Evidence map›Paper›PMID 42671644›Full record

ArticleJournal of neurology2026

Immune-mediated necrotizing myopathies: clinico-serological features and treatment outcomes of a large Italian cohort of patients.

Silvia Bonanno, Erika Salvi, Marta Cheli, Franco Salerno, Matteo Lucchini, Alessandra Cicia, Vincenzo Carlomagno, Antonio Lauletta, Laura Tufano, Francesco Girolamo and 33 more

Abstract readMulticenter Study
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In one paragraph

Article in Journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

43 authors.

Silvia BonannoNeuroimmunology and Neuromuscular Disease Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133, Milan, Italy.
Erika SalviData Science Center and Computational multi-Omics of Neurological Disorders (MIND) Lab, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Marta CheliNeuroimmunology and Neuromuscular Disease Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133, Milan, Italy.
Franco SalernoNeuroimmunology and Neuromuscular Disease Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133, Milan, Italy.
Matteo LucchiniFondazione Policlinico Universitario A. Gemelli IRCCS, Università Cattolica, Roma, Italy.
Alessandra CiciaFondazione Policlinico Universitario A. Gemelli IRCCS, Università Cattolica, Roma, Italy.
Vincenzo CarlomagnoFondazione Policlinico Universitario A. Gemelli IRCCS, Università Cattolica, Roma, Italy.
Antonio LaulettaSapienza Università di Roma, Ospedale Sant'Andrea, Roma, Italy.
Laura TufanoSapienza Università di Roma, Ospedale Sant'Andrea, Roma, Italy.
Francesco GirolamoDepartment of Translational Biomedicine and Neuroscience (DiBraiN), University of Bari Aldo Moro, Bari, Italy.
Lucia Nicolini De GaetanoNeuroimmunology and Neuromuscular Disease Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133, Milan, Italy.
Marco FornaroUnit of Rheumatology, Department of Precision and Regenerative Medicine, Area Jonica (DiMePRe-J), University of Bari, Bari, Italy.
Elia PancheriDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Federico ZaottiniDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics and Maternal Infantile Sciences, University of Genoa, Genova, Italy.
Elena FaedoDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics and Maternal Infantile Sciences, University of Genoa, Genova, Italy.
Patrizia Rovere QueriniSan Raffaele Vita-Salute University, Milan, Italy.
Rebecca De LorenzoInternal Medicine Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Marina ScarlatoNeuromuscular Repair Unit, Institute of Experimental Neurology (InSpe), Division of Neuroscience, IRCCS Ospedale San Raffaele, Milan, Italy.
Francesca BottazziFondazione IRCCS Policlinico San Matteo, Università degli studi di Pavia, Pavia, Italy.
Pietro RiguzziDepartment of Neurosciences, University of Padova, Padua, Italy.
Sara GibertiniNeuroimmunology and Neuromuscular Disease Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133, Milan, Italy.
Barbara RisiDepartment of Clinical and Experimental Sciences, University of Brescia, NeMO-Brescia Clinical Center for Neuromuscular Diseases, Brescia, Italy.
Alessia PuglieseDepartment of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Dario ZoppiDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, Naples, Italy.
Lucia RuggieroDepartment of Neurosciences, Reproductive Sciences and Odontostomatology, University of Naples Federico II, Naples, Italy.
Giulia RicciDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Paolo ManganottiClinical Unit of Neurology, Department of Medicine, Surgery and Health Sciences, University Hospital and Health Services of Trieste, ASUGI, University of Trieste, Trieste, Italy.
Gabriele SicilianoDepartment of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Carmelo RodolicoDepartment of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Massimiliano FilostoDepartment of Clinical and Experimental Sciences, University of Brescia, NeMO-Brescia Clinical Center for Neuromuscular Diseases, Brescia, Italy.
Luca BelloDepartment of Neurosciences, University of Padova, Padua, Italy.
Elena PegoraroDepartment of Neurosciences, University of Padova, Padua, Italy.
Lorenzo CavagnaFondazione IRCCS Policlinico San Matteo, Università degli studi di Pavia, Pavia, Italy.
Stefano Carlo PrevitaliSan Raffaele Vita-Salute University, Milan, Italy.
Chiara FiorilloDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics and Maternal Infantile Sciences, University of Genoa, Genova, Italy.
Marina GrandisDepartment of Neurosciences, Rehabilitation, Ophthalmology, Genetics and Maternal Infantile Sciences, University of Genoa, Genova, Italy.
Gaetano VattemiDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Paola ToninDepartment of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.
Florenzo IannoneUnit of Rheumatology, Department of Precision and Regenerative Medicine, Area Jonica (DiMePRe-J), University of Bari, Bari, Italy.
Giovanni AntoniniSapienza Università di Roma, Ospedale Sant'Andrea, Roma, Italy.
Matteo GaribaldiSapienza Università di Roma, Ospedale Sant'Andrea, Roma, Italy.
Massimiliano MirabellaFondazione Policlinico Universitario A. Gemelli IRCCS, Università Cattolica, Roma, Italy.
Lorenzo MaggiNeuroimmunology and Neuromuscular Disease Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133, Milan, Italy. lorenzo.maggi@istituto-besta.it.ORCID http://orcid.org/0000-0002-0932-5173

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune-mediated necrotizing myopathy (IMNM) is a distinct entity with limited large-cohort data. We aimed to characterize clinico-serological features and treatment outcomes of anti-SRP, anti-HMGCR, and seronegative IMNM in a large Italian cohort.

methodsRetrospective multicenter study of adults diagnosed with IMNM (224th ENMC criteria) across 14 Italian neuromuscular centers between 2019 and 2022 was performed.

resultsWe included 159 subjects (57% female, median age 62 years): 40 SRP+, 71 HMGCR+, 41 seronegative, and 7 untested. SRP+ more frequently presented with proximal upper limb weakness and axial involvement versus HMGCR+ (OR = 3.89, padj = 0.007, OR = 3.47, padj = 0.04) and seronegative (OR = 4.00, padj = 0.014, OR = 15.2, padj = 0.005). Lung involvement was higher in SRP+ (7.5%), vs none in HMGCR+ and 2.4% in seronegative (p=0.028). Extramuscular features were more frequent in HMGCR+ (OR = 3.78, p = 0.019, padj = 0.057). SRP+ had higher odds of loss of motor independence (OR=4.22, padj =0.011) and relapse (OR = 14.4, padj = 0.010) than HMGCR+. Seronegative had better functional outcomes than SRP+ (p=0.047). Cancer associated myositis predicted worse disability (OR = 6.93, p = 0.0044). Overall, 71.7% improved with corticosteroids (OR=3.83, padj =0.01) and immunosuppressants (OR=2.296, padj =0.037), without serotype differences. CK decreased in 81.8% and normalized in 40.3% of patients; ΔCK was associated with improvement (p=0.017), clinical remission (p=0.002) and correlated with post-treatment functional scores (R=0.19, p= 0.044).

conclusionSubtype-specific differences and prognostic factors emerge. Exploratory functional assessment and ΔCK may capture treatment response in real-world settings.

Indexed as

Hydroxymethylglutaryl CoA ReductasesMuscular DiseasesMyositisAdultAgedAutoantibodiesCohort StudiesFemaleHumansItalyMaleMiddle AgedNecrosisRetrospective StudiesTreatment OutcomeAutoantibodiesHMGCR protein, humanHydroxymethylglutaryl CoA ReductasesAnti-HMGCR antibodiesAnti-SRP antibodiesCreatine kinaseImmune-mediated necrotizing myopathySeronegative myopathy

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