Evidence map›Paper›PMID 29312149›Full record

ArticleFrontiers in endocrinology2017

Effect of Osteocyte-Ablation on Inorganic Phosphate Metabolism: Analysis of Bone-Kidney-Gut Axis.

Osamu Fujii, Sawako Tatsumi, Mao Ogata, Tomohiro Arakaki, Haruna Sakaguchi, Kengo Nomura, Atsumi Miyagawa, Kayo Ikuta, Ai Hanazaki, Ichiro Kaneko and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2017. 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
0.7field-weighted citation impact, top 29% 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, 9 citations in OpenAlex.

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

12 authors at 1 institution in 1 country.

Osamu FujiiDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Sawako TatsumiDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Mao OgataDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Tomohiro ArakakiDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Haruna SakaguchiDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Kengo NomuraDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Atsumi MiyagawaDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Kayo IkutaDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Ai HanazakiDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Ichiro KanekoDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Hiroko SegawaDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Ken-Ichi MiyamotoDepartment of Molecular Nutrition, Institution of Biomedical Science, Tokushima University Graduate School, Tokushima, Japan.
Tokushima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In response to kidney damage, osteocytes increase the production of several hormones critically involved in mineral metabolism. Recent studies suggest that osteocyte function is altered very early in the course of chronic kidney disease. In the present study, to clarify the role of osteocytes and the canalicular network in mineral homeostasis, we performed four experiments. In Experiment 1, we investigated renal and intestinal Pi handling in osteocyte-less (OCL) model mice [transgenic mice with the dentin matrix protein-1 promoter-driven diphtheria toxin (DT)-receptor that were injected with DT]. In Experiment 2, we administered granulocyte colony-stimulating factor to mice to disrupt the osteocyte canalicular network. In Experiment 3, we investigated the role of osteocytes in dietary Pi signaling. In Experiment 4, we analyzed gene expression level fluctuations in the intestine and liver by comparing mice fed a high Pi diet and OCL mice. Together, the findings of these experiments indicate that osteocyte ablation caused rapid renal Pi excretion (

Indexed as

bile acidfibroblast growth factor 23intestinekidneyKlotholiverosteocytephosphate

Identifiers

PMID29312149
PMCPMC5742590
OpenAlexW2777599602

What OpenQuestion holds

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LicenceCC BY
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.