Evidence map›Paper›PMID 31745229›Full record

ArticleScientific reports2019

Effect of food on the pharmacokinetics and therapeutic efficacy of 4-phenylbutyrate in progressive familial intrahepatic cholestasis.

Satoshi Nakano, Shuhei Osaka, Yusuke Sabu, Kei Minowa, Saeko Hirai, Hiroki Kondou, Takeshi Kimura, Yoshihiro Azuma, Satoshi Watanabe, Ayano Inui and 11 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
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

21 authors at 11 institutions in 1 country.

Satoshi NakanoLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Science, The University of Tokyo, Tokyo, Japan.
Shuhei OsakaLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Science, The University of Tokyo, Tokyo, Japan.
Yusuke SabuLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Science, The University of Tokyo, Tokyo, Japan.
Kei MinowaDepartment of Pediatrics, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Saeko HiraiDepartment of Pediatrics, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Hiroki KondouDepartment of Pediatrics, Kindai University Nara Hospital, Nara, Japan.ORCID http://orcid.org/0000-0002-2461-1303
Takeshi KimuraDepartment of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.
Yoshihiro AzumaDepartment of Pediatrics, Yamaguchi University Graduate School of Medicine, Yamaguchi, Japan.
Satoshi WatanabeDepartment of Pediatrics, Nagasaki University Hospital, Nagasaki, Japan.ORCID http://orcid.org/0000-0003-1878-1717
Ayano InuiDepartment of Pediatric Hepatology and Gastroenterology, Saiseikai Yokohama City Tobu Hospital, Kanagawa, Japan.
Kazuhiko BesshoDepartment of Pediatrics, Osaka University Graduate School of Medicine, Osaka, Japan.
Hidefumi NakamuraClinical Research Center, National Center for Child Health and Development, Tokyo, Japan.
Hironori KusanoDepartment of Pathology, Kurume University School of Medicine, Fukuoka, Japan.
Atsuko NakazawaDepartment of Clinical Research, Saitama Children's Medical Center, Saitama, Japan.
Ken TanikawaDepartment of Diagnostic Pathology, Kurume University Hospital, Fukuoka, Japan.
Masayoshi KageKurume University Research Center for Innovative Cancer Therapy, Fukuoka, Japan.
Toshiaki ShimizuDepartment of Pediatrics, Juntendo University Graduate School of Medicine, Tokyo, Japan.
Hiroyuki KusuharaLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Science, The University of Tokyo, Tokyo, Japan.
Yoh ZenDepartment of Diagnostic Pathology, Kobe University, Hyogo, Japan.
Mitsuyoshi SuzukiDepartment of Pediatrics, Juntendo University Graduate School of Medicine, Tokyo, Japan.ORCID http://orcid.org/0000-0002-9969-3454
Hisamitsu HayashiLaboratory of Molecular Pharmacokinetics, Graduate School of Pharmaceutical Science, The University of Tokyo, Tokyo, Japan. hayapi@mol.f.u-tokyo.ac.jp.ORCID http://orcid.org/0000-0002-5247-895X
Juntendo University · JPThe University of Tokyo · JPKurume University · JPThe University of Osaka · JPKobe University · JPKurume University Hospital · JPNagasaki University Hospital · JPNara Medical University Hospital · JPNational Center For Child Health and Development · JPSaitama Children's Medical Center · JPYamaguchi University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progressive familial intrahepatic cholestasis (PFIC), a rare inherited disorder, progresses to liver failure in childhood. We have shown that sodium 4-phenylbutyrate (NaPB), a drug approved for urea cycle disorders (UCDs), has beneficial effects in PFIC. However, there is little evidence to determine an optimal regimen for NaPB therapy. Herein, a multicenter, open-label, single-dose study was performed to investigate the influence of meal timing on the pharmacokinetics of NaPB. NaPB (150 mg/kg) was administered orally 30 min before, just before, and just after breakfast following overnight fasting. Seven pediatric PFIC patients were enrolled and six completed the study. Compared with postprandial administration, an approved regimen for UCDs, preprandial administration significantly increased the peak plasma concentration and area under the plasma concentration-time curve of 4-phenylbutyrate by 2.5-fold (95% confidential interval (CI), 2.0-3.0;P = 0.003) and 2.4-fold (95% CI, 1.7-3.2;P = 0.005). The observational study over 3 years in two PFIC patients showed that preprandial, but not prandial or postprandial, oral treatment with 500 mg/kg/day NaPB improved liver function tests and clinical symptoms and suppressed the fibrosis progression. No adverse events were observed. Preprandial oral administration of NaPB was needed to maximize its potency in PFIC patients.

Indexed as

DietDrug SynergismAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 11ChildChild, PreschoolCholestasis, IntrahepaticFemaleHumansInfantMaleMutationPhenylbutyratesPrognosisTissue Distribution4-phenylbutyric acidABCB11 protein, humanAntineoplastic AgentsATP Binding Cassette Transporter, Subfamily B, Member 11Phenylbutyrates

Identifiers

PMID31745229
PMCPMC6863819
OpenAlexW2990552804

What OpenQuestion holds

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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.