Evidence map›Paper›PMID 36773176›Full record

ArticleClinical and experimental nephrology2023

Intimal growth on the luminal surface of arteriovenous grafts in rats.

Sumihisa Ono, Naoyuki Hatayama, Kanyu Miyamoto, Munekazu Naito, Takuji Ishimoto, Yasuhiko Ito

Abstract read
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In one paragraph

Article in Clinical and experimental nephrology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 58% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

6 authors at 2 institutions in 1 country.

Sumihisa OnoDepartment of Nephrology, Central Japan International Medical Center, 1-1, Kenkounomachi, Minokamoshi, Gifu, Japan.
Naoyuki HatayamaDepartment of Anatomy, Aichi Medical University, 1-1, Yazakokarimata, Nagakute, Aichi, Japan. nhatayama416@gmail.com.ORCID http://orcid.org/0000-0003-3652-1046
Kanyu MiyamotoDepartment of Nephrology, Central Japan International Medical Center, 1-1, Kenkounomachi, Minokamoshi, Gifu, Japan.
Munekazu NaitoDepartment of Anatomy, Aichi Medical University, 1-1, Yazakokarimata, Nagakute, Aichi, Japan.
Takuji IshimotoDivision of Nephrology and Rheumatology, Department of Internal Medicine, Aichi Medical University School of Medicine, 1-1, Yazakokarimata, Nagakute, Aichi, Japan.
Yasuhiko ItoDivision of Nephrology and Rheumatology, Department of Internal Medicine, Aichi Medical University School of Medicine, 1-1, Yazakokarimata, Nagakute, Aichi, Japan. yasuito@aichi-med-u.ac.jp.
Aichi Medical University · JPSaitama International Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEndothelial cells are known to grow on the luminal surface of arteriovenous grafts (AVGs) used in hemodialysis. Although endothelial cells are important for preventing infection, a detailed growth of endothelial cells in AVGs is unknown. This study sought to create a simpler animal model of AVGs and to investigate how endothelial cells form on the luminal surface.

methodsPolyethylene grafts were placed between the cervical artery and vein of Wistar rats. The grafts were removed at 6 h, 24 h, 3 days, or 7 days after placement. The luminal surface was observed under optical and polarizing microscopy and stained with endothelial cell markers (LEL, CD31), the progenitor cell marker CD34, and the macrophage marker ED-1.

resultsMicroscopy demonstrated many diffuse vascular endothelial cells on the luminal surface of AVGs after placement. While there was no difference in the number of LEL-positive cells between the arterial side (AS) and venous side (VS) at 6 h or 7 days, there were significantly more of these cells on the VS at both 24 h and 3 days (p < 0.05). Analysis at 24 h showed some CD31-positive cells and few CD34-positive cells.

conclusionsThis was the first study to use a simple rat model of AVG placement. Endothelial cell formation was initially more active on the VS than on the AS, but these cells subsequently increased in number across the luminal surface. Future clinical studies might contribute clinically by confirming whether AS versus VS puncture results in different infection rates.

Indexed as

Arteriovenous Shunt, SurgicalAnimalsEndothelial CellsRatsRats, WistarRenal DialysisTunica IntimaVeinsArteriovenous graftNeointimaRat

Identifiers

PMID36773176
OpenAlexW4320033178

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.