Evidence map›Paper›PMID 28478589›Full record

ArticleHistochemistry and cell biology2017

Preoperative factors predicting saphenous vein graft occlusion in coronary artery bypass grafting: a multivariate analysis.

Agnieszka Malinska, Zuzanna Podemska, Bartlomiej Perek, Marek Jemielity, Piotr Buczkowski, Malgorzata Grzymislawska, Patrycja Sujka-Kordowska, Michal Nowicki

Open access · hybridAbstract read
In one paragraph

Article in Histochemistry and cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. In focus in HCB.Histochemistry and cell biology · 2017
    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

8 authors at 2 institutions in 1 country.

Agnieszka MalinskaDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
Zuzanna PodemskaDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
Bartlomiej PerekDepartment of Cardiac Surgery and Transplantology, Poznan University of Medical Sciences, Dluga 1/2 St., 60-101, Poznan, Poland.
Marek JemielityDepartment of Cardiac Surgery and Transplantology, Poznan University of Medical Sciences, Dluga 1/2 St., 60-101, Poznan, Poland.
Piotr BuczkowskiDepartment of Cardiac Surgery and Transplantology, Poznan University of Medical Sciences, Dluga 1/2 St., 60-101, Poznan, Poland.
Malgorzata GrzymislawskaDepartment of Anatomy, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
Patrycja Sujka-KordowskaDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland. psujka@ump.edu.pl.
Michal NowickiDepartment of Histology and Embryology, Poznan University of Medical Sciences, Swiecickiego 6 St., 60-781, Poznan, Poland.
Poznan University of Medical Sciences · PLHeliodor Swiecicki Clinical Hospital · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Saphenous vein segments are frequently used as aortocoronary bypass grafts, particularly in patients over 65 years of age. In the majority of patients, venous grafts maintain their patency for 5-6 years; however, some become occluded within 12 months after surgery. There are some defined predictive biological factors used to assess saphenous vein graft long-term patency rates, but little is known about molecular parameters for estimating the risk of early vein occlusion. The pathogenesis of this process involves the proliferation of stem cells, as well as progenitor cells, in the graft wall. Histologically, this is reflected by CD34 and CD133 expression in endothelial and smooth muscle cells. Thus, the aim of present work was to perform a multivariate analysis of stem cell and progenitor cell markers in saphenous vein graft walls before transplantation to arterial circulation and correlate these results with early graft occlusion. A total of 718 patients, who underwent coronary artery bypass grafting using a saphenous vein graft, were enrolled in this prospective study. CD34, CD133 and von Willebrand factor expression was evaluated via immunohistochemistry. A multivariate analysis revealed that strong CD133 expression in smooth muscle cells can be considered a risk factor for early graft failure. Our findings suggest that CD133 expression in smooth muscle cells of the tunica media in saphenous vein grafts obtained from coronary artery bypass graft patients before graft transplantation to coronary circulation might predict the possibility of early graft occlusion.

Indexed as

Coronary Artery BypassAgedAged, 80 and overFemaleHumansImmunohistochemistryMaleMiddle AgedMultivariate AnalysisSaphenous VeinCD133Coronary artery bypass graftingPrognosisSaphenous veinSmooth muscle cells

Identifiers

PMID28478589
PMCPMC5602051
OpenAlexW2611250105

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.