Evidence map›Paper›PMID 29799952›Full record

ArticleJAMA dermatology2018

Whole-Body Distribution and Clinical Association of Telangiectases in Systemic Sclerosis.

Mathieu Jouvray, David Launay, Sylvain Dubucquoi, Vincent Sobanski, Céline Podevin, Marc Lambert, Sandrine Morell-Dubois, Hélène Maillard, Pierre-Yves Hatron, Eric Hachulla and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in JAMA dermatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 4 pooled it
0.8field-weighted citation impact, top 28% 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, 4 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Management of pulmonary arterial hypertension in systemic sclerosis: from classical treatments to new horizons.European respiratory review : an official journal of the European Respiratory Society · 2026
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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 4 institutions in 1 country.

Mathieu JouvrayUniversity Lille, Lille Inflammation Research International Center, Lille, France.
David LaunayUniversity Lille, Lille Inflammation Research International Center, Lille, France.
Sylvain DubucquoiUniversity Lille, Lille Inflammation Research International Center, Lille, France.
Vincent SobanskiUniversity Lille, Lille Inflammation Research International Center, Lille, France.
Céline PodevinUniversity Lille, Lille Inflammation Research International Center, Lille, France.
Marc LambertUniversity Lille, Lille Inflammation Research International Center, Lille, France.
Sandrine Morell-DuboisCHU Lille, Département De Médecine Interne et Immunologie Clinique, Lille, France.
Hélène MaillardCHU Lille, Département De Médecine Interne et Immunologie Clinique, Lille, France.
Pierre-Yves HatronCHU Lille, Département De Médecine Interne et Immunologie Clinique, Lille, France.
Eric HachullaUniversity Lille, Lille Inflammation Research International Center, Lille, France.
Jonathan GiovannelliUniversity Lille, Lille Inflammation Research International Center, Lille, France.
Centre Hospitalier Universitaire de Lille · FRInserm · FRLille Inflammation Research International Center · FRUniversité Lille Nord de France · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: In systemic sclerosis (SSc), to date, no study has precisely described the total number and fine distribution of telangiectases (TAs), their clinical association with the disease, and the biological mechanisms causing their development. Objectives: To describe the whole-body distribution of TAs and assess the association between the whole-body TA number and the characteristics of patients with SSc. Design, Setting, and Participants: A single-center, cross-sectional study was conducted between July 11, 2016, and March 15, 2017, at the National Referral Centre for Rare Systemic and Autoimmune Diseases in France. A population-based sample of 106 adults who fulfilled the 2013 American College of Rheumatology/European League Against Rheumatism criteria for SSc were included; 8 patients who had previously received laser treatment for TAs were excluded. Main Outcomes and Measures: The number of TAs on the whole body (total and those >5 mm) and TA distribution in different areas were recorded. The association with clinical and biological data was studied using univariate and multivariate linear regression. Results: A total of 106 patients (83 [78.3%] women) were enrolled, including 12 with precapillary pulmonary hypertension (PH). Mean (SD) age was 60.6 (13.5) years. Telangiectasia distribution was 37.2% on the face, 33.2% on the upper limbs, including 26.4% on the hands, 28.1% on the trunk, including 17.1% for the upper part of the trunk, and 1.5% on the lower limbs. In analysis using the multivariate linear regression model, the whole-body TA number was independently associated with male sex (percentage change, 144.4%; 95% CI, 7.5% to 455.9%; P = .03), PH (162.8%; 95% CI, 5.6% to 553.8%; P = .04), history of pulmonary embolism (336.4%; 95% CI, 39.0% to 1270.1%; P = .01), glomerular filtration rate (-1.6%; 95% CI, -3.2% to -0.1% per 1-mL/min/1.73 m2 increase; P = .04), and soluble endoglin level (28.2%; 95% CI, 1.2% to 62.5% per 1-ng/mL increase; P = .04). Receiver operating characteristic analyses assessing the ability of TAs to identify the presence of PH revealed that the area under the curve was significant for the TA number on the whole body (0.77; 95% CI, 0.57 to 0.88), on the hands and face (0.81; 95% CI, 0.57 to 0.91), and on the hands (95% CI, 0.77; 95% CI, 0.57 to 0.89). Conclusions and Relevance: In the patients in this study with SSc, TAs were predominantly located on the face, hands, and the upper part of the trunk. Telangiectases appeared to be associated with vasculopathy features of SSc, particularly with PH and soluble endoglin levels.

Indexed as

AgedArea Under CurveCross-Sectional StudiesEndoglinFacial DermatosesFemaleGlomerular Filtration RateHand DermatosesHumansHypertension, PulmonaryLower ExtremityMaleMiddle AgedPulmonary EmbolismROC CurveScleroderma, SystemicEndoglinVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID29799952
PMCPMC6128493
OpenAlexW2803581127

What OpenQuestion holds

Textmetadata
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.