Evidence map›Paper›PMID 24375159›Full record

Trial reportIranian biomedical journal2014

Pentoxifylline decreases serum level of adhesion molecules in atherosclerosis patients.

Amir Hooshang Mohammadpour, Homa Falsoleiman, Jamal Shamsara, Ghazaleh Allah Abadi, Ramin Rasooli, Mohammad Ramezani

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Iranian biomedical journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact, top 86% 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

8 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Inflammatory Targets in Diabetic Nephropathy.Journal of clinical medicine · 2020
    Review
  7. Review
  8. 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 1 institution in 1 country.

Amir Hooshang MohammadpourDept. of Pharmacodynamy and Toxicology, School of Pharmacy, Mashhad University of Medical Science, Mashhad, Iran.
Homa FalsoleimanCardiovascular Research Center, Ghaem Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Jamal ShamsaraPharmaceutical Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Ghazaleh Allah AbadiNanotechnology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Ramin RasooliPharmaceutical Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Mohammad RamezaniPharmaceutical Research Center, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Mashhad University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammation is involved in development, progression, and complications of atherosclerotic disease. Clinical studies have indicated that the level of monocyte chemoattractant protein 1 (MCP-1), IL-18, and adhesion molecules correlates with the severity of atherosclerosis and can predict future cardiovascular events. Experimental studies have shown pentoxifylline (PTX) reduces these factors in animal models. The purpose of the present pilot study was to evaluate effect of PTX on a group of inflammatory biomarkers in patients with coronary artery disease (CAD).

methodsForty patients with angiographically documented CAD, who fulfilled inclusion and exclusion criteria, were entered in the double-blind, randomized, pilot clinical study. The patients were randomly given PTX (400 mg three times daily) or placebo (3 tab/day) for 2 months. Serum concentrations of MCP-1, IL-18, intercellular adhesion Molecule 1 (ICAM-1), and vascular cell adhesion molecule 1 (VCAM-1) were measured before and at the end of intervention by enzyme-linked immunosorbant assay.

resultsOur study showed that the serum levels of ICAM-1 and VCAM-1 was decreased in the study population after two-month treatment (P<0.05).

conclusionBased on the results of our pilot study, administration of PTX in CAD patients significantly decreases adhesion molecules levels.

Indexed as

AtherosclerosisCell Adhesion MoleculesChemokine CCL2Double-Blind MethodFemaleHumansInflammationIntercellular Adhesion Molecule-1Interleukin-18MaleMiddle AgedPentoxifyllinePilot ProjectsPlacebosPlatelet Aggregation InhibitorsVascular Cell Adhesion Molecule-1CCL2 protein, humanCell Adhesion MoleculesChemokine CCL2ICAM1 protein, humanIL18 protein, humanIntercellular Adhesion Molecule-1Interleukin-18PentoxifyllinePlacebosPlatelet Aggregation InhibitorsVascular Cell Adhesion Molecule-1AtherosclerosisInflammationPentoxifylline

Identifiers

PMID24375159
PMCPMC3892136
OpenAlexW2101292486

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.