Evidence map›Paper›PMID 24385750›Full record

ArticleTurkish journal of haematology : official journal of Turkish Society of Haematology2013

Antiphospholipid antibodies and systemic scleroderma.

Awa Oumar Touré, Fatimata Ly, Abibatou Sall, Alassane Diatta, Macoura Gadji, Moussa Seck, Blaise Faye, Tandakha Dieye, Saliou Diop

Open access · diamondAbstract read
In one paragraph

Article in Turkish journal of haematology : official journal of Turkish Society of Haematology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
0.9field-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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

  1. Pooled it
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  11. Antiphospholipid antibodies and systemic scleroderma.Turkish journal of haematology : official journal of Turkish Society of Haematology · 2013
    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

9 authors at 2 institutions in 2 countries.

Awa Oumar Tourélaboratoire d'hématologie; Université Cheikh Anta Diop de Dakar (UCAD).
Fatimata LyService de dermatologie UCAD.
Abibatou Salllaboratoire d'hématologie; Université Cheikh Anta Diop de Dakar (UCAD).
Alassane DiattaLaboratoire de biochimie UCAD.
Macoura Gadjilaboratoire d'hématologie; Université Cheikh Anta Diop de Dakar (UCAD).
Moussa Secklaboratoire d'hématologie; Université Cheikh Anta Diop de Dakar (UCAD).
Blaise Fayelaboratoire d'hématologie; Université Cheikh Anta Diop de Dakar (UCAD).
Tandakha Dieyelaboratoire d'hématologie; Université Cheikh Anta Diop de Dakar (UCAD).
Saliou Dioplaboratoire d'hématologie; Université Cheikh Anta Diop de Dakar (UCAD).
Cheikh Anta Diop University · SNUniversidad Cristiana de las Asambleas de Dios · SV

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAntiphospholipid antibodies (APLs) could be associated with an increased risk of vascular pathologies in systemic scleroderma. The aim of our study was to search for APLs in patients affected by systemic scleroderma and to evaluate their involvement in the clinical manifestations of this disease. MATERIALS AND

methodsWe conducted a cross-sectional descriptive study, from January 2009 until August 2010, with patients received at the Department of Dermatology (Dakar, Senegal). Blood samples were taken at the hematology laboratory and were analyzed for the presence of APLs.

resultsForty patients were recruited. Various types of either isolated or associated APLs were found in 23 patients, i.e. 57.5% of the study population. The most frequently encountered antibody was IgG anti-β2 GPI (37.5% of the patients), followed by anticardiolipins (17.5%) and lupus anticoagulants (5%). No statistically significant association of positive antiphospholipid-related tests to any of the scleroderma complications could be demonstrated.

conclusionA high proportion of patients showing association of systemic scleroderma and APLs suggests the presence of a morbid correlation between these 2 pathologies. It would be useful to follow a cohort of patients affected by systemic scleroderma in order to monitor vascular complications following confirmation of the presence of antiphospholipid syndrome. CONFLICT OF INTEREST: None declared.

Indexed as

AntiphospholipidscomplicationSenegalSystemic scleroderma

Identifiers

PMID24385750
PMCPMC3781654
OpenAlexW2090913597

What OpenQuestion holds

Textmetadata
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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.