated. The mean difference (MD) and 95% confidence interval (CI) were applied to assess the strength of the relationship.

resultsA total of 12 studies involving 1996 related East Asia epilepsy patients were assessed. We found that the UGT2B7 G211T polymorphism was associated with adjusted plasma VPA concentration (GG versus TT: P = 0.01, I

conclusionsThe results of this meta-analysis demonstrated that UGT2B7 G211T and C161T polymorphisms were able to affect the pharmacokinetics in epilepsy patients treated with VPA, which provide further evidence for genetic effects of UGT2B7 gene on pharmacokinetics and pharmacodynamics of VPA. Epilepsy patients with these genotypes may be necessary to increase (or decrease) VPA dose to ensure its therapeutic effect.

Indexed as

Pharmacogenomic VariantsPolymorphism, GeneticAnticonvulsantsChi-Square DistributionEpilepsyGene FrequencyGlucuronosyltransferaseHeterozygoteHomozygoteHumansPharmacogeneticsPhenotypeValproic AcidAnticonvulsantsGlucuronosyltransferaseUGT2B7 protein, humanValproic AcidMeta-analysisPharmacokineticsPlasma concentrationSingle-nucleotide polymorphismUGT2B7Valproic acid

Identifiers

PMID29243113
OpenAlexW2773107542

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.