Nicolò Pipitone

ORCID: 0000-0002-2002-7185
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About
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Research Areas
  • Vasculitis and related conditions
  • Otitis Media and Relapsing Polychondritis
  • Systemic Lupus Erythematosus Research
  • Inflammatory Myopathies and Dermatomyositis
  • Cell Adhesion Molecules Research
  • Coagulation, Bradykinin, Polyphosphates, and Angioedema
  • Rheumatoid Arthritis Research and Therapies
  • Ocular Diseases and Behçet’s Syndrome
  • Systemic Sclerosis and Related Diseases
  • Spondyloarthritis Studies and Treatments
  • Atherosclerosis and Cardiovascular Diseases
  • IgG4-Related and Inflammatory Diseases
  • Sarcoidosis and Beryllium Toxicity Research
  • Eosinophilic Disorders and Syndromes
  • Retinal and Optic Conditions
  • Renal Diseases and Glomerulopathies
  • Autoimmune and Inflammatory Disorders Research
  • Inflammasome and immune disorders
  • Urticaria and Related Conditions
  • Psoriasis: Treatment and Pathogenesis
  • Immunodeficiency and Autoimmune Disorders
  • Skin Diseases and Diabetes
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Chemokine receptors and signaling
  • Cerebrovascular and Carotid Artery Diseases

Azienda Sanitaria Unità Locale di Reggio Emilia
2015-2024

University of Modena and Reggio Emilia
2014-2024

Istituti di Ricovero e Cura a Carattere Scientifico
2015-2024

Medizinische Hochschule Brandenburg Theodor Fontane
2024

Azienda Ospedaliera S.Maria
2011-2023

Santa Maria Nuova Hospital
2006-2023

Center for Rheumatology
2007-2020

ASM International
2014-2018

Ospedale Santa Maria
2007-2017

Villa Maria Hospital
2017

Abstract Objective Behçet's disease ( BD ) is a chronic, relapsing, inflammatory vascular with no pathognomonic test. Low sensitivity of the currently applied International Study Group ISG clinical diagnostic criteria led to their reassessment. Methods An Team for Revision Criteria (from 27 countries) submitted data from 2556 clinically diagnosed patients and 1163 controls ‐mimicking diseases or presenting at least one major sign. These were randomly divided into training validation sets....

10.1111/jdv.12107 article EN Journal of the European Academy of Dermatology and Venereology 2013-02-26

The objective of this study was to develop EULAR/ACR classification criteria for polymyalgia rheumatica (PMR). Candidate were evaluated in a 6-month prospective cohort 125 patients with new onset PMR and 169 non-PMR comparison subjects conditions mimicking PMR. A scoring algorithm developed based on morning stiffness >45 minutes (2 points), hip pain/limited range motion (1 point), absence RF and/or ACPA peripheral joint pain point). score ≥4 had 68% sensitivity 78% specificity discriminating...

10.1136/annrheumdis-2011-200329 article EN Annals of the Rheumatic Diseases 2012-03-02

Abstract The objective of this study was to develop European League Against Rheumatism/American College Rheumatology classification criteria for polymyalgia rheumatica (PMR). Candidate were evaluated in a 6‐month prospective cohort 125 patients with new‐onset PMR and 169 non‐PMR comparison subjects conditions mimicking PMR. A scoring algorithm developed based on morning stiffness >45 minutes (2 points), hip pain/limited range motion (1 point), absence rheumatoid factor and/or...

10.1002/art.34356 article EN Arthritis & Rheumatism 2012-03-02

Aims The EuroMyositis Registry facilitates collaboration across the idiopathic inflammatory myopathy (IIM) research community. This inaugural report examines pooled data. Methods Cross-sectional analysis of IIM cases from 11 countries was performed. Associations between clinical subtypes, extramuscular involvement, environmental exposures and medications were investigated. Results Of 3067 cases, 69% female. most common subtype dermatomyositis (DM) (31%). Smoking more frequent in connective...

10.1136/annrheumdis-2017-211868 article EN cc-by Annals of the Rheumatic Diseases 2017-08-30
Lorenzo Cavagna Ernesto Trallero‐Araguás Federica Meloni Ilaria Cavazzana Jorge Rojas‐Serrano and 95 more Eugen Feist Giovanni Zanframundo Valentina Morandi Alain Meyer José António Pereira da Silva Catarina Costa Øyvind Molberg Helena Andersson Veronica Codullo Marta Mosca Simone Barsotti R Neri Carlo Alberto Scirè Marcello Govoni Federica Furini Francisco Javier López-Longo Julia Martínez‐Barrio Udo Schneider Hanns‐Martin Lorenz Andrea Doria Anna Ghirardello Norberto Ortego‐Centeno Marco Confalonieri Paola Tomietto Nicolò Pipitone Ana Rodriguez Cambron María Ángeles Blázquez-Cañamero Reinhard Voll Sarah K. Wendel Salvatore Scarpato F. Maurier Massimiliano Limonta Paolo Luigi Colombelli Margherita Giannini Bernard Gény Eugenio Arrigoni Elena Bravi Paola Migliorini Alessandro Mathieu Matteo Piga Ulrich Drott Christiane Delbrueck Jutta Bauhammer Giovanni Cagnotto Carlo Vancheri Gianluca Sambataro Ellen De Langhe Pier Paolo Sainaghi Maria Cristina Monti Francesca Gigli Berzolari Mariaeva Romano Francesco Bonella Christof Specker Andreas Schwarting Ignacio Villa Blanco Carlo Selmi Angela Ceribelli Laura Nuño Antonio Mera Nair Pérez Gómez Enrico Fusaro Simone Parisi L. Sinigaglia Nicoletta Del Papa Maurizio Benucci Marco A. Cimmino Valeria Riccieri Fabrizio Conti Gian Domenico Sebastiani Anna Iuliano Giacomo Emmi Daniele Cammelli Marco Sebastiani Andreina Manfredi Javier Bachiller‐Corral Walter Alberto Sifuentes Giraldo Giuseppe Paolazzi Lesley Ann Saketkoo Roberto Giorgi Fausto Salaffi José Manuel Cifrián Roberto Caporali Francesco Locatelli Enrico Marchioni Alberto Pesci Giulia Dei Maria Rosa Pozzi Claudia Lomater Jörg H. W. Distler Johannes Knitza George Schett Florenzo Iannone Marco Fornaro Franco Franceschini Luca Quartuccio

Antisynthetase syndrome (ASSD) is a rare clinical condition that characterized by the occurrence of classic triad, encompassing myositis, arthritis, and interstitial lung disease (ILD), along with specific autoantibodies are addressed to different aminoacyl tRNA synthetases (ARS). Until now, it has been unknown whether presence ARS might affect presentation, evolution, outcome ASSD. In this study, we retrospectively recorded time onset, characteristics, clustering triad findings, survival...

10.3390/jcm8112013 article EN Journal of Clinical Medicine 2019-11-18

To evaluate the frequency of visual manifestations at presentation in an Italian population-based cohort patients with biopsy-proven giant cell arteritis (GCA), and to investigate predictors for development permanent loss.We identified 136 Reggio Emilia (Italy) residents GCA diagnosed between 1986 2002. Medical records these were reviewed, demographic, clinical, laboratory data collected.Multivariate analysis multiple logistic regression models was performed identify best loss.Visual...

10.1002/art.21075 article EN Arthritis Care & Research 2005-04-07

<b>BACKGROUND AND PURPOSE:</b> Wernicke encephalopathy (WE) is a severe neurologic disorder resulting from dietary vitamin B<sub>1</sub> deficiency. This study was undertaken to analyze and compare MR imaging findings manifestations at clinical presentations of patients with WE without history alcohol abuse. <b>MATERIALS METHODS:</b> were identified using diagnostic data bases. Fifty-six (29 females, 27 males) diagnosed between 1999 2008 who improved within 1 month the onset thiamine...

10.3174/ajnr.a1280 article EN cc-by American Journal of Neuroradiology 2008-10-22

We reviewed 888 temporal artery biopsies (TAB) performed in 871 patients a single institution from January 1986 to December 2013. Forty-four (4.9%) were inadequate, 490 (55.2%) devoid of inflammation and considered negative, 354 (39.9%) showed positive. On the basis localization inflammation, positive TABs further classified into 4 categories: small vessel vasculitis (SVV), which was limited periadventitial vessels muscular coat, with sparing (32 cases, 9% biopsies); vasa vasorum (VVV),...

10.1097/pas.0000000000000244 article EN The American Journal of Surgical Pathology 2014-05-22

To evaluate the impact of traditional cardiovascular risk factors, carotid atherosclerosis and effect anti-platelet/anti-coagulant therapy on occurrence severe cranial ischaemic events (CIEs) in GCA.We identified 180 Reggio Emilia (Italy) residents with biopsy-proven GCA diagnosed between 1986 2005. We evaluated data demographics, clinical features, laboratory investigations, use atherosclerosis.Systemic signs/symptoms were significantly less frequent (P = 0.004) ESR C-reactive protein (CRP)...

10.1093/rheumatology/ken465 article EN Lara D. Veeken 2008-10-17

This study evaluated the frequency, timing, and characteristics of flares in a large cohort Italian patients with biopsy-proven giant cell arteritis (GCA) to identify factors at diagnosis able predict occurrence flares. We 157 transmural GCA diagnosed followed Rheumatology Unit Reggio Emilia Hospital (Italy) for whom sufficient information was available from time until least 4 years follow-up. Fifty-seven (36.5%) experienced ≥1 Fifty-one (46.4%) 110 total (88 relapses 22 recurrences) were...

10.1097/md.0000000000003524 article EN cc-by-nc Medicine 2016-05-01

To characterize the 10 year relationship between anti-transcriptional intermediary factor 1 antibody (anti-TIF1-Ab) positivity and cancer onset in a large UK-based adult DM cohort.Data from anti-TIF1-Ab-positive/-negative adults with verified diagnoses of UK Myositis Network register were analysed. Each patient was followed up until they developed cancer. Kaplan-Meier methods Cox proportional hazard modelling employed to estimate cumulative incidence.Data 263 cases analysed, total 3252...

10.1093/rheumatology/key357 article EN cc-by Lara D. Veeken 2018-10-24

To identify patients with VEXAS syndrome (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome) from a single-center cohort of Italian vasculitis, using clinically oriented phenotype-first approach.We retrospectively reviewed the clinical records 147 consecutive male followed up in our vasculitis clinic 2013 to date. All diagnosis and treatment-resistant manifestations inflammation, persistently elevated inflammation markers, hematologic abnormalities were identified. Bone...

10.1002/art.41992 article EN cc-by-nc-nd Arthritis & Rheumatology 2021-10-08

To evaluate the presence and extent of large-vessel inflammation in patients with chronic periaortitis (CP) using (18)F-fluorodeoxyglucose-positron emission tomography (FDG-PET).A consecutive case series consisting 7 CP seen over a 3-year period control group 14 malignancy were evaluated FDG-PET. For every we selected 2 age- sex-matched controls who underwent PET imaging for malignancy. The diagnosis was made by means computed tomography. performed at before therapy started. Measurement...

10.1002/art.21074 article EN Arthritis Care & Research 2005-04-07

Abstract Objective To test the hypothesis that oral creatine supplements with exercise are more effective than alone in improving muscle function patients established dermatomyositis or polymyositis receiving chronic medical therapies who clinically weak yet stable. Methods In a 6‐month, 2‐center, double‐blind, randomized controlled trial, were to receive (8 days, 20 gm/day then 3 gm/day) placebo. All followed home program. The primary outcome was aggregate functional performance time...

10.1002/art.22687 article EN Arthritis Care & Research 2007-04-30

To evaluate the inflammatory involvement of cervical interspinous bursae in patients with polymyalgia rheumatica (PMR) using MRI.In all, 12 consecutive, untreated new PMR were investigated. Five fibromyalgia, two osteoarthritis and six spondyloarthritis neck pain served as controls. MRI spine was performed all case 13 control patients. Two four pelvic girdle also had lumbar spine.MRI evidence bursitis found PMR, three psoriatic spondylitis one osteoarthritis. A moderate to marked (grade...

10.1136/ard.2007.084723 article EN Annals of the Rheumatic Diseases 2008-01-21

To investigate the epidemiology and clinical course of Behçet's disease (BD) over a 17-year period in defined area northern Italy.All patients with incident BD diagnosed (from January 1, 1988 to December 31, 2004) living Reggio Emilia were identified through following sources: physicians at Hospital, medical practitioners, community-based specialists. We all registered centralized index district database for rare diseases. Patients followed up from time diagnosis until either their death or...

10.1002/art.22500 article EN Arthritis Care & Research 2007-01-31
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