Evidence map›Paper›PMID 25624859›Full record

ArticleArchives of medical science : AMS2014

Effect of common single nucleotide polymorphisms in COX-1 gene on related metabolic activity in diabetic patients treated with acetylsalicylic acid.

Marek Postula, Piotr K Janicki, Marek Rosiak, Agnieszka Kaplon-Cieslicka, Agnieszka Kondracka, Ewa Trzepla, Krzysztof J Filipiak, Dariusz A Kosior, Andrzej Czlonkowski, Grzegorz Opolski

Open access · goldAbstract read
In one paragraph

Article in Archives of medical science : AMS, 2014. 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
0.6field-weighted citation impact, top 26% 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, 2 citations in OpenAlex.

  1. 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

10 authors at 3 institutions in 2 countries.

Marek PostulaDepartment of Cardiology and Hypertension, Central Clinical Hospital, the Ministry of the Interior, Warsaw, Poland ; Department of Clinical and Experimental Pharmacology, Medical University of Warsaw, Warsaw, Poland.
Piotr K JanickiPerioperative Genomics Laboratory, Department of Anesthesiology, Penn State College of Medicine, Hershey, Pennsylvania, USA.
Marek RosiakDepartment of Cardiology and Hypertension, Central Clinical Hospital, the Ministry of the Interior, Warsaw, Poland ; Department of Clinical and Experimental Pharmacology, Medical University of Warsaw, Warsaw, Poland.
Agnieszka Kaplon-CieslickaDepartment of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Agnieszka KondrackaDepartment of Internal Medicine and Endocrinology, Medical University of Warsaw, Warsaw, Poland.
Ewa TrzeplaDepartment of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Krzysztof J FilipiakDepartment of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Dariusz A KosiorDepartment of Cardiology and Hypertension, Central Clinical Hospital, the Ministry of the Interior, Warsaw, Poland ; Mossakowski Medical Research Centre Polish Academy of Sciences, Warsaw, Poland.
Andrzej CzlonkowskiDepartment of Clinical and Experimental Pharmacology, Medical University of Warsaw, Warsaw, Poland.
Grzegorz OpolskiDepartment of Cardiology, Medical University of Warsaw, Warsaw, Poland.
Medical University of Warsaw · PLPenn State Milton S. Hershey Medical Center · USPolish Academy of Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe objective of this study was to investigate the effect of common single nucleotide genomic polymorphisms in the cyclooxygenase-1 (COX-1) gene on the thromboxane A2 (TxA2) metabolite concentrations in serum and urine, as well as on prostaglandin F2α (PGF2α) urinary excretion in the diabetic population on acetylsalicylic acid (ASA) therapy. MATERIAL AND

methodsThe study cohort consisted of 284 Caucasians with diabetes type 2 who had been taking ASA tablets at the dose of 75 mg/day for at least 3 months. Genotyping for the 4 selected SNPs within the COX-1 gene (two nonsynonymous-coding variants, rs3842787 [C50T, P17L] and rs5789 [C174A, L237M]; and two other synonymous SNPs, rs3842788 [G128A, Q41Q] and rs5788 [C644A]) was performed using the Sequenom iPLEX platform.

resultsNo statistically significant results were observed for the investigated SNPs and measured metabolites in the investigated cohort of patients. Statistically significant differences in S-TxB2 could however be observed for rs5788 in the subgroup of patients with very high S-TxB2 concentrations. In particular, more patients who were carriers of the minor allele for this polymorphism were observed in the group with S-TxB2 levels > 95(th) percentile, when compared with similar carriers in the group with S-TxB2 < 95(th) percentile (20% vs. 1.1%, respectively, p < 0.001, Mann-Whitney test).

conclusionsThe results of our study suggest that the four investigated common SNPs in the COX1 gene are not associated with obviously altered TxA2 metabolism and PGF2α synthesis in the investigated diabetic cohort treated with ASA.

Indexed as

8-iso-prostaglandin F2αacetylsalicylic acidcyclooxygenase-1diabetes mellitusthromboxane

Identifiers

PMID25624859
PMCPMC4296057
OpenAlexW2323829441

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.