Evidence map›Paper›PMID 24979700›Full record

ArticlePloS one2014

Antiphospholipid antibodies predict progression of abdominal aortic aneurysms.

Christina Duftner, Rüdiger Seiler, Christian Dejaco, Iris Chemelli-Steingruber, Harald Schennach, Werner Klotz, Michael Rieger, Manfred Herold, Jürgen Falkensammer, Gustav Fraedrich and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 17% 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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  11. Inflammatory cell phenotypes in AAAs: their role and potential as targets for therapy.Arteriosclerosis, thrombosis, and vascular biology · 2015
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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 3 institutions in 1 country.

Christina DuftnerDepartment of Internal Medicine, Clinic of Internal Medicine VI, Innsbruck Medical University, Innsbruck, Austria; Department of Internal Medicine, General Hospital Kufstein, Kufstein, Austria.
Rüdiger SeilerDepartment of Operative Medicine, Clinic of Vascular Surgery, Innsbruck Medical University, Innsbruck, Austria.
Christian DejacoDepartment of Internal Medicine, Clinic of Internal Medicine VI, Innsbruck Medical University, Innsbruck, Austria; Department of Rheumatology, Medical University Graz, Graz, Austria.
Iris Chemelli-SteingruberDepartment of Radiology, Innsbruck Medical University, Innsbruck, Austria.
Harald SchennachInstitute of Blood Transfusion and Immunology, Innsbruck Medical University, Innsbruck, Austria.
Werner KlotzDepartment of Internal Medicine, Clinic of Internal Medicine VI, Innsbruck Medical University, Innsbruck, Austria.
Michael RiegerDepartment of Radiology, Innsbruck Medical University, Innsbruck, Austria.
Manfred HeroldDepartment of Internal Medicine, Clinic of Internal Medicine VI, Innsbruck Medical University, Innsbruck, Austria.
Jürgen FalkensammerDepartment of Operative Medicine, Clinic of Vascular Surgery, Innsbruck Medical University, Innsbruck, Austria; Department of Vascular and Endovascular Surgery, Wilhelminenhospital, Vienna, Austria.
Gustav FraedrichDepartment of Operative Medicine, Clinic of Vascular Surgery, Innsbruck Medical University, Innsbruck, Austria.
Michael SchirmerDepartment of Internal Medicine, Clinic of Internal Medicine VI, Innsbruck Medical University, Innsbruck, Austria.
Innsbruck Medical University · ATUniversity of Applied Sciences Kufstein · ATWilhelminen Hospital · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antiphospholipid antibodies (aPLs) frequently occur in autoimmune and cardiovascular diseases and correlate with a worse clinical outcome. In the present study, we evaluated the association between antiphospholipid antibodies (aPLs), markers of inflammation, disease progression and the presence of an intra-aneurysmal thrombus in abdominal aortic aneurysm (AAA) patients. APLs ELISAs were performed in frozen serum samples of 96 consecutive AAA patients and 48 healthy controls yielding positive test results in 13 patients (13.5%) and 3 controls (6.3%; n.s.). Nine of the 13 aPL-positive AAA patients underwent a second antibody testing >12 weeks apart revealing a positive result in 6 cases. APL-positive patients had increased levels of inflammatory markers compared to aPL-negative patients. Disease progression was defined as an increase of the AAA diameter >0.5 cm/year measured by sonography. Follow-up was performed in 69 patients identifying 41 (59.4%) patients with progressive disease. Performing multipredictor logistic regression analysis adjusting for classical AAA risk factors as confounders, the presence of aPLs at baseline revealed an odds ratio of 9.4 (95% CI 1.0-86.8, p = 0.049) to predict AAA progression. Fifty-five patients underwent a computed tomography in addition to ultrasound assessment indicating intra-aneurysmal thrombus formation in 82.3%. Median thrombus volume was 46.7 cm3 (1.9-377.5). AAA diameter correlated with the size of the intra-aneurysmal thrombus (corrcoeff = 0.721, p<0.001), however neither the presence nor the size of the intra-aneurysmal thrombus were related to the presence of aPLs. In conclusion, the presence of aPLs is associated with elevated levels of inflammatory markers and is an independent predictor of progressive disease in AAA patients.

Indexed as

AgedAged, 80 and overAntibodies, AntiphospholipidAortic Aneurysm, AbdominalBiomarkersCase-Control StudiesFemaleHumansMaleMiddle AgedUltrasonographyAntibodies, AntiphospholipidBiomarkers

Identifiers

PMID24979700
PMCPMC4076179
OpenAlexW1980615815

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.