Evidence map›Paper›PMID 32585971›Full record

ArticleCells2020

Cytokine Profile in Striated Muscle Laminopathies: New Promising Biomarkers for Disease Prediction.

Cristina Cappelletti, Irene Tramacere, Paola Cavalcante, Elisa Schena, Luisa Politano, Nicola Carboni, Alessandra Gambineri, Adele D'Amico, Lucia Ruggiero, Giulia Ricci and 11 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Sterile inflammation in laminopathies.European journal of cell biology · 2025
    Review
  2. Article
  3. Anti-myogenic and profibrotic effect of serum from patients affected by muscular laminopathies.Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
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

21 authors at 11 institutions in 1 country.

Cristina CappellettiNeurology IV-Neuroimmunology and Neuromuscular Diseases Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
Irene TramacereDepartment of Research and Clinical Development, Fondazione IRCCS Istituto Neurologico "Carlo Besta", 20133 Milan, Italy.
Paola CavalcanteNeurology IV-Neuroimmunology and Neuromuscular Diseases Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
Elisa SchenaCNR Institute of Molecular Genetics, Unit of Bologna, 40136 Bologna, Italy.
Luisa PolitanoCardiomyology and Medical Genetics, Department of Experimental Medicine, University of Campania, Luigi Vanvitelli, 80138 Naples, Italy.ORCID 0000-0002-0925-7158
Nicola CarboniNeurology Department, Hospital San Francesco of Nuoro, 08100 Nuoro, Italy.ORCID 0000-0003-3245-9169
Alessandra GambineriEndocrinology Unit, Department of Clinical and Medical Science, S. Orsola-Malpighi Hospital, University of Bologna, 40138 Bologna, Italy.
Adele D'AmicoUnit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, 00165 Rome, Italy.
Lucia RuggieroDepartment of Neurosciences and Reproductive and Odontostomatologic Sciences, University Federico II, 80137 Naples, Italy.ORCID 0000-0002-7756-9567
Giulia RicciDepartment of Clinical and Experimental Medicine, Neurological Clinic, 56126 Pisa, Italy.
Gabriele SicilianoDepartment of Clinical and Experimental Medicine, Neurological Clinic, 56126 Pisa, Italy.
Giuseppe BorianiCardiology Division, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Policlinico di Modena, 41121 Modena, Italy.
Tiziana Enrica MonginiDepartment of Neurosciences "Rita Levi Montalcini", University of Turin, 10124 Turin, Italy.
Liliana VercelliDepartment of Neurosciences "Rita Levi Montalcini", University of Turin, 10124 Turin, Italy.ORCID 0000-0001-8352-1087
Elena BiaginiAzienda Ospedaliero Universitaria - Policlinico di St. Orsola, Cardiology Unit, Cardio-Thoracic-Vascular Department, 40138 Bologna, Italy.ORCID 0000-0003-0295-0440
Matteo ZiacchiAzienda Ospedaliero Universitaria - Policlinico di St. Orsola, Cardiology Unit, Cardio-Thoracic-Vascular Department, 40138 Bologna, Italy.
Maria Rosaria D'ApiceMedical Genetics Unit, Policlinico Tor Vergata University Hospital, 00133 Rome, Italy.
Giovanna LattanziCNR Institute of Molecular Genetics, Unit of Bologna, 40136 Bologna, Italy.ORCID 0000-0002-7103-8722
Renato MantegazzaNeurology IV-Neuroimmunology and Neuromuscular Diseases Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
Lorenzo MaggiNeurology IV-Neuroimmunology and Neuromuscular Diseases Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.ORCID 0000-0002-0932-5173
Pia BernasconiNeurology IV-Neuroimmunology and Neuromuscular Diseases Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.ORCID 0000-0003-0869-2104
Fondazione IRCCS Istituto Neurologico Carlo Besta · ITIRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITUniversity of Turin · ITAssociazione Istituzione Libera Università Nuorese · ITBambino Gesù Children's Hospital · ITFederico II University Hospital · ITIstituto Ortopedico Rizzoli · ITPoliclinico Tor Vergata · ITUniversity of Bologna · ITUniversity of Campania "Luigi Vanvitelli" · ITUniversity of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Laminopathies are a wide and heterogeneous group of rare human diseases caused by mutations of the LMNA gene or related nuclear envelope genes. The variety of clinical phenotypes and the wide spectrum of histopathological changes among patients carrying an identical mutation in the LMNA gene make the prognostic process rather difficult, and classical genetic screens appear to have limited predictive value for disease development. The aim of this study was to evaluate whether a comprehensive profile of circulating cytokines may be a useful tool to differentiate and stratify disease subgroups, support clinical follow-ups and contribute to new therapeutic approaches. Serum levels of 51 pro- and anti-inflammatory molecules, including cytokines, chemokines and growth factors, were quantified by a Luminex multiple immune-assay in 53 patients with muscular laminopathy (Musc-LMNA), 10 with non-muscular laminopathy, 22 with other muscular disorders and in 35 healthy controls. Interleukin-17 (IL-17), granulocyte colony-stimulating factor (G-CSF) and transforming growth factor beta (TGF-β2) levels significantly discriminated Musc-LMNA from controls; interleukin-1β (IL-1β), interleukin-4 (IL-4) and interleukin-8 (IL-8) were differentially expressed in Musc-LMNA patients compared to those with non-muscular laminopathies, whereas IL-17 was significantly higher in Musc-LMNA patients with muscular and cardiac involvement. These findings support the hypothesis of a key role of the immune system in Musc-LMNA and emphasize the potential use of cytokines as biomarkers for these disorders.

Indexed as

AdultBiomarkersCytokinesFemaleHumansLaminopathiesMaleMuscle, StriatedMuscular DiseasesBiomarkersCytokinescytokineslaminopathiesmacrophagesmuscle damageskeletal muscle

Identifiers

PMID32585971
PMCPMC7348753
OpenAlexW3036727997

What OpenQuestion holds

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LicenceCC BY
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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.