Evidence map›Paper›PMID 31674929›Full record

Trial reportAnatolian journal of cardiology2019

Comparative effects of atorvastatin 80 mg and rosuvastatin 40 mg on the levels of serum endocan, chemerin, and galectin-3 in patients with acute myocardial infarction.

Abdullah Tunçez, Bülent Behlül Altunkeser, Bahadır Öztürk, Muhammed Salih Ateş, Hüseyin Tezcan, Canan Aydoğan, Emre Can Kırık, Ulvi Yalçın, Nazif Aygül, Kenan Demir and 1 more

Open access · diamondAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Anatolian journal of cardiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 3 pooled it
1.0field-weighted citation impact, top 24% 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

21 citing papers in PubMed, 3 syntheses or guidelines pooled it, 24 citations in OpenAlex.

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  20. Endocan: A Key Player of Cardiovascular Disease.Frontiers in cardiovascular medicine · 2021
    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

11 authors at 1 institution in 1 country.

Abdullah TunçezDepartment of Cardiology, Faculty of Medicine, Selçuk University; Konya-Turkey.
Bülent Behlül AltunkeserDepartment of Cardiology, Faculty of Medicine, Selçuk University; Konya-Turkey.
Bahadır ÖztürkDepartment of Biochemistry, Faculty of Medicine, Selçuk University; Konya-Turkey.
Muhammed Salih AteşDepartment of Cardiology, Faculty of Medicine, Selçuk University; Konya-Turkey.
Hüseyin TezcanDepartment of Cardiology, Faculty of Medicine, Selçuk University; Konya-Turkey.
Canan AydoğanDepartment of Cardiology, Faculty of Medicine, Selçuk University; Konya-Turkey.
Emre Can KırıkDepartment of Cardiology, Faculty of Medicine, Selçuk University; Konya-Turkey.
Ulvi YalçınDepartment of Cardiology, Faculty of Medicine, Selçuk University; Konya-Turkey.
Nazif AygülDepartment of Cardiology, Faculty of Medicine, Selçuk University; Konya-Turkey.
Kenan DemirDepartment of Cardiology, Faculty of Medicine, Selçuk University; Konya-Turkey.
Fikret AkyürekDepartment of Biochemistry, Faculty of Medicine, Selçuk University; Konya-Turkey.
Selçuk University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveEndocan, chemerin, and galectin-3 are discrete biomarkers associated with cardiovascular diseases and acting through different pathophysiological pathways. The aim of this study is to investigate and compare the effects of high doses of atorvastatin and rosuvastatin on serum endocan, chemerin, and galectin-3 levels in patients with acute myocardial infarction (AMI).

methodsSixty-three patients with AMI were randomized to receive atorvastatin (80 mg/day) or rosuvastatin (40 mg/day) after percutaneous revascularization. Serum levels of endocan, chemerin, and galectin-3 were evaluated at baseline and after 4-week therapy.

resultsEndocan levels were not decreased statistically significantly with atorvastatin 80 mg, but rosuvastatin 40 mg markedly decreased the levels of endocan according to baseline [from 110.27 (86.03-143.69) pg/mL to 99.22 (78.30-122.87) pg/mL with atorvastatin 80 mg and from 110.73 (77.28-165.22) pg/mL to 93.40 (70.48-115.13) pg/mL with rosuvastatin 40 mg, p=0.242 for atorvastatin 80 mg and p=0.014 for rosuvastatin 40 mg]. Chemerin levels significantly decreased in both groups according to baseline [from 264.90 (196.00-525.95) ng/mL to 135.00 (105.95-225.65) ng/mL with atorvastatin 80 mg and from 309.95 (168.87-701.27) ng/mL to 121.25 (86.60-212.65) ng/mL with rosuvastatin 40 mg, p<0.001, respectively, for both groups]. Galectin-3 levels did not change markedly with atorvastatin 80 mg, but they decreased with rosuvastatin 40 mg [from 17.00 (13.10-22.25) ng/mL to 19.30 (15.25-23.45) ng/mL with atorvastatin 80 mg, p=0.721, and from 18.25 (12.82-23.82) ng/mL to 16.60 (10.60-20.15) ng/mL with rosuvastatin 40 mg, p=0.074]. There were no significant between-group differences in terms of absolute and percentage changes of endocan, chemerin, and galectin-3 at 4 weeks.

conclusionWe reported that both statins similarly decreased the endocan levels, whereas rosuvastatin seems to have more prominent effects on the reduction of the chemerin and galectin-3 levels in patients with AMI.

Indexed as

AngioplastyAtorvastatinBiomarkersBlood ProteinsChemokinesFemaleGalectin 3GalectinsHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMiddle AgedMyocardial InfarctionNeoplasm ProteinsProteoglycansRosuvastatin CalciumAtorvastatinBiomarkersBlood ProteinsChemokinesESM1 protein, humanGalectin 3GalectinsHydroxymethylglutaryl-CoA Reductase InhibitorsLGALS3 protein, humanNeoplasm ProteinsProteoglycansRARRES2 protein, humanRosuvastatin Calcium

Identifiers

PMID31674929
PMCPMC6955059
OpenAlexW2964727817

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.