Evidence map›Paper›PMID 28154599›Full record

ArticleKorean circulation journal2017

Effect of Stents Coated with Artemisinin or Dihydroartemisinin in a Porcine Coronary Restenosis Model.

Suyoung Jang, Myung Ho Jeong, Kyung Seob Lim, In Ho Bae, Jun-Kyu Park, Dae Sung Park, Jae Won Shim, Jung Ha Kim, Hyun Kuk Kim, Doo Sun Sim and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Korean circulation journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

13 authors at 3 institutions in 1 country.

Suyoung JangKorea Cardiovascular Stent Research Institute, Jangsung, Korea.; Cardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.
Myung Ho JeongKorea Cardiovascular Stent Research Institute, Jangsung, Korea.; Cardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.; Regeneromics Research Center, Chonnam National University, Gwangju, Gwangju, Korea.
Kyung Seob LimCardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.
In Ho BaeKorea Cardiovascular Stent Research Institute, Jangsung, Korea.; Cardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.
Jun-Kyu ParkCardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.
Dae Sung ParkCardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.
Jae Won ShimCardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.
Jung Ha KimCardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.
Hyun Kuk KimCardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.
Doo Sun SimCardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.
Young Joon HongCardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.
Youngkeun AhnCardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.
Jung Chaee KangCardiovascular Convergence Research Center Nominated by Korea Ministry of Health and Welfare, Gwangju, Korea.; Cardiovascular Research Center, Chonnam National University Hospital, Gwangju, Korea.
Chonnam National University Hospital · KRMinistry of Health and Welfare · KRJangsung (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesArtemisinin and dihydroartemisinin are drugs used to treat malaria. These drugs suppress inflammatory reactions. The aim of this study was to examine the anti-intima hyperplasia effect of a novel drug-eluting stent with artemisinin or dihydroartemisinin in a porcine coronary restenosis model. MATERIALS AND

methodsPigs were randomized into four groups; in the first, the coronary arteries (20 pigs, a total of 40 coronary arteries, with 10 coronary arteries in each group) was implanted with bare metal stents (BMS, n=10); the second group was given polymer-coated stents (PCS, n=10); the third group was treated with artemisinin-eluting stents (AES, n=10); and the fourth group was given dihydroartemisinin-eluting stents (DAES, n=10). Histopathologic analysis was performed 28 days after stenting.

resultsThe injury and fibrin scores among the four groups were not significantly different. However, the internal elastic lamina, lumen area, and neointima area were significantly different. Moreover, the percent area of stenosis (46.2±18.66% in BMS vs. 89.4±10.92% in PCS vs. 83.3±17.07% in AES vs. 36.7±11.20% in DAES, p<0.0001) and inflammation score (1.0 [range: 1.0-1.0] vs. 3.0 [range: 2.25-3.0] vs. 3.0 [range: 1.0-3.0] vs. 2.0 [range: 1.75-3.0] in BMS, PCS, AES, and DAES, respectively; p<0.001) were markedly decreased in the DAES group compared to the PCS group.

conclusionDES, which uses a natural substance, dihydroartemisinin, showed a neointima and inflammatory suppressive effect in a porcine coronary restenosis model.

Indexed as

Coronary restenosisInflammationStents

Identifiers

PMID28154599
PMCPMC5287173
OpenAlexW2548011323

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.