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Cutaneous Manifestations, Clinical Characteristics, and Prognosis of Patients With Systemic Sclerosis Sine Scleroderma

2023· article· en· W4382344802 on OpenAlexaff
Alain Lescoat, Suiyuan Huang, Patrícia Carreira, Elise Siegert, Jeska de Vries‐Bouwstra, Jörg H. W. Distler, Vanessa Smith, Francesco Del Galdo, Branimir Anić, Nemanja Damjanov, Simona Rednic, Camillo Ribi, Dominique Farge Bancel, Anna‐Maria Hoffmann‐Vold, Armando Gabrielli, Oliver Distler, Dinesh Khanna, Yannick Allanore, Marco Matucci‐Cerinic, Ulrich A. Walker, Florenzo Iannone, Radim Bečvář, Otylia Kowal Bielecka, Carmen Pizzorni, Francesco Ciccia, Panayiotis G. Vlachoyiannopoulos, Jiří Štork, Murat İnanç, Srđan Novak, László Czirják, Michele Iudici, Katja Perdan Pirkmajer, Bernard Coleiro, Gianluca Moroncini, Roger Hesselstrand, Mislav Radić, Alexandra Balbir‐Gurman, Andrea Lo Monaco, Raffaele Pellerito, Alessandro Giollo, Jadranka Morović‐Vergles, Christopher P. Denton, Madelon C Vonk, Jörg Henes, Vera Ortiz-Santamaría, Stefan Heitmann, Dorota Krasowska, Paul Hasler, Michaela Köhm, Ivan Foeldvari, Gianluigi Bajocchi, Maria João Salvador, Bojana Stamenković, Carlo Selmi, Mohammed Tikly, Lidia P Ananieva, Ariane L. Herrick, Ulf Müller‐Ladner, Klaus Søndergaard, Francesco Puppo, Merete Engelhart, G Szücs, Carlos de la Puente, Valeria Riccieri, Ruxandra Ionescu, Ami Sha, Ana Maria Gheorghiu, Cord Sunderkötter, Francesca Ingegnoli, Luc Mouthon, Francesco Paolo Cantatore, Susanne Ullman, Carlos Alberto von Mühlen, Maria Rosa Pozzi, Kilian Eyerich, Piotr Wiland, Marie Vanthuyne, Juan José Alegre Sancho, Kristine Herrmann, Ellen De Langhe, Marko Barešić, Miroslav Mayer, Maria Üprus, Kati Otsa, Şule Yavuz, B. Granel, Carolina de Souza Müller, Svetlana Agachi, Simon Stebbings, Alessandro Mathieu, Alessandra Vacca, Percival D. Sampaio‐Barros, Lisa K. Stamp, Kamal Solanki, Douglas J. Veale, Esthela Loyo, Carmen Tineo, Sergio Toloza, Mengtao Li, Walid Ahmed Abdel Atty Mohamed, Jacek Olas, Fahrettin Öksel, Figen Yargucu, Cristina-Mihaela Tănăseanu, Rosario Foti, Codrina Ancuța, Daniel E. Furst, Britta Maurer, Jacob M. van Laar, Marzena Olesińska, Cristiane Kayser, Nihal Fathi, Paloma García de la Peña Lefebvre, Jorge Juan González Martín, Patrick Carpentier, B. Imbert, Camille Françès, Patricia Senet, Jean Sibilia, Ira Litinsky, Jean Sénécal, Martial Koenig, France Joval, Tamara Grodzicky, Goda Šeškutė, Lesley Ann Saketkoo, Eduardo Kerzberg, Washington Bianchi, Breno Valdetaro Bianchi, I. Castellví, Jasminka Milas-Ahic, Roberta Višević, Massimiliano Limonta, Doron Rimar, Maura Couto, François Spertini, Antonella Marcoccia, Sarah Kahl, Vivien Hsu, Thierry Martin, Sergey Moiseev, Pavel Novikov, Tim Schmeiser, Dominik Majewski, Zbigniew Zdrojewski, Julia Martínez‐Barrio, Vera Bernardino, Lelita Santo, Yair Levy, Elena Rezuş, Ömer Pamuk, Daniel Brito de Araújo, Piercarlo Sarzi‐Puttini, Marek Brzosko, Hadi Poormoghim, Marta Maman, Ina Kötter, Giovanna Cuomo, F. Gaches, Laura Belloli, Petros P. Sfikakis, Juliana Markus, Ana-Maria Ramazan, Marie‐Elise Truchetet, P. Jégo, Lorenzo Dagna, L. F. Voigt, Susana Oliveira, Fabiola Atzeni, Masataka Kuwana, A. Mékinian, M. Martin, Yoshiya Tanaka, Hidekata Yasuoka, Carmen Pilar Simeón‐Aznar, Tatsuya Atsumi, Magda Pârvu, Inês Cordeiro, Nicoletta Del Papa, Thomas Karonitsch, Anna Bazela-Ostromecka, Enrico Selvi, Yasushi Kawaguchi, T. Soukup, Ignasi Rodríguez‐Pintó, Marija Geroldinger‐Simić, Gerard Espinosa, Karen Voigt, Torsten Kubacki, Olena Garmish, Marta Mosca, Ulrich Gerth, Ludmila Antonenko, Fabian A. Mendoza, Paolo Airó, Gabriela Riemekasten, É. Hachulla, Andrea Doria, Edoardo Rosato, Nicolas Hunzelmann, Carlomaurizio Montecucco, Maurizio Cutolo

Bibliographic record

VenueJAMA Dermatology · 2023
Typearticle
Languageen
FieldMedicine
TopicSystemic Sclerosis and Related Diseases
Canadian institutionsMcGill University
Fundersnot available
KeywordsMedicineScleroderma (fungus)DermatologyInternal medicineNatural historyInterstitial lung diseaseCohortPathologyLung

Abstract

fetched live from OpenAlex

Importance: Systemic sclerosis (SSc) sine scleroderma (ssSSc) is a subset of SSc defined by the absence of skin fibrosis. Little is known about the natural history and skin manifestations among patients with ssSSc. Objective: To characterize the clinical phenotype of patients with ssSSc compared with patients with limited cutaneous SSc (lcSSc) and diffuse cutaneous SSc (dcSSc) within the EUSTAR database. Design, Setting, and Participants: This longitudinal observational cohort study based on the international EUSTAR database included all patients fulfilling the classification criteria for SSc assessed by the modified Rodnan Skin score (mRSS) at inclusion and with at least 1 follow-up visit; ssSSc was defined by the absence of skin fibrosis (mRSS = 0 and no sclerodactyly) at all available visits. Data extraction was performed in November 2020, and data analysis was performed from April 2021 to April 2023. Main Outcomes and Measures: Main outcomes were survival and skin manifestations (onset of skin fibrosis, digital ulcers, telangiectasias, puffy fingers). Results: Among the 4263 patients fulfilling the inclusion criteria, 376 (8.8%) were classified as having ssSSc (mean [SD] age, 55.3 [13.9] years; 345 [91.8%] were female). At last available visit, in comparison with 708 patients with lcSSc and 708 patients with dcSSc with the same disease duration, patients with ssSSc had a lower prevalence of previous or current digital ulcers (28.2% vs 53.1% in lcSSc; P < .001; and 68.3% in dcSSc; P < .001) and puffy fingers (63.8% vs 82.4% in lcSSc; P < .001; and 87.6% in dcSSc; P < .001). By contrast, the prevalence of interstitial lung disease was similar in ssSSc and lcSSc (49.8% and 57.1%; P = .03) but significantly higher in dcSSc (75.0%; P < .001). Skin telangiectasias were associated with diastolic dysfunction in patients with ssSSc (odds ratio, 4.778; 95% CI, 2.060-11.081; P < .001). The only independent factor for the onset of skin fibrosis in ssSSc was the positivity for anti-Scl-70 antibodies (odds ratio, 3.078; 95% CI, 1.227-7.725; P = .02). Survival rate was higher in patients with ssSSc (92.4%) compared with lcSSc (69.4%; P = .06) and dcSSc (55.5%; P < .001) after up to 15 years of follow-up. Conclusions and Relevance: Systemic sclerosis sine scleroderma should not be neglected considering the high prevalence of interstitial lung disease (>40%) and SSc renal crisis (almost 3%). Patients with ssSSc had a higher survival than other subsets. Dermatologists should be aware that cutaneous findings in this subgroup may be associated with internal organ dysfunction. In particular, skin telangiectasias in ssSSc were associated with diastolic heart dysfunction.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.003
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.003
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.027
GPT teacher head0.269
Teacher spread0.242 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations37
Published2023
Admission routes1
Has abstractyes

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