Evidence map›Paper›PMID 26247037›Full record

ArticleJournal of diabetes research2015

Impact of Inherited Prothrombotic Disorders on the Long-Term Clinical Outcome of Percutaneous Transluminal Angioplasty in Patients with Diabetes.

Michal Dubský, Alexandra Jirkovská, Libuše Pagáčová, Robert Bém, Andrea Němcová, Vladimíra Fejfarová, Veronika Wosková, Edward B Jude

Open access · goldAbstract readControlled Clinical Trial
In one paragraph

Article in Journal of diabetes research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Thrombophilia in 153 Patients With Premature Cardiovascular Disease ≤Age 45.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis · 2018
    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 2 countries.

Michal DubskýDiabetes Centre, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.
Alexandra JirkovskáDiabetes Centre, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.
Libuše PagáčováDiabetes Centre, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.
Robert BémDiabetes Centre, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.
Andrea NěmcováDiabetes Centre, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.
Vladimíra FejfarováDiabetes Centre, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.
Veronika WoskováDiabetes Centre, Institute for Clinical and Experimental Medicine, 140 21 Prague, Czech Republic.
Edward B JudeDiabetes Centre, Tameside Hospital NHS Foundation Trust and University of Manchester, Ashton-Under-Lyne OL6 9RW, UK.
Institute of Clinical and Experimental Medicine · CZTameside and Glossop Integrated Care NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of our study was to analyse inherited thrombotic disorders that influence the long-term outcome of PTA. Methods. Diabetic patients with peripheral arterial disease (PAD) treated by PTA in our centre between 2008 and 2011 were included in the study. Patients were divided into unsuccessful PTA group (75 patients), successful PTA group (58 patients), and control group (65 patients, with diabetes but no PAD). Diagnosis of inherited thrombotic disorders included mutation in factor V (Leiden), factor II (prothrombin), and mutation in genes for methylenetetrahydrofolate reductase-MTHFR (C677T and A1298C). Results. The genotypic frequency of Leiden allele G1691A was significantly associated with a risk of unsuccessful PTA in comparison with successful PTA group and control group (OR 8.8 (1.1-70.6), p = 0.041, and OR 9.8 (1.2-79.2), p = 0.032, resp.). However, we only observed a trend for the association of the prothrombin allele G20210A and risk of PTA failure. The frequencies of alleles of MTHFR 677 or 1298 did not differ significantly among the groups. Conclusion. Our study showed higher frequency of heterozygous form of Leiden mutation in diabetic patients with unsuccessful outcome of PTA in comparison with patients with successful PTA and diabetic patients without PAD.

Indexed as

Point MutationAgedAmino Acid SubstitutionAngioplastyArmCross-Sectional StudiesCzech RepublicDiabetic AngiopathiesFactor VFemaleGenetic Association StudiesHumansIschemiaLegMaleMethylenetetrahydrofolate Reductase (NADPH2)Factor Vfactor V LeidenMethylenetetrahydrofolate Reductase (NADPH2)MTHFR protein, humanProthrombin

Identifiers

PMID26247037
PMCPMC4515498
OpenAlexW1569390192

What OpenQuestion holds

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LicenceCC BY
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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.