Evidence map›Paper›PMID 33114187›Full record

ArticleInternational journal of molecular sciences2020

Paradoxical Psoriasis Induced by Anti-TNFα Treatment: Evaluation of Disease-Specific Clinical and Genetic Markers.

Agostino Bucalo, Federica Rega, Arianna Zangrilli, Valentina Silvestri, Virginia Valentini, Giorgia Scafetta, Federica Marraffa, Sara Grassi, Elena Rogante, Arianna Piccolo and 5 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

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  17. Focus on Anti-Tumour Necrosis Factor (TNF)-α-Related Autoimmune Diseases.International journal of molecular sciences · 2023
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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

15 authors at 2 institutions in 1 country.

Agostino BucaloDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
Federica RegaClinic of Dermatology Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, 00161 Rome, Italy.
Arianna ZangrilliDermatology Unit, Policlinico Tor Vergata, Tor Vergata University of Rome, 00133 Rome, Italy.ORCID 0000-0003-4983-4420
Valentina SilvestriDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.ORCID 0000-0003-0712-9379
Virginia ValentiniDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
Giorgia ScafettaDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
Federica MarraffaClinic of Dermatology Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, 00161 Rome, Italy.
Sara GrassiClinic of Dermatology Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, 00161 Rome, Italy.
Elena RoganteClinic of Dermatology Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, 00161 Rome, Italy.
Arianna PiccoloDermatology Unit, Policlinico Tor Vergata, Tor Vergata University of Rome, 00133 Rome, Italy.
Salvatore CucchiaraPediatric Gastroenterology and Liver Unit, Maternal and Child Health Department, Sapienza University of Rome, 00161 Rome, Italy.
Franca ViolaPediatric Gastroenterology and Liver Unit, Maternal and Child Health Department, Sapienza University of Rome, 00161 Rome, Italy.
Luca BianchiDermatology Unit, Policlinico Tor Vergata, Tor Vergata University of Rome, 00133 Rome, Italy.ORCID 0000-0001-8697-6896
Laura OttiniDepartment of Molecular Medicine, Sapienza University of Rome, 00161 Rome, Italy.
Antonio RichettaClinic of Dermatology Department of Clinical Internal, Anesthesiological and Cardiovascular Sciences, Sapienza University of Rome, 00161 Rome, Italy.
Sapienza University of Rome · ITPoliclinico Tor Vergata · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG2018-21389Fellowship FIRC-AIRC three-years fellowship "Carlo Zanotti" 24107
6 · The paper itself

Abstract

Paradoxical psoriasis (PP) may occur during treatment with anti-tumor necrosis factor-alpha (TNF-α) drugs in various chronic immune-mediated diseases, mainly inflammatory bowel diseases (IBD) and psoriasis. In this study, clinical and genetic characteristics of PP arising in IBD and psoriatic patients were investigated to identify disease-specific markers of the paradoxical effect. A total of 161 IBD and psoriatic patients treated with anti-TNF-α drugs were included in the study. Of these patients, 39 developed PP. All patients were characterized for the main clinical-pathologic characteristics and genotyped for six candidate single nucleotide polymorphisms (SNPs) selected for their possible role in PP susceptibility. In IBD patients, the onset of PP was associated with female sex, presence of comorbidities, and use of adalimumab. IBD patients with PP had a higher frequency of the

Indexed as

Polymorphism, Single NucleotideAdalimumabChildFemaleGenetic MarkersGenetic Predisposition to DiseaseHLA-C AntigensHumansInflammatory Bowel DiseasesMalePsoriasisSex CharacteristicsTumor Necrosis Factor-alphaAdalimumabGenetic MarkersHLA-C AntigensTNF protein, humanTumor Necrosis Factor-alphagenetic polymorphismsinflammatory bowel diseaseparadoxical psoriasispsoriasistumor necrosis factor-alpha inhibitors

Identifiers

PMID33114187
PMCPMC7660646
OpenAlexW3094028440

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.