Evidence map›Paper›PMID 31666542›Full record

ArticleScientific reports2019

AST-120, an Oral Carbon Absorbent, Protects against the Progression of Atherosclerosis in a Mouse Chronic Renal Failure Model by Preserving sFlt-1 Expression Levels.

Yasuki Nakada, Kenji Onoue, Tomoya Nakano, Satomi Ishihara, Takuya Kumazawa, Hitoshi Nakagawa, Tomoya Ueda, Taku Nishida, Tsunenari Soeda, Satoshi Okayama and 3 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 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. sFlt-1 in Chronic Kidney Disease: Friend or Foe?International journal of molecular sciences · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Advances in biomarker development and potential application for preeclampsia based on pathogenesis.European journal of obstetrics & gynecology and reproductive biology: X · 2021
    Review
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  16. 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

13 authors at 1 institution in 1 country.

Yasuki NakadaDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Kenji OnoueDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan. konoue@naramed-u.ac.jp.
Tomoya NakanoDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Satomi IshiharaDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Takuya KumazawaDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Hitoshi NakagawaDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Tomoya UedaDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Taku NishidaDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Tsunenari SoedaDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Satoshi OkayamaDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Makoto WatanabeDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Rika KawakamiDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Yoshihiko SaitoDepartment of Cardiovascular Medicine, Nara Medical University, Kashihara, Nara, 634-8522, Japan.
Nara Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Soluble Flt-1 (sFlt-1), an endogenous antagonist of the proatherogenic cytokine placental growth factor, is decreased in chronic kidney disease (CKD), leading to atherosclerotic progression. In this study, we investigated the effect of AST-120, an oral carbon adsorbent which can remove uremic toxins, on sFlt-1 expression levels and atherosclerosis progression. Atherosclerotic apolipoprotein E-deficient mice underwent a 5/6 nephrectomy (5/6 NR) or a sham operation (sham) at 8 weeks of age and were then treated or not with oral AST-120 for 12 weeks. sFlt-1 expression levels and the degree of atherosclerosis were assessed at 22 weeks of age in each of the four groups (sham; n = 7, 5/6 NR; n = 10, sham + AST-120: n = 8, 5/6 NR + AST-120; n = 8). The expression levels of sFlt-1 mRNA in the kidney were significantly lower in the 5/6 NR group than in the sham group, but AST-120 treatment prevented this decrease in sFlt-1 levels. Similarly, the atherosclerotic plaque area of the thoracoabdominal aorta was significantly larger in the 5/6 NR group than in the sham group, and AST-120 treatment prevented this increase in atherosclerosis. AST-120 could, therefore, be used as a therapeutic to treat atherosclerosis in patients with CKD.

Indexed as

Administration, OralAnimalsAtherosclerosisCarbonDisease Models, AnimalDisease ProgressionGene Expression RegulationHumansHuman Umbilical Vein Endothelial CellsKidney Failure, ChronicMiceOxidesRNA, MessengerSolubilityVascular Endothelial Growth Factor Receptor-1AST 120CarbonFlt1 protein, mouseOxidesRNA, MessengerVascular Endothelial Growth Factor Receptor-1

Identifiers

PMID31666542
PMCPMC6821698
OpenAlexW2982441224

What OpenQuestion holds

Textmetadata
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.